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Your search keyword '"Bourgeat, P"' showing total 11 results
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11 results on '"Bourgeat, P"'

1. Subjective Memory Complaints in APOE epsilon 4 Carriers are Associated with High Amyloid-beta Burden

Author

Zwan, M.D., Villemagne, V.L., Dore, V., Buckley, R., Bourgeat, P., Veljanoski, R., Salvado, O., Williams, R., Margison, L., Rembach, A., Macaulay, S.L., Martins, R., Amesh, D., van der Flier, W.M., Ellis, K.A., Scheltens, P., Masters, C.L., Rowe, C.C., Amsterdam Neuroscience - Neurodegeneration, and Neurology

Abstract

Background:APOE ɛ4 genotype and aging have been identified as risk factors for Alzheimer’s disease (AD). In addition, subjective memory complaints (SMC) might be a first clinical expression of the effect of AD pathology on cognitive functioning. Objective:To assess whether APOE ɛ4 genotype, age, SMC, and episodic memory are risk factors for high amyloid-β (Aβ) burden in cognitively normal elderly. Methods:307 cognitively normal participants (72.7 ± 6.8 years, 53% female, 55% SMC) from the Australian Imaging, Biomarkers and Lifestyle (AIBL) study underwent amyloid PET and APOE genotyping. Logistic regression analyses were performed to determine the association of APOE ɛ4 genotype, age, SMC, and episodic memory with Aβ pathology. Results:Odds of high Aβ burden were greater at an older age (OR = 3.21; 95% CI = 1.68–6.14), when SMC were present (OR = 1.90; 95% CI = 1.03–3.48), and for APOE ɛ4 carriers (OR = 7.49; 95% CI = 3.96–14.15), while episodic memory was not associated with odds of high Aβ burden. Stratified analyses showed that odds of SMC for high Aβ burden were increased in specifically APOE ɛ4 carriers (OR = 4.58, 95% CI = 1.83–11.49) and younger participants (OR = 3.73, 95% CI = 1.39–10.01). Conclusion:Aging, APOE ɛ4 genotype, and SMC were associated with high Aβ burden. SMC were especially indicative of high Aβ burden in younger participants and in APOE ɛ4 carriers. These findings suggest that selection based on the presence of SMC, APOE ɛ4 genotype and age may help identify healthy elderly participants with high Aβ burden eligible for secondary prevention trials.

Published
2016
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2. A radioimmunoassay for the tripeptide Gly-Trp-Met, a major metabolite of endogenous cholecystokinin in brain

Author

Froylan Vargas, Bourgeat P, Christiane Rose, and J.-C. Schwartz

Subjects
Isoflurophate, Metabolite, Radioimmunoassay, Neuropeptide, Endogeny, Tripeptide, Cross Reactions, Sensitivity and Specificity, Serine, Cellular and Molecular Neuroscience, chemistry.chemical_compound, Endocrinology, Benzoquinones, Animals, Amino Acid Sequence, Derivatization, Chromatography, High Pressure Liquid, Cholecystokinin, Cerebral Cortex, Endocrine and Autonomic Systems, Chemistry, Sulfhydryl Reagents, Reproducibility of Results, General Medicine, Hydrogen-Ion Concentration, Rats, Neurology, Biochemistry, Indicators and Reagents, Oligopeptides
Abstract

We developed a specific and sensitive radioimmunoassay for the tripeptide Gly-Trp-Met (GWM) after its derivatization with p -benzoquinone. Measurable amounts of endogenous GWM-like immunoreactivity (GWM-ir), co-eluting in HPLC with authentic GMW were detected in the medium of depolarized slices of rat cerebral cortex. The tripeptide GWM appears as the major inactive CCK-8 metabolite since a major fraction of CCK-8-ir released from the slices was apparently recovered in the medium as GWM. In addition, in the presence of the serine reagent diisopropylfluorophosphate, a strong decrease of GWM formation was observed to accompany the corresponding increase of CCK-8-ir recovery in medium. The present study confirms that (a) serine peptidase(s) is(are) responsible for inactivating endogenous CCK-8 in brain as previously proposed (Rose et al. Proc Natl Acad Sci USA 1988; 85: 8326).

Published
1996
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10. High content, multi-parameter analyses in buccal cells to identify alzheimer’s disease

Author

François, M., Fenech, M. F., Thomas, P., Hor, M., Rembach, A., Martins, R. N., Rainey-Smith, S. R., Masters, C. L., Ames, D., Rowe, C. C., Lance Macaulay, S., Hill, A. F., Leifert, W. R., Appannah, A., Barnes, M., Barnham, K., Bedo, J., Bellingham, S., Bon, L., Bourgeat, P., Brown, B., Buckley, R., Burnham, S., Bush, A., Chandler, G., Chen, K., Clarnette, R., Collins, S., Cooke, I., Cowie, T., Cox, K., Cuningham, E., Cyarto, E., Dang, P. A. V., Darby, D., Desmond, P., Doecke, J., Dore, V., Downing, H., Dridan, B., Duesing, K., Fahey, M., Farrow, M., Faux, N., Fenech, M., Fernandez, S., Fernando, B., Fowler, C., Francois, M., Fripp, J., Frost, S., Gardener, S., Gibson, S., Graham, P., Gupta, V., Hansen, D., Harrington, K., Hill, A., Hone, E., Horne, M., Huckstepp, B., Jones, A., Jones, G., Kamer, A., Kanagasingam, Y., Keam, L., Kowalczyk, A., Krivdic, B., Lam, C. P., Lamb, F., Lautenschlager, N., Laws, S., Leifert, W., Lenzo, N., Leroux, H., Lftikhar, F., Li, Q. -X, Lim, F., Lim, L., Lockett, L., Lucas, K., Mano, M., Marczak, C., Martins, G., Maruff, P., Matsumoto, Y., Bird, S., Mcbride, S., Mckay, R., Mulligan, R., Nash, T., Nigro, J., O Keefe, G., Ong, K., Parker, B., Pedrini, S., Peiffer, J., Pejoska, S., Penny, L., Perez, K., Pertile, K., Phal, P., Porter, T., Rainey-Smith, S., Raniga, P., Restrepo, C., Riley, M., Roberts, B., Robertson, J., Rodrigues, M., Rooney, A., Rumble, R., Ryan, T., Salvado, O., Samuel, M., Saunders, I., Savage, G., Silbert, B., Sohrabi, H., Syrette, J., Cassandra Szoeke, Taddei, K., Taddei, T., Tan, S., Tegg, M., Trivedi, D., Trounson, B., Veljanovski, R., Verdile, G., Villemagne, V., Volitakis, I., Vockler, C., Vovos, M., Vrantsidis, F., Walker, S., Watt, A., Weinborn, M., Wilson, B., Woodward, M., Yastrubetskaya, O., Yates, P., Zhang, P., Chatterjee, P., Creegan, R., Ruyck, K., Ding, H., Groth, D., Head, R., Krause, D., Lachovitzki, R., Lim, Y. Y., Lintern, T., Mondal, A., Nuttall, S., O Callaghan, N., Osborne, L., Pang, C., Patten, G., Tuckfield, A., Varghese, J., Wilson, A., and Zhang, Q.

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