37 results on '"Rutten, B P F"'
Search Results
2. Differential associations of childhood adversity subtypes and psychopathology in men and women
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Prachason, T., primary, Mutlu, I., additional, Fusar-Poli, L., additional, Menne-Lothmann, C., additional, Decoster, J., additional, van Winkel, R., additional, Collip, D., additional, Delespaul, P., additional, De Hert, M., additional, Derom, C., additional, Thiery, E., additional, Jacobs, N., additional, Wichers, M., additional, van Os, J., additional, Rutten, B. P. F., additional, Pries, L.-K., additional, and Gülöksüz, S., additional
- Published
- 2023
- Full Text
- View/download PDF
3. Taalachterstand en psychose onder mensen met een migratieachtergrond
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Jongsma, H E, van der Ven, E M A, Velthorst, E, de Haan, L, Rutten, B P F, van Os, J, Jongsma, H E, van der Ven, E M A, Velthorst, E, de Haan, L, Rutten, B P F, and van Os, J
- Abstract
BACKGROUND: Ethnic minorities in the Netherlands face an excess psychosis risk, and understanding of causality remains limited. Linguistic disadvantage and other indicators of societal exclusion might play a role, and offer potential targets for public health interventions.AIM: To establish the contribution of linguistic disadvantage, indicators of social distance and perceived discrimination to the increased risk of psychoses in migrants and ethnic minorities.METHODS: We used the Dutch data from an international case-control study into psychotic disorders (the EU-GEI study). A first episode of psychosis was our outcome variable, and we used well-defined data on established confounders (e.g. age and sex) and indicators of ethnicity, social distance, linguistic disadvantage and perceived discrimination as our predictor variables.RESULTS: Ethnic minorities face an increased psychosis risk. This appears to be the case for both first- and second- generation migrants and so-called ‘Western’ and non-Western migrants. Though confounders and social distance appear to contribute, linguistic disadvantage appears to play a role in the excess psychosis risk in first-generation migrants.CONCLUSION: Reducing the social consequences of linguistic disadvantage or social distance might be a starting point for concrete public health interventions aimed at preventing the increased psychosis risk faced by first-generation migrants.
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- 2023
4. Taalachterstand en psychose onder mensen met een migratieachtergrond
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Hersenen-Medisch 1, Brain, Jongsma, H E, van der Ven, E M A, Velthorst, E, de Haan, L, Rutten, B P F, van Os, J, Hersenen-Medisch 1, Brain, Jongsma, H E, van der Ven, E M A, Velthorst, E, de Haan, L, Rutten, B P F, and van Os, J
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- 2023
5. Linguistic distance and psychosis in ethnic minorities
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Jongsma, H E, van der Ven, E M A, Velthorst, E, de Haan, L, Rutten, B P F, van Os, J, Clinical Developmental Psychology, APH - Mental Health, and World Health Organization (WHO) Collaborating Center
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SDG 16 - Peace ,SDG 16 - Peace, Justice and Strong Institutions ,SDG 10 - Reduced Inequalities ,Justice and Strong Institutions - Abstract
BACKGROUND: Ethnic minorities in the Netherlands face an excess psychosis risk, and understanding of causality remains limited. Linguistic disadvantage and other indicators of societal exclusion might play a role, and offer potential targets for public health interventions.AIM: To establish the contribution of linguistic disadvantage, indicators of social distance and perceived discrimination to the increased risk of psychoses in migrants and ethnic minorities.METHODS: We used the Dutch data from an international case-control study into psychotic disorders (the EU-GEI study). A first episode of psychosis was our outcome variable, and we used well-defined data on established confounders (e.g. age and sex) and indicators of ethnicity, social distance, linguistic disadvantage and perceived discrimination as our predictor variables.RESULTS: Ethnic minorities face an increased psychosis risk. This appears to be the case for both first- and second- generation migrants and so-called ‘Western’ and non-Western migrants. Though confounders and social distance appear to contribute, linguistic disadvantage appears to play a role in the excess psychosis risk in first-generation migrants.CONCLUSION: Reducing the social consequences of linguistic disadvantage or social distance might be a starting point for concrete public health interventions aimed at preventing the increased psychosis risk faced by first-generation migrants.
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- 2023
6. Epigenetic dysregulation of brainstem nuclei in the pathogenesis of Alzheimer’s disease: looking in the correct place at the right time?
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Iatrou, A., Kenis, G., Rutten, B. P. F., Lunnon, K., and van den Hove, D. L. A.
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- 2017
- Full Text
- View/download PDF
7. Genome-wide association analyses of symptom severity among clozapine-treated patients with schizophrenia spectrum disorders
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Okhuijsen-Pfeifer, C., van der Horst, M. Z., Bousman, C. A., Lin, B., van Eijk, K. R., Ripke, S., Ayhan, Y., Babaoglu, M. O., Bak, M., Alink, W., van Beek, H., Beld, E., Bouhuis, A., Edlinger, M., Erdogan, I. M., Ertuğrul, A., Yoca, G., Everall, I. P., Görlitz, T., van Amelsvoort, T., Bartels-Velthuis, A. A., Bruggeman, R., Cahn, W., Guloksuz, S., de Haan, L., Kahn, R. S., Schirmbeck, F., Simons, C. J. P., van Os, J., Alizadeh, B. Z., Luykx, J. J., Rutten, B. P. F., van Winkel, R., Grootens, K. P., Gutwinski, S., Hallikainen, T., Jeger-Land, E., de Koning, M., Lähteenvuo, M., Legge, S. E., Leucht, S., Morgenroth, C., Müderrisoğlu, A., Narang, A., Pantelis, C., Pardiñas, A. F., Oviedo-Salcedo, T., Schneider-Thoma, J., Schreiter, S., Repo-Tiihonen, E., Tuppurainen, H., Veereschild, M., Veerman, S., de Vos, M., Wagner, E., Cohen, D., Bogers, J. P. A. M., Walters, J. T. R., Yağcıoğlu, A. E. Anil, Tiihonen, J., Hasan, A., Clinical Cognitive Neuropsychiatry Research Program (CCNP), Life Course Epidemiology (LCE), Real World Studies in PharmacoEpidemiology, -Genetics, -Economics and -Therapy (PEGET), Psychiatrie & Neuropsychologie, RS: MHeNs - R3 - Neuroscience, Adult Psychiatry, APH - Mental Health, ANS - Complex Trait Genetics, and ANS - Mood, Anxiety, Psychosis, Stress & Sleep
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POLYGENIC RISK SCORE ,GENETIC RISK ,N-DESMETHYLCLOZAPINE ,Schizophrenia/chemically induced ,Cytochrome P-450 CYP1A2/genetics ,Cellular and Molecular Neuroscience ,Cytochrome P-450 CYP1A2 ,Humans ,ddc:610 ,CYP2C19 ,BRAIN ,Clozapine ,POLYMORPHISMS ,Biological Psychiatry ,IDENTIFICATION ,PHARMACOGENETICS ,CYTOCHROME-P450 ,Clozapine/therapeutic use ,Cytochrome P-450 CYP2C19 ,Psychiatry and Mental health ,Cytochrome P-450 CYP2D6 ,Schizophrenia ,Cytochrome P-450 CYP2C19/genetics ,Antipsychotic Agents/therapeutic use ,Cytochrome P-450 CYP2D6/genetics ,PHARMACOLOGICAL-TREATMENT ,Antipsychotic Agents ,Genome-Wide Association Study - Abstract
Clozapine is the most effective antipsychotic for patients with treatment-resistant schizophrenia. However, response is highly variable and possible genetic underpinnings of this variability remain unknown. Here, we performed polygenic risk score (PRS) analyses to estimate the amount of variance in symptom severity among clozapine-treated patients explained by PRSs (R2) and examined the association between symptom severity and genotype-predicted CYP1A2, CYP2D6, and CYP2C19 enzyme activity. Genome-wide association (GWA) analyses were performed to explore loci associated with symptom severity. A multicenter cohort of 804 patients (after quality control N = 684) with schizophrenia spectrum disorder treated with clozapine were cross-sectionally assessed using the Positive and Negative Syndrome Scale and/or the Clinical Global Impression-Severity (CGI-S) scale. GWA and PRS regression analyses were conducted. Genotype-predicted CYP1A2, CYP2D6, and CYP2C19 enzyme activities were calculated. Schizophrenia-PRS was most significantly and positively associated with low symptom severity (p = 1.03 × 10−3; R2 = 1.85). Cross-disorder-PRS was also positively associated with lower CGI-S score (p = 0.01; R2 = 0.81). Compared to the lowest tertile, patients in the highest schizophrenia-PRS tertile had 1.94 times (p = 6.84×10−4) increased probability of low symptom severity. Higher genotype-predicted CYP2C19 enzyme activity was independently associated with lower symptom severity (p = 8.44×10−3). While no locus surpassed the genome-wide significance threshold, rs1923778 within NFIB showed a suggestive association (p = 3.78×10−7) with symptom severity. We show that high schizophrenia-PRS and genotype-predicted CYP2C19 enzyme activity are independently associated with lower symptom severity among individuals treated with clozapine. Our findings open avenues for future pharmacogenomic projects investigating the potential of PRS and genotype-predicted CYP-activity in schizophrenia.
