Serotonin Transporter Gene, Depressive Symptoms, and Interleukin-6

  • Shaoyong Su
  • , Jinying Zhao
  • , J. Douglas Bremner
  • , Andrew H. Miller
  • , Weining Tang
  • , Mark Bouzyk
  • , Harold Snieder
  • , Olga Novik
  • , Nadeem Afzal
  • , Jack Goldberg
  • , Viola Vaccarino*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

57 Citations (Scopus)

Abstract

Background-We explored the relationship of genetic variants of the serotonin transporter gene SLC6A4, a key regulator of the serotonergic neurotransmission, with both depressive symptoms and plasma interleukin-6 (IL-6) levels.

Methods and Results-We genotyped 20 polymorphisms in 360 male twins (mean age, 54 years) from the Vietnam Era Twin Registry. Current depressive symptoms were measured with the Beck Depression Inventory II. IL-6 was assessed using a commercially available ELISA kit. Genotype associations were analyzed using generalized estimating equations. To study how SLC6A4 genetic vulnerability influences the relationship between depressive symptoms and IL-6, bivariate models were constructed using structural equation modeling. Of the 20 polymorphisms examined, the effective number of independent tests was 6, and the threshold of significance after Bonferroni correction was 0.008. There were 6 single-nucleotide polymorphisms significantly associated with Beck Depression Inventory (P

Conclusions-Genetic vulnerability involving the SLC6A4 gene is significantly associated with both increased depressive symptoms and elevated IL-6 plasma levels. Common pathophysiological processes may link depression and inflammation, and implicate the serotonin pathway in neural-immune interactions. (Circ Cardiovasc Genet. 2009;2:614-620.)

Original languageEnglish
Pages (from-to)614-U205
Number of pages12
JournalCirculation-Cardiovascular Genetics
Volume2
Issue number6
DOIs
Publication statusPublished - Dec-2009

Keywords

  • atherosclerosis
  • epidemiology
  • genetics
  • inflammation
  • depression
  • CORONARY-ARTERY-DISEASE
  • HEART-DISEASE
  • AFFECTIVE-DISORDERS
  • RISK-FACTOR
  • ASSOCIATION
  • POLYMORPHISM
  • TRAITS
  • INFLAMMATION
  • MECHANISMS
  • HAPLOTYPES

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