Alan R. Gaby, MD
Wednesday, October 03, 2012
by: Alan R. Gaby, MD
Retrospective observational study
247,574 individuals of all ages from Copenhagen, Denmark, whose serum 25-hydroxyvitamin D level had been measured by their general practitioner between April 2004 and January 2010
Serum 25-hydroxyvitamin D levels and all-cause mortality
Primary Outcome Measures
The association between serum 25-hydroxyvitamin D levels and all-cause mortality
During a median follow-up period of 3.07 years, 15,198 subjects (6.1%) died. A reverse J-shaped association between serum 25-hydroxyvitamin D and mortality was observed. A level of 50-60 nmol/L was associated with the lowest mortality. Compared with 50 nmol/L, the hazard ratios (95% confidence intervals) of all-cause mortality at very low (10 nmol/L) and high (140 nmol/L) serum levels of 25-hydroxyvitamin D were 2.13 (2.02-2.24) and 1.42 (1.31-1.53), respectively. After exclusion of subjects who died within 1 year of blood collection, the reverse J-shaped association remained, although the hazard ratios for all-cause mortality at both the highest and lowest levels of 25-hydroxyvitamin D decreased slightly.
Observational studies do not prove cause-and-effect. A number of factors other than vitamin D nutritional status influence serum 25-hydroxyvitamin D levels. For example, 25-hydroxyvitamin D is an acute-phase reactant that declines in the serum in response to inflammation.1 In addition, a substantial amount of 25-hydroxylation of vitamin D occurs in the gonads, and serum 25-hydroxyvitamin D levels appear to be influenced by gonadal function.2 Observational studies on 25-hydroxyvitamin D levels and health outcomes may therefore be confounded by differences in levels of testosterone, estrogen, and DHEA, each of which may influence health outcomes. Although less is known about factors that might increase serum 25-hydroxyvitamin D levels, such increases could conceivably occur in response to certain disease states.
Despite these limitations, the results of the present study are consistent with the possibility that both deficiency and excess of vitamin D are harmful. 3
1. Reid D, Toole BJ, Knox S, et al. The relation between acute changes in the systemic inflammatory response and plasma 25-hydroxyvitamin D concentrations after elective knee arthroplasty. Am J Clin Nutr. 2011;93:1006-1011.
2. Foresta C, Selice R, Di Mambro A, Strapazzon G. Testiculopathy and vitamin D insufficiency. Lancet. 2010;376:1301.
3. Grimnes G, Joakimsen R, Figenschau Y, et al. The effect of high-dose vitamin D on bone mineral density and bone turnover markers in postmenopausal women with low bone mass – a randomized controlled 1-year trial. Osteoporos Int. 2012;23:201-211.