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- 2022
8. Cognitive functioning throughout adulthood and illness stages in individuals with psychotic disorders and their unaffected siblings
- Author
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Velthorst E., Mollon J., Murray R. M., de Haan L., Germeys I. M., Glahn D. C., Arango C., van der Ven E., Di Forti M., Bernardo M., Guloksuz S., Delespaul P., Mezquida G., Amoretti S., Bobes J., Saiz P. A., Garcia-Portilla M. P., Santos J. L., Jimenez-Lopez E., Sanjuan J., Aguilar E. J., Arrojo M., Carracedo A., Lopez G., Gonzalez-Penas J., Parellada M., Atbasoglu C., Saka M. C., Ucok A., Alptekin K., Akdede B., Binbay T., Altinyazar V., Ulas H., Yalincetin B., Gumus-Akay G., Beyaz B. C., Soygur H., Cankurtaran E. S., Kaymak S. U., Maric N. P., Mihaljevic M. M., Petrovic S. A., Mirjanic T., Del-Ben C. M., Ferraro L., Gayer-Anderson C., Jones P. B., Jongsma H. E., Kirkbride J. B., La Cascia C., Lasalvia A., Tosato S., Llorca P. -M., Menezes P. R., Morgan C., Quattrone D., Menchetti M., Selten J. -P., Szoke A., Tarricone I., Tortelli A., McGuire P., Valmaggia L., Kempton M. J., van der Gaag M., Riecher-Rossler A., Bressan R. A., Barrantes-Vidal N., Nelson B., McGorry P., Pantelis C., Krebs M. -O., Ruhrmann S., Sachs G., Rutten B. P. F., van Os J., Alizadeh B. Z., van Amelsvoort T., Bartels-Velthuis A. A., Bruggeman R., van Beveren N. J., Luykx J. J., Cahn W., Simons C. J. P., Kahn R. S., Schirmbeck F., van Winkel R., Calem M., Tognin S., Modinos G., Pisani S., Kraan T. C., van Dam D. S., Burger N., Amminger G. P., Politis A., Goodall J., Borgwardt S., Studerus E., Gadelha A., Brietzke E., Asevedo G., Asevedo E., Zugman A., Dominguez-Martinez T., Monsonet M., Cristobal-Narvaez P., Racioppi A., Kwapil T. R., Kazes M., Daban C., Bourgin J., Gay O., Mam-Lam-Fook C., Nordholm D., Rander L., Krakauer K., Glenthoj L. B., Glenthoj B., Gebhard D., Arnhold J., Klosterkotter J., Lasser I., Winklbaur B., Reichenberg A., Velthorst E., Mollon J., Murray R.M., de Haan L., Germeys I.M., Glahn D.C., Arango C., van der Ven E., Di Forti M., Bernardo M., Guloksuz S., Delespaul P., Mezquida G., Amoretti S., Bobes J., Saiz P.A., Garcia-Portilla M.P., Santos J.L., Jimenez-Lopez E., Sanjuan J., Aguilar E.J., Arrojo M., Carracedo A., Lopez G., Gonzalez-Penas J., Parellada M., Atbasoglu C., Saka M.C., Ucok A., Alptekin K., Akdede B., Binbay T., Altinyazar V., Ulas H., Yalincetin B., Gumus-Akay G., Beyaz B.C., Soygur H., Cankurtaran E.S., Kaymak S.U., Maric N.P., Mihaljevic M.M., Petrovic S.A., Mirjanic T., Del-Ben C.M., Ferraro L., Gayer-Anderson C., Jones P.B., Jongsma H.E., Kirkbride J.B., La Cascia C., Lasalvia A., Tosato S., Llorca P.-M., Menezes P.R., Morgan C., Quattrone D., Menchetti M., Selten J.-P., Szoke A., Tarricone I., Tortelli A., McGuire P., Valmaggia L., Kempton M.J., van der Gaag M., Riecher-Rossler A., Bressan R.A., Barrantes-Vidal N., Nelson B., McGorry P., Pantelis C., Krebs M.-O., Ruhrmann S., Sachs G., Rutten B.P.F., van Os J., Alizadeh B.Z., van Amelsvoort T., Bartels-Velthuis A.A., Bruggeman R., van Beveren N.J., Luykx J.J., Cahn W., Simons C.J.P., Kahn R.S., Schirmbeck F., van Winkel R., Calem M., Tognin S., Modinos G., Pisani S., Kraan T.C., van Dam D.S., Burger N., Amminger G.P., Politis A., Goodall J., Borgwardt S., Studerus E., Gadelha A., Brietzke E., Asevedo G., Asevedo E., Zugman A., Dominguez-Martinez T., Monsonet M., Cristobal-Narvaez P., Racioppi A., Kwapil T.R., Kazes M., Daban C., Bourgin J., Gay O., Mam-Lam-Fook C., Nordholm D., Rander L., Krakauer K., Glenthoj L.B., Glenthoj B., Gebhard D., Arnhold J., Klosterkotter J., Lasser I., Winklbaur B., Reichenberg A., RS: MHeNs - R2 - Mental Health, Psychiatrie & Neuropsychologie, RS: MHeNs - R1 - Cognitive Neuropsychiatry and Clinical Neuroscience, Neurosciences, Psychiatry, Clinical Developmental Psychology, World Health Organization (WHO) Collaborating Center, Life Course Epidemiology (LCE), Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Clinical Cognitive Neuropsychiatry Research Program (CCNP), Real World Studies in PharmacoEpidemiology, -Genetics, -Economics and -Therapy (PEGET), Adult Psychiatry, APH - Mental Health, Amsterdam Neuroscience - Complex Trait Genetics, and Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep
