49 results on '"Cook, M. B"'
Search Results
2. Sex steroid hormones in relation to Barrettʼs esophagus: an analysis of the FINBAR Study
- Author
-
Cook, M. B., Wood, S., Hyland, P. L., Caron, P., Drahos, J., Falk, R. T., Pfeiffer, R. M., Dawsey, S. M., Abnet, C. C., Taylor, P. R., Guillemette, C., Murray, L. J., and Anderson, L. A.
- Published
- 2017
- Full Text
- View/download PDF
3. Corrigendum to 'Measures of body fatness and height in early and mid-to-late adulthood and prostate cancer : risk and mortality in The Pooling Project of Prospective Studies of Diet and Cancer'
- Author
-
Genkinger, J M, Wu, K, Wang, M, Albanes, D, Black, A, van den Brandt, P A, Burke, K A, Cook, M B, Gapstur, S M, Giles, G G, Giovannucci, E, Goodman, G G, Goodman, P J, Håkansson, N, Key, T J, Männistö, S, Le Marchand, L, Liao, L M, MacInnis, R J, Neuhouser, M L, Platz, E A, Sawada, N, Schenk, J M, Stevens, V L, Travis, R C, Tsugane, S, Visvanathan, K, Wilkens, L R, Wolk, Alicja, Smith-Warner, S A, Genkinger, J M, Wu, K, Wang, M, Albanes, D, Black, A, van den Brandt, P A, Burke, K A, Cook, M B, Gapstur, S M, Giles, G G, Giovannucci, E, Goodman, G G, Goodman, P J, Håkansson, N, Key, T J, Männistö, S, Le Marchand, L, Liao, L M, MacInnis, R J, Neuhouser, M L, Platz, E A, Sawada, N, Schenk, J M, Stevens, V L, Travis, R C, Tsugane, S, Visvanathan, K, Wilkens, L R, Wolk, Alicja, and Smith-Warner, S A
- Abstract
Background: Advanced prostate cancer etiology is poorly understood. Few studies have examined associations ofanthropometric factors (e.g. early adulthood obesity) with advanced prostate cancer risk. Patients and methods: We carried out pooled analyses to examine associations between body fatness, height, andprostate cancer risk. Among 830 772 men, 51 734 incident prostate cancer cases were identified, including 4762advanced (T4/N1/M1 or prostate cancer deaths) cases, 2915 advanced restricted (same as advanced, but excludinglocalized cancers that resulted in death) cases, 9489 high-grade cases, and 3027 prostate cancer deaths. Coxproportional hazards models were used to calculate study-specific hazard ratios (HR) and 95% confidence intervals(CI); results were pooled using random effects models. Results: No statistically significant associations were observed for body mass index (BMI) in early adulthood for advanced,advanced restricted, and high-grade prostate cancer, and prostate cancer mortality. Positive associations were shown forBMI at baseline with advanced prostate cancer (HR ¼ 1.30, 95% CI ¼ 0.95e1.78) and prostate cancer mortality (HR ¼1.52, 95% CI ¼ 1.12e2.07) comparing BMI 35.0 kg/m2 with 21e22.9 kg/m2. When considering early adulthood andbaseline BMI together, a 27% higher prostate cancer mortality risk (95% CI ¼ 9% to 49%) was observed for men withBMI <25.0 kg/m2 in early adulthood and BMI 30.0 kg/m2 at baseline compared with BMI <25.0 kg/m2 in earlyadulthood and BMI <30.0 kg/m2 at baseline. Baseline waist circumference, comparing 110 cm with <90 cm, andwaist-to-hip ratio, comparing 1.00 with <0.90, were associated with significant 14%e16% increases in high-gradeprostate cancer risk and suggestive or significant 20%e39% increases in prostate cancer mortality risk. Height wasassociated with suggestive or significant 33%e56% risks of advanced or advanced restricted prostate cancer andprostate cancer mortality, comparing 1.90 m with <1.65 m, [Annals of Oncology Volume 31, Issue 1, January 2020, Pages 103-114]
- Published
- 2021
- Full Text
- View/download PDF
4. Gonadal and extragonadal germ cell tumours in the United States, 1973–2007
- Author
-
Stang, A., Trabert, B., Wentzensen, N., Cook, M. B., Rusner, C., Oosterhuis, J. W., and McGlynn, K. A.
- Published
- 2012
- Full Text
- View/download PDF
5. Impact of classification of mixed germ-cell tumours on incidence trends of non-seminoma
- Author
-
Trabert, B., Stang, A., Cook, M. B., Rusner, C., and McGlynn, K. A.
- Published
- 2011
- Full Text
- View/download PDF
6. Organochlorine compounds and testicular dysgenesis syndrome: human data
- Author
-
Cook, M. B., Trabert, B., and McGlynn, K. A.
- Published
- 2011
- Full Text
- View/download PDF
7. Endogenous DNA damage and testicular germ cell tumors
- Author
-
Cook, M. B., Sigurdson, A. J., Jones, I. M., Thomas, C. B., Graubard, B. I., Korde, L., Greene, M. H., and McGlynn, K. A.
- Published
- 2009
- Full Text
- View/download PDF
8. Mortality risks associated with Barrettʼs oesophagus
- Author
-
COOK, M. B., WILD, C. P., EVERETT, S. M., HARDIE, L. J., BANI-HANI, K. E., MARTIN, I. G., and FORMAN, D.
- Published
- 2008
9. Advanced Materials for Exploration Task Research Results
- Author
-
Cook, M. B, Murphy, K. L, and Schneider, T
- Subjects
Chemistry And Materials (General) - Abstract
The Advanced Materials for Exploration (AME) Activity in Marshall Space Flight Center s (MSFC s) Exploration Science and Technology Directorate coordinated activities from 2001 to 2006 to support in-space propulsion technologies for future missions. Working together, materials scientists and mission planners identified materials shortfalls that are limiting the performance of long-term missions. The goal of the AME project was to deliver improved materials in targeted areas to meet technology development milestones of NASA s exploration-dedicated activities. Materials research tasks were targeted in five areas: (1) Thermal management materials, (2) propulsion materials, (3) materials characterization, (4) vehicle health monitoring materials, and (5) structural materials. Selected tasks were scheduled for completion such that these new materials could be incorporated into customer development plans.
- Published
- 2008
10. Measures of body fatness and height in early and mid-to-late adulthood and prostate cancer : risk and mortality in The Pooling Project of Prospective Studies of Diet and Cancer
- Author
-
Genkinger, J. M., Wu, K., Wang, M., Albanes, D., Black, A., van den Brandt, P. A., Burke, K. A., Cook, M. B., Gapstur, S. M., Giles, G. G., Giovannucci, E., Goodman, G. G., Goodman, P. J., Håkansson, N., Key, T. J., Mannistö, S., Le Marchand, L., Liao, L. M., MacInnis, R. J., Neuhouser, M. L., Platz, E. A., Sawada, N., Schenk, J. M., Stevens, V. L., Travis, R. C., Tsugane, S., Visvanathan, K., Wilkens, L. R., Wolk, Alicja, Smith-Warner, S. A., Genkinger, J. M., Wu, K., Wang, M., Albanes, D., Black, A., van den Brandt, P. A., Burke, K. A., Cook, M. B., Gapstur, S. M., Giles, G. G., Giovannucci, E., Goodman, G. G., Goodman, P. J., Håkansson, N., Key, T. J., Mannistö, S., Le Marchand, L., Liao, L. M., MacInnis, R. J., Neuhouser, M. L., Platz, E. A., Sawada, N., Schenk, J. M., Stevens, V. L., Travis, R. C., Tsugane, S., Visvanathan, K., Wilkens, L. R., Wolk, Alicja, and Smith-Warner, S. A.
