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Higher magnesium intake is associated with lower fasting glucose and insulin, with no evidence of interaction with select genetic loci, in a meta-analysis of 15 CHARGE Consortium Studies.

TitleHigher magnesium intake is associated with lower fasting glucose and insulin, with no evidence of interaction with select genetic loci, in a meta-analysis of 15 CHARGE Consortium Studies.
Publication TypeJournal Article
Year of Publication2013
AuthorsHruby, A, Ngwa, JS, Renstrom, F, Wojczynski, MK, Ganna, A, Hallmans, G, Houston, DK, Jacques, PF, Kanoni, S, Lehtimäki, T, Lemaitre, RN, Manichaikul, A, North, KE, Ntalla, I, Sonestedt, E, Tanaka, T, van Rooij, FJA, Bandinelli, S, Djoussé, L, Grigoriou, E, Johansson, I, Lohman, KK, Pankow, JS, Raitakari, OT, Riserus, U, Yannakoulia, M, Zillikens, CM, Hassanali, N, Liu, Y, Mozaffarian, D, Papoutsakis, C, Syvänen, A-C, Uitterlinden, AG, Viikari, J, Groves, CJ, Hofman, A, Lind, L, McCarthy, MI, Mikkilä, V, Mukamal, K, Franco, OH, Borecki, IB, Cupples, AL, Dedoussis, GV, Ferrucci, L, Hu, FB, Ingelsson, E, Kähönen, M, Kao, LWH, Kritchevsky, SB, Orho-Melander, M, Prokopenko, I, Rotter, JI, Siscovick, DS, Witteman, JCM, Franks, PW, Meigs, JB, McKeown, NM, Nettleton, JA
JournalJ Nutr
Volume143
Issue3
Pagination345-53
Date Published2013 Mar
ISSN1541-6100
KeywordsBlood Glucose, Female, Genetic Loci, Humans, Insulin, Magnesium, Male, Polymorphism, Single Nucleotide, Trace Elements, TRPM Cation Channels
Abstract<p>Favorable associations between magnesium intake and glycemic traits, such as fasting glucose and insulin, are observed in observational and clinical studies, but whether genetic variation affects these associations is largely unknown. We hypothesized that single nucleotide polymorphisms (SNPs) associated with either glycemic traits or magnesium metabolism affect the association between magnesium intake and fasting glucose and insulin. Fifteen studies from the CHARGE (Cohorts for Heart and Aging Research in Genomic Epidemiology) Consortium provided data from up to 52,684 participants of European descent without known diabetes. In fixed-effects meta-analyses, we quantified 1) cross-sectional associations of dietary magnesium intake with fasting glucose (mmol/L) and insulin (ln-pmol/L) and 2) interactions between magnesium intake and SNPs related to fasting glucose (16 SNPs), insulin (2 SNPs), or magnesium (8 SNPs) on fasting glucose and insulin. After adjustment for age, sex, energy intake, BMI, and behavioral risk factors, magnesium (per 50-mg/d increment) was inversely associated with fasting glucose [β = -0.009 mmol/L (95% CI: -0.013, -0.005), P < 0.0001] and insulin [-0.020 ln-pmol/L (95% CI: -0.024, -0.017), P < 0.0001]. No magnesium-related SNP or interaction between any SNP and magnesium reached significance after correction for multiple testing. However, rs2274924 in magnesium transporter-encoding TRPM6 showed a nominal association (uncorrected P = 0.03) with glucose, and rs11558471 in SLC30A8 and rs3740393 near CNNM2 showed a nominal interaction (uncorrected, both P = 0.02) with magnesium on glucose. Consistent with other studies, a higher magnesium intake was associated with lower fasting glucose and insulin. Nominal evidence of TRPM6 influence and magnesium interaction with select loci suggests that further investigation is warranted.</p>
DOI10.3945/jn.112.172049
Alternate JournalJ. Nutr.
PubMed ID23343670
PubMed Central IDPMC3713023
Grant ListR01 DK078616 / DK / NIDDK NIH HHS / United States
UL1 TR000124 / TR / NCATS NIH HHS / United States
R01 HL105756 / HL / NHLBI NIH HHS / United States
P30 DK063491 / DK / NIDDK NIH HHS / United States
K24 DK080140 / DK / NIDDK NIH HHS / United States
090532 / / Wellcome Trust / United Kingdom
R01 HL087700 / HL / NHLBI NIH HHS / United States