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0301 basic medicine ,validity ,medicine.medical_treatment ,CHILDHOOD ,Neuropsychological Tests ,FAMÍLIA ,episode ,Cognition ,0302 clinical medicine ,DEFICITS ,Settore MED/48 -Scienze Infermierist. e Tecn. Neuro-Psichiatriche e Riabilitat ,Medicine ,Cognitive impairment ,Psychiatry ,Symptom severity ,Cannabis use ,IMPAIRMENT ,ABILITY ,Psychiatry and Mental health ,Schizophrenia ,RELIABILITY ,Neuropsychological Test ,Life Sciences & Biomedicine ,Human ,Clinical psychology ,Adult ,Biochemistry & Molecular Biology ,impairment ,schizophrenia-patients ,ability ,GENETIC RISK ,Psychotic Disorder ,SCHIZOPHRENIA-PATIENTS ,03 medical and health sciences ,Cellular and Molecular Neuroscience ,SDG 3 - Good Health and Well-being ,Settore M-PSI/08 - Psicologia Clinica ,Humans ,In patient ,Cognitive skill ,VALIDITY ,Antipsychotic ,Molecular Biology ,Settore MED/25 - Psichiatria ,Aged ,Cross-Sectional Studie ,DECLINE ,Science & Technology ,reliability ,business.industry ,Working memory ,Siblings ,Neurosciences ,Diagnostic markers ,medicine.disease ,Cross-Sectional Studies ,030104 developmental biology ,deficits ,Psychotic Disorders ,PSYCHOSIS, COGNITION, MULTICENTRIC STUDY ,Neurosciences & Neurology ,business ,EPISODE ,030217 neurology & neurosurgery - Abstract
The European Community’s Seventh Framework Programme under grant agreement No. HEALTH-F2-2010-241909 (EUGEI); The Spanish sample was supported by the Spanish Ministry of Science and Innovation, Instituto de Salud Carlos III (SAM16PE07CP1, PI16/02012, PI19/024) (...), Velthorst, E., Mollon, J., Murray, R.M., de Haan, L., Germeys, I.M., Glahn, D.C., Arango, C., van der Ven, E., Di Forti, M., Bernardo, M., Guloksuz, S., Delespaul, P., Mezquida, G., Amoretti, S., Bobes, J., Saiz, P.A., García-Portilla, M.P., Santos, J.L., Jiménez-López, E., Sanjuan, J., Aguilar, E.J., Arrojo, M., Carracedo, A., López, G., González-Peñas, J., Parellada, M., Atbaşoğlu, C., Saka, M.C., Üçok, A., Alptekin, K., Akdede, B., Binbay, T., Altınyazar, V., Ulaş, H., Yalınçetin, B., Gümüş-Akay, G., Beyaz, B.C., Soygür, H., Cankurtaran, E.Ş., Kaymak, S.U., Maric, N.P., Mihaljevic, M.M., Petrovic, S.A., Mirjanic, T., Del-Ben, C.M., Ferraro, L., Gayer-Anderson, C., Jones, P.B., Jongsma, H.E., Kirkbride, J.B., La Cascia, C., Lasalvia, A., Tosato, S., Llorca, P.-M., Menezes, P.R., Morgan, C., Quattrone, D., Menchetti, M., Selten, J.-P., Szöke, A., Tarricone, I., Tortelli, A., McGuire, P., Valmaggia, L., Kempton, M.J., van der Gaag, M., Riecher-Rössler, A., Bressan, R.A., Barrantes-Vidal, N., Nelson, B., McGorry, P., Pantelis, C., Krebs, M.-O., Ruhrmann, S., Sachs, G., Rutten, B.P.F., van Os, J., Alizadeh, B.Z., van Amelsvoort, T., Bartels-Velthuis, A.A., Bruggeman, R., van Beveren, N.J., Luykx, J.J., Cahn, W., Simons, C.J.P., Kahn, R.S., Schirmbeck, F., van Winkel, R., Calem, M., Tognin, S., Modinos, G., Pisani, S., Kraan, T.C., van Dam, D.S., Burger, N., Amminger, G.P., Politis, A., Goodall, J., Borgwardt, S., Studerus, E., Gadelha, A., Brietzke, E., Asevedo, G., Asevedo, E., Zugman, A., Domínguez-Martínez, T., Monsonet, M., Cristóbal-Narváez, P., Racioppi, A., Kwapil, T.R., Kazes, M., Daban, C., Bourgin, J., Gay, O., Mam-Lam-Fook, C., Nordholm, D., Rander, L., Krakauer, K., Glenthøj, L.B., Glenthøj, B., Gebhard, D., Arnhold, J., Klosterkötter, J., Lasser, I., Winklbaur, B., Reichenberg, A., EU-GEI High Risk Study
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- 2021
9. Genetic vulnerability to DUSP22 promoter hypermethylation is involved in the relation between in utero famine exposure and schizophrenia
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Boks, M. P., Houtepen, L. C., Xu, Z., He, Y., Ursini, G., Maihofer, A. X., Rajarajan, P., Yu, Q., Xu, H., Wu, Y., Wang, S., Shi, J. P., Hulshoff Pol, H. E., Strengman, E., Rutten, B. P. F., Jaffe, A. E., Kleinman, J. E., Baker, D. G., Hol, E. M., Akbarian, S., Nievergelt, C. M., De Witte, L. D., Vinkers, C. H., Weinberger, D. R., Yu, J., and Kahn, R. S.
