کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5842569 1560630 2013 4 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Response to citalopram is not associated with SLC6A4 genotype in African-Americans and Caucasians with major depression
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی کاردیولوژی و پزشکی قلب و عروق
پیش نمایش صفحه اول مقاله
Response to citalopram is not associated with SLC6A4 genotype in African-Americans and Caucasians with major depression
چکیده انگلیسی

AimsEthnic differences in genotype frequency provide a natural condition for assessing the contribution of gene variations to the causes and treatments of disease. Accordingly, the purpose of this study was to determine whether ethnic variations in allele frequencies of the serotonin transporter gene-linked polymorphic region (5-HTTLPR) of the SLC6A4 gene were related to the response to the treatment of depression.Main methodsAfrican-Americans (n = 101) and Caucasians (n = 100) with major depressive disorder were treated with the antidepressant citalopram (20-60 mg/day) for 8 weeks. Genotyping for the long (L) and short (s) alleles (LL, Ls, and ss) of the SLC6A4 gene was performed and the association between genotype and treatment response was assessed.Key findingsSubjects in both ethnic groups showed a significant reduction in depression scores over time (p < .0001). However, in spite of a significantly greater frequency of the L allele in African-Americans as compared to Caucasians, a comparable clinical response between the two groups was found with 5-HTTLPR polymorphism not significantly associated with clinical response in either ethnic group.SignificanceThe results are consistent with a previous finding and in accord with most of the results obtained in Caucasian subjects that SLC6A4 genotype is not related, at least by itself, to a response to treatment in either ethnic group to any clinically significant degree.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Life Sciences - Volume 92, Issues 20–21, 30 May 2013, Pages 967-970
نویسندگان
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