Postpartum Depression in Women with the FMR1 Premutation

被引:4
作者
Obadia, Roberta W. [1 ]
Iosif, Ana-Maria [2 ]
Seritan, Andreea L. [3 ]
机构
[1] Univ Calif Davis, Sch Med, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Dept Publ Hlth Sci, Davis, CA 95616 USA
[3] Univ Calif Davis, Med Ctr, Dept Psychiat & Behav Sci, Sacramento, CA 95817 USA
基金
美国国家卫生研究院;
关键词
Female carriers; FMR1; premutation; Fragile X syndrome (FXS); Major depressive disorder; Postpartum depression;
D O I
10.2174/157340013805289680
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Psychiatric disorders in women with the FMR1 premutation are common and include attention deficit hyperactivity disorder, anxiety, depression, and eating disorders. This pilot study explored the risk factors for postpartum depression (PPD) in women with the premutation. Methods: We conducted a chart review of 50 women premutation carriers with major depressive disorder who had children. Of these, 7 women had a history of major depressive episodes in the postpartum period. The PPD and non-PPD groups were characterized descriptively based on women's age at the time of the psychiatric evaluation, race, ethnicity, education level, IQ, CGG repeat size, comorbid psychiatric conditions, parity, and number of children with fragile X syndrome (FXS). Exact logistic regression was used to analyze the relationship between the number of children with FXS and the risk of PPD. Results: The PPD and non-PPD groups were similar on all variables examined, with the exception of the number of affected children. Each of the 7 women with PPD had at least one child with FXS, whereas a third of the women without PPD had no affected children. For each additional affected child, the risk of PPD increased by 158% (exact odds ratio 2.58, 95% CI 0.99-7.59). Further studies are needed to replicate these findings and to better characterize PPD in female premutation carriers.
引用
收藏
页码:72 / 77
页数:6
相关论文
共 45 条
  • [1] Abbeduto L, 2004, AM J MENT RETARD, V109, P237, DOI 10.1352/0895-8017(2004)109<237:PWACIM>2.0.CO
  • [2] 2
  • [3] Allingham-Hawkins SJ, 1999, AM J MED GENET, V83, P322, DOI 10.1002/(SICI)1096-8628(19990402)83:4<322::AID-AJMG17>3.0.CO
  • [4] 2-B
  • [5] American College of Obstetricians and Gynecologists Committee on Genetics, 2006, Obstet Gynecol, V107, P1483
  • [6] American Psychiatric Association, 2000, DIAGN CRIT DSM IV TR, P204
  • [7] No Change in the Age of Diagnosis for Fragile X Syndrome: Findings From a National Parent Survey
    Bailey, Donald B., Jr.
    Raspa, Melissa
    Bishop, Ellen
    Holiday, David
    [J]. PEDIATRICS, 2009, 124 (02) : 527 - 533
  • [8] Baker JK, 2007, AM J MENT RETARD, V112, P375, DOI 10.1352/0895-8017(2007)112[0375:POSSIY]2.0.CO
  • [9] 2
  • [10] Lifetime Prevalence of Mood and Anxiety Disorders in Fragile X Premutation Carriers
    Bourgeois, James A.
    Seritan, Andreea L.
    Casillas, E. Melina
    Hessl, David
    Schneider, Andrea
    Yang, Ying
    Kaur, Inderjeet
    Cogswell, Jennifer B.
    Nguyen, Danh V.
    Hagerman, Randi J.
    [J]. JOURNAL OF CLINICAL PSYCHIATRY, 2011, 72 (02) : 175 - 182