Search

Your search keyword '"Zitman, F"' showing total 428 results
Start Over Author "Zitman, F"
428 results on '"Zitman, F"'

2. Utility of the Brief Symptom Inventory (BSI) in Psychiatric Outpatients with Intellectual Disabilities

Author

Wieland, J., Wardenaar, K. J., Fontein, E., and Zitman, F. G.

Abstract

Background: Diagnostics and care for people with intellectual disabilities (ID) and psychiatric disorders need to be improved. This can be done by using assessment instruments to routinely measure the nature and severity of psychiatric symptoms. Up until now, in the Netherlands, assessment measures are seldom used in the psychiatric care for this population. The objective of the present paper is to evaluate the use of the Brief Symptom Inventory (BSI), a widely used standardised questionnaire in general psychiatry, in a well-defined sample of people with borderline intellectual functioning or mild ID diagnosed with one or more psychiatric disorders. Methods: A total of 224 psychiatric outpatients with either borderline intellectual functioning or mild ID participated in this study. All participants were new patients of Kristal, Centre for Psychiatry and Intellectual Disability in the Netherlands, in the period between 1 April 2008 and 1 October 2009. All participants were assessed by a multidisciplinary team, including a certified psychiatrist. Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) criteria were applied. The mean total intelligence quotient was measured with the Wechsler Adult Intelligence Scale (WAIS-III). The BSI was administered in an assisted fashion. Utility and psychometric properties of the BSI were investigated. Internal consistency coefficients (Cronbach's alphas) were computed. Bivariate correlations between the sub-scales were computed to assess differentiation between the scales. Mean sub-scale scores were compared between different DSM-IV-TR subgroups to investigate the discriminant abilities of the scales. A confirmatory factor analysis was conducted. Results: The results suggest that the BSI is practically useful. Internal consistencies ranged from 0.70 to 0.96 and thus are considered good to adequate. Sub-scale inter-correlations showed there is a degree of differentiation between the sub-scales. Discriminant validity was shown for the sub-scales "depression," "anxiety" and "phobic anxiety." Confirmatory factor analysis showed that the underlying structure of the BSI could be described by the same nine-factor model as reported in previous studies. Conclusions: As a result of the psychometric properties illustrated, this study supports the use of the BSI as a screener for psychopathology and a general outcome measure in people with ID. (Contains 3 tables and 4 figures.)

Published
2012
Full Text
View/download PDF

6. Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

Author

Sullivan, P F, de Geus, E J C, Willemsen, G, James, M R, Smit, J H, Zandbelt, T, Arolt, V, Baune, B T, Blackwood, D, Cichon, S, Coventry, W L, Domschke, K, Farmer, A, Fava, M, Gordon, S D, He, Q, Heath, A C, Heutink, P, Holsboer, F, Hoogendijk, W J, Hottenga, J J, Hu, Y, Kohli, M, Lin, D, Lucae, S, MacIntyre, D J, Maier, W, McGhee, K A, McGuffin, P, Montgomery, G W, Muir, W J, Nolen, W A, Nöthen, M M, Perlis, R H, Pirlo, K, Posthuma, D, Rietschel, M, Rizzu, P, Schosser, A, Smit, A B, Smoller, J W, Tzeng, J-Y, van Dyck, R, Verhage, M, Zitman, F G, Martin, N G, Wray, N R, Boomsma, D I, and Penninx, B W J H

Published
2009
Full Text
View/download PDF

41. Red ROM als kwaliteitsinstrument

Author

de Jong, Kim, Tiemens, Bea, Verbraak, Marc, Beekman, A. F. T., Bockting, C. L. H., Bouman, T. K., Castelein, S., van Dyck, R., Emmelkamp, P. M. G., van der Feltz-Cornelis, C. M., van der Gaag, M., Huibers, M. J. H., Hutschemaekers, G. J. M., de Keijser, A., Keijsers, G. P. J., Koekkoek, B., Korrelboom, K., van Minnen, A., van Oppen, P. C., Oudejans, S. C. C., Oude Voshaar, R. C., Schippers, G. M., Scholing, A., Spijker, J., Spinhoven, Ph., van Straten, A., Vermeiren, R. R. J. M., Zitman, F. G., Experimental Psychotherapy & Psychopathology, Clinical Cognitive Neuropsychiatry Research Program (CCNP), and Interdisciplinair Centrum voor Psychopathologie en Emotieregulatie