- Abstract
Background: Advanced prostate cancer etiology is poorly understood. Few studies have examined associations of anthropometric factors (e.g. early adulthood obesity) with advanced prostate cancer risk. Patients and methods: We carried out pooled analyses to examine associations between body fatness, height, and prostate cancer risk. Among 830 772 men, 51 734 incident prostate cancer cases were identified, including 4762 advanced (T4/N1/M1 or prostate cancer deaths) cases, 2915 advanced restricted (same as advanced, but excluding localized cancers that resulted in death) cases, 9489 high-grade cases, and 3027 prostate cancer deaths. Cox proportional hazards models were used to calculate study-specific hazard ratios (HR) and 95% confidence intervals (CI); results were pooled using random effects models. Results: No statistically significant associations were observed for body mass index (BMI) in early adulthood for advanced, advanced restricted, and high-grade prostate cancer, and prostate cancer mortality. Positive associations were shown for BMI at baseline with advanced prostate cancer (HR = 1.30, 95% CI = 0.95-1.78) and prostate cancer mortality (HR = 1.52, 95% CI = 1.12-2.07) comparing BMI >= 35.0 kg/m(2) with 21-22.9 kg/m(2). When considering early adulthood and baseline BMI together, a 27% higher prostate cancer mortality risk (95% CI = 9% to 49%) was observed for men with BMI <25.0 kg/m(2) in early adulthood and BMI >= 30.0 kg/m(2) at baseline compared with BMI <25.0 kg/m(2) in early adulthood and BMI <30.0 kg/m(2) at baseline. Baseline waist circumference, comparing >= 110 cm with <90 cm, and waist-to-hip ratio, comparing >= 1.00 with <0.90, were associated with significant 14%-16% increases in high-grade prostate cancer risk and suggestive or significant 20%-39% increases in prostate cancer mortality risk. Height was associated with suggestive or significant 33%-56% risks of advanced or advanced restricted prostate cancer and prostat, Correction in: Annals of Oncology, Vol. 32, Issue 9, page 1201DOI: 10.1016/j.annonc.2021.07.001
- Published
- 2020
- Full Text
- View/download PDF
11. A Systematic Review and Meta-Analysis of the Sex Ratio for Barrettʼs Esophagus, Erosive Reflux Disease, and Nonerosive Reflux Disease
- Author
-
Cook, M. B., Wild, C. P., and Forman, D.
- Published
- 2005
12. 5th Conference on Aerospace Materials, Processes, and Environmental Technology
- Author
-
Cook, M. B and Stanley, D. Cross
- Subjects
Chemistry And Materials (General) - Abstract
Records are presented from the 5th Conference on Aerospace Materials, Processes, and Environmental Technology. Topics included pollution prevention, inspection methods, advanced materials, aerospace materials and technical standards,materials testing and evaluation, advanced manufacturing,development in metallic processes, synthesis of nanomaterials, composite cryotank processing, environmentally friendly cleaning, and poster sessions.
- Published
- 2003
13. Associations between circulating sex steroid hormones and leukocyte telomere length in men in the National Health and Nutrition Examination Survey
- Author
-
Coburn, S. B., primary, Graubard, B. I., additional, Trabert, B., additional, McGlynn, K. A., additional, and Cook, M. B., additional
- Published
- 2018
- Full Text
- View/download PDF
14. A Meta-analysis of Individual Participant Data Reveals an Association between Circulating Levels of IGF-I and Prostate Cancer Risk
- Author
-
Travis, RC, Appleby, P N, Martin, RM, Holly, JMP, Albanes, D, Black, A, Bueno-de-Mesquita, HB, Chan, JM, Chen, C (Christopher Li Hsian), Chirlaque, MD, Cook, M B, Deschasaux, M, Donovan, JL, Ferrucci, L, Galan, P, Giles, GG, Giovannucci, E L, Gunter, MJ, Habel, L A, Hamdy, FC, Helzlsouer, K J, Hercberg, S, Hoover, RN, Janssen, J.A.M.J.L., Kaaks, R, Kubo, T, Le Marchand, L, Metter, EJ, Mikami, K, Morris, J K, Neal, DE, Neuhouser, ML, Ozasa, K, Palli, D, Platz, EA, Pollak, MN, Price, AJ, Roobol - Bouts, Monique, Schaefer, C, Schenk, J M, Severi, G, Stampfer, MJ, Stattin, P, Tamakoshi, A, Tangen, C M, Touvier, M, Wald, N J, Weiss, NS, Ziegler, RG, Key, TJ, Allen, NE, Endogenous Hormones, Nutr, Internal Medicine, and Urology
- Subjects
SDG 3 - Good Health and Well-being - Published
- 2016
15. Marijuana use and serum testosterone concentrations among U.S. males
- Author
-
Thistle, J. E., primary, Graubard, B. I., additional, Braunlin, M., additional, Vesper, H., additional, Trabert, B., additional, Cook, M. B., additional, and McGlynn, K. A., additional
- Published
- 2017
- Full Text
- View/download PDF
16. Childhood height and birth weight in relation to future prostate cancer risk in the Copenhagen Schoo
- Author
-
Cook, M. B, Gamborg, M, Aarestrup, J, Sxf8rensen, T. I.A, and Baker, J. L.
- Published
- 2013
17. Childhood body mass index in relation to future risk of oesophageal adenocarcinoma
- Author
-
Cook, M B, Freedman, N D, Gamborg, M, Sørensen, T I A, Baker, Jennifer Lyn, Cook, M B, Freedman, N D, Gamborg, M, Sørensen, T I A, and Baker, Jennifer Lyn
- Abstract
BACKGROUND: Middle-aged obese adults are at substantially elevated risk of oesophageal adenocarcinoma. It is unclear whether this risk originates earlier in life.METHODS: We assessed associations between childhood body mass index (BMI) and height-measured annually between ages 7 and 13-with adult oesophageal adenocarcinoma in a cohort from the Copenhagen School Health Records Register. Analyses included 255 053 children born during 1930-1971. Danish Cancer Registry linkage provided outcomes. We calculated hazard ratios (HRs) and 95% confidence intervals (CIs) using Cox proportional hazards regression.RESULTS: During 5.4 million person-years of follow-up, 254 (216 males) incident oesophageal adenocarcinomas occurred. At each examined age, cancer risk increased linearly per unit BMI z-score, although associations were only statistically significant for ages 9-13. The HR for the age of 13 years was 1.31 (95% CI: 1.13, 1.51) per unit BMI z-score. Associations were similar in men and women and across birth cohorts. Childhood height was not related to cancer risk in men but was in women, although these analyses included just 38 female cases. HRs per unit height z-score at the age of 13 years were 1.04 (0.90, 1.19) in males and 1.77 (1.27, 2.47) in females, with similar results observed at the other examined ages.CONCLUSION: Individuals with higher childhood BMI were at elevated risk of oesophageal adenocarcinoma, even though these cancers occurred many decades later in life. Although the mechanisms require further investigation, our findings provide additional evidence for the long-term health risks of childhood obesity.
