Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation study

Publication Description
Summary Background Low plasma 25-hydroxyvitamin D (25[OH]D) concentration is associated with high arterial blood pressure and hypertension risk, but whether this association is causal is unknown. We used a mendelian randomisation approach to test whether 25(OH)D concentration is causally associated with blood pressure and hypertension risk. Methods In this mendelian randomisation study, we generated an allele score (25[OH]D synthesis score) based on variants of genes that affect 25(OH)D synthesis or substrate availability ( CYP2R1 and DHCR7 ), which we used as a proxy for 25(OH)D concentration. We meta-analysed data for up to 108 173 individuals from 35 studies in the D-CarDia collaboration to investigate associations between the allele score and blood pressure measurements. We complemented these analyses with previously published summary statistics from the International Consortium on Blood Pressure (ICBP), the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium, and the Global Blood Pressure Genetics (Global BPGen) consortium. Findings In phenotypic analyses (up to n=49 363), increased 25(OH)D concentration was associated with decreased systolic blood pressure (β per 10% increase, −0·12 mm Hg, 95% CI −0·20 to −0·04; p=0·003) and reduced odds of hypertension (odds ratio [OR] 0·98, 95% CI 0·97–0·99; p=0·0003), but not with decreased diastolic blood pressure (β per 10% increase, −0·02 mm Hg, −0·08 to 0·03; p=0·37). In meta-analyses in which we combined data from D-CarDia and the ICBP (n=146 581, after exclusion of overlapping studies), each 25(OH)D-increasing allele of the synthesis score was associated with a change of −0·10 mm Hg in systolic blood pressure (−0·21 to −0·0001; p=0·0498) and a change of −0·08 mm Hg in diastolic blood pressure (−0·15 to −0·02; p=0·01). When D-CarDia and consortia data for hypertension were meta-analysed together (n=142 255), the synthesis score was associated with a reduced odds of hypertension (OR per allele, 0·98, 0·96–0·99; p=0·001). In instrumental variable analysis, each 10% increase in genetically instrumented 25(OH)D concentration was associated with a change of −0·29 mm Hg in diastolic blood pressure (−0·52 to −0·07; p=0·01), a change of −0·37 mm Hg in systolic blood pressure (−0·73 to 0·003; p=0·052), and an 8·1% decreased odds of hypertension (OR 0·92, 0·87–0·97; p=0·002). Interpretation Increased plasma concentrations of 25(OH)D might reduce the risk of hypertension. This finding warrants further investigation in an independent, similarly powered study. Funding British Heart Foundation, UK Medical Research Council, and Academy of Finland.

Primary Author
Vimaleswaran,Karani S., PhD
Cavadino,Alana, MSc
Berry,Diane J., PhD
Jorde,Rolf, Prof
Dieffenbach,Aida Karina, PhD
Lu,Chen, PhD
Alves,Alexessander Couto, PhD
Heerspink, Hiddo J Lambers, PhD
Tikkanen,Emmi, PhD
Eriksson,Joel, MD
Wong,Andrew, PhD
Mangino,Massimo, PhD
Jablonski,Kathleen A., PhD
Nolte,Ilja M., PhD
Houston,Denise K., PhD
Ahluwalia,Tarunveer Singh, PhD
van der Most, Peter J, MSc
Pasko,Dorota, MSc
Zgaga,Lina, PhD
Thiering,Elisabeth, MSc
Vitart,Veronique, PhD
Fraser,Ross M., PhD
Huffman,Jennifer E., MSc
de Boer, Rudolf A, Prof
Schöttker,Ben, PhD
Saum,Kai-Uwe, MPH
McCarthy,Mark I., Prof
Dupuis,Josée, Prof
Herzig,Karl-Heinz, Prof
Sebert,Sylvain, PhD
Pouta,Anneli, MD
Laitinen,Jaana, PhD
Kleber,Marcus E., PhD
Navis,Gerjan, Prof
Lorentzon,Mattias, Prof
Jameson,Karen, MSc
Arden,Nigel, Prof
Cooper,Jackie A., MSc
Acharya,Jayshree, PhD
Hardy,Rebecca, Prof
Raitakari,Olli, Prof
Ripatti,Samuli, Prof
Billings,Liana K., MD
Lahti,Jari, PhD
Osmond,Clive, Prof
Penninx,Brenda W., Prof
Rejnmark,Lars, MD
Lohman,Kurt K., MStat
Paternoster,Lavinia, PhD
Stolk,Ronald P., Prof
Hernandez,Dena G., MS
Byberg,Liisa, PhD
Hagström,Emil, MD
Melhus,Håkan, Prof
Ingelsson,Erik, Prof
Mellström,Dan, Prof
Ljunggren,Östen, Prof
Tzoulaki,Ioanna, PhD
McLachlan,Stela, MD
Theodoratou,Evropi, PhD
Tiesler, Carla M T, MSc
Jula,Antti, MD
Navarro,Pau, PhD
Wright,Alan F., Prof
Polasek,Ozren, MD
Wilson,James F., DPhil
Rudan,Igor, Prof
Salomaa,Veikko, Prof
Heinrich,Joachim, PhD
Campbell,Harry, Prof
Price,Jacqueline F., MD
Karlsson,Magnus, Prof
Lind,Lars, MD
Michaëlsson,Karl, Prof
Bandinelli,Stefania
Frayling,Timothy M., Prof
Hartman,Catharina A., PhD
Sørensen, Thorkild I A, Prof
Kritchevsky,Stephen B., Prof
Langdahl,Bente Lomholt, Prof
Eriksson,Johan G., Prof
Florez,Jose C., Prof
Spector,Tim D., Prof
Lehtimäki,Terho, Prof
Kuh,Diana, Prof
Humphries,Steve E., Prof
Cooper,Cyrus, Prof
Ohlsson,Claes, Prof
März,Winfried, Prof
de Borst, Martin H, MD
Kumari,Meena, Prof
Kivimaki,Mika, Prof
Wang,Thomas J., Prof
Power,Chris, Prof
Brenner,Hermann, Prof
Grimnes,Guri, MD
van der Harst, Pim, MD
Snieder,Harold, Prof
Hingorani,Aroon D., Prof
Pilz,Stefan, Prof
...

Volume
2

Issue
9

Start Page
719

Other Pages
729

Publisher
Elsevier Ltd

URL
https://www.clinicalkey.es/playcontent/1-s2.0-S2213858714701135

PMID
24974252

PMCID
PMC4582411



Reference Type
Journal Article

Periodical Full
Lancet Diabetes & Endocrinology, The

Publication Year
2014

Place of Publication
England

ISSN/ISBN
2213-8587

Document Object Index
10.1016/S2213-8587(14)70113-5