Published
2017

43. The association between lower educational attainment and depression owing to shared genetic effects? Results in ∼25 000 subjects: Results in ~25,000 subjects

Author

Peyrot, W. J., Lee, S. H., Milaneschi, Y., Abdellaoui, A., Byrne, E. M., Esko, T., de Geus, E. J. C., Hemani, G., Hottenga, J. J., Kloiber, S., Levinson, D. F., Lucae, S., Martin, N. G., Medland, S. E., Metspalu, A., Milani, L., Noethen, M. M., Potash, J. B., Rietschel, M., Rietveld, C. A., Ripke, S., Shi, J., Willemsen, G., Zhu, Z., Boomsma, D. I., Wray, N. R., Penninx, B. W. J. H., Lewis, C. M., Hamilton, S. P., Weissman, M. M., Breen, G., Blackwood, D. H., Cichon, S., Heath, A. C., Holsboer, F., Madden, Pamela A., McGuffin, P., Muglia, P., Pergadia, M. L., Lin, D., Müller-Myhsok, B., Steinberg, S., Grabe, H. J., Lichtenstein, P., Magnusson, P., Perlis, R. H., Preisig, M., Smoller, J. W., Stefansson, K., Uher, R., Kutalik, Z., Tansey, K. E., Teumer, A., Viktorin, A., Barnes, M. R., Bettecken, T., Binder, E. B., Breuer, R., Castro, V. M., Churchill, S. E., Coryell, W. H., Craddock, N., Craig, I. W., Czamara, D., Degenhardt, F., Farmer, A. E., Fava, M., Frank, J., Gainer, V. S., Gallagher, P. J., Gordon, S. D., Goryachev, S., Gross, M., Guipponi, M., Henders, A. K., Herms, S., Hickie, I. B., Hoefels, S., Hoogendijk, W., Iosifescu, D. V., Ising, M., Jones, I., Jones, L., Jung-Ying, T., Knowles, J. A., Kohane, I. S., Kohli, M. A., Korszun, A., Landen, M., Lawson, W. B., Lewis, G., Macintyre, D., Maier, W., Mattheisen, M., McGrath, P. J., McIntosh, A., McLean, A., Middeldorp, C. M., Middleton, L., Montgomery, G. M., Murphy, S. N., Nauck, M., Nolen, W. A., Nyholt, Dale R., O'Donovan, M., Oskarsson, H., Pedersen, N., Scheftner, W. A., Schulz, A., Schulze, T. G., Shyn, S. I., Sigurdsson, E., Slager, S. L., Smit, J. H., Stefansson, H., Steffens, M., Thorgeirsson, T., Tozzi, F., Treutlein, J., Uhr, M., van den Oord, E. J., van Grootheest, G., Völzke, H., Weilburg, J. B., Zitman, F. G., Neale, B., Daly, M., Sullivan, P. F., Agrawal, Arpana, Albrecht, Eva, Z Alizadeh, Behrooz, Allik, J. ri, Amin, Najaf, Attia, John R., Bandinelli, Stefania, Barnard, John, Bastardot, Franois, e Baumeister, Sebastian, Beauchamp, Jonathan, Benjamin, Daniel J., Benke, Kelly S., Bennett, David A., Berger, Klaus, Bielak, Lawrence F., Bierut, Laura J., Boatman, Jeffrey A., Boyle, Patricia A., Bültmann, Ute, Campbell, Harry, Cesarini, David, Chabris, Christopher F., Cherkas, Lynn, Chung, Mina K., Conley, Dalton, Cucca, Francesco, Davey-Smith, George, Davies, Gail, de Andrade, Mariza, de Jager, Philip L., de Leeuw, Christiaan, de Neve, Jan-Emmanuel, Deary, Ian J., Dedoussis, George V., Deloukas, Panos, Derringer, Jaime, Dimitriou, Maria, Eiriksdottir, Gudny, Eklund, Niina, Elderson, Martin F., Eriksson, Johan G., Evans, Daniel S., Evans, David M., Faul, Jessica D., Fehrmann, Rudolf, Ferrucci, Luigi, Fischer, Krista, Franke, Lude, Garcia, Melissa