Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence

被引:9
作者
St Pourcain, Beate [1 ,2 ,3 ,4 ]
Haworth, C. M. A. [5 ,6 ]
Davis, O. S. P. [6 ,7 ]
Wang, Kai [8 ,9 ,10 ]
Timpson, Nicholas J. [1 ,4 ]
Evans, David M. [1 ,4 ,11 ]
Kemp, John P. [1 ,4 ,11 ]
Ronald, Angelica [12 ]
Price, Tom [13 ]
Meaburn, Emma [12 ]
Ring, Susan M. [1 ,4 ]
Golding, Jean [4 ,14 ]
Hakonarson, Hakon [8 ]
Plomin, R. [6 ]
Smith, George Davey [1 ,4 ]
机构
[1] Univ Bristol, MRC IEU, Bristol BS8 2BN, Avon, England
[2] Univ Bristol, Sch Oral & Dent Sci, Bristol BS8 2BN, Avon, England
[3] Univ Bristol, Sch Expt Psychol, Bristol BS8 2BN, Avon, England
[4] Univ Bristol, Sch Social & Community Med, Bristol BS8 2BN, Avon, England
[5] Univ Warwick, Dept Psychol, Coventry CV4 7AL, W Midlands, England
[6] Kings Coll London, Inst Psychiat, MRC Social Genet & Dev Psychiat Ctr, London WC2R 2LS, England
[7] UCL, Dept Genet Evolut & Environm, Genet Inst, London, England
[8] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[9] Univ So Calif, ZilkhaNeurogenet Inst, Los Angeles, CA USA
[10] Univ So Calif, Dept Psychiat, Los Angeles, CA USA
[11] Univ Queensland, Translat Res Inst, Diamantina Inst, Brisbane, Qld, Australia
[12] Univ London, Dept Psychol Sci, London, England
[13] Univ Penn, Sch Med, Inst Translat Med & Therapeut, Philadelphia, PA 19104 USA
[14] Univ Bristol, Ctr Child & Adolescent Hlth, Bristol BS8 2BN, Avon, England
基金
美国国家卫生研究院; 英国医学研究理事会; 英国惠康基金; 欧洲研究理事会;
关键词
DIFFICULTIES QUESTIONNAIRE; GENETIC INFLUENCES; AUTISTIC TRAITS; SPECTRUM; ASSOCIATION; ADJUSTMENT; STRENGTHS; POPULATION; FRIENDSHIP; PHENOTYPES;
D O I
10.1007/s00439-014-1514-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Peer behaviour plays an important role in the development of social adjustment, though little is known about its genetic architecture. We conducted a twin study combined with a genome-wide complex trait analysis (GCTA) and a genome-wide screen to characterise genetic influences on problematic peer behaviour during childhood and adolescence. This included a series of longitudinal measures (parent-reported Strengths-and-Difficulties Questionnaire) from a UK population-based birth-cohort (ALSPAC, 4-17 years), and a UK twin sample (TEDS, 4-11 years). Longitudinal twin analysis (TEDS; N currency sign 7,366 twin pairs) showed that peer problems in childhood are heritable (4-11 years, 0.60 < twin-h (2) currency sign 0.71) but genetically heterogeneous from age to age (4-11 years, twin-r (g) = 0.30). GCTA (ALSPAC: N currency sign 5,608, TEDS: N currency sign 2,691) provided furthermore little support for the contribution of measured common genetic variants during childhood (4-12 years, 0.02 < GCTA-h (2)(Meta) currency sign 0.11) though these influences become stronger in adolescence (13-17 years, 0.14 < GCTA-h (2)(ALSPAC) currency sign 0.27). A subsequent cross-sectional genome-wide screen in ALSPAC (N currency sign 6,000) focussed on peer problems with the highest GCTA-heritability (10, 13 and 17 years, 0.0002 < GCTA-P currency sign 0.03). Single variant signals (P currency sign 10(-5)) were followed up in TEDS (N currency sign 2835, 9 and 11 years) and, in search for autism quantitative trait loci, explored within two autism samples (AGRE: N (Pedigrees) = 793; ACC: N (Cases) = 1,453/N (Controls) = 7,070). There was, however, no evidence for association in TEDS and little evidence for an overlap with the autistic continuum. In summary, our findings suggest that problematic peer relationships are heritable but genetically complex and heterogeneous from age to age, with an increase in common measurable genetic variation during adolescence.
引用
收藏
页码:539 / 551
页数:13
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