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Genetic variation in stearoyl-CoA desaturase 1 is associated with metabolic syndrome prevalence in Costa Rican adults
UMass Center for Clinical and Translational Science Supported Publications
  • Jian Gong, Brown University
  • Hannia Campos, Harvard School of Public Health
  • Stephen T. McGarvey, Brown University
  • Zhijin Wu, Brown University
  • Robert J. Goldberg, University of Massachusetts Medical School
  • Ana Baylin, Brown University
UMMS Affiliation
Department of Quantitative Health Sciences; Meyers Primary Care Institute
Publication Date
Document Type
Adipose Tissue; Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Costa Rica; Fatty Acids; Female; Gene Expression Regulation; Genotype; Haplotypes; Humans; Male; Metabolic Syndrome X; Middle Aged; *Polymorphism, Single Nucleotide; Prevalence; Stearoyl-CoA Desaturase; Young Adult; alpha-Linolenic Acid

Stearoyl-CoA desaturase 1 (SCD1) activity, a key regulator of lipid metabolism, may be associated with the development of metabolic syndrome (MetS). We examined the association of genetic variation in the SCD1 gene with the occurrence of MetS and its five components in a population of Costa Rican adults (n = 2152; mean age, 58 y; range, 18-86 y). Associations of tag single nucleotide polymorphisms (tagSNP) of the SCD1 gene with prevalence of MetS and its five components were analyzed by use of log-Poisson models with robust variance estimates and linear regression models, respectively. The likelihood ratio was used to test potential gene-fatty acid interactive effects with adipose tissue alpha-linolenic acid. One tagSNP (rs1502593) was significantly associated with an increased prevalence of MetS in the total study sample. Compared with the common homozygous CC genotype, the CT and TT genotypes for rs1502593 were associated with higher prevalence ratios (PR) of MetS for CT vs. CC: [PR = 1.22 (95% CI = 1.03, 1.44)] and for TT vs. CC [PR = 1.24 (95% CI = 1.01, 1.52)]. Among women, we observed borderline positive associations between systolic blood pressure and fasting blood sugar levels and rs1502593 (P = 0.05 and 0.06). Compared to the common haplotype (frequency >/= 5%) with no minor alleles of SCD1 tagSNP, the other two observed common haplotypes carrying the rs1502593 minor allele were significantly associated with elevated prevalence of MetS. No gene-fatty acid interactive effects were observed. Our results suggest that genetic variation in the SCD1 gene may play a role in the development of MetS.

  • UMCCTS funding
DOI of Published Version

J Nutr. 2011 Dec;141(12):2211-8. Epub 2011 Nov 2. doi 10.3945/jn.111.143503

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Link to Article in PubMed

PubMed ID
Citation Information
Jian Gong, Hannia Campos, Stephen T. McGarvey, Zhijin Wu, et al.. "Genetic variation in stearoyl-CoA desaturase 1 is associated with metabolic syndrome prevalence in Costa Rican adults" Vol. 141 Iss. 12 (2011) ISSN: 0022-3166 (Linking)
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