Brain-derived neurotrophic factor val66met genotype and early life stress effects upon bipolar course

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• 作者：Shefali Miller^a ; ^b ; ^{shefalis@stanford.edu} ; ^{shefalimiller1@gmail.com} ; Joachim Hallmayer^a ; Po W. Wang^a ; Shelley J. Hill^a ; Sheri L. Johnson^c ; Terence A. Ketter^a
• 关键词：Bipolar disorder ; Brain-derived neurotrophic factor ; Childhood abuse ; Early life stress ; Illness course ; Gene-environment interaction
• 刊名：Journal of Psychiatric Research
• 出版年：2013
• 出版时间：February, 2013
• 年：2013
• 卷：47
• 期：2
• 页码：252-258
• 全文大小：265 K

文摘

Background

Gene-environment interactions may contribute to bipolar disorder (BD) clinical course variability. We examined effects of brain-derived neurotrophic factor (BDNF) val66met genotype and early life stress (ELS) upon illness severity and chronicity in adult BD patients.

Methods

80 patients (43 BD I, 33 BD II, 4 BD not otherwise specified, mean?¡À?SD age 46.4?¡À?14.0 years, 63.7 % female) receiving open evidence-based and measurement-based care in the Stanford Bipolar Disorders Clinic for at least 12 months underwent BDNF val66met genotyping and completed the Childhood Trauma Questionnaire. BDNF met?allele carrier genotype and history of childhood sexual and physical abuse were evaluated in relation to mean prior-year Clinical Global Impressions-Bipolar Version-Overall Severity of Illness (MPY-CGI-BP-OS) score and clinical and demographic characteristics.

Results

BDNF met?allele carriers (but not non-met?allele carriers) with compared to without childhood sexual abuse had 21 % higher MPY-CGI-BP-OS scores (3.5?¡À?0.7 versus 2.9?¡À?0.7, respectively, t?=??2.4, df?=?28, p?=?0.025) and 35 % earlier BD onset age (14.6?¡À?5.7 versus 22.8?¡À?7.9 years, respectively, t?=?3.0, df?=?27, p?=?0.006). Regression analysis, however, was non-significant for a BDNF-childhood sexual abuse interaction.

Limitations

small sample of predominantly female Caucasian insured outpatients taking complex medication regimens; only one gene polymorphism considered.

Conclusions

Between group comparisons suggested BDNF met?allele carrier genotype might amplify negative effects of ELS upon BD illness severity/chronicity, although with regression analysis, there was not a significant gene-environment interaction. Further studies with larger samples are warranted to assess whether BDNF met?allele carriers with ELS are at risk for more severe/chronic BD illness course.