E., Gieger, Christian, Gjessing, Hkon K., Groenen, Patrick J. F., Grönberg, Henrik, Gudnason, Vilmundur, Hägg, Sara, Hall, Per, Harris, Jennifer R., Harris, Juliette M., Harris, Tamara B., Hastie, Nicholas D., Hayward, Caroline, Hernandez, Dena G., Hoffmann, Wolgang, Hofman, Adriaan, Hofman, Albert, Holle, Rolf, Holliday, Elizabeth G., Holzapfel, Christina, Iacono, William G., Ibrahim-Verbaas, Carla A., Illig, Thomas, Ingelsson, Erik, Jacobsson, Bo, Järvelin, Marjo-Riitta, Jhun, Min A., Johannesson, Magnus, Joshi, Peter K., Jugessur, Astanand, Kaakinen, Marika, Kähönen, Mika, Kanoni, Stavroula, Kaprio, Jaakkko, Kardia, Sharon L. R., Karjalainen, Juha, Kirkpatrick, Robert M., Koellinger, Philipp D., Kolcic, Ivana, Kowgier, Matthew, Kristiansson, Kati, Krueger, Robert F., Kutalik, Z. ltan, Lahti, Jari, Laibson, David, Latvala, Antti, Launer, Lenore J., Lawlor, Debbie A., Lethimäki, Terho, Li, Jingmei, Lichtenstein, Paul, Lichtner, Peter K., Liewald, David C., Lin, Peng, Lind, Penelope A., Liu, Yongmei, Lohman, Kurt, Loitfelder, Marisa, Magnusson, Patrick K. E., Mäkinen, Tomi E., Vidal, Pedro Marques, Martin, Nicolas W., Masala, Marco, McGue, Matt, McMahon, George, Meirelles, Osorio, Meyer, Michelle N., Mielck, Andreas, Miller, Michael B., Montgomery, Grant W., Mukherjee, Sutapa, Myhre, Ronny, Nuotio, Marja-Liisa, J Oldmeadow, Christopher, Oostra, Ben A., Palmer, Lyle J., Palotie, Aarno, Perola, Markus, Petrovic, Katja E., Peyser, Patricia A., Polašek, Ozren, Posthuma, Danielle, Preisig, Martin, Quaye, Lydia, Räikkönen, Katri, Raitakari, Olli T., Realo, Anu, Reinmaa, Eva, Rice, John P., Ring, Susan M., Ripatti, Samuli, Rivadeneira, Fernando, Rizzi, Thais S., Rudan, Igor, Rustichini, Aldo, Salomaa, Veikko, Sarin, Antti-Pekka, Schlessinger, David, Schmidt, Helena, Schmidt, Reinhold, Scott, Rodney J., Shakhbazov, Konstantin, Smith, Albert V., Smith, Jennifer A., Snieder, Harold, St Pourcain, Beate, Starr, John M., Sul, Jae Hoon, Surakka, Ida, Svento, Rauli, Tanaka, Toshiko, Terracciano, Antonio, Teumer, Alexander, Thurik, A. Roy, Tiemeier, Henning, Timpson, Nicholas J., Uitterlinden, André G., van der Loos, Matthijs J. H. M., van Duijn, Cornelia M., van Rooij, Frank J. A., van Wagoner, David R., Vartiainen, Erkki, Viikari, Jorma, Visscher, Peter M., Vitart, Veronique, Vollenweider, Peter K., Völzke, Henry, Vonk, Judith M., Waeber, G. rard, Weir, David R., Wellmann, J. rgen, Westra, Harm-Jan, Wichmann, H. Erich, Widen, Elisabeth, Wilson, James F., Wright, Alan F., Yang, Jian, Yu, Lei, Zhao, Wei, and Academic Medical Center

Subjects
Adult, Male, Psychiatric Status Rating Scales, Likelihood Functions, Genotype, Estonia/epidemiology, Netherlands/epidemiology, Depressive Disorder, Major/epidemiology, Middle Aged, Polymorphism, Single Nucleotide/genetics, Cohort Studies, Odds Ratio, Educational Status, Humans, Regression Analysis, Female, Gene-Environment Interaction, Genetic Association Studies, Aged
Abstract

