Guangdong Provincial Key Laboratory of Food, Nutrition and Health, School of Public Health, Sun Yat-sen University, No. 74 Zhongshan Road 2, Guangdong, 510080, China.
Chronic Disease Epidemiology Laboratory, Pennington Biomedical Research Center, 6400 Perkins Road, Baton Rouge, LA, 70808, USA.
Eur J Nutr. 2018 Oct;57(7):2457-2467. doi: 10.1007/s00394-017-1518-8. Epub 2017 Aug 14.
Serum calcium and phosphorus abnormalities are associated with cardiovascular disorders in general population, but evidence among patients with established coronary heart disease (CHD) is limited and controversial. This study aimed to investigate the associations of baseline serum calcium and phosphorus levels with long-term mortality risk among patients with CHD.
We conducted a prospective cohort study among 3187 patients with CHD from October 2008 and December 2011 in China. Cox proportional hazards model was used to assess the associations of serum calcium and phosphorus at baseline with the risk of death.
During follow-up (mean, 4.9 years), 295 patients died, 193 of which resulted from cardiovascular causes. Multivariable-adjusted hazard ratios (HR) for each 1 mmol/L increase in serum calcium at baseline were 0.27 (95% confidence interval (CI) 0.14-0.51) for all-cause mortality and 0.26 (95% CI 0.12-0.54) for cardiovascular mortality. Patients in the highest compared to the lowest quartile of serum calcium were at lower risk of all-cause mortality (HR, 95% CI 0.57, 0.40-0.82) and cardiovascular mortality (0.50, 0.32-0.79) (both P < 0.001). This inverse association between serum calcium and the risk of mortality did not change when participants were stratified by sex, age groups, level of overweight, types of CHD, and history of diabetes. We also observed a graded positive association between baseline serum phosphorus and the risks of mortality.
The present study is the first to report that lower serum calcium at baseline is associated with an increased risk of all-cause and cardiovascular mortality in a Chinese coronary heart disease cohort. Further studies are required to investigate the causal relationship and actual mechanisms.
血清钙和磷异常与一般人群的心血管疾病有关,但在已确诊的冠心病(CHD)患者中的证据有限且存在争议。本研究旨在探讨基线血清钙和磷水平与 CHD 患者长期死亡风险的关系。
我们在中国进行了一项前瞻性队列研究,纳入了 2008 年 10 月至 2011 年 12 月期间的 3187 例 CHD 患者。Cox 比例风险模型用于评估基线时血清钙和磷与死亡风险的关系。
在随访期间(平均 4.9 年),有 295 例患者死亡,其中 193 例死于心血管原因。多变量调整后的风险比(HR)显示,基线时血清钙每增加 1mmol/L,全因死亡率的 HR 为 0.27(95%置信区间[CI] 0.14-0.51),心血管死亡率的 HR 为 0.26(95% CI 0.12-0.54)。与血清钙最低四分位数相比,血清钙最高四分位数的患者全因死亡率(HR,95%CI 0.57,0.40-0.82)和心血管死亡率(0.50,0.32-0.79)均较低(均 P<0.001)。这种血清钙与死亡率风险之间的负相关关系在按性别、年龄组、超重程度、CHD 类型和糖尿病史分层的患者中并未改变。我们还观察到基线血清磷与死亡率风险之间存在分级正相关关系。
本研究首次报道,中国冠心病队列中,基线时血清钙较低与全因和心血管死亡风险增加相关。需要进一步研究以探讨因果关系和实际机制。