- Published
- 2015
18. Childhood height increases the risk of prostate cancer mortality
- Author
-
Aarestrup, J, Gamborg, M, Cook, M B, Baker, J L, Aarestrup, J, Gamborg, M, Cook, M B, and Baker, J L
- Abstract
BACKGROUND: Adult body size is positively associated with aggressive and fatal prostate cancers. It is unknown whether these associations originate in early life. Therefore, we investigated if childhood height, body mass index (BMI; kg/m(2)) and growth are associated with prostate cancer-specific mortality and survival.METHODS: Subjects were 125,208 men from the Copenhagen School Health Records Register, born 1930-1969 with height and weight measurements at ages 7-13years. Linkage to the Danish Cancer Registry and the Register of Causes of Death enabled identification of incident and fatal prostate cancers. Cox proportional hazards regressions were performed.RESULTS: 630 men had prostate cancer recorded as the underlying cause of death. Childhood height at age 13years was positively associated with prostate cancer-specific mortality (hazard ratio [HR]per z-score=1.2, 95% confidence interval [CI]: 1.1-1.3). Associations were significant at all other childhood ages. Growth analyses showed that height at age 13years had a stronger association with prostate cancer-specific mortality than height at age 7, suggesting the association at age 7 is largely mediated through later childhood height. The tallest boys at age 13years had a significantly worse survival, but only when restricted to a diagnosis at <60years of age (HRz-score of 1=1.7, 95% CI: 1.3-2.4). These associations were significant at all other childhood ages. Childhood BMI was not associated with prostate cancer mortality or survival.CONCLUSION: Childhood height was positively associated with the hard end-point of prostate cancer-specific mortality, which strengthens prior epidemiologic observations of a positive association with prostate cancer incidence.
- Published
- 2015
19. Nitrogen dioxide observations from the Geostationary Trace gas and Aerosol Sensor Optimization (GeoTASO) airborne instrument: retrieval algorithm and measurements during DISCOVER-AQ Texas 2013
- Author
-
Nowlan, C. R., primary, Liu, X., additional, Leitch, J. W., additional, Chance, K., additional, González Abad, G., additional, Liu, C., additional, Zoogman, P., additional, Cole, J., additional, Delker, T., additional, Good, W., additional, Murcray, F., additional, Ruppert, L., additional, Soo, D., additional, Follette-Cook, M. B., additional, Janz, S. J., additional, Kowalewski, M. G., additional, Loughner, C. P., additional, Pickering, K. E., additional, Herman, J. R., additional, Beaver, M. R., additional, Long, R. W., additional, Szykman, J. J., additional, Judd, L. M., additional, Kelley, P., additional, Luke, W. T., additional, Ren, X., additional, and Al-Saadi, J. A., additional
- Published
- 2015
- Full Text
- View/download PDF
20. Childhood body mass index in relation to future risk of oesophageal adenocarcinoma
- Author
-
Cook, M B, primary, Freedman, N D, additional, Gamborg, M, additional, Sørensen, T I A, additional, and Baker, J L, additional
- Published
- 2015
- Full Text
- View/download PDF
21. Childhood body mass index and the risk of prostate cancer in adult men
- Author
-
Aarestrup, J, Gamborg, M, Cook, M B, Sørensen, T I A, Baker, J L, Aarestrup, J, Gamborg, M, Cook, M B, Sørensen, T I A, and Baker, J L
- Abstract
BACKGROUND: Prostate cancer aetiology is poorly understood. It may have origins early in life; previously we found a positive association with childhood height. The effects of early life body mass index (BMI; kg m(-2)) on prostate cancer remain equivocal. We investigated if childhood BMI, independently and adjusted for height, is positively associated with adult prostate cancer.METHODS: Subjects were a cohort of 125208 boys formed from the Copenhagen School Health Records Register, born 1930-1969 with height and weight measurements at 7-13 years. Cases were identified through linkage to the Danish Cancer Registry. Cox proportional hazards regressions were performed.RESULTS: Overall, 3355 men were diagnosed with prostate cancer. Body mass index during childhood was positively associated with adult prostate cancer. The hazard ratio of prostate cancer was 1.06 (95% confidence interval (CI): 1.01-1.10) per BMI z-score at age 7, and 1.05 (95% CI: 1.01-1.10) per BMI z-score at age 13. Estimates were similar and significant at all other ages. However, adjustment for childhood height attenuated the associations at all but the youngest ages as most estimates became nonsignificant.CONCLUSIONS: These results suggest that at most childhood ages, BMI does not confer an additional risk for prostate cancer beyond that of height.
- Published
- 2014
22. Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33
- Author
-
Wang, Z., primary, Zhu, B., additional, Zhang, M., additional, Parikh, H., additional, Jia, J., additional, Chung, C. C., additional, Sampson, J. N., additional, Hoskins, J. W., additional, Hutchinson, A., additional, Burdette, L., additional, Ibrahim, A., additional, Hautman, C., additional, Raj, P. S., additional, Abnet, C. C., additional, Adjei, A. A., additional, Ahlbom, A., additional, Albanes, D., additional, Allen, N. E., additional, Ambrosone, C. B., additional, Aldrich, M., additional, Amiano, P., additional, Amos, C., additional, Andersson, U., additional, Andriole, G., additional, Andrulis, I. L., additional, Arici, C., additional, Arslan, A. A., additional, Austin, M. A., additional, Baris, D., additional, Barkauskas, D. A., additional, Bassig, B. A., additional, Beane Freeman, L. E., additional, Berg, C. D., additional, Berndt, S. I., additional, Bertazzi, P. A., additional, Biritwum, R. B., additional, Black, A., additional, Blot, W., additional, Boeing, H., additional, Boffetta, P., additional, Bolton, K., additional, Boutron-Ruault, M.-C., additional, Bracci, P. M., additional, Brennan, P., additional, Brinton, L. A., additional, Brotzman, M., additional, Bueno-de-Mesquita, H. B., additional, Buring, J. E., additional, Butler, M. A., additional, Cai, Q., additional, Cancel-Tassin, G., additional, Canzian, F., additional, Cao, G., additional, Caporaso, N. E., additional, Carrato, A., additional, Carreon, T., additional, Carta, A., additional, Chang, G.-C., additional, Chang, I.-S., additional, Chang-Claude, J., additional, Che, X., additional, Chen, C.-J., additional, Chen, C.-Y., additional, Chen, C.-H., additional, Chen, C., additional, Chen, K.-Y., additional, Chen, Y.-M., additional, Chokkalingam, A. P., additional, Chu, L. W., additional, Clavel-Chapelon, F., additional, Colditz, G. A., additional, Colt, J. S., additional, Conti, D., additional, Cook, M. B., additional, Cortessis, V. K., additional, Crawford, E. D., additional, Cussenot, O., additional, Davis, F. G., additional, De Vivo, I., additional, Deng, X., additional, Ding, T., additional, Dinney, C. P., additional, Di Stefano, A. L., additional, Diver, W. R., additional, Duell, E. J., additional, Elena, J. W., additional, Fan, J.-H., additional, Feigelson, H. S., additional, Feychting, M., additional, Figueroa, J. D., additional, Flanagan, A. M., additional, Fraumeni, J. F., additional, Freedman, N. D., additional, Fridley, B. L., additional, Fuchs, C. S., additional, Gago-Dominguez, M., additional, Gallinger, S., additional, Gao, Y.