An association between lower educational attainment (EA) and an increased risk for depression has been confirmed in various western countries. This study examines whether pleiotropic genetic effects contribute to this association. Therefore, data were analyzed from a total of 9662 major depressive disorder (MDD) cases and 14 949 controls (with no lifetime MDD diagnosis) from the Psychiatric Genomics Consortium with additional Dutch and Estonian data. The association of EA and MDD was assessed with logistic regression in 15 138 individuals indicating a significantly negative association in our sample with an odds ratio for MDD 0.78 (0.75-0.82) per standard deviation increase in EA. With data of 884 105 autosomal common single-nucleotide polymorphisms (SNPs), three methods were applied to test for pleiotropy between MDD and EA: (i) genetic profile risk scores (GPRS) derived from training data for EA (independent meta-analysis on ∼120 000 subjects) and MDD (using a 10-fold leave-one-out procedure in the current sample), (ii) bivariate genomic-relationship-matrix restricted maximum likelihood (GREML) and (iii) SNP effect concordance analysis (SECA). With these methods, we found (i) that the EA-GPRS did not predict MDD status, and MDD-GPRS did not predict EA, (ii) a weak negative genetic correlation with bivariate GREML analyses, but this correlation was not consistently significant, (iii) no evidence for concordance of MDD and EA SNP effects with SECA analysis. To conclude, our study confirms an association of lower EA and MDD risk, but this association was not because of measurable pleiotropic genetic effects, which suggests that environmental factors could be involved, for example, socioeconomic status.

Published
2015

45. The metabolic syndrome and related characteristics in major depression: inpatients and outpatients compared metabolic differences across treatment settings

Author

Luppino, F.S., Bouvy, P.F., Giltay, E.J., Penninx, B.W.J.H., Zitman, F. G., Psychiatry, EMGO - Mental health, and EMGO+ - Mental Health

Subjects
Inpatients, INSULIN-RESISTANCE, LATE-LIFE, Metabolic characteristics, BLOOD-PRESSURE, Major depressive disorder, ASSOCIATION, Metabolic syndrome, DISEASE RISK-FACTORS, BODY-MASS INDEX, SDG 3 - Good Health and Well-being, CARDIOVASCULAR-DISEASE, Outpatients, ANTIDEPRESSANT USE, ANXIETY, FOLLOW-UP
Abstract

Objective: We aimed to systematically compare patients with major depressive disorder from three different treatment settings (a primary care outpatient, a secondary care outpatient and one inpatient sample), with regard to metabolic syndrome (MetSyn) prevalences, individual MetSyn components and related metabolic variables. Method: The outpatient samples were drawn from the ongoing Netherlands Study of Depression and Anxiety (302 primary care and 445 secondary care outpatients). The inpatient sample (n=80) was recruited from five Dutch mental health hospitals. The assessments of MetSyn and related variables [waist circumference (WC), high-density lipoprotein (HDL) and low-density lipoprotein (LDL) cholesterol, triglycerides, glucose, systolic and diastolic blood pressure (SBP, DBP), body mass index (BMI), waist-hip ratio (WHR), LDL and total cholesterol (TC)] were compared using analysis of (co)variance and regression analysis, whereas medication analyses examined the extent to which clinical differences (e. g., depression severity or medication use) mediated the observed metabolic differences across setting. Results: MetSyn prevalences (26% primary, 24% secondary care and 28% inpatients) did not significantly differ (P=.71). WC, BMI, LDL cholesterol, glucose and DBP were not significantly different across settings. However, WHR, TC and triglyceride levels were higher in inpatients than in both outpatients groups, while HDL cholesterol levels and SBP were lower. There was some mediating role for tricyclic and non-selective serotonin-reuptake inhibitor antidepressant use, but overall, the mediating role of clinical differences was limited. Conclusions: Although overall MetSyn prevalences did not differ, patterns of individual MetSyn-related variables differed more markedly across depressed inpatients and outpatients. Inpatients showed more adverse WHR and serum lipid profiles, while SBP levels were lower. (C) 2014 Elsevier Inc. All rights reserved.