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- 2018
- Full Text
- View/download PDF
10. Predicting the functional states of human iPSC-derived neurons with single-cell RNA-seq and electrophysiology
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Bardy, C, van den Hurk, M, Kakaradov, B, Erwin, J A, Jaeger, B N, Hernandez, R V, Eames, T, Paucar, A A, Gorris, M, Marchand, C, Jappelli, R, Barron, J, Bryant, A K, Kellogg, M, Lasken, R S, Rutten, B P F, Steinbusch, H W M, Yeo, G W, and Gage, F H
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- 2016
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11. Genetic and psychosocial stressors have independent effects on the level of subclinical psychosis: findings from the multinational EU-GEI study
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Hersenen-Medisch 1, Brain, Pignon, B, Peyre, H, Ayrolles, A, Kirkbride, J B, Jamain, S, Ferchiou, A, Richard, J R, Baudin, G, Tosato, S, Jongsma, H, de Haan, L, Tarricone, I, Bernardo, M, Velthorst, E, Braca, M, Arango, C, Arrojo, M, Bobes, J, Del-Ben, C M, Di Forti, M, Gayer-Anderson, C, Jones, P B, La Cascia, C, Lasalvia, A, Menezes, P R, Quattrone, D, Sanjuán, J, Selten, J P, Tortelli, A, Llorca, P M, van Os, J, Rutten, B P F, Murray, R M, Morgan, C, Leboyer, M, Szöke, A, Schürhoff, F, Hersenen-Medisch 1, Brain, Pignon, B, Peyre, H, Ayrolles, A, Kirkbride, J B, Jamain, S, Ferchiou, A, Richard, J R, Baudin, G, Tosato, S, Jongsma, H, de Haan, L, Tarricone, I, Bernardo, M, Velthorst, E, Braca, M, Arango, C, Arrojo, M, Bobes, J, Del-Ben, C M, Di Forti, M, Gayer-Anderson, C, Jones, P B, La Cascia, C, Lasalvia, A, Menezes, P R, Quattrone, D, Sanjuán, J, Selten, J P, Tortelli, A, Llorca, P M, van Os, J, Rutten, B P F, Murray, R M, Morgan, C, Leboyer, M, Szöke, A, and Schürhoff, F
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- 2022
12. Samenspel tussen genetische achtergrond en omgevingsfactoren in de psychiatrie: stand van zaken en toekomstperspectief
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Onderzoeksgroep 2, Brain, Hersenen-Medisch 1, Onderzoek, Rutten, B P F, Guloksuz, S, Boks, M, van Os, J, Luykx, J J, van Winkel, R, Onderzoeksgroep 2, Brain, Hersenen-Medisch 1, Onderzoek, Rutten, B P F, Guloksuz, S, Boks, M, van Os, J, Luykx, J J, and van Winkel, R
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- 2022
13. Genetic and psychosocial stressors have independent effects on the level of subclinical psychosis: findings from the multinational EU-GEI study
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Pignon, B., primary, Peyre, H., additional, Ayrolles, A., additional, Kirkbride, J. B., additional, Jamain, S., additional, Ferchiou, A., additional, Richard, J. R., additional, Baudin, G., additional, Tosato, S., additional, Jongsma, H., additional, de Haan, L., additional, Tarricone, I., additional, Bernardo, M., additional, Velthorst, E., additional, Braca, M., additional, Arango, C., additional, Arrojo, M., additional, Bobes, J., additional, Del-Ben, C. M., additional, Di Forti, M., additional, Gayer-Anderson, C., additional, Jones, P. B., additional, La Cascia, C., additional, Lasalvia, A., additional, Menezes, P. R., additional, Quattrone, D., additional, Sanjuán, J., additional, Selten, J. P., additional, Tortelli, A., additional, Llorca, P. M., additional, van Os, J., additional, Rutten, B. P. F., additional, Murray, R. M., additional, Morgan, C., additional, Leboyer, M., additional, Szöke, A., additional, and Schürhoff, F., additional
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- 2022
- Full Text
- View/download PDF
14. An environmental analysis of genes associated with schizophrenia: hypoxia and vascular factors as interacting elements in the neurodevelopmental model
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Schmidt-Kastner, R, van Os, J, Esquivel, G, Steinbusch, H W M, and Rutten, B P F
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- 2012
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15. The association between genome-wide polymorphisms and chronic postoperative pain: a prospective observational study
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van Reij, R. R., Hoofwijk, D. M. N., Rutten, B. P. F., Weinhold, L., Leber, M., Joosten, E. A. J., Ramirez, A., van den Hoogen, N. J., Allegri, M., Bassoricci, E., Bettinelli, S., Bugada, D., Cedrati, V. L. E., Cappelleri, G., Compagnone, C., De Gregori, M., Fumagalli, R., Grimaldi, S., Mantelli, M., Molinaro, M., Zorzetto, M., Anesthesiologie, RS: MHeNs - R3 - Neuroscience, MUMC+: MA Psychiatrie (3), Psychiatrie & Neuropsychologie, and MUMC+: MA Anesthesiologie (9)
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EXPRESSION ,medicine.medical_specialty ,GENES ,SURGERY ,medicine.medical_treatment ,LOCI ,Genome-wide association study ,Polymorphism, Single Nucleotide ,Quality of life ,Internal medicine ,IMPUTATION ,Medicine ,Humans ,risk factors ,Prospective Studies ,CHRONIC POSTSURGICAL PAIN ,Genetic association ,Aged ,genome‐wide association study ,Pain, Postoperative ,Hysterectomy ,genome-wide association study ,business.industry ,Chronic pain ,Articles ,Middle Aged ,medicine.disease ,NERVOUS-SYSTEM ,Advances in Peri‐operative Care ,PREVALENCE ,Anesthesiology and Pain Medicine ,DISEASES ,Cohort ,RISK-FACTORS ,Observational study ,Female ,Original Article ,business ,chronic pain ,Abdominal surgery ,Follow-Up Studies - Abstract
Summary Chronic postoperative pain is common and can have a negative impact on quality of life. Recent studies show that genetic risk factors are likely to play a role, although only gene‐targeted analysis has been used to date. This is the first genome‐wide association study to identify single‐nucleotide polymorphisms associated with the development of chronic postoperative pain based on two independent cohorts. In a discovery cohort, 330 women scheduled for hysterectomy were genotyped. A case–control association analysis compared patients without chronic postoperative pain and the 34 who had severe chronic postoperative pain 3 months after surgery. No single‐nucleotide polymorphisms reached genome‐wide significance, but several showed suggestive associations with chronic postoperative pain (p
- Published
- 2020
16. The association between genome-wide polymorphisms and chronic postoperative pain: a prospective observational study
- Author
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van Reij, R. R., I, Hoofwijk, D. M. N., Rutten, B. P. F., Weinhold, L., Leber, M., Joosten, E. A. J., Ramirez, A., van den Hoogen, N. J., Allegri, M., Bassoricci, E., Bettinelli, S., Bugada, D., Cedrati, V. L. E., Cappelleri, G., Compagnone, C., De Gregori, M., Fumagalli, R., Grimaldi, S., Mantelli, M., Molinaro, M., Zorzetto, M., van Reij, R. R., I, Hoofwijk, D. M. N., Rutten, B. P. F., Weinhold, L., Leber, M., Joosten, E. A. J., Ramirez, A., van den Hoogen, N. J., Allegri, M., Bassoricci, E., Bettinelli, S., Bugada, D., Cedrati, V. L. E., Cappelleri, G., Compagnone, C., De Gregori, M., Fumagalli, R., Grimaldi, S., Mantelli, M., Molinaro, M., and Zorzetto, M.
- Abstract
Chronic postoperative pain is common and can have a negative impact on quality of life. Recent studies show that genetic risk factors are likely to play a role, although only gene-targeted analysis has been used to date. This is the first genome-wide association study to identify single-nucleotide polymorphisms associated with the development of chronic postoperative pain based on two independent cohorts. In a discovery cohort, 330 women scheduled for hysterectomy were genotyped. A case-control association analysis compared patients without chronic postoperative pain and the 34 who had severe chronic postoperative pain 3 months after surgery. No single-nucleotide polymorphisms reached genome-wide significance, but several showed suggestive associations with chronic postoperative pain (p < 1 x 10(-5)). Single-nucleotide polymorphisms with significance p NAV3 was significantly replicated with chronic postoperative pain in the replication cohort (p = 0.009). Meta-analysis revealed that two loci (IQGAP1 and CRTC3) were significantly associated with chronic postoperative pain at 3 months (IQGAP1 p = 3.93 x 10(-6) beta = 2.3863, CRTC3 p = 2.26 x 10(-6), beta = 2.4209). The present genome-wide association study provides initial evidence for genetic risk factors of chronic postoperative pain and supports follow-up studies.