-T., additional, Gapstur, S. M., additional, Garcia-Closas, M., additional, Garcia-Closas, R., additional, Gastier-Foster, J. M., additional, Gaziano, J. M., additional, Gerhard, D. S., additional, Giffen, C. A., additional, Giles, G. G., additional, Gillanders, E. M., additional, Giovannucci, E. L., additional, Goggins, M., additional, Gokgoz, N., additional, Goldstein, A. M., additional, Gonzalez, C., additional, Gorlick, R., additional, Greene, M. H., additional, Gross, M., additional, Grossman, H. B., additional, Grubb, R., additional, Gu, J., additional, Guan, P., additional, Haiman, C. A., additional, Hallmans, G., additional, Hankinson, S. E., additional, Harris, C. C., additional, Hartge, P., additional, Hattinger, C., additional, Hayes, R. B., additional, He, Q., additional, Helman, L., additional, Henderson, B. E., additional, Henriksson, R., additional, Hoffman-Bolton, J., additional, Hohensee, C., additional, Holly, E. A., additional, Hong, Y.-C., additional, Hoover, R. N., additional, Hosgood, H. D., additional, Hsiao, C.-F., additional, Hsing, A. W., additional, Hsiung, C. A., additional, Hu, N., additional, Hu, W., additional, Hu, Z., additional, Huang, M.-S., additional, Hunter, D. J., additional, Inskip, P. D., additional, Ito, H., additional, Jacobs, E. J., additional, Jacobs, K. B., additional, Jenab, M., additional, Ji, B.-T., additional, Johansen, C., additional, Johansson, M., additional, Johnson, A., additional, Kaaks, R., additional, Kamat, A. M., additional, Kamineni, A., additional, Karagas, M., additional, Khanna, C., additional, Khaw, K.-T., additional, Kim, C., additional, Kim, I.-S., additional, Kim, J. H., additional, Kim, Y. H., additional, Kim, Y.-C., additional, Kim, Y. T., additional, Kang, C. H., additional, Jung, Y. J., additional, Kitahara, C. M., additional, Klein, A. P., additional, Klein, R., additional, Kogevinas, M., additional, Koh, W.-P., additional, Kohno, T., additional, Kolonel, L. N., additional, Kooperberg, C., additional, Kratz, C. P., additional, Krogh, V., additional, Kunitoh, H., additional, Kurtz, R. C., additional, Kurucu, N., additional, Lan, Q., additional, Lathrop, M., additional, Lau, C. C., additional, Lecanda, F., additional, Lee, K.-M., additional, Lee, M. P., additional, Le Marchand, L., additional, Lerner, S. P., additional, Li, D., additional, Liao, L. M., additional, Lim, W.-Y., additional, Lin, D., additional, Lin, J., additional, Lindstrom, S., additional, Linet, M. S., additional, Lissowska, J., additional, Liu, J., additional, Ljungberg, B., additional, Lloreta, J., additional, Lu, D., additional, Ma, J., additional, Malats, N., additional, Mannisto, S., additional, Marina, N., additional, Mastrangelo, G., additional, Matsuo, K., additional, McGlynn, K. A., additional, McKean-Cowdin, R., additional, McNeill, L. H., additional, McWilliams, R. R., additional, Melin, B. S., additional, Meltzer, P. S., additional, Mensah, J. E., additional, Miao, X., additional, Michaud, D. S., additional, Mondul, A. M., additional, Moore, L. E., additional, Muir, K., additional, Niwa, S., additional, Olson, S. H., additional, Orr, N., additional, Panico, S., additional, Park, J. Y., additional, Patel, A. V., additional, Patino-Garcia, A., additional, Pavanello, S., additional, Peeters, P. H. M., additional, Peplonska, B., additional, Peters, U., additional, Petersen, G. M., additional, Picci, P., additional, Pike, M. C., additional, Porru, S., additional, Prescott, J., additional, Pu, X., additional, Purdue, M. P., additional, Qiao, Y.-L., additional, Rajaraman, P., additional, Riboli, E., additional, Risch, H. A., additional, Rodabough, R. J., additional, Rothman, N., additional, Ruder, A. M., additional, Ryu, J.-S., additional, Sanson, M., additional, Schned, A., additional, Schumacher, F. R., additional, Schwartz, A. G., additional, Schwartz, K. L., additional, Schwenn, M., additional, Scotlandi, K., additional, Seow, A., additional, Serra, C., additional, Serra, M., additional, Sesso, H. D., additional, Severi, G., additional, Shen, H., additional, Shen, M., additional, Shete, S., additional, Shiraishi, K., additional, Shu, X.-O., additional, Siddiq, A., additional, Sierrasesumaga, L., additional, Sierri, S., additional, Loon Sihoe, A. D., additional, Silverman, D. T., additional, Simon, M., additional, Southey, M. C., additional, Spector, L., additional, Spitz, M., additional, Stampfer, M., additional, Stattin, P., additional, Stern, M. C., additional, Stevens, V. L., additional, Stolzenberg-Solomon, R. Z., additional, Stram, D. O., additional, Strom, S. S., additional, Su, W.-C., additional, Sund, M., additional, Sung, S. W., additional, Swerdlow, A., additional, Tan, W., additional, Tanaka, H., additional, Tang, W., additional, Tang, Z.-Z., additional, Tardon, A., additional, Tay, E., additional, Taylor, P. R., additional, Tettey, Y., additional, Thomas, D. M., additional, Tirabosco, R., additional, Tjonneland, A., additional, Tobias, G. S., additional, Toro, J. R., additional, Travis, R. C., additional, Trichopoulos, D., additional, Troisi, R., additional, Truelove, A., additional, Tsai, Y.-H., additional, Tucker, M. A., additional, Tumino, R., additional, Van Den Berg, D., additional, Van Den Eeden, S. K., additional, Vermeulen, R., additional, Vineis, P., additional, Visvanathan, K., additional, Vogel, U., additional, Wang, C., additional, Wang, J., additional, Wang, S. S., additional, Weiderpass, E., additional, Weinstein, S. J., additional, Wentzensen, N., additional, Wheeler, W., additional, White, E., additional, Wiencke, J. K., additional, Wolk, A., additional, Wolpin, B. M., additional, Wong, M. P., additional, Wrensch, M., additional, Wu, C., additional, Wu, T., additional, Wu, X., additional, Wu, Y.-L., additional, Wunder, J. S., additional, Xiang, Y.-B., additional, Xu, J., additional, Yang, H. P., additional, Yang, P.-C., additional, Yatabe, Y., additional, Ye, Y., additional, Yeboah, E. D., additional, Yin, Z., additional, Ying, C., additional, Yu, C.-J., additional, Yu, K., additional, Yuan, J.-M., additional, Zanetti, K. A., additional, Zeleniuch-Jacquotte, A., additional, Zheng, W., additional, Zhou, B., additional, Mirabello, L., additional, Savage, S. A., additional, Kraft, P., additional, Chanock, S. J., additional, Yeager, M., additional, Landi, M. T., additional, Shi, J., additional, Chatterjee, N., additional, and Amundadottir, L. T., additional
- Published
- 2014
- Full Text
- View/download PDF
23. Childhood body mass index and the risk of prostate cancer in adult men
- Author
-
Aarestrup, J, primary, Gamborg, M, additional, Cook, M B, additional, Sørensen, T I A, additional, and Baker, J L, additional
- Published
- 2014
- Full Text
- View/download PDF
24. Testicular germ cell tumor susceptibility associated with the UCK2 locus on chromosome 1q23
- Author
-
Schumacher, F. R., primary, Wang, Z., additional, Skotheim, R. I., additional, Koster, R., additional, Chung, C. C., additional, Hildebrandt, M. A. T., additional, Kratz, C. P., additional, Bakken, A. C., additional, Timothy Bishop, D., additional, Cook, M. B., additional, Erickson, R. L., additional, Fossa, S. D., additional, Greene, M. H., additional, Jacobs, K. B., additional, Kanetsky, P. A., additional, Kolonel, L. N., additional, Loud, J. T., additional, Korde, L. A., additional, Le Marchand, L., additional, Pablo Lewinger, J., additional, Lothe, R. A., additional, Pike, M. C., additional, Rahman, N., additional, Rubertone, M. V., additional, Schwartz, S. M., additional, Siegmund, K. D., additional, Skinner, E. C., additional, Turnbull, C., additional, Van Den Berg, D. J., additional, Wu, X., additional, Yeager, M., additional, Nathanson, K. L., additional, Chanock, S. J., additional, Cortessis, V. K., additional, and McGlynn, K. A., additional
