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PMID: 12629534 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Serotonin-related gene polymorphisms and central nervous system serotonin function.

Williams RB, Marchuk DA, Gadde KM, Barefoot JC, Grichnik K, Helms MJ, Kuhn CM, Lewis JG, Schanberg SM, Stafford-Smith M, Suarez EC, Clary GL, Svenson IK, Siegler IC

Abstract

Central nervous system (CNS) serotonergic function affects a wide range of biological and behavioral functions affecting health and disease. Our objective in this study was to determine whether functional polymorphisms of the genes that encode for the serotonin transporter promoter (5HTTLPR) and monoamine oxidase A (MAOA-uVNTR) are associated with CNS serotonin turnover-indexed by cerebrospinal fluid levels of 5-hydroxyindoleacetic acid (5-HIAA)-in a community sample of healthy adults. Subjects were 165 community volunteers without current medical or psychiatric illness, stratified with respect to ethnicity, gender, and socioeconomic status who underwent inpatient evaluation in the General Clinical Research Center of a university medical center. A significant ethnicity x genotype interaction (P=0.008) indicated that, compared to the long/long and long/short genotypes, the 5HTTLPR short/short genotype was associated with higher CSF 5-HIAA levels in African Americans, but with lower levels in Caucasians. A gender x genotype interaction (P=0.04) indicated that 5HTTLPR short/short genotype was associated with higher 5-HIAA levels in women but with lower levels in men. MAOA-uVNTR 3.5 and 4 repeat alleles were associated with higher 5-HIAA (P=0.03) levels in men, but were unrelated to 5-HIAA levels in women. These findings suggest that effects of serotonin-related gene polymorphisms on CNS serotonergic function vary as a function of both ethnicity and gender. Further research will be required to determine the mechanism(s) underlying these differential effects. In the meanwhile, both ethnicity and gender should be taken into account in research evaluating effects of these and related polymorphisms on CNS serotonergic function, as well as the broad range of biological and behavioral functions that are regulated by CNS serotonergic function.

MeSH Terms
Adult Analysis of Variance Carrier Proteins/genetics Central Nervous System/metabolism Ethnicity/psychology,statistics & numerical data Female Genotype Humans Hydroxyindoleacetic Acid/cerebrospinal fluid Male Membrane Glycoproteins/genetics Membrane Transport Proteins Middle Aged Monoamine Oxidase/genetics Nerve Tissue Proteins Polymorphism, Genetic/genetics Serotonin/genetics,metabolism Serotonin Plasma Membrane Transport Proteins Sex Factors Socioeconomic Factors
Chemicals
Carrier Proteins Membrane Glycoproteins Membrane Transport Proteins Nerve Tissue Proteins SLC6A4 protein, human Serotonin Plasma Membrane Transport Proteins Serotonin Hydroxyindoleacetic Acid Monoamine Oxidase
Authors & Affiliations
14 authors, click to expand affiliations / ORCID
Williams Redford B
Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Box 3926, Durham, NC 27710, USA. [email protected]
Marchuk Douglas A
Gadde Kishore M
Barefoot John C
Grichnik Katherine
Helms Michael J
Kuhn Cynthia M
Lewis James G
Schanberg Saul M
Stafford-Smith Mark
Suarez Edward C
Clary Greg L
Svenson Ingrid K
Siegler Ilene C
Article Info
Journal
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology
Abbr.
Neuropsychopharmacology
ISSN
0893-133X
Published
2003-03-00
Epub
2002-00-29
Pages
533-41
Language
English
Region
England
NLM ID
8904907
Subset
IM
Grants
NHLBI NIH HHS · P01 HL036587 · United States
NIMH NIH HHS · K05MH79482 · United States
NCRR NIH HHS · M01RR30 · United States
NHLBI NIH HHS · P01HL36587 · United States
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