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GWAS Study

Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes.

Corre T, Arjona FJ, Hayward C et al.

29093028 PubMed ID
GWAS Study Type
9099 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CT
Corre T
AF
Arjona FJ
HC
Hayward C
YS
Youhanna S
DB
de Baaij JHF
BH
Belge H
NN
Nägele N
DH
Debaix H
BM
Blanchard MG
TM
Traglia M
HS
Harris SE
US
Ulivi S
RR
Rueedi R
LD
Lamparter D
MA
Macé A
SC
Sala C
LS
Lenarduzzi S
PB
Ponte B
PM
Pruijm M
AD
Ackermann D
EG
Ehret G
BD
Baptista D
PO
Polasek O
RI
Rudan I
HT
Hurd TW
HN
Hastie ND
VV
Vitart V
WG
Waeber G
KZ
Kutalik Z
BS
Bergmann S
VR
Vargas-Poussou R
KM
Konrad M
GP
Gasparini P
DI
Deary IJ
SJ
Starr JM
TD
Toniolo D
VP
Vollenweider P
HJ
Hoenderop JGJ
BR
Bindels RJM
BM
Bochud M
DO
Devuyst O
Chapter II

Abstract

Summary of the research findings

Magnesium (Mg2+) homeostasis is critical for metabolism. However, the genetic determinants of the renal handling of Mg2+, which is crucial for Mg2+ homeostasis, and the potential influence on metabolic traits in the general population are unknown. We obtained plasma and urine parameters from 9099 individuals from seven cohorts, and conducted a genome-wide meta-analysis of Mg2+ homeostasis. We identified two loci associated with urinary magnesium (uMg), rs3824347 (P=4.4×10-13) near TRPM6, which encodes an epithelial Mg2+ channel, and rs35929 (P=2.1×10-11), a variant of ARL15, which encodes a GTP-binding protein. Together, these loci account for 2.3% of the variation in 24-hour uMg excretion. In human kidney cells, ARL15 regulated TRPM6-mediated currents. In zebrafish, dietary Mg2+ regulated the expression of the highly conserved ARL15 ortholog arl15b, and arl15b knockdown resulted in renal Mg2+ wasting and metabolic disturbances. Finally, ARL15 rs35929 modified the association of uMg with fasting insulin and fat mass in a general population. In conclusion, this combined observational and experimental approach uncovered a gene-environment interaction linking Mg2+ deficiency to insulin resistance and obesity.

up to 5,810 European ancestry individuals, up to 1,541 Val Borbera (founder/genetic isolate) individuals, up to 281 Carlantino (founder/genetic isolate) individuals, up to 889 Korcula (founder/genetic isolate) individuals, up to 489 Split (founder/genetic isolate) individuals, up to 195 Vis (founder/genetic isolate) individuals

Chapter III

Study Statistics

Key metrics and study information

9099
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Switzerland, U.K., Croatia, Italy
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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