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- 2020
17. Polygenic liability for schizophrenia and childhood adversity influences daily-life emotion dysregulation and psychosis proneness
- Author
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TN groep Adan, Neurogenetica, Brain, Hersenen-Medisch 1, Pries, L-K, Klingenberg, B, Menne-Lothmann, C, Decoster, J, van Winkel, R, Collip, D, Delespaul, P, De Hert, M, Derom, C, Thiery, E, Jacobs, N, Wichers, M, Cinar, O, Lin, B D, Luykx, J J, Rutten, B P F, van Os, J, Guloksuz, S, TN groep Adan, Neurogenetica, Brain, Hersenen-Medisch 1, Pries, L-K, Klingenberg, B, Menne-Lothmann, C, Decoster, J, van Winkel, R, Collip, D, Delespaul, P, De Hert, M, Derom, C, Thiery, E, Jacobs, N, Wichers, M, Cinar, O, Lin, B D, Luykx, J J, Rutten, B P F, van Os, J, and Guloksuz, S
- Published
- 2020
18. Genetic vulnerability to DUSP22 promoter hypermethylation is involved in the relation between in utero famine exposure and schizophrenia
- Author
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Boks, M P, Houtepen, L C, Xu, Z, He, Y, Ursini, G, Maihofer, A X, Rajarajan, P, Yu, Q, Xu, H, Wu, Y, Wang, S, Shi, J P, Hulshoff Pol, H E, Strengman, E, Rutten, B P F, Jaffe, A E, Kleinman, J E, Baker, D G, Hol, E M, Akbarian, S, Nievergelt, C M, De Witte, L D, Vinkers, C H, Weinberger, D R, Yu, J, Kahn, R S, Boks, M P, Houtepen, L C, Xu, Z, He, Y, Ursini, G, Maihofer, A X, Rajarajan, P, Yu, Q, Xu, H, Wu, Y, Wang, S, Shi, J P, Hulshoff Pol, H E, Strengman, E, Rutten, B P F, Jaffe, A E, Kleinman, J E, Baker, D G, Hol, E M, Akbarian, S, Nievergelt, C M, De Witte, L D, Vinkers, C H, Weinberger, D R, Yu, J, and Kahn, R S
- Published
- 2018
19. Transgenerational Epigenetics of Traumatic Stress
- Author
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Rutten, Bart P F; https://orcid.org/0000-0002-9834-6346, Rutten, B P F ( Bart P F ), Jawaid, Ali; https://orcid.org/0000-0002-5126-6744, Roszkowski, Martin; https://orcid.org/0000-0002-8896-5514, Mansuy, Isabelle M; https://orcid.org/0000-0001-7785-5371, Rutten, Bart P F; https://orcid.org/0000-0002-9834-6346, Rutten, B P F ( Bart P F ), Jawaid, Ali; https://orcid.org/0000-0002-5126-6744, Roszkowski, Martin; https://orcid.org/0000-0002-8896-5514, and Mansuy, Isabelle M; https://orcid.org/0000-0001-7785-5371
- Abstract
Traumatic stress is a type of environmental experience that can modify behavior, cognition and physiological functions such as metabolism, in mammals. Many of the effects of traumatic stress can be transmitted to subsequent generations even when individuals from these generations are not exposed to any traumatic stressor. This book chapter discusses the concept of epigenetic/non-genomic inheritance of such traits involving the germline in mammals. It includes a comprehensive review of animal and human studies on inter- and transgenerational inheritance of the effects of traumatic stress, some of the epigenetic changes in the germline currently known to be associated with traumatic stress, and possible mechanisms for their induction and maintenance during development and adulthood. We also describe some experimental interventions that attempted to prevent the transmission of these effects, and consider the evolutionary importance of transgenerational inheritance and future outlook of the field.
- Published
- 2018
20. Genetic vulnerability to DUSP22 promoter hypermethylation is involved in the relation between in utero famine exposure and schizophrenia
- Author
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Onderzoeksgroep 2, Brain, Onderzoeksgroep 11, Affectieve & Psychotische Med., Onderzoeksgroep 1, Pathologie, TN groep Hol, Onderzoeksgroep 5, Psychiatrie_Medisch, Boks, M P, Houtepen, L C, Xu, Z, He, Y, Ursini, G, Maihofer, A X, Rajarajan, P, Yu, Q, Xu, H, Wu, Y, Wang, S, Shi, J P, Hulshoff Pol, H E, Strengman, E, Rutten, B P F, Jaffe, A E, Kleinman, J E, Baker, D G, Hol, E M, Akbarian, S, Nievergelt, C M, De Witte, L D, Vinkers, C H, Weinberger, D R, Yu, J, Kahn, R S, Onderzoeksgroep 2, Brain, Onderzoeksgroep 11, Affectieve & Psychotische Med., Onderzoeksgroep 1, Pathologie, TN groep Hol, Onderzoeksgroep 5, Psychiatrie_Medisch, Boks, M P, Houtepen, L C, Xu, Z, He, Y, Ursini, G, Maihofer, A X, Rajarajan, P, Yu, Q, Xu, H, Wu, Y, Wang, S, Shi, J P, Hulshoff Pol, H E, Strengman, E, Rutten, B P F, Jaffe, A E, Kleinman, J E, Baker, D G, Hol, E M, Akbarian, S, Nievergelt, C M, De Witte, L D, Vinkers, C H, Weinberger, D R, Yu, J, and Kahn, R S
- Published
- 2018
21. Longitudinal changes in glucocorticoid receptor exon 1F methylation and psychopathology after military deployment
- Author
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Schür, R R, primary, Boks, M P, additional, Rutten, B P F, additional, Daskalakis, N P, additional, de Nijs, L, additional, van Zuiden, M, additional, Kavelaars, A, additional, Heijnen, C J, additional, Joëls, M, additional, Kahn, R S, additional, Geuze, E, additional, Vermetten, E, additional, and Vinkers, C H, additional
- Published
- 2017
- Full Text
- View/download PDF
22. Longitudinal analyses of the DNA methylome in deployed military servicemen identify susceptibility loci for post-traumatic stress disorder
- Author
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Rutten, B P F, primary, Vermetten, E, additional, Vinkers, C H, additional, Ursini, G, additional, Daskalakis, N P, additional, Pishva, E, additional, de Nijs, L, additional, Houtepen, L C, additional, Eijssen, L, additional, Jaffe, A E, additional, Kenis, G, additional, Viechtbauer, W, additional, van den Hove, D, additional, Schraut, K G, additional, Lesch, K-P, additional, Kleinman, J E, additional, Hyde, T M, additional, Weinberger, D R, additional, Schalkwyk, L, additional, Lunnon, K, additional, Mill, J, additional, Cohen, H, additional, Yehuda, R, additional, Baker, D G, additional, Maihofer, A X, additional, Nievergelt, C M, additional, Geuze, E, additional, and Boks, M P M, additional
- Published
- 2017
- Full Text
- View/download PDF
23. Epigenetic dysregulation of brainstem nuclei in the pathogenesis of Alzheimer’s disease: looking in the correct place at the right time?