Published
2014
Full Text
View/download PDF

46. Clinical pharmacological meeting

Author

Lubsen, J., Tijssen, J. G. P., Sluiter, H. E., Huysmans, F. Th. H., Thien, Th. A., Koene, R. A. P., Vincent, H. H., Derkx, F. H. M., Veld, A. J. Man in 't, Boomsma, F., Schalekamp, H. A. D. H., Hoefnagels, W. H. L., Lenders, J. W. M., Thien, Th., Smits, P., van 't Laar, A., v. Wijk, L. M., Kingma, J. H., Dunselman, P. H. J. M., v. Gilst, W. H., Lie, K. I., Wesseling, H., Lohman, J. J. H. M., Hooymans, P. M., Koten, M. L. P., Verhey, M. T. J. M., Merkus, F. W. H. M., Koopmans, P., Gribnau, F., Demacker, P., Jonkman, J. H. G., Van der Boon, W. J. V., Schoenmaker, R., Holtkamp, A., Hempenius, J., Edelbroek, P. M., Linssen, A. C. G., Zitman, F. G., Rooymans, H. G. M., de Wolff, F. A., Speth, P. A. J., Linssen, P. L. M., Wessels, J. H. C., Haanen, C., Elferink, F., van der Vijgh, W. J. F., van der Poort, S. E. J. M., Vermorken, J. B., Pinedo, H. M., Sonneveld, P., Nooter, K., van den Engh, G. J., Schurgers, N., de Blaey, C. J., and Crommelin, D. J. A.

Published
1984
Full Text
View/download PDF

47. Abstracts of papers

Author

Kleinbloesem, C. H., van Brummelen, P., van de Linde, J. A., Breimer, D. D., Kerremans, A. L. M., Cremers, H. J., Rodrigues de Miranda, J. F., van Ginneken, C. A. M., Gribnau, F. W. J., Schols, M., Mooy, J., van Hooff, M., van Baak, M. A., Rahn, K. H., Soeterboek, A. M., van Thiel, M., Westra, P., Vermeer, G. A., van Rooy, H. H., Pirovano, I. M., Soudijn, W., Lohman, J. J. H. M., Hooymans, P. M., Verhey, M. T. J. M., Pluym, B. F. M., Merkus, F. W. H. M., Thijssen, H. H. W., Baars, L. G., Reijnders, M. J., Wagenvoort, J. H. T., Fieren, M. W. J. A., Goessens, W. H. F., Michel, M. F., Edelbroek, P. M., Zitman, F. G., Schreuder, J. N., Rooymans, H. G. M., de Wolff, F. A., Hekster, Ch. A., Vree, T. B., van Baak, M. A., Jennen, W. H. J., Verstappen, F. T. J., Salemans, J., Lenders, J. W. M., Fennis, J., Thien, Th., Houben, H., Binkhorst, R. A., van 't Laar, A., Koopmans, P. P., van Hees, P. A. M., Hoefnagels, W. H. L., Huysmans, F. T. M., Woittiez, A. J. J., Wenting, G. J., Derkx, F. H. M., Schalekamp, M. A. D. H., Storms, G. E. M. G., Lutterman, J. A., de Nobel, E., van 't Laar, A., Sitsen, J. M. A., de Jong, W., Stuyt, P. M. J., Stalenhoef, A. F. H., Demacker, P. N. M., van 't Laar, A., Oosterhuis, B., Berge, R. J. M.ten, Sauerwein, N. P., Endert, E., Schellekens, P. Th. A., van Boxtel, C. J., Terpstra G. K., Raaijmakers, J. A. M., Wassink, G. A., Kreukniet, J., Bakker, J. C., de Vries-v. Rossen, A., Bleeker, W. K., Ufkes, J. G. R., van Rosevelt, R. F., van Mourik, J. A., Loos, J. A., Brummelhuis, H. G. J., Schalken, J. J., Lammers, J. W. J., Beld, A. J., and van Herwaarden, C. L. A.

