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Dietary magnesium, C-reactive protein and interleukin-6: The Strong Heart Family Study.
Rao, Nandana D; Lemaitre, Rozenn N; Sitlani, Colleen M; Umans, Jason G; Haack, Karin; Handeland, Veronica; Navas-Acien, Ana; Cole, Shelley A; Best, Lyle G; Fretts, Amanda M.
Afiliación
  • Rao ND; Institute of Public Health Genetics, University of Washington, Seattle, Washington, United States of America.
  • Lemaitre RN; Department of Medicine, University of Washington, Seattle, Washington, United States of America.
  • Sitlani CM; Cardiovascular Research Health Unit, University of Washington, Seattle, Washington, United States of America.
  • Umans JG; Department of Medicine, University of Washington, Seattle, Washington, United States of America.
  • Haack K; Cardiovascular Research Health Unit, University of Washington, Seattle, Washington, United States of America.
  • Handeland V; MedStar Health Research Institute, Hyattsville, Maryland, United States of America.
  • Navas-Acien A; Department of Medicine, Georgetown University, Washington, DC, United States of America.
  • Cole SA; Texas Biomedical Research Institute, San Antonio, Texas, United States of America.
  • Best LG; Indian Health Services, Rockville, Maryland, United States of America.
  • Fretts AM; Department of Environmental Health Science, Columbia University, New York, New York, United States of America.
PLoS One ; 18(12): e0296238, 2023.
Article en En | MEDLINE | ID: mdl-38128021
ABSTRACT

OBJECTIVES:

To examine the associations of dietary Mg intake with inflammatory biomarkers (C-reactive protein (CRP) and interleukin 6 (IL-6)), and the interaction of dietary Mg intake with single nucleotide polymorphism (SNP) rs3740393, a SNP related to Mg metabolism and transport, on CRP and IL-6 among American Indians (AIs).

METHODS:

This cross-sectional study included AI participants (n = 1,924) from the Strong Heart Family Study (SHFS). Mg intake from foods and dietary supplements was ascertained using a 119-item Block food frequency questionnaire, CRP and IL-6 were measured from blood, and SNP rs3740393 was genotyped using MetaboChip. Generalized estimating equations were used to examine associations of Mg intake, and the interaction between rs3740393 and dietary Mg, with CRP and IL-6.

RESULTS:

Reported Mg intake was not associated with CRP or IL-6, irrespective of genotype. A significant interaction (p-interaction = 0.018) was observed between Mg intake and rs3740393 on IL-6. Among participants with the C/C genotype, for every 1 SD higher in log-Mg, log-IL-6 was 0.04 (95% CI -0.10 to 0.17) pg/mL higher. Among participants with the C/G genotype, for every 1 SD higher in log-Mg, log-IL-6 was 0.08 (95% CI -0.21 to 0.05) pg/mL lower, and among participants with the G/G genotype, for every 1 SD higher in log-Mg, log-IL-6 was 0.19 (95% CI -0.38 to -0.01) pg/mL lower.

CONCLUSIONS:

Mg intake may be associated with lower IL-6 with increasing dosage of the G allele at rs3740393. Future research is necessary to replicate this finding and examine other Mg-related genes that influence associations of Mg intake with inflammation.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteína C-Reactiva / Interleucina-6 Límite: Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteína C-Reactiva / Interleucina-6 Límite: Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos