TY - JOUR
T1 - Vitamin D and mortality
T2 - Individual participant data meta-analysis of standardized 25-hydroxyvitamin D in 26916 individuals from a European consortium
AU - Gaksch, Martin
AU - Jorde, Rolf
AU - Grimnes, Guri
AU - Joakimsen, Ragnar
AU - Schirmer, Henrik
AU - Wilsgaard, Tom
AU - Mathiesen, Ellisiv B
AU - Njølstad, Inger
AU - Løchen, Maja-Lisa
AU - März, Winfried
AU - Kleber, Marcus E
AU - Tomaschitz, Andreas
AU - Grübler, Martin
AU - Eiriksdottir, Gudny
AU - Gudmundsson, Elias F
AU - Harris, Tamara B
AU - Cotch, Mary F
AU - Aspelund, Thor
AU - Gudnason, Vilmundur
AU - Rutters, Femke
AU - Beulens, Joline W J
AU - van 't Riet, Esther
AU - Nijpels, Giel
AU - Dekker, Jacqueline M
AU - Grove-Laugesen, Diana
AU - Rejnmark, Lars
AU - Busch, Markus A
AU - Mensink, Gert B M
AU - Scheidt-Nave, Christa
AU - Thamm, Michael
AU - Swart, Karin M A
AU - Brouwer, Ingeborg A
AU - Lips, Paul
AU - van Schoor, Natasja M
AU - Sempos, Christopher T
AU - Durazo-Arvizu, Ramón A
AU - Škrabáková, Zuzana
AU - Dowling, Kirsten G
AU - Cashman, Kevin D
AU - Kiely, Mairead
AU - Pilz, Stefan
PY - 2017
Y1 - 2017
N2 - BACKGROUND: Vitamin D deficiency may be a risk factor for mortality but previous meta-analyses lacked standardization of laboratory methods for 25-hydroxyvitamin D (25[OH]D) concentrations and used aggregate data instead of individual participant data (IPD). We therefore performed an IPD meta-analysis on the association between standardized serum 25(OH)D and mortality.METHODS: In a European consortium of eight prospective studies, including seven general population cohorts, we used the Vitamin D Standardization Program (VDSP) protocols to standardize 25(OH)D data. Meta-analyses using a one step procedure on IPD were performed to study associations of 25(OH)D with all-cause mortality as the primary outcome, and with cardiovascular and cancer mortality as secondary outcomes. This meta-analysis is registered at ClinicalTrials.gov, number NCT02438488.FINDINGS: We analysed 26916 study participants (median age 61.6 years, 58% females) with a median 25(OH)D concentration of 53.8 nmol/L. During a median follow-up time of 10.5 years, 6802 persons died. Compared to participants with 25(OH)D concentrations of 75 to 99.99 nmol/L, the adjusted hazard ratios (with 95% confidence interval) for mortality in the 25(OH)D groups with 40 to 49.99, 30 to 39.99, and <30 nmol/L were 1.15 (1.00-1.29), 1.33 (1.16-1.51), and 1.67 (1.44-1.89), respectively. We observed similar results for cardiovascular mortality, but there was no significant linear association between 25(OH)D and cancer mortality. There was also no significantly increased mortality risk at high 25(OH)D levels up to 125 nmol/L.INTERPRETATION: In the first IPD meta-analysis using standardized measurements of 25(OH)D we observed an association between low 25(OH)D and increased risk of all-cause mortality. It is of public health interest to evaluate whether treatment of vitamin D deficiency prevents premature deaths.
AB - BACKGROUND: Vitamin D deficiency may be a risk factor for mortality but previous meta-analyses lacked standardization of laboratory methods for 25-hydroxyvitamin D (25[OH]D) concentrations and used aggregate data instead of individual participant data (IPD). We therefore performed an IPD meta-analysis on the association between standardized serum 25(OH)D and mortality.METHODS: In a European consortium of eight prospective studies, including seven general population cohorts, we used the Vitamin D Standardization Program (VDSP) protocols to standardize 25(OH)D data. Meta-analyses using a one step procedure on IPD were performed to study associations of 25(OH)D with all-cause mortality as the primary outcome, and with cardiovascular and cancer mortality as secondary outcomes. This meta-analysis is registered at ClinicalTrials.gov, number NCT02438488.FINDINGS: We analysed 26916 study participants (median age 61.6 years, 58% females) with a median 25(OH)D concentration of 53.8 nmol/L. During a median follow-up time of 10.5 years, 6802 persons died. Compared to participants with 25(OH)D concentrations of 75 to 99.99 nmol/L, the adjusted hazard ratios (with 95% confidence interval) for mortality in the 25(OH)D groups with 40 to 49.99, 30 to 39.99, and <30 nmol/L were 1.15 (1.00-1.29), 1.33 (1.16-1.51), and 1.67 (1.44-1.89), respectively. We observed similar results for cardiovascular mortality, but there was no significant linear association between 25(OH)D and cancer mortality. There was also no significantly increased mortality risk at high 25(OH)D levels up to 125 nmol/L.INTERPRETATION: In the first IPD meta-analysis using standardized measurements of 25(OH)D we observed an association between low 25(OH)D and increased risk of all-cause mortality. It is of public health interest to evaluate whether treatment of vitamin D deficiency prevents premature deaths.
KW - Journal Article
UR - http://www.scopus.com/inward/record.url?scp=85012982827&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85012982827&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0170791
DO - 10.1371/journal.pone.0170791
M3 - Article
C2 - 28207791
SN - 1932-6203
VL - 12
SP - e0170791
JO - PLoS ONE
JF - PLoS ONE
IS - 2
M1 - e0170791
ER -