- Author
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Iatrou, A., primary, Kenis, G., additional, Rutten, B. P. F., additional, Lunnon, K., additional, and van den Hove, D. L. A., additional
- Published
- 2016
- Full Text
- View/download PDF
24. Stagering van psychotische stoornissen
- Author
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de Haan, L., Klaassen, R., van Beveren, N., Wunderink, L., Rutten, B. P. F., van Os, J., Amsterdam Neuroscience, and Adult Psychiatry
- Abstract
In psychotic disorders it is the stage of development of the disease which mainly determines the prognosis and the effectiveness of treatment. To describe and to refine the current staging and profiling of psychotic disorders and to propose a way in which to describe the course of dimensions of psychoses. We searched the literature for articles relating to the staging of psychotic disorders. McGorry e.a. developed a simple classification into stages which is currently applicable to research and clinical practice. We propose a further refinement in the form of a graph from which one can see in a glance the history of clinically relevant variation. Research into the prodromal stages of diseases is needed in order to elucidate the pathophysiological mechanisms that the stages have in common and to reveal the pathways of differential development
- Published
- 2012
25. Longitudinal analyses of the DNA methylome in deployed military servicemen identify susceptibility loci for post-traumatic stress disorder
- Author
-
Rutten, B P F, Vermetten, E, Vinkers, C H, Ursini, G, Daskalakis, N P, Pishva, E, de Nijs, L, Houtepen, L C, Eijssen, L, Jaffe, A E, Kenis, G, Viechtbauer, W, van den Hove, D, Schraut, K G, Lesch, K-P, Kleinman, J E, Hyde, T M, Weinberger, D R, Schalkwyk, L, Lunnon, K, Mill, J, Cohen, H, Yehuda, R, Baker, D G, Maihofer, A X, Nievergelt, C M, Geuze, E, and Boks, M P M
- Abstract
In order to determine the impact of the epigenetic response to traumatic stress on post-traumatic stress disorder (PTSD), this study examined longitudinal changes of genome-wide blood DNA methylation profiles in relation to the development of PTSD symptoms in two prospective military cohorts (one discovery and one replication data set). In the first cohort consisting of male Dutch military servicemen (n=93), the emergence of PTSD symptoms over a deployment period to a combat zone was significantly associated with alterations in DNA methylation levels at 17 genomic positions and 12 genomic regions. Evidence for mediation of the relation between combat trauma and PTSD symptoms by longitudinal changes in DNA methylation was observed at several positions and regions. Bioinformatic analyses of the reported associations identified significant enrichment in several pathways relevant for symptoms of PTSD. Targeted analyses of the significant findings from the discovery sample in an independent prospective cohort of male US marines (n=98) replicated the observed relation between decreases in DNA methylation levels and PTSD symptoms at genomic regions in ZFP57, RNF39 and HIST1H2APS2. Together, our study pinpoints three novel genomic regions where longitudinal decreases in DNA methylation across the period of exposure to combat trauma marks susceptibility for PTSD.
- Published
- 2018
- Full Text
- View/download PDF
26. Gene-Environment Interaction Research and Transgenic Mouse Models of Alzheimer's Disease
- Author
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Chouliaras, L., primary, Sierksma, A. S. R., additional, Kenis, G., additional, Prickaerts, J., additional, Lemmens, M. A. M., additional, Brasnjevic, I., additional, van Donkelaar, E. L., additional, Martinez-Martinez, P., additional, Losen, M., additional, De Baets, M. H., additional, Kholod, N., additional, van Leeuwen, F., additional, Hof, P. R., additional, van Os, J., additional, Steinbusch, H. W. M., additional, van den Hove, D. L. A., additional, and Rutten, B. P. F., additional
- Published
- 2010
- Full Text
- View/download PDF
27. Epigenetic Mediation of Environmental Influences in Major Psychotic Disorders
- Author
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Rutten, B. P. F., primary and Mill, J., additional
- Published
- 2009
- Full Text
- View/download PDF
28. Examining the independent and joint effects of genomic and exposomic liabilities for schizophrenia across the psychosis spectrum
- Author
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Pries, L.-K., Dal Ferro, G. A., van Os, J., Delespaul, P., Kenis, G., Lin, B. D., Luykx, J. J., Richards, A. L., Akdede, B., Binbay, T., Altınyazar, V., Yalınçetin, B., Gümüş-Akay, G., Cihan, B., Soygür, H., Ulaş, H., Şahin Cankurtaran, E., Ulusoy Kaymak, S., Mihaljevic, M. M., Andric Petrovic, S., Mirjanic, T., Bernardo, M., Mezquida, G., Amoretti, S., Bobes, J., Saiz, P. A., García-Portilla, M. Paz, Sanjuan, J., Aguilar, E. J., Santos, J. L., Jiménez-López, E., Arrojo, M., Carracedo, A., López, G., González-Peñas, J., Parellada, M., Maric, N. P., Atbaşoğlu, C., Ucok, A., Alptekin, K., Can Saka, M., Arango, C., O'Donovan, M., Tosato, S., Rutten, B. P. F., and Guloksuz, S.
- Abstract
AbstractAimsPsychosis spectrum disorder has a complex pathoetiology characterised by interacting environmental and genetic vulnerabilities. The present study aims to investigate the role of gene–environment interaction using aggregate scores of genetic (polygenic risk score for schizophrenia (PRS-SCZ)) and environment liability for schizophrenia (exposome score for schizophrenia (ES-SCZ)) across the psychosis continuum.MethodsThe sample consisted of 1699 patients, 1753 unaffected siblings, and 1542 healthy comparison participants. The Structured Interview for Schizotypy-Revised (SIS-R) was administered to analyse scores of total, positive, and negative schizotypy in siblings and healthy comparison participants. The PRS-SCZ was trained using the Psychiatric Genomics Consortiums results and the ES-SCZ was calculated guided by the approach validated in a previous report in the current data set. Regression models were applied to test the independent and joint effects of PRS-SCZ and ES-SCZ (adjusted for age, sex, and ancestry using 10 principal components).ResultsBoth genetic and environmental vulnerability were associated with case-control status. Furthermore, there was evidence for additive interaction between binary modes of PRS-SCZ and ES-SCZ (above 75% of the control distribution) increasing the odds for schizophrenia spectrum diagnosis (relative excess risk due to interaction = 6.79, [95% confidential interval (CI) 3.32, 10.26], p< 0.001). Sensitivity analyses using continuous PRS-SCZ and ES-SCZ confirmed gene–environment interaction (relative excess risk due to interaction = 1.80 [95% CI 1.01, 3.32], p= 0.004). In siblings and healthy comparison participants, PRS-SCZ and ES-SCZ were associated with all SIS-R dimensions and evidence was found for an interaction between PRS-SCZ and ES-SCZ on the total (B= 0.006 [95% CI 0.003, 0.009], p< 0.001), positive (B= 0.006 [95% CI, 0.002, 0.009], p= 0.002), and negative (B= 0.006, [95% CI 0.004, 0.009], p< 0.001) schizotypy dimensions.ConclusionsThe interplay between exposome load and schizophrenia genetic liability contributing to psychosis across the spectrum of expression provide further empirical support to the notion of aetiological continuity underlying an extended psychosis phenotype.
