Literature DB >> 11702054

Genetic survival analysis of age-at-onset of bipolar disorder: evidence for anticipation or cohort effect in families.

P M Visscher1, M H Yazdi, A D Jackson, M Schalling, K Lindblad, Q P Yuan, D Porteous, W J Muir, D H Blackwood.   

Abstract

Age-at-onset (AAO) in a number of extended families ascertained for bipolar disorder was analysed using survival analysis techniques, fitting proportional hazards models to estimate the fixed effects of sex, year of birth, and generation, and a random polygenic genetic effect. Data comprised the AAO (for 171 affecteds) or age when last seen (ALS) for 327 unaffecteds, on 498 individuals in 27 families. ALS was treated as the censored time in the statistical analyses. The majority of individuals classified as affected were diagnosed with bipolar I and II (n = 103) or recurrent major depressive disorder (n = 68). In addition to the significant effects of sex and year of birth, a fitted 'generation' effect was highly significant, which could be interpreted as evidence for an anticipation effect. The risk of developing bipolar or unipolar disorder increased twofold with each generation descended from the oldest founder. However, although information from both affected and unaffected individuals was used to estimate the relative risk of subsequent generations, it is possible that the results are biased because of the 'Penrose effect'. Females had a twofold increased risk in developing depressive disorder relative to males. The risk of developing bipolar or unipolar disorder increased by approximately 4% per year of birth. A polygenic component of variance was estimated, resulting in a 'heritability' of AAO of approximately 0.52. In a family showing strong evidence of linkage to chromosome 4p (family 22), the 'affected haplotype' increased the relative risk of being affected by a factor of 46. In this family, there was strong evidence of a time trend in the AAO. When either year of birth or generation was fitted in the model, these effects were highly significant, but neither was significant in the presence of the other. For this family, there was no increase in trinucleotide repeats measured by the repeat expansion detection method in affected individuals compared with control subjects. Proportional hazard models appear appropriate to analyse AAO data, and the methodology will be extended to map quantitative trait loci (QTL) for AAO.

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Year:  2001        PMID: 11702054     DOI: 10.1097/00041444-200109000-00004

Source DB:  PubMed          Journal:  Psychiatr Genet        ISSN: 0955-8829            Impact factor:   2.458


  4 in total

Review 1.  Anticipation and CAG*CTG repeat expansion in schizophrenia and bipolar affective disorder.

Authors:  M Teresa Fortune; James L Kennedy; John B Vincent
Journal:  Curr Psychiatry Rep       Date:  2003-06       Impact factor: 5.285

Review 2.  The genetics of early-onset bipolar disorder: A systematic review.

Authors:  Kevin P Kennedy; Kathryn R Cullen; Colin G DeYoung; Bonnie Klimes-Dougan
Journal:  J Affect Disord       Date:  2015-05-15       Impact factor: 4.839

3.  Familiality and SNP heritability of age at onset and episodicity in major depressive disorder.

Authors:  P Ferentinos; A Koukounari; R Power; M Rivera; R Uher; N Craddock; M J Owen; A Korszun; L Jones; I Jones; M Gill; J P Rice; M Ising; W Maier; O Mors; M Rietschel; M Preisig; E B Binder; K J Aitchison; J Mendlewicz; D Souery; J Hauser; N Henigsberg; G Breen; I W Craig; A E Farmer; B Müller-Myhsok; P McGuffin; C M Lewis
Journal:  Psychol Med       Date:  2015-02-20       Impact factor: 7.723

4.  Heritability, SNP- and Gene-Based Analyses of Cannabis Use Initiation and Age at Onset.

Authors:  Camelia C Minică; Conor V Dolan; Jouke-Jan Hottenga; René Pool; Iryna O Fedko; Hamdi Mbarek; Charlotte Huppertz; Meike Bartels; Dorret I Boomsma; Jacqueline M Vink
Journal:  Behav Genet       Date:  2015-05-19       Impact factor: 2.805

  4 in total

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