Xiong Kai, Lu Linjie, Ge Pingyu, Yuan Shenglan, Che Bangwei, Zhai Jiancheng, Tang Kaifa, Zhang Hongyan
Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China.
Department of Urology & Andrology, The First Affiliated Hospital of Guizhou University of Traditional Chinese Medicine, Guiyang 550001, China.
J Trace Elem Med Biol. 2025 Jun;89:127652. doi: 10.1016/j.jtemb.2025.127652. Epub 2025 Apr 10.
The association between high calcium intake and prostate cancer (PCa) risk is only weak, and the dose-response relationship between the two remains unclear. Therefore, we conducted a systematic review and dose-response meta-analysis to evaluate the relationship between calcium intake and PCa risk.
The databases were searched up to September 2024. Random-effects models were employed to pool effect sizes (ESs) with 95 % confidence intervals (CIs) for the highest versus lowest intakes of total, dietary, supplemental, dairy and non-dairy calcium. Linear and non-linear dose-response analyses were performed to assess the relationships between them.
21 prospective cohort studies were included in this meta-analysis. High intakes of total, dietary, and dairy calcium were associated with an increased risk of PCa. The summary ESs were 1.08 (95 % CI 1.01-1.15), 1.16 (95 % CI 1.08-1.24), and 1.13 (95 % CI 1.02-1.24), respectively. Supplemental calcium and non-dairy calcium intakes were not significantly associated with PCa risk. Linear dose-response analysis indicated that dietary (P-linear < 0.001) and dairy calcium intakes (P-linear = 0.02) were positively associated with PCa risk, and total calcium intake was possibly linearly related to PCa risk (P-linear = 0.06). An additional intake of 300 mg/day of total, dietary, and dairy calcium is linked to approximately 2 %, 6 %, and 5 % increases in PCa risk, respectively. No non-linear dose-response relationships were observed between calcium intake and PCa risk.
These results demonstrate higher intakes of total, dietary, and dairy calcium were associated with an increased risk of PCa. Future research should provide more detailed results, including risks between different sources of calcium and PCa subtypes.
高钙摄入量与前列腺癌(PCa)风险之间的关联较弱,两者之间的剂量反应关系仍不明确。因此,我们进行了一项系统评价和剂量反应荟萃分析,以评估钙摄入量与PCa风险之间的关系。
检索数据库至2024年9月。采用随机效应模型合并最高与最低总钙、膳食钙、补充剂钙、乳制品钙和非乳制品钙摄入量的效应量(ESs)及其95%置信区间(CIs)。进行线性和非线性剂量反应分析以评估它们之间的关系。
本荟萃分析纳入了21项前瞻性队列研究。总钙、膳食钙和乳制品钙的高摄入量与PCa风险增加相关。汇总ESs分别为1.08(95%CI 1.01 - 1.15)、1.16(95%CI 1.08 - 1.24)和1.13(95%CI 1.02 - 1.24)。补充剂钙和非乳制品钙摄入量与PCa风险无显著关联。线性剂量反应分析表明,膳食钙摄入量(P线性<0.001)和乳制品钙摄入量(P线性 = 0.02)与PCa风险呈正相关,总钙摄入量可能与PCa风险呈线性相关(P线性 = 0.06)。总钙、膳食钙和乳制品钙每日额外摄入300 mg分别与PCa风险增加约2%、6%和5%相关。未观察到钙摄入量与PCa风险之间的非线性剂量反应关系。
这些结果表明,总钙、膳食钙和乳制品钙的较高摄入量与PCa风险增加相关。未来的研究应提供更详细的结果,包括不同钙源与PCa亚型之间的风险。