RETRACTED: Non-linear Mendelian randomization analyses support a role for vitamin D deficiency in cardiovascular disease risk (Retracted article. See vol. 46, pg. 1456, 2025)

被引:136
作者
Zhou, Ang [1 ,2 ]
Selvanayagam, Joseph B. [2 ,3 ]
Hypponen, Elina [1 ,2 ,4 ]
机构
[1] Univ South Australia, Australian Ctr Precis Hlth, Canc Res Inst, GPO Box 2471, Adelaide, SA 5001, Australia
[2] South Australian Hlth & Med Res Inst, North Terrace, Adelaide, SA 5000, Australia
[3] Flinders Med Ctr, Dept Cardiovasc Med, Adelaide, SA 5042, Australia
[4] UCL Great Ormond St Inst Child Hlth, Populat Policy & Practice, 30 Guilford St, London, England
基金
英国医学研究理事会;
关键词
Non-linear Mendelian randomization; Vitamin D; Serum 25-hydroxyvitamin Dconcentration; Cardiovascular diseases; Systolic blood pressure; Diastolic blood pressure; Cardiac-imaging phenotypes; RENIN-ANGIOTENSIN SYSTEM; UK BIOBANK; 25-HYDROXYVITAMIN D; BLOOD-PRESSURE; INSTRUMENTAL VARIABLES; ASSOCIATION; PARTICIPANTS;
D O I
10.1093/eurheartj/ehab809
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Low vitamin D status is associated with a higher risk for cardiovascular diseases (CVDs). Although most existing linear Mendelian randomization (MR) studies reported a null effect of vitamin D on CVD risk, a non-linear effect cannot be excluded. Our aim was to apply the non-linear MR design to investigate the association of serum 25-hydroxyvitamin D [25(OH)D] concentration with CVD risk. Methods and results The non-linear MR analysis was conducted in the UK Biobank with 44 519 CVD cases and 251 269 controls. Blood pressure (BP) and cardiac-imaging-derived phenotypes were included as secondary outcomes. Serum 25(OH)D concentration was instrumented using 35 confirmed genome-wide significant variants. We also estimated the potential reduction in CVD incidence attributable to correction of low vitamin D status. There was a L-shaped association between genetically predicted serum 25(OH)D and CVD risk (Pnon-linear = 0.007), where CVD risk initially decreased steeply with increasing concentrations and levelled off at around 50 nmol/L. A similar association was seen for systolic (Pnon-linear = 0.03) and diastolic (Pnon-linear = 0.07) BP. No evidence of association was seen for cardiac-imaging phenotypes (P = 0.05 for all). Correction of serum 25(OH)D level below 50 nmol/L was predicted to result in a 4.4% reduction in CVD incidence (95% confidence interval: 1.8- 7.3%). Conclusion Vitamin D deficiency can increase the risk of CVD. Burden of CVD could be reduced by population-wide correction of low vitamin D status.
引用
收藏
页码:1731 / +
页数:10
相关论文
共 57 条
[1]   Vitamin D and Cardiovascular Disease Controversy Unresolved [J].
Al Mheid, Ibhar ;
Quyyumi, Arshed A. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2017, 70 (01) :89-100
[2]   Vitamin D deficiency 2.0: an update on the current status worldwide [J].
Amrein, Karin ;
Scherkl, Mario ;
Hoffmann, Magdalena ;
Neuwersch-Sommeregger, Stefan ;
Koestenberger, Markus ;
Berisha, Adelina Tmava ;
Martucci, Gennaro ;
Pilz, Stefan ;
Malle, Oliver .
EUROPEAN JOURNAL OF CLINICAL NUTRITION, 2020, 74 (11) :1498-1513
[3]   Whole grain consumption and risk of cardiovascular disease, cancer, and all cause and cause specific mortality: systematic review and dose-response meta-analysis of prospective studies [J].
Aune, Dagfinn ;
Keum, NaNa ;
Giovannucci, Edward ;
Fadnes, Lars T. ;
Boffetta, Paolo ;
Greenwood, Darren C. ;
Tonstad, Serena ;
Vatten, Lars J. ;
Riboli, Elio ;
Norat, Teresa .
BMJ-BRITISH MEDICAL JOURNAL, 2016, 353
[4]  
Australian Government Department of Health, 2021, VIT D STAT
[5]   Vitamin D Supplementation and Cardiovascular Disease Risks in More Than 83000 Individuals in 21 Randomized Clinical Trials: A Meta-analysis [J].
Barbarawi, Mahmoud ;
Kheiri, Babikir ;
Zayed, Yazan ;
Barbarawi, Owais ;
Dhillon, Harsukh ;
Swaid, Bakr ;
Yelangi, Anitha ;
Sundus, Saira ;
Bachuwa, Ghassan ;
Alkotob, Mohammad Luay ;
Manson, JoAnn E. .
JAMA CARDIOLOGY, 2019, 4 (08) :765-775
[6]   Categorical versus continuous risk factors and the calculation of potential impact fractions [J].
Barendregt, Jan J. ;
Veerman, J. Lennert .
JOURNAL OF EPIDEMIOLOGY AND COMMUNITY HEALTH, 2010, 64 (03) :209-212
[7]   Comparison of risk factor associations in UK Biobank against representative, general population based studies with conventional response rates: prospective cohort study and individual participant meta-analysis [J].
Batty, G. David ;
Gale, Catharine R. ;
Kivimaki, Mika ;
Deary, Ian J. ;
Bell, Steven .
BMJ-BRITISH MEDICAL JOURNAL, 2020, 368
[8]  
Bhaskaran K, 2018, LANCET DIABETES ENDO, V6, P944, DOI [10.1016/s2213-8587(18)30288-2, 10.1016/S2213-8587(18)30288-2]
[9]   25-Hydroxyvitamin D Levels and Risk of Ischemic Heart Disease, Myocardial Infarction, and Early Death Population-Based Study and Meta-Analyses of 18 and 17 Studies [J].
Brondum-Jacobsen, Peter ;
Benn, Marianne ;
Jensen, Gorm B. ;
Nordestgaard, Borge G. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2012, 32 (11) :2794-+
[10]   Use of allele scores as instrumental variables for Mendelian randomization [J].
Burgess, Stephen ;
Thompson, Simon G. .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2013, 42 (04) :1134-1144