- Published
- 2013
- Full Text
- View/download PDF
25. Alcohol intake and risk of oesophageal adenocarcinoma: a pooled analysis from the BEACON Consortium
- Author
-
Freedman, N. D., primary, Murray, L. J., additional, Kamangar, F., additional, Abnet, C. C., additional, Cook, M. B., additional, Nyren, O., additional, Ye, W., additional, Wu, A. H., additional, Bernstein, L., additional, Brown, L. M., additional, Ward, M. H., additional, Pandeya, N., additional, Green, A. C., additional, Casson, A. G., additional, Giffen, C., additional, Risch, H. A., additional, Gammon, M. D., additional, Chow, W.-H., additional, Vaughan, T. L., additional, Corley, D. A., additional, and Whiteman, D. C., additional
- Published
- 2011
- Full Text
- View/download PDF
26. Broad-scale latitudinal patterns of genetic diversity among native European and introduced house sparrow (Passer domesticus) populations
- Author
-
SCHREY, A. W., primary, GRISPO, M., additional, AWAD, M., additional, COOK, M. B., additional, McCOY, E. D., additional, MUSHINSKY, H. R., additional, ALBAYRAK, T., additional, BENSCH, S., additional, BURKE, T., additional, BUTLER, L. K., additional, DOR, R., additional, FOKIDIS, H. B., additional, JENSEN, H., additional, IMBOMA, T., additional, KESSLER-RIOS, M. M., additional, MARZAL, A., additional, STEWART, I. R. K., additional, WESTERDAHL, H., additional, WESTNEAT, D. F., additional, ZEHTINDJIEV, P., additional, and MARTIN, L. B., additional
- Published
- 2011
- Full Text
- View/download PDF
27. Genetic contributions to the association between adult height and testicular germ cell tumors
- Author
-
Cook, M. B., primary, Chia, V. M., additional, Berndt, S. I., additional, Graubard, B. I., additional, Chanock, S. J., additional, Rubertone, M. V., additional, Erickson, R. L., additional, Hayes, R. B., additional, and McGlynn, K. A., additional
- Published
- 2011
- Full Text
- View/download PDF
28. A systematic review and meta-analysis of the relationship between body size and testicular cancer
- Author
-
Lerro, C C, primary, McGlynn, K A, additional, and Cook, M B, additional
- Published
- 2010
- Full Text
- View/download PDF
29. Classification of Northern Hemisphere stratospheric ozone and water vapor profiles by meteorological regime
- Author
-
Follette-Cook, M. B., primary, Hudson, R. D., additional, and Nedoluha, G. E., additional
- Published
- 2009
- Full Text
- View/download PDF
30. Oesophageal cancer incidence in the United States by race, sex, and histologic type, 1977–2005
- Author
-
Cook, M B, primary, Chow, W-H, additional, and Devesa, S S, additional
- Published
- 2009
- Full Text
- View/download PDF
31. Human Factors of the Confirmation Bias in Intelligence Analysis: Decision Support From Graphical Evidence Landscapes
- Author
-
Cook, M. B., primary and Smallman, H. S., additional
- Published
- 2008
- Full Text
- View/download PDF
32. Risk of testicular germ-cell tumours in relation to childhood physical activity
- Author
-
Cook, M B, primary, Zhang, Y, additional, Graubard, B I, additional, Rubertone, M V, additional, Erickson, R L, additional, and McGlynn, K A, additional
- Published
- 2007
- Full Text
- View/download PDF
33. A Systematic Review and Meta-Analysis of the Risk of Excess Adiposity on Barrett's Esophagus
- Author
-
Cook, M B, primary, Greenwood, D, additional, Hardie, L J, additional, Wild, C P, additional, and Forman, D, additional
- Published
- 2006
- Full Text
- View/download PDF
34. Risk of testicular germ-cell tumours in relation to childhood physical activity.
- Author
-
Cook, M. B., Zhang, Y., Graubard, B. I., Rubertone, M. V., Erickson, R. L., and McGlynn, K. A.
- Subjects
- *
RESEARCH , *MILITARY personnel , *TUMORS , *SPERMATIC cord torsion , *MOTHERS , *INFORMATION resources , *PHYSICAL fitness - Abstract
The US Servicemen's Testicular Tumor Environmental and Endocrine Determinants (STEED) case–control study of testicular germ-cell tumours (TGCTs) enrolled participants and their mothers in 2002–2005. Hours of sports or vigorous childhood physical activity per week were ascertained for three time periods; 1st–5th grades, 6th–8th grades and 9th–12th grades. Son- and mother-reports were analysed separately and included 539 control son–mother pairs and 499 case son–mother pairs. Odds ratios and 95% confidence intervals were produced. The analysis of the sons' responses found no relationship between childhood physical activity and TGCT, while the mothers' analysis found an inverse association, which was solely due to nonseminoma. Future studies should seek to validate responses further using recorded information sources such as school records.British Journal of Cancer (2008) 98, 174–178. doi:10.1038/sj.bjc.6604109 www.bjcancer.com Published online 20 November 2007 [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
35. Physical Activity from Adolescence through Midlife and Associations with Obesity and Endometrial Cancer Risk.
- Author
-
Saint-Maurice, P. F., Sampson, J. N., Michels, K. A., Moore, S. C., Loftfield, E., McClain, K., Cook, M. B., Trabert, B., and Matthews, C. E.
- Abstract
PURPOSE: This study sought to describe the physical activity-endometrial cancer association and potential mediation of this relationship by obesity in midlife. METHODS: Participants were 67,705 women (aged 50-71 years) enrolled in the NIH-AARP cohort who reported their historical leisure-time physical activity patterns starting at age 15-18 years. We identified five long-term physical activity patterns between adolescence and cohort entry (i.e., inactive, maintained-low, maintained-high, increasers, decreasers). We used Cox regression (Hazard ratio - HR [95% CI]) to assess the relationship between these patterns and midlife obesity and endometrial cancer, adjusting for covariates. Mediation analysis was used to decompose the physical activity patterns-endometrial cancer association to estimate the proportion of the physical activity-endometrial cancer association mediated by midlife obesity. RESULTS: During an average 12.3 years of follow-up 1,468 endometrial cancers occurred. Long-term physical activity patterns were inactive, maintained-low, maintained-high, increasers, and decreasers. Compared to long-term inactive women, women who maintained-high or increased activity levels had a 19-26% lower risk for endometrial cancer (maintained-high: HR = 0.81 [0.67, 0.98]; increasers: HR = 0.74 [0.61, 0.91]). They also had a 45-77% lower risk for obesity in midlife (e.g., maintained-high, BMI 30-39.9: HR = 0.50 [0.46, 0.55]; maintained-high, BMI 40+: HR = 0.32 [0.26, 0.39]). Obesity was a significant mediator and appeared to account for 55-63% of the physical activity-endometrial cancer associations observed. CONCLUSIONS: Both initiating and maintaining physical activity throughout adulthood can play a role in preventing obesity and in turn, lowering the risk for endometrial cancer. [ABSTRACT FROM AUTHOR]
- Published
- 2021
- Full Text
- View/download PDF
36. Survival for oesophageal, stomach and small intestine cancers in Europe 1999-2007: Results from EUROCARE-5.
- Author
-
Anderson, L. A., Tavilla, A., Brenner, H., Luttmann, S., Navarro, C., Gavin, A. T., Holleczek, B., Johnston, B. T., Cook, M. B., Bannon, F., and Sant, M.
