Calcium, Its Regulatory Hormones, and Their Causal Role on Blood Pressure: A Two-Sample Mendelian Randomization Study.


Journal

The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362

Informations de publication

Date de publication:
23 11 2022
Historique:
received: 03 06 2022
pubmed: 6 9 2022
medline: 25 11 2022
entrez: 5 9 2022
Statut: ppublish

Résumé

Vitamin D (Vit-D), parathyroid hormone (PTH), and fibroblast growth factor 23 (FGF23) are the major calciotropic hormones involved in the regulation of blood calcium levels from the intestine, kidney, and bone through a tight endocrine feedback loop system. Altered levels of calcium itself or through the effect of its regulatory hormones could affect blood pressure (BP), but the exact mechanisms remain unclear. To evaluate whether a causal relationship exists between serum calcium level and/or the regulatory hormones involved in its homeostasis with BP, we performed a two-sample Mendelian randomization (MR) study. From 4 large genome-wide association studies (GWAS) we obtained independent (r2 < 0.001) single nucleotide polymorphisms (SNPs) associated with serum calcium (119 SNPs), Vit-D (78 SNPs), PTH (5 SNPs), and FGF23 (5 SNPs), to investigate through MR their association with systolic BP (SBP) and diastolic BP (DBP) in a Swedish urban-based study, the Malmö Diet and Cancer study (n = 29 298). Causality was evaluated by the inverse variance weighted method (IVW) and weighted median, while MR Egger and MR-PRESSO were used as sensitivity analyses. Genetically predicted serum calcium level was found to be associated with DBP (IVW: beta = 0.10, SE = 0.04, P = 0.007) and SBP (IVW: beta = 0.07, SE = 0.04, P = 0.04). Genetically predicted Vit-D and PTH showed no association with the traits, while FGF23 was inversely associated with SBP (IVW: beta = -0.11, SE = 0.04, P = 0.01), although this association lost statistical significance in sensitivity analysis. Our study shows a direct association between genetically predicted calcium level and DBP, and a weaker association with SBP. No such clear association was found for genetically predicted calciotropic hormone levels. It is of interest to detect which target genes involved in calcium homeostasis mediate the effect of calcium on BP, particularly for improving personalized intervention strategies.

Identifiants

pubmed: 36062972
pii: 6692281
doi: 10.1210/clinem/dgac501
doi:

Substances chimiques

Calcium SY7Q814VUP
Calcium, Dietary 0
Parathyroid Hormone 0
Vitamin D 1406-16-2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3080-3085

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Alice Giontella (A)

Department of Medicine, University of Verona, Verona 37124, Italy.
Department of Clinical Sciences, Clinical Research Center, Lund University, Malmö 21428, Sweden.

Luca A Lotta (LA)

Regeneron Genetics Center, Tarrytown, NY 10591, USA.

Aris Baras (A)

Regeneron Genetics Center, Tarrytown, NY 10591, USA.

Pietro Minuz (P)

Department of Medicine, University of Verona, Verona 37124, Italy.

Dipender Gill (D)

Department of Epidemiology and Biostatistics, Imperial College London, London SW72AZ, UK.
Novo Nordisk Research Centre Oxford, Old Road Campus OX37FZ, UK.

Olle Melander (O)

Department of Clinical Sciences, Clinical Research Center, Lund University, Malmö 21428, Sweden.
Department of Emergency and Internal Medicine, Skåne University Hospital, Malmö 21428, Sweden.

Cristiano Fava (C)

Department of Medicine, University of Verona, Verona 37124, Italy.
Department of Clinical Sciences, Clinical Research Center, Lund University, Malmö 21428, Sweden.

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Classifications MeSH