Published
1983
Full Text
View/download PDF

48. Abstract of papers

Author

Konings, A. W. T., Joenje, H., Bast, A., Julicher, R., Van Iersel, A. A. J., Blaauboer, B. J., Balfoort, H. W., Ronbout, P. J. A., Borm, P. J. A., Engelen, J. J. M., Wouters, E. F. M., Swaen, C. M. H., de Boorder, Tj., Bos, R. P., Prinsen, W. J. C., Jongeneelen, F. J., Theuws, J. L. G., Henderson, P. Th., Cervantes, A., Schuurhuis, G. J., Pinedo, H. M., Lankelma, J., Commandeur, J. N. M., Oostendorp, R. A. J., Schoofs, P. R., Xu, B., Vermeulen, N. P. E., Coosen, R., van Leeuwen, F. X. R., Vos, J. G., Thijssen, J. H. H., Loeber, J. G., de Mol, N. J., Becht, A. B. C., Koenen, J., Lodder, G., de Wolff, F. A., van Ginkel, M. F., van der Voet, G. B., Dogterom, P., Nagelkerke, J. F., Mulder, G. J., Edelbroek, P. M., Zitman, F. G., Evelo, C. T. A., Niessen, H. J. J. M., Roelofs, H. M. J., Falke, H. E., De Groot, A. P., Willems, M. I., Franken, M. A. M., Kapteijn, R., Krajnc, E. I., Haenen, G. R. M. M., Plug, J. P. M., Timmerman, H., Hageman, G. J., Verhagen, H., Kleinjans, J. C. S., Herweijer, M. A., Bootsman, T. C., Scholte, B. J., Planta, R. J., Kroese, E. D., Tijdens, R. B., Meerman, J. H. N., Lusthof, K. J., Decuyper, J. G. A., Groothuis-Pielage, I. L., de Mol, N. J., Rietjens, I. M. C. M., Vos, R. M. E., Alink, G. M., van Bladeren, P. J., Rietveld, E. C., Ketels, H. H. T. M., Wetzer, A. M. A. C., Seutter-Berlage, F., Rombout, P., Dormans, J., van Bree, L., Marra, M., Til, H. P., Woutersen, R. A., Feron, V. J., Clary, J. J., Brandsma, A. E., de Wofff, F. A., van de Straat, R., de Vries, J., Boere, A. J. F., Rombout, P. J. A., Rietjens, I., Alink, G., van Erp, Yvette H. M., Heirbaut, Petra R. C. M., Koopmans, Marion J. E., Weterings, Peter J. J. M., van Loveren, H., de Klerk, A., Hakkert, B., Vertagen, H., Thijssen, H. H. W., Wester, P. W., Canton, J. H., Weterings, Peter J. J. M., and van Erp, Yvette H. M.

Published
1987
Full Text
View/download PDF

49. [Staging and profiling of unipolar depression]

Author

Peeters, F.P., Ruhe, H.G., Beekman, A.T., Spijker, J., Schoevers, R.A., Zitman, F., and Schene, A.H.

Subjects
Mental health [NCEBP 9]
Abstract

Contains fulltext : 110312.pdf (Publisher’s version ) (Open Access) BACKGROUND: Not only is the heterogeneous concept of depression too comprehensive, it is also insufficiently differentiated. This serves as a barrier to scientific research and obscures the symptoms that should indicate what treatment is required. AIM: To describe an accurate model for staging and profiling depression. METHOD: We placed depressive disorders in the context of the entire course of the disorder and we regarded the course as a continuum of psychopathology. RESULTS: First of all we distinguish five stages: (1) the prodromal phase, (2) the first depressive episode, (3) residual symptoms following an episode, (4) the relapse episode and (5) the chronic and/or treatment-resistant depression. The higher the stage, the greater the need for complex and specialised treatment. As characteristics for profiling we distinguish (a) aetiological and pathophysiological variables and (b) clinical factors. The latter are the ones that mainly influence treatment from stage 2 onwards. CONCLUSION: In our article we give a tentative overview of possible characteristics for profiling. At the moment the clinical factors are the ones used most for assessment. Current research into the value of aetiological characteristics for profiling will increase the applicability of a staging and profiling model.

Published
2012

Catalog

Books, media, physical & digital resources
See catalog results