Sun Yi-Qian, Langhammer Arnulf, Skorpen Frank, Chen Yue, Mai Xiao-Mei
Department of Laboratory Medicine, Children's and Women's Health (LBK), Trondheim, Norway.
Department of Public Health and Nursing, Norwegian University of Science and Technology, NTNU, Trondheim, Norway.
BMJ Open. 2017 Jul 3;7(6):e017256. doi: 10.1136/bmjopen-2017-017256.
To investigate the association of vitamin D status with all-cause mortality in a Norwegian population and the potential influences of existing chronic diseases on the association.
A population-based prospective cohort study.
Nord-Trøndelag County, Norway.
A random sample (n=6613) of adults aged 20 years or older in a cohort.
Serum 25-hydroxyvitamin D (25(OH)D) levels were measured in blood samples collected at baseline (n=6377). Mortality was ascertained from the Norwegian National Registry. Cox regression models were applied to estimate the HRs with 95% CIs for all-cause mortality in association with serum 25(OH)D levels after adjustment for a wide spectrum of confounding factors as well as chronic diseases at baseline.
The median follow-up time was 18.5 years, during which 1539 subjects died. The HRs for all-cause mortality associated with the first quartile level of 25(OH)D (<34.5 nmol/L) as compared with the fourth quartile (≥58.1 nmol/L) before and after adjustment for chronic diseases at baseline were 1.30 (95% CI 1.11 to 1.51) and 1.27 (95% CI 1.09 to 1.48), respectively. In the subjects without chronic diseases at baseline and with further exclusion of the first 3 years of follow-up, the corresponding adjusted HR was 1.34 (95% CI 1.09 to 1.66).
Low serum 25(OH)D level was associated with increased all-cause mortality in a general Norwegian population. The association was not notably influenced by existing chronic diseases.
研究挪威人群中维生素D状态与全因死亡率之间的关联,以及现有慢性疾病对该关联的潜在影响。
基于人群的前瞻性队列研究。
挪威北特伦德拉格郡。
队列中20岁及以上成年人的随机样本(n = 6613)。
在基线时采集的血样中测量血清25-羟维生素D(25(OH)D)水平(n = 6377)。从挪威国家登记处确定死亡率。应用Cox回归模型,在对一系列混杂因素以及基线时的慢性疾病进行调整后,估计与血清25(OH)D水平相关的全因死亡率的HR及95%CI。
中位随访时间为18.5年,在此期间有1539名受试者死亡。在对基线时的慢性疾病进行调整前后,与25(OH)D第一四分位数水平(<34.5 nmol/L)相比,第四四分位数(≥58.1 nmol/L)的全因死亡率HR分别为1.30(95%CI 1.11至1.51)和1.27(95%CI 1.09至1.48)。在基线时无慢性疾病且进一步排除随访前3年的受试者中,则相应的调整后HR为1.34(95%CI 1.09至1.66)。
在挪威普通人群中,低血清25(OH)D水平与全因死亡率增加相关。该关联未受到现有慢性疾病显著影响。