- Subjects
- *
CANCER patients , *REPORTING of diseases , *ESOPHAGEAL tumors , *INTESTINAL tumors , *LIFE expectancy , *POPULATION geography , *STATISTICS , *STOMACH tumors , *SURVIVAL analysis (Biometry) , *SURVIVAL - Abstract
Background: European regional variation in cancer survival was reported in the EUROCARE-4 study for patients diagnosed in 1995-1999. Relative survival (RS) estimates are here updated for patients diagnosed with cancer of the oesophagus, stomach and small intestine from 2000 to 2007. Trends in RS from 1999-2001 to 2005-2007 are presented to monitor and discuss improvements in patient survival in Europe. Materials and methods: EUROCARE-5 data from 29 countries (87 cancer registries) were used to investigate 1- and 5-year RS. Using registry-specific life-tables stratified by age, gender and calendar year, age-standardised 'complete analysis' RS estimates by country and region were calculated for Northern, Southern, Eastern and Central Europe, and for Ireland and United Kingdom (UK). Survival trends of patients in periods 1999-2001, 2002-2004 and 2005-2007 were investigated using the 'period' RS approach. We computed the 5-year RS conditional on surviving the first year (5-year conditional survival), as the ratio of age-standardised 5-year RS to 1-year RS. Results: Oesophageal cancer 1- and 5-year RS (40% and 12%, respectively) remained poor in Europe. Patient survival was worst in Eastern (8%), Northern (11%) and Southern Europe (10%). Europe-wide, there was a 3% improvement in oesophageal cancer 5-year survival by 2005-2007, with Ireland and the UK (3%), and Central Europe (4%) showing large improvements. Europe-wide, stomach cancer 5-year RS was 25%. Ireland and UK (17%) and Eastern Europe (19%) had the poorest 5-year patient survival. Southern Europe had the best 5-year survival (30%), though only showing an improvement of 2% by 2005-2007. Small intestine cancer 5-year RS for Europe was 48%, with Central Europe having the best (54%), and Ireland and UK the poorest (37%). Five-year patient survival improvement for Europe was 8% by 2005-2007, with Central, Southern and Eastern Europe showing the greatest increases (P9%). Conclusions: Survival for these cancer sites, particularly oesophageal cancer, remains poor in Europe with wide variation. Further investigation into the wide variation, including analysis by histology and anatomical sub-site, will yield insights to better monitor and explain the improvements in survival observed over time. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
- View/download PDF
37. Corrigendum to 'Measures of body fatness and height in early and mid-to-late adulthood and prostate cancer: risk and mortality in The Pooling Project of Prospective Studies of Diet and Cancer': [Annals of Oncology Volume 31, Issue 1, January 2020, Pages 103-114].
- Author
-
Genkinger JM, Wu K, Wang M, Albanes D, Black A, van den Brandt PA, Burke KA, Cook MB, Gapstur SM, Giles GG, Giovannucci E, Goodman GG, Goodman PJ, Håkansson N, Key TJ, Männistö S, Le Marchand L, Liao LM, MacInnis RJ, Neuhouser ML, Platz EA, Sawada N, Schenk JM, Stevens VL, Travis RC, Tsugane S, Visvanathan K, Wilkens LR, Wolk A, and Smith-Warner SA
- Published
- 2021
- Full Text
- View/download PDF
38. Measures of body fatness and height in early and mid-to-late adulthood and prostate cancer: risk and mortality in The Pooling Project of Prospective Studies of Diet and Cancer.
- Author
-
Genkinger JM, Wu K, Wang M, Albanes D, Black A, van den Brandt PA, Burke KA, Cook MB, Gapstur SM, Giles GG, Giovannucci E, Goodman GG, Goodman PJ, Håkansson N, Key TJ, Männistö S, Le Marchand L, Liao LM, MacInnis RJ, Neuhouser ML, Platz EA, Sawada N, Schenk JM, Stevens VL, Travis RC, Tsugane S, Visvanathan K, Wilkens LR, Wolk A, and Smith-Warner SA
- Subjects
- Adult, Body Height, Body Mass Index, Diet, Humans, Male, Proportional Hazards Models, Prospective Studies, Risk Factors, Waist Circumference, Prostatic Neoplasms
- Abstract
Background: Advanced prostate cancer etiology is poorly understood. Few studies have examined associations of anthropometric factors (e.g. early adulthood obesity) with advanced prostate cancer risk., Patients and Methods: We carried out pooled analyses to examine associations between body fatness, height, and prostate cancer risk. Among 830 772 men, 51 734 incident prostate cancer cases were identified, including 4762 advanced (T4/N1/M1 or prostate cancer deaths) cases, 2915 advanced restricted (same as advanced, but excluding localized cancers that resulted in death) cases, 9489 high-grade cases, and 3027 prostate cancer deaths. Cox proportional hazards models were used to calculate study-specific hazard ratios (HR) and 95% confidence intervals (CI); results were pooled using random effects models., Results: No statistically significant associations were observed for body mass index (BMI) in early adulthood for advanced, advanced restricted, and high-grade prostate cancer, and prostate cancer mortality. Positive associations were shown for BMI at baseline with advanced prostate cancer (HR = 1.30, 95% CI = 0.95-1.78) and prostate cancer mortality (HR = 1.52, 95% CI = 1.12-2.07) comparing BMI ≥35.0 kg/m
2 with 21-22.9 kg/m2 . When considering early adulthood and baseline BMI together, a 27% higher prostate cancer mortality risk (95% CI = 9% to 49%) was observed for men with BMI <25.0 kg/m2 in early adulthood and BMI ≥30.0 kg/m2 at baseline compared with BMI <25.0 kg/m2 in early adulthood and BMI <30.0 kg/m2 at baseline. Baseline waist circumference, comparing ≥110 cm with <90 cm, and waist-to-hip ratio, comparing ≥1.00 with <0.90, were associated with significant 14%-16% increases in high-grade prostate cancer risk and suggestive or significant 20%-39% increases in prostate cancer mortality risk. Height was associated with suggestive or significant 33%-56% risks of advanced or advanced restricted prostate cancer and prostate cancer mortality, comparing ≥1.90 m with <1.65 m., Conclusion: Our findings suggest that height and total and central adiposity in mid-to-later adulthood, but not early adulthood adiposity, are associated with risk of advanced forms of prostate cancer. Thus, maintenance of healthy weight may help prevent advanced prostate cancer., (Copyright © 2019 European Society for Medical Oncology. All rights reserved.)- Published
- 2020
- Full Text
- View/download PDF
39. MANAGEMENT OF PROSTATE CANCER IN ACCRA, GHANA.
- Author
-
Yeboah ED, Hsing AW, Mante S, Mensah JE, Kyei MY, Yarney J, Vanderpuye V, Beecham K, Tettey Y, Biritwum RB, Adjei AA, Gyasi R, Asante K, Ampadu KN, Klufio GO, Gepi-Attee S, Owoo C, Kwami D, Ahiaku, Pandra R, and Cook MB
- Abstract
Introduction: Africans living with prostate cancer in Africa face problems of early diagnosis and appropriate treatment., Aim: To study the clinical incidence of prostate cancer, risk factors, TNM stage, their management and outcomes., Methods: A prospective study of Prostate Cancer cases managed at Korle Bu Teaching Hospital and hospitals in Accra, diagnosed by history, abnormal PSA/DRE, physical examination and histologically confirmed by biopsy from 2004 to 2013 was carried out. The cases were TNM staged and managed by approved protocol., Results: There were 669 cases with a mean age 70±0.045SE years, median Gleason Score of 7, organ confined Prostate Cancer(PC) in 415(62%), locally advanced in 167(25%) and metastatic Prostate Cancer in 87(13%) cases. The cases were followed for median of 10 months to ≥ 84 months. Organ confined cases were managed by: Radical Prostatectomy (RP) 92 (13.8%) with a mortality of 0.3%; brachytherapy 70 (10.5%) with a mortality of 0.1% and External Beam Radiotherapy (EBRT) 155 (23%) with a mortality 0.7%. In all, 98 men constituting (14.1%) cases with a mean age of 75+0.25SE years, life expectancy <10 years were treated by hormonal therapy with a mortality of 1.7%. Twenty cases who were for active surveillance (GS6), PSA <10ng/ml, life expectancy <10 years later all opted for EBRT. Locally advanced cases 25% all had neoadjuvant hormonal therapy then Brachytherapy in 3 (0.4%) mortality 0.15% and EBRT in 64 (9.5%), mortality 0.59%. Hormonal therapy was given in 100 (15%) locally advanced cases, mortality 5%. Metastatic prostate cancer cases (13%) were managed by hormonal therapy, mortality 6%., Conclusion: Improved facilities and dedicated skilled teams led to a significant rise in proportion of organ confined Prostate Cancer from 15.3% to 62% curable by Radical Prostatectomy, brachytherapy or EBRT with longer disease free survival.