- Published
- 2020
- Full Text
- View/download PDF
29. Genetic and psychosocial stressors have independent effects on the level of subclinical psychosis: findings from the multinational EU-GEI study
- Author
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B. Pignon, H. Peyre, A. Ayrolles, J. B. Kirkbride, S. Jamain, A. Ferchiou, J. R. Richard, G. Baudin, S. Tosato, H. Jongsma, L. de Haan, I. Tarricone, M. Bernardo, E. Velthorst, M. Braca, C. Arango, M. Arrojo, J. Bobes, C. M. Del-Ben, M. Di Forti, C. Gayer-Anderson, P. B. Jones, C. La Cascia, A. Lasalvia, P. R. Menezes, D. Quattrone, J. Sanjuán, J. P. Selten, A. Tortelli, P. M. Llorca, J. van Os, B. P. F. Rutten, R. M. Murray, C. Morgan, M. Leboyer, A. Szöke, F. Schürhoff, Pignon B., Peyre H., Ayrolles A., Kirkbride J.B., Jamain S., Ferchiou A., Richard J.R., Baudin G., Tosato S., Jongsma H., de Haan L., Tarricone I., Bernardo M., Velthorst E., Braca M., Arango C., Arrojo M., Bobes J., Del-Ben C.M., Di Forti M., Gayer-Anderson C., Jones P.B., La Cascia C., Lasalvia A., Menezes P.R., Quattrone D., Sanjuan J., Selten J.P., Tortelli A., Llorca P.M., van Os J., Rutten B.P.F., Murray R.M., Morgan C., Leboyer M., Szoke A., Schurhoff F., Pignon, B [0000-0003-0526-3136], Ayrolles, A [0000-0002-3202-0781], Kirkbride, JB [0000-0003-3401-0824], Tosato, S [0000-0002-9665-7538], Lasalvia, A [0000-0001-9963-6081], Morgan, C [0000-0002-1386-2369], Apollo - University of Cambridge Repository, Pignon, B, Peyre, H, Ayrolles, A, Kirkbride, J B, Jamain, S, Ferchiou, A, Richard, J R, Baudin, G, Tosato, S, Jongsma, H, de Haan, L, Tarricone, I, Bernardo, M, Velthorst, E, Braca, M, Arango, C, Arrojo, M, Bobes, J, Del-Ben, C M, Di Forti, M, Gayer-Anderson, C, Jones, P B, La Cascia, C, Lasalvia, A, Menezes, P R, Quattrone, D, Sanjuán, J, Selten, J P, Tortelli, A, Llorca, P M, van Os, J, Rutten, B P F, Murray, R M, Morgan, C, Leboyer, M, Szöke, A, Schürhoff, F, Adult Psychiatry, APH - Mental Health, ANS - Complex Trait Genetics, ANS - Mood, Anxiety, Psychosis, Stress & Sleep, Psychiatrie & Neuropsychologie, RS: MHeNs - R2 - Mental Health, MUMC+: Hersen en Zenuw Centrum (3), MUMC+: VPK Flexteam IC (9), MUMC+: MA Psychiatrie (3), and RS: MHeNs - R3 - Neuroscience
- Subjects
Schizophrenia/genetics ,Environmental effects on human beings ,Risk factors in diseases ,Epidemiology ,Psicosi ,psychosi ,Pathological psychology ,Genes × environment interaction ,Risk Factors ,Settore MED/48 -Scienze Infermierist. e Tecn. Neuro-Psichiatriche e Riabilitat ,psychosocial stressors ,Humans ,psychosis ,Psychotic Disorders/genetics ,Settore MED/25 - Psichiatria ,Influència del medi ambient en l'home ,Genètica de la conducta ,Factors de risc en les malalties ,Genes × environment interactions ,Public Health, Environmental and Occupational Health ,Psychoses ,polygenic risk score for schizophrenia ,Psicopatologia ,Psychiatry and Mental health ,Psychotic Disorders ,Behavior genetics ,Schizophrenia ,Esquizofrènia ,Gene-Environment Interaction - Abstract
the Spanish Ministry of Science and Innovation. Instituto de Salud Carlos III (SAM16PE07CP1, PI16/02012, PI19/024), co-financed by ERDF Funds from the European Commission, ‘A way of making Europe’, CIBERSAM. Madrid Regional Government (B2017/BMD-3740 AGES-CM-2), European Union Structural Funds. European Union Seventh Framework Program under grant agreements FP7-4-HEALTH-2009-2.2.1-2-241909 (Project EU-GEI) and FP7-HEALTH-2013-2.2.1-2-603196 (Project PSYSCAN); and European Union H2020 Program under the Innovative Medicines Initiative 2 Joint Undertaking (grant agreement No 115916, Project PRISM, and grant agreement No 777394, Project AIMS-2-TRIALS) (...), Pignon B, Peyre H, Ayrolles A, Kirkbride JB, Jamain S, Ferchiou A, Richard JR, Baudin G, Tosato S, Jongsma H, de Haan L, Tarricone I, Bernardo M, Velthorst E, Braca M, Arango C, Arrojo M, Bobes J, Del-Ben CM, Di Forti M, Gayer-Anderson C, Jones PB, La Cascia C, Lasalvia A, Menezes PR, Quattrone D, Sanjuán J, Selten JP, Tortelli A, Llorca PM, van Os J, Rutten BPF, Murray RM, Morgan C, Leboyer M, Szöke A, Schürhoff F
- Published
- 2022
- Full Text
- View/download PDF
30. [Linguistic distance and psychosis in ethnic minorities].
- Author
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Jongsma HE, van der Ven EMA, Velthorst E, de Haan L, Rutten BPF, and van Os J
- Subjects
- Humans, Case-Control Studies, Ethnicity, Netherlands, Ethnic and Racial Minorities, Psychotic Disorders
- Abstract
Background: Ethnic minorities in the Netherlands face an excess psychosis risk, and understanding of causality remains limited. Linguistic disadvantage and other indicators of societal exclusion might play a role, and offer potential targets for public health interventions., Aim: To establish the contribution of linguistic disadvantage, indicators of social distance and perceived discrimination to the increased risk of psychoses in migrants and ethnic minorities., Methods: We used the Dutch data from an international case-control study into psychotic disorders (the EU-GEI study). A first episode of psychosis was our outcome variable, and we used well-defined data on established confounders (e.g. age and sex) and indicators of ethnicity, social distance, linguistic disadvantage and perceived discrimination as our predictor variables., Results: Ethnic minorities face an increased psychosis risk. This appears to be the case for both first- and second- generation migrants and so-called ‘Western’ and non-Western migrants. Though confounders and social distance appear to contribute, linguistic disadvantage appears to play a role in the excess psychosis risk in first-generation migrants., Conclusion: Reducing the social consequences of linguistic disadvantage or social distance might be a starting point for concrete public health interventions aimed at preventing the increased psychosis risk faced by first-generation migrants.
- Published
- 2023
31. [Zorgvraagtypering met de HoNOS+: kijken in een glazen bol?]
- Author
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Bremer-Hoeve S, de Groot E, van Wel EB, Rutten BPF, and van Bronswijk SC
- Published
- 2022
32. [Interplay between genetic background and environmental factors in psychiatry: current situation and future prospects].
- Author
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Rutten BPF, Guloksuz S, Boks M, van Os J, Luykx JJ, and van Winkel R
- Subjects
- Humans, Mental Disorders genetics, Environment, Genetic Background, Psychiatry methods
- Abstract
Background: The hypothesis that etiopathogeneses of psychiatric disorders are determined by interplay between genetic background and environmental factors, as well their interactions can increasingly be put to direct scientific test, based on a wave of methodological, technological and knowledge developments.
AIM: To provide insight into and to provide perspective on some important scientific developments and facilitate challenges in this area.
METHOD: Narrative overview of the scientific literature and formulation of a concept and future perspective.
RESULTS: The overview points to concrete progress in the fields of genetic epidemiology, environmental analyses, gene-environment interactions and epigenetics in psychiatry. For example, recent studies have provided evidence for the existence of interactions and correlations between genetic and environmental factors, interdependence of risk-influencing effects of environmental factors, and translational neurobiological studies have identified biological processes that influence the impact of (or the response to) environmental influences on individuals mediate. These important steps to translate epidemiological research into testable biological hypotheses are facilitated by new techniques and the availability of large and relevant clinical and biological datasets.
CONCLUSION: Scientific progress on the interplay between genetic background and environmental factors enriches the conceptual framework of the etiopathogenesis of mental disorders and provides a future perspective in which we are likely to receive answers to a number of clinically relevant questions in the coming decade.
