What is familial about familial bipolar disorder? Resemblance among relatives across a broad spectrum of phenotypic characteristics

被引:89
作者
Schulze, Thomas G. [1 ]
Hedeker, Donald
Zandi, Peter
Rietschel, Marcella
McMahon, Francis J.
机构
[1] Heidelberg Univ, Div Genet Epidemiol Psychiat, Cent Inst Mental Hlth, D-68159 Mannheim, Germany
[2] NIMH, Mood & Anxiety Disorders Program, NIH, Bethesda, MD 20892 USA
[3] Univ Illinois, Div Epidemiol & Biostat, Sch Publ Hlth, Chicago, IL USA
[4] Johns Hopkins Univ, Dept Mental Hlth, Bloomberg Sch Publ Hlth, Baltimore, MD USA
关键词
D O I
10.1001/archpsyc.63.12.1368
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Context: Current diagnostic criteria for bipolar affective disorder define a phenotype that is highly heritable, yet clinically variable. A more homogeneous definition might facilitate genetic and other studies, but the best approach is unclear. Familial features of bipolar disorder should help define more homogeneous subtypes, but there are few data indicating which clinical features of bipolar disorder are the most familial. Objective: To study the familiality of phenotypic features in families ascertained through individuals with bipolar affective disorder. Design: The study comprises 1246 individuals in 172 multiplex families ascertained for genetic linkage studies of bipolar disorder. The familiality of 40 diverse phenotypic features was studied using mixed-effects regression analysis. Results: Substance abuse, alcoholism, psychosis, history of suicide attempt, and the level of social functioning were all strongly familial in this sample. Several other traits, including clinical subtype, earliest age at onset, and comorbid panic disorder, showed a suggestion of familiality that did not hold up to conservative correction for multiple testing. Conclusions: This is the largest and most comprehensive study to assess the familiality of phenotypic features in bipolar disorder. Our results suggest that comorbid conditions and social functioning should be considered along with other familial clinical features in formulating subtypes of bipolar disorder suitable for further studies. Familial variables may help reduce diagnostic heterogeneity in genetic and other biological studies.
引用
收藏
页码:1368 / 1376
页数:9
相关论文
共 77 条
  • [21] Familial variation in episode frequency in bipolar affective disorder
    Fisfalen, ME
    Schulze, TG
    DePaulo, JR
    DeGroot, LJ
    Badner, JA
    McMahon, FJ
    [J]. AMERICAN JOURNAL OF PSYCHIATRY, 2005, 162 (07) : 1266 - 1272
  • [22] Human nonsyndromic sensorineural deafness
    Friedman, TB
    Griffith, AJ
    [J]. ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, 2003, 4 : 341 - 402
  • [23] GERSHON ES, 1982, ARCH GEN PSYCHIAT, V39, P1157
  • [24] GOLDBERG JF, 1995, AM J PSYCHIAT, V152, P379
  • [25] Consistency of remission and outcome in bipolar and unipolar mood disorders: a 10-year prospective follow-up
    Goldberg, JF
    Harrow, M
    [J]. JOURNAL OF AFFECTIVE DISORDERS, 2004, 81 (02) : 123 - 131
  • [26] Goodwin F.K., 2007, MANIC DEPRESSIVE ILL
  • [27] The mixed or multilevel model for behavior genetic analysis
    Guo, G
    Wang, JM
    [J]. BEHAVIOR GENETICS, 2002, 32 (01) : 37 - 49
  • [28] Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series
    Hattori, E
    Liu, CY
    Badner, JA
    Bonner, TI
    Christian, SL
    Maheshwari, M
    Detera-Wadleigh, SD
    Gibbs, RA
    Gershon, ES
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (05) : 1131 - 1140
  • [29] Social functioning and personality of subjects at familial risk for affective disorder
    Hecht, H
    Genzwürker, S
    Helle, M
    van Calker, D
    [J]. JOURNAL OF AFFECTIVE DISORDERS, 2005, 84 (01) : 33 - 42
  • [30] MIXREG: A computer program for mixed-effects regression analysis with autocorrelated errors
    Hedeker, D
    Gibbons, RD
    [J]. COMPUTER METHODS AND PROGRAMS IN BIOMEDICINE, 1996, 49 (03) : 229 - 252