- Published
- 2016
40. Childhood height increases the risk of prostate cancer mortality.
- Author
-
Aarestrup J, Gamborg M, Cook MB, and Baker JL
- Subjects
- Adolescent, Body Mass Index, Child, Cohort Studies, Denmark epidemiology, Humans, Male, Risk Factors, Body Height, Prostatic Neoplasms mortality
- Abstract
Background: Adult body size is positively associated with aggressive and fatal prostate cancers. It is unknown whether these associations originate in early life. Therefore, we investigated if childhood height, body mass index (BMI; kg/m(2)) and growth are associated with prostate cancer-specific mortality and survival., Methods: Subjects were 125,208 men from the Copenhagen School Health Records Register, born 1930-1969 with height and weight measurements at ages 7-13years. Linkage to the Danish Cancer Registry and the Register of Causes of Death enabled identification of incident and fatal prostate cancers. Cox proportional hazards regressions were performed., Results: 630 men had prostate cancer recorded as the underlying cause of death. Childhood height at age 13years was positively associated with prostate cancer-specific mortality (hazard ratio [HR]per z-score=1.2, 95% confidence interval [CI]: 1.1-1.3). Associations were significant at all other childhood ages. Growth analyses showed that height at age 13years had a stronger association with prostate cancer-specific mortality than height at age 7, suggesting the association at age 7 is largely mediated through later childhood height. The tallest boys at age 13years had a significantly worse survival, but only when restricted to a diagnosis at <60years of age (HRz-score of 1=1.7, 95% CI: 1.3-2.4). These associations were significant at all other childhood ages. Childhood BMI was not associated with prostate cancer mortality or survival., Conclusion: Childhood height was positively associated with the hard end-point of prostate cancer-specific mortality, which strengthens prior epidemiologic observations of a positive association with prostate cancer incidence., (Copyright © 2015 Elsevier Ltd. All rights reserved.)
- Published
- 2015
- Full Text
- View/download PDF
41. Burden of extragonadal germ cell tumours in Europe and the United States.
- Author
-
Stang A, Trabert B, Wentzensen N, Cook MB, Rusner C, Oosterhuis JW, and McGlynn KA
- Subjects
- Female, Humans, Male, Neoplasms, Germ Cell and Embryonal epidemiology, Rare Diseases epidemiology, Testicular Neoplasms epidemiology
- Published
- 2012
- Full Text
- View/download PDF
42. Financial appraisal of wet mesophilic AD technology as a renewable energy and waste management technology.
- Author
-
Dolan T, Cook MB, and Angus AJ
- Subjects
- Anaerobiosis, Conservation of Energy Resources methods, Financing, Government, United Kingdom, Waste Management methods, Waste Products economics, Waste Products statistics & numerical data, Conservation of Energy Resources economics, Waste Management economics
- Abstract
Anaerobic digestion (AD) has the potential to support diversion of organic waste from landfill and increase renewable energy production. However, diffusion of this technology has been uneven, with countries such as Germany and Sweden taking the lead, but limited diffusion in other countries such as the UK. In this context, this study explores the financial viability of AD in the UK to offer reasons why it has not been more widely used. This paper presents a model that calculates the Internal Rate of Return (IRR) on a twenty year investment in a 30,000 tonnes per annum wet mesophilic AD plant in the UK for the treatment of source separated organic waste, which is judged to be a suitable technology for the UK climate. The model evaluates the financial significance of the different alternative energy outputs from this AD plant and the resulting economic subsidies paid for renewable energy. Results show that renewable electricity and renewable heat sales supported by renewable electricity and renewable heat tariffs generates the greatest IRR (31.26%). All other uses of biogas generate an IRR in excess of 15%, and are judged to be a financially viable investment. Sensitivity analysis highlights the financial significance of: economic incentive payments and a waste management gate fee; and demonstrates that the fate of the digestate by-product is a source of financial uncertainty for AD investors., (Copyright © 2011 Elsevier B.V. All rights reserved.)
- Published
- 2011
- Full Text
- View/download PDF
43. Interobserver reliability in the endoscopic diagnosis and grading of Barrett's esophagus: an Asian multinational study.
- Author
-
Lee YC, Cook MB, Bhatia S, Chow WH, El-Omar EM, Goto H, Lin JT, Li YQ, Rhee PL, Sharma P, Sung JJ, Wong JY, Wu JC, and Ho KY
- Subjects
- Asia, Barrett Esophagus diagnosis, Humans, Observer Variation, Reproducibility of Results, Barrett Esophagus pathology, Clinical Competence statistics & numerical data, Esophagoscopy standards
- Abstract
Background and Study Aim: The establishment of precise and valid diagnostic criteria is important for any disease. We determined the interobserver reliability in the endoscopic diagnosis and grading of Barrett's esophagus., Patients and Methods: Video clips of endoscopy in 21 patients with/without Barrett's esophagus were used for training (n = 3) and for diagnosis/grading (n = 18) of Barrett's esophagus by endoscopists from seven hospitals in Asia. Barrett's esophagus was graded using the Prague C & M Criteria whereby the circumferential extent of the Barrett's segment (C value), maximum extent of Barrett's segment (M value), location of the gastroesophageal junction, and location of the diaphragmatic hiatus were scored. The intraclass correlation coefficients (ICC) were calculated as a measure of interobserver reliability., Results: A total of 34 endoscopists participated. ICC values for the scores of the C value, M value, location of the gastroesophageal junction, and location of the diaphragmatic hiatus were: 0.92 (95 % confidence interval [CI] 0.88 - 0.97), 0.94 (95 %CI 0.90 - 0.98), 0.86 (95 %CI 0.78 - 0.94), and 0.81 (95 %CI 0.71 - 0.92), respectively, indicating excellent interobserver agreement. The differences in region/country, endoscopists' experience, case volume of participating centers, or primary practice type had no significant effect on the reliability. The ICC values for recognition of Barrett's esophagus of > or = 1 cm were 0.90 (95 %CI 0.80 - 1.00) and 0.92 (95 %CI 0.87 - 0.98) for the C and M values, respectively, whereas the corresponding ICC values for Barrett's segment of < 1 cm were 0.18 (95 %CI 0.03 - 0.32) and 0.21 (95 %CI 0.00 - 0.51), respectively., Conclusions: Despite the uncommon occurrence of Barrett's esophagus in Asia, our endoscopists exhibited excellent agreement in the endoscopic diagnosis and grading of Barrett's esophagus using the Prague C & M Criteria. However, in view of the low interobserver reliability in recognizing Barrett's segments of < 1 cm, future studies in Asia should take this into account when selecting the study population., (Copyright Georg Thieme Verlag KG Stuttgart . New York.)
- Published
- 2010
- Full Text
- View/download PDF
44. Identification and characterization of segments 3 and 4 of the ISAV genome.
- Author
-
Ritchie RJ, Heppell J, Cook MB, Jones S, and Griffiths SG
- Subjects
- Animals, Base Sequence, Blotting, Northern, Blotting, Southern, Cell Line, Cloning, Molecular, DNA Primers, Molecular Sequence Data, Open Reading Frames, Reverse Transcriptase Polymerase Chain Reaction, Genome, Viral, Orthomyxoviridae genetics, Salmon virology
- Abstract
Infectious Salmon Anaemia is a serious disease of farmed Atlantic Salmon on three continents. The disease causes severe anaemia and haemorrphagic liver necrosis, and carries major economic consequences for affected areas. Nevertheless, the causative agent, a novel orthomyxo-like Virus (Infectious Salmon Anaemia Virus - ISAV), is only partially characterized at the molecular level. We report the isolation and characterization of two novel ISAV segments at the genomic and proteomic levels. These segments are the third and fourth largest of the (ISAV) genome and may code for a nucleocapsid protein (NP) and a polymerase (PA). Western blot analysis using an ISAV polyclonal antibody identified one of these novel proteins as being the major tissue antigen. We discuss the implications of our findings for vaccine development and surveillance of Infectious Salmon Anaemia.
