Stratifying empiric risk of schizophrenia among first degree relatives using multiple predictors in two independent Indian samples

被引:4
作者
Bhatia, Triptish [1 ]
Gettig, Elizabeth A. [2 ]
Gottesman, Irving I. [3 ,4 ,5 ]
Berliner, Jonathan [6 ]
Mishra, N. N. [7 ]
Nimgaonkar, Vishwajit L. [8 ,9 ,10 ]
Deshpande, Smita N. [11 ]
机构
[1] PGIMER Dr Ram Manohar Lohia Hosp, Dept Psychiat, Indo US Projects, Pk St, New Delhi 110001, India
[2] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Human Genet, Pittsburgh, PA 15261 USA
[3] Univ Minnesota, Med School Twin Cities, Charlottesville, VA USA
[4] Univ Virginia, Dept Psychol, Gilmer Hall, Charlottesville, VA 22903 USA
[5] Univ Virginia, Psychol Emeritus, Gilmer Hall, Charlottesville, VA 22903 USA
[6] Princeton Univ, Greater Philadelphia Area, Philadelphia, PA USA
[7] BRA Bihar Univ, LS Coll, Dept Psychol, Muzaffarpur, Bihar, India
[8] Univ Pittsburgh, Sch Med, Dept Psychiat, Pittsburgh, PA 15213 USA
[9] Univ Pittsburgh, Sch Med, Dept Human Genet, Pittsburgh, PA 15213 USA
[10] Univ Pittsburgh, Grad Sch Publ Hlth, Pittsburgh, PA 15213 USA
[11] PGIMER Dr Ram Manohar Lohia Hosp, Dept Psychiat, Pk St, New Delhi 110001, India
关键词
Schizophrenia; Genetic counseling; Familial; Risk; FAMILY-HISTORY; PSYCHIATRIC GENETICS; DIAGNOSTIC INTERVIEW; CANNABIS USE; PSYCHOSIS; TWIN; PREVENTION; DISORDERS; HEALTH; URBANICITY;
D O I
10.1016/j.ajp.2016.08.015
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Schizophrenia (SZ) has an estimated heritability of 64-88%, with the higher values based on twin studies. Conventionally, family history of psychosis is the best individual-level predictor of risk, but reliable risk estimates are unavailable for Indian populations. Genetic, environmental, and epigenetic factors are equally important and should be considered when predicting risk in 'at risk' individuals. Objective: To estimate risk based on an Indian schizophrenia participant's family history combined with selected demographic factors. Methods: To incorporate variables in addition to family history, and to stratify risk, we constructed a regression equation that included demographic variables in addition to family history. The equation was tested in two independent Indian samples: (i) an initial sample of SZ participants (N = 128) with one sibling or offspring; (ii) a second, independent sample consisting of multiply affected families (N = 138 families, with two or more sibs/offspring affected with SZ). Results: The overall estimated risk was 4.31 +/- 0.27 (mean +/- standard deviation). There were 19 (14.8%) individuals in the high risk group, 75 (58.6%) in the moderate risk and 34 (26.6%) in the above average risk (in Sample A). In the validation sample, risks were distributed as: high (45%), moderate (38%) and above average (17%). Consistent risk estimates were obtained from both samples using the regression equation. Conclusions: Familial risk can be combined with demographic factors to estimate risk for SZ in India. If replicated, the proposed stratification of risk may be easier and more realistic for family members. (C) 2016 Published by Elsevier B.V.
引用
收藏
页码:79 / 84
页数:6
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