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Adiposity and immune-muscle crosstalk in South Asians &Europeans: A cross-sectional study.
Samaan, M Constantine; Anand, Sonia S; Sharma, Arya M; Bonner, Ashley; Beyene, Joseph; Samjoo, Imtiaz; Tarnopolsky, Mark A.
Afiliação
  • Samaan MC; Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
  • Anand SS; Division of Pediatric Endocrinology, McMaster Children's Hospital, Hamilton, Ontario, Canada.
  • Sharma AM; Population Genomics Program, Chanchlani Research Centre, McMaster University, Hamilton, ON, Canada.
  • Bonner A; Population Health Research Institute, Hamilton Health Sciences and McMaster University, Hamilton, Ontario, Canada.
  • Beyene J; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Samjoo I; Department of Clinical Epidemiology/Biostatistics, McMaster University, Hamilton, Ontario, Canada.
  • Tarnopolsky MA; University of Alberta, Edmonton, Alberta, Canada.
Sci Rep ; 5: 14521, 2015 Oct 12.
Article em En | MEDLINE | ID: mdl-26455502
ABSTRACT
South Asians (SA) are at higher risk of cardiometabolic disorders than Europeans (EU), yet the potential determinants of this risk are poorly understood. We tested the hypotheses that 1) South Asians (SA) have greater muscle inflammation compared to Europeans (EU) at similar fat mass 2) differential regional adiposity in SA compared to EU is associated with enhanced muscle inflammation in SA. This cross-sectional study was conducted at a tertiary academic center in Hamilton, Ontario, Canada. The study included 29 EU and 26 SA. Quantitative real-time PCR and western blot were used to measure muscle inflammation. Statistical analysis was done using a General Linear Model. Despite having similar macrophage content to EU, SA muscle had lower levels of chemokine CCL2 compared to EU at gene expression (ß -1.099, SE ß 0.521, p-value 0.04) and protein (0.84 ± 0.69 versus 1.10 ± 0.60, p-value 0.052) levels. SA had more pronounced abdominal and hepatic adiposity, with smaller Intramyocellular lipid particles compared to EU (0.26 ± 0.12 µm(2) versus 0.15 ± 0.06 µm(2), p-value 0.02). In conclusion, CCL2 downregulation in SA may be an attempt to protect muscle against macrophage infiltration, and defects in fatty acid partitioning to muscle may lead to the disproportionate adiposity and adverse cardiometabolic profile in SA.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Músculo Esquelético / Quimiocina CCL2 / Gordura Intra-Abdominal / Ácidos Graxos / Obesidade Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies País como assunto: America do norte Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Músculo Esquelético / Quimiocina CCL2 / Gordura Intra-Abdominal / Ácidos Graxos / Obesidade Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies País como assunto: America do norte Idioma: En Ano de publicação: 2015 Tipo de documento: Article