- Published
- 2001
- Full Text
- View/download PDF
45. The adult growth hormone deficiency syndrome.
- Author
-
Cook DM, Ludlam WH, and Cook MB
- Subjects
- Adult, Diagnosis, Differential, Drug Monitoring, Female, Human Growth Hormone adverse effects, Human Growth Hormone blood, Human Growth Hormone therapeutic use, Humans, Insulin-Like Growth Factor I analysis, Male, Middle Aged, Patient Satisfaction, Physician-Patient Relations, Syndrome, Human Growth Hormone deficiency
- Abstract
The diagnosis of the adult GH deficiency syndrome from a clinical and laboratory standpoint has been reviewed. Therapy guidelines and monitoring should focus on the patient's symptoms and IGF-1 concentrations from a laboratory standpoint. Successful patient/physician interaction depends on physician awareness of the symptoms of the deficiency syndrome and symptoms associated with therapy. Successful therapy with GH almost always results in an extremely satisfied patient, family, and physician.
- Published
- 2000
46. Route of estrogen administration helps to determine growth hormone (GH) replacement dose in GH-deficient adults.
- Author
-
Cook DM, Ludlam WH, and Cook MB
- Subjects
- Administration, Cutaneous, Administration, Oral, Adult, Female, Hormone Replacement Therapy, Human Growth Hormone therapeutic use, Humans, Insulin-Like Growth Factor I metabolism, Male, Middle Aged, Prospective Studies, Estradiol administration & dosage, Human Growth Hormone administration & dosage, Human Growth Hormone deficiency
- Abstract
We prospectively studied two groups of GH-deficient patients during GH therapy based upon exposure of the liver to elevated (oral estrogen) or not elevated (endogenous or transdermal) sources of estrogen. We wondered whether higher concentrations of estrogen at the liver level (oral estrogen) might inhibit insulin-like growth factor I (IGF-I) secretion and alter exogenous GH requirements. In this study we compared GH replacement requirements in these two groups of women as well as with GH-treated adult hypopituitary males. The final GH dose was based upon maintenance IGF-I levels in the mid- to high normal range adjusted for age and sex or symptom tolerance. Each group [women taking oral estrogen (n = 12), women not taking oral estrogen (n = 13), and men (n = 12)] was similar in age and final IGF-I concentration. Women taking oral estrogen required 10.6 +/- 0.7 microg/kg x day or 867 +/- 45 microg/day GH, women not taking oral estrogen required 5.0 +/- 0.7 microg/kg x day or 424 +/- 57 microg/day, and men required 4.1 +/- 0.6 microg/kg x day or 376 +/- 49 microg/day to achieve similar IGF-I concentrations. GH requirements in men were not different from those in women not taking oral estrogen, but the GH requirements in both groups were significantly different from GH requirements in women taking oral estrogen. These observations may be useful in anticipating appropriate starting and final doses of GH in adult hypopituitary patients.
- Published
- 1999
- Full Text
- View/download PDF
47. Rapid, low-technology MIC determination with clinical Mycobacterium tuberculosis isolates by using the microplate Alamar Blue assay.
- Author
-
Franzblau SG, Witzig RS, McLaughlin JC, Torres P, Madico G, Hernandez A, Degnan MT, Cook MB, Quenzer VK, Ferguson RM, and Gilman RH
- Subjects
- Bacteriological Techniques, Coloring Agents metabolism, Culture Media metabolism, Drug Resistance, Microbial, Drug Resistance, Multiple, Ethambutol pharmacology, Humans, Isoniazid pharmacology, Microbial Sensitivity Tests economics, Peru epidemiology, Rifampin pharmacology, Sensitivity and Specificity, Streptomycin pharmacology, Tuberculosis epidemiology, Antibiotics, Antitubercular pharmacology, Antitubercular Agents pharmacology, Microbial Sensitivity Tests methods, Mycobacterium tuberculosis drug effects, Oxazines, Tuberculosis drug therapy, Xanthenes
- Abstract
A colorimetric, microplate-based Alamar Blue assay (MABA) method was used to determine the MICs of isoniazid (INH), rifampin, streptomycin (SM), and ethambutol (EMB) for 34 Peruvian Mycobacterium tuberculosis isolates (including both pansensitive and multidrug-resistant strains) and the H37Rv strain by using bacterial suspensions prepared directly from solid media. Results for all isolates were available within 8 days. Discordant results were observed on initial tests for 3 of 16 INH-susceptible isolates, 5 of 31 EMB-susceptible isolates, and 2 of 4 SM-resistant isolates (by the BACTEC 460 system). The overall agreements between the MICs obtained by MABA and the results obtained with the BACTEC 460 system were 87.9% for initial results and 93.6% after retesting 12 of 17 samples with discrepant results. Interpretation of MABA endpoints improved with technical experience. The MABA is a simple, rapid, low-cost, appropriate technology which does not require expensive instrumentation and which makes use of a nontoxic, temperature-stable reagent.
- Published
- 1998
- Full Text
- View/download PDF
48. Pediatric blood culture evaluation of the BACTEC PEDS Plus and the DuPont Isolator 1.5 systems.
- Author
-
Eisenach K, Dyke J, Boehme M, Johnson B, and Cook MB
- Subjects
- Anti-Bacterial Agents pharmacology, Anti-Bacterial Agents therapeutic use, Bacteremia diagnosis, Bacteremia drug therapy, Bacteria drug effects, Bacteria growth & development, Child, Colony Count, Microbial, Culture Media, Evaluation Studies as Topic, Humans, Bacteremia microbiology, Bacteria isolation & purification
- Abstract
A new nonradiometric BACTEC medium has been developed for culturing pediatric blood samples. The BACTEC PEDS Plus medium (BACTEC PED) consists of 20 ml of an enriched broth with resins. In contrast to the other aerobic BACTEC media, there is a lower concentration of sodium polyanetholesulfonate in the medium and more CO2 in the headspace of the vial. This study was conducted in two different pediatric settings to compare the performance of the BACTEC PED medium with the Du Pont Isolator 1.5 system (ISO 1.5) in terms of overall organism recovery and time to detection. Equal volumes of up to 1.5 ml were tested in both systems. A total of 4063 culture sets were analyzed, yielding 301 (7.4%) clinically significant isolates. Of these, 86 (29%) were recovered only from the BACTEC PED and 12 (4%) only from the ISO 1.5 (p less than 0.001). BACTEC PED recovered significantly more staphylococci and Enterobacteriaceae than ISO 1.5 (p less than 0.001 and p less than 0.005, respectively). Detection times of isolates recovered in both systems were comparable. For those patients on antibiotic therapy at the time of culture, 21 (37%) were positive only in the BACTEC PED, whereas two (4%) were positive only in the ISO 1.5. The nontherapy group had 61 (27%) organisms that were detected in BACTEC PED only and 9 (4%) in ISO 1.5 only. These results indicate that BACTEC PED is a significant advance in blood culture systems that will provide a sensitive method for detecting pediatric bacteremias.
- Published
- 1992
- Full Text
- View/download PDF
49. Editorial: Bad news, good news.
- Author
-
Cook MB
- Published
- 1987
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.