.- Published
- 2022
33. Longitudinal changes in glucocorticoid receptor exon 1 F methylation and psychopathology after military deployment.
- Author
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Schür RR, Boks MP, Rutten BPF, Daskalakis NP, de Nijs L, van Zuiden M, Kavelaars A, Heijnen CJ, Joëls M, Kahn RS, Geuze E, Vermetten E, and Vinkers CH
- Subjects
- Adolescent, Adult, Afghan Campaign 2001-, Epigenesis, Genetic, Exons, Humans, Longitudinal Studies, Male, Mental Health, Middle Aged, Military Personnel, Prospective Studies, Psychiatric Status Rating Scales, Stress Disorders, Post-Traumatic genetics, Stress, Psychological, Young Adult, DNA Methylation, Exposure to Violence, Mental Disorders genetics, Receptors, Glucocorticoid genetics
- Abstract
Several cross-sectional studies have demonstrated the relevance of DNA methylation of the glucocorticoid receptor exon 1
F region (GR-1F ) for trauma-related psychopathology. We conducted a longitudinal study to examine GR-1F methylation changes over time in relation to trauma exposure and the development of post-deployment psychopathology. GR-1F methylation (52 loci) was quantified using pyrosequencing in whole blood of 92 military men 1 month before and 6 months after a 4-month deployment period to Afghanistan. GR-1F methylation overall (mean methylation and the number of methylated loci) and functional methylation (methylation at loci associated with GR exon 1F expression) measures were examined. We first investigated the effect of exposure to potentially traumatic events during deployment on these measures. Subsequently, changes in GR-1F methylation were related to changes in mental health problems (total Symptom Checklist-90 score) and posttraumatic stress disorder (PTSD) symptoms (Self-Report Inventory for PTSD). Trauma exposure during deployment was associated with an increase in all methylation measures, but development of mental health problems 6 months after deployment was only significantly associated with an increased functional methylation. Emergence of post-deployment PTSD symptoms was not related to increased functional methylation over time. Pre-deployment methylation levels did not predict post-deployment psychopathology. To our knowledge, this is the first study to prospectively demonstrate trauma-related increases in GR-1F methylation, and it shows that only increases at specific functionally relevant sites predispose for post-deployment psychopathology.- Published
- 2017
- Full Text
- View/download PDF
34. [Auto-immune disorders as a possible cause of neuropsychiatric syndromes].
- Author
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Martinez-Martinez P, Molenaar PC, Losen M, Hoffmann C, Stevens J, de Witte LD, van Amelsvoort T, van Os J, and Rutten BP
- Subjects
- Humans, Mental Disorders metabolism, Nervous System Diseases metabolism, Nervous System Diseases physiopathology, Potassium Channels, Voltage-Gated immunology, Antibodies metabolism, Autoimmune Diseases psychology, Mental Disorders immunology, Nervous System Diseases immunology
- Abstract
Background: Changes that occur in the behaviour of voltage-gated ion channels and ligand-gated receptor channels due to gene mutations or auto-immune attack are the cause of channelopathies in the central and peripheral nervous system. Although the relation between molecular channel defects and clinical symptoms has been explained in the case of many neuromuscular channelopathies, the pathophysiology of auto-immunity in neuropsychiatric syndromes is still unclear., Aim: To review recent findings regarding neuronal auto-immune reactions in severe neuropsychiatric syndromes., Method: Using PubMed, we consulted the literature published between 1990 and August 2014 relating to the occurrence of auto-immune antibodies in severe and persistent neuropsychiatric syndromes., Results: Auto-antibodies have only limited access to the central nervous system, but if they do enter the system they can, in some cases, cause disease. We discuss recent findings regarding the occurrence of auto-antibodies against ligand-activated receptor channels and potassium channels in neuropsychiatric and neurological syndromes, including schizophrenia and limbic encephalitis., Conclusion: Although the occurrence of several auto-antibodies in schizophrenia has been confirmed, there is still no proof of a causal relationship in the syndrome. We still have no evidence of the prevalence of auto-immunity in neuropsychiatric syndromes. The discovery that an antibody against an ion channel is associated with some neuropsychiatric disorders may mean that in future it will be possible to treat patients by means of immunosuppression, which could lead to an improvement in a patient's cognitive abilities.
- Published
- 2015
35. [Body dysmorphic disorder in cosmetic surgery - prevalence, psychiatric comorbidity and outcome].
- Author
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Hundscheid T, van der Hulst RR, Rutten BP, and Leue C
- Subjects
- Body Dysmorphic Disorders diagnosis, Body Dysmorphic Disorders epidemiology, Comorbidity, Humans, Patient Satisfaction, Prevalence, Body Dysmorphic Disorders psychology, Body Dysmorphic Disorders surgery, Surgery, Plastic
- Abstract
Background: Patients suffering from body dysmorphic disorder (bdd) are preoccupied with a slight or imagined defect in appearance., Aim: First of all, to review the literature on the prevalence of bdd in cosmetic surgery and thereafter to review the literature on psychiatric comorbidity and the outcome of surgical interventions., Method: We based our search strategy on Embase, Medline and PubMed, using the search terms 'body dysmorphic disorder', 'cosmetic surgery', 'prevalence', 'comorbidity' and 'outcome'. Our search covered English and Dutch literature published after the introduction of bdd in dsm-iii-r and before 1 November, 2013. A study of the relevant articles enabled us to access additional articles mentioned in these texts., Results: Our initial search strategy turned out to be too narrow. It was therefore broadened to include 'body dysmorphic disorder', 'cosmetic surgery', and 'prevalence'. Eventually we included 23 original articles. In 11 of these the prevalence of bdd varied from 3.2 to 53.6%. Twelve articles on psychiatric comorbidity revealed predominantly mood and anxiety disorders on axis I and cluster C personality disorders on axis II. Only two studies reported on the outcome of cosmetic surgery performed on bdd patients; surgical interventions, however, seemed to result in new preoccupations with the prolongation of psychiatric comorbidity., Conclusion: bdd is a common psychiatric disorder that can sometimes lead to cosmetic surgery. However, pre-operative screening of bdd patients is vital so that efficient psychiatric treatment can be initiated and patients are not subjected to surgical interventions which may be ineffective or even harmful.
- Published
- 2014
36. [Psychotic disorders: the need for staging].
- Author
-
de Haan L, Klaassen R, van Beveren N, Wunderink L, Rutten BP, and van Os J
- Subjects
- Disease Progression, Early Diagnosis, Humans, Prognosis, Psychotic Disorders therapy, Treatment Outcome, Psychotic Disorders classification, Psychotic Disorders diagnosis
- Abstract
Background: In psychotic disorders it is the stage of development of the disease which mainly determines the prognosis and the effectiveness of treatment., Aim: To describe and to refine the current staging and profiling of psychotic disorders and to propose a way in which to describe the course of dimensions of psychoses., Method: We searched the literature for articles relating to the staging of psychotic disorders., Results: McGorry e.a. developed a simple classification into stages which is currently applicable to research and clinical practice. We propose a further refinement in the form of a graph from which one can see in a glance the history of clinically relevant variation., Conclusion: Research into the prodromal stages of diseases is needed in order to elucidate the pathophysiological mechanisms that the stages have in common and to reveal the pathways of differential development.
- Published
- 2012
37. Erratum: gene-environment interaction research and transgenic mouse models of Alzheimer's disease.
- Author
-
Chouliaras L, Sierksma AS, Kenis G, Prickaerts J, Lemmens MA, Brasnjevic I, van Donkelaar EL, Martinez-Martinez P, Losen M, De Baets MH, Kholod N, van Leeuwen FW, Hof PR, van Os J, Steinbusch HW, van den Hove DL, and Rutten BP
- Published
- 2011
- Full Text
- View/download PDF
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