Department of Medicine, University of Wisconsin, Madison, WI, USA.
J Bone Miner Res. 2010 Dec;25(12):2786-95. doi: 10.1002/jbmr.166. Epub 2010 Jun 24.
Proton pump inhibitors (PPIs) increase osteoporotic fracture risk presumably via hypochlorhydria and consequent reduced fractional calcium absorption (FCA). Existing studies provide conflicting information regarding the direct effects of PPIs on FCA. We evaluated the effect of PPI therapy on FCA. We recruited women at least 5 years past menopause who were not taking acid suppressants. Participants underwent three 24-hour inpatient FCA studies using the dual stable isotope method. Two FCA studies were performed 1 month apart to establish baseline calcium absorption. The third study occurred after taking omeprazole (40 mg/day) for 30 days. Each participant consumed the same foods during all FCA studies; study meals replicated subjects' dietary habits based on 7-day diet diaries. Twenty-one postmenopausal women ages 58 ± 7 years (mean ± SD) completed all study visits. Seventeen women were white, and 2 each were black and Hispanic. FCA (mean ± SD) was 20% ± 10% at visit 1, 18% ± 10% at visit 2, and 23% ± 10% following 30 ± 3 days of daily omeprazole (p = .07, ANOVA). Multiple linear regression revealed that age, gastric pH, serum omeprazole levels, adherence to omeprazole, and 25-hydroxyvitamin D levels were unrelated to changes in FCA between study visits 2 and 3. The 1,25-dihydroxyvitamin D(3) level at visit 2 was the only variable (p = .049) associated with the change in FCA between visits 2 and 3. PPI-associated hypochlorhydria does not decrease FCA following 30 days of continuous use. Future studies should focus on identifying mechanisms by which PPIs increase the risk of osteoporotic fracture.
质子泵抑制剂(PPIs)通过低胃酸和随后的钙吸收分数减少(FCA)增加骨质疏松性骨折风险。现有研究对 PPI 对 FCA 的直接影响提供了相互矛盾的信息。我们评估了 PPI 治疗对 FCA 的影响。我们招募了绝经后至少 5 年且未服用抑酸剂的女性。参与者接受了三次 24 小时住院 FCA 研究,使用双稳定同位素法。两次 FCA 研究相隔一个月进行,以确定钙吸收的基线。第三次研究在服用奥美拉唑(40mg/天)30 天后进行。所有 FCA 研究期间,每位参与者都食用相同的食物;研究餐根据 7 天饮食日记复制了受试者的饮食习惯。21 名绝经后女性年龄 58±7 岁(平均值±标准差)完成了所有研究访问。17 名女性为白人,2 名女性为黑人,2 名女性为西班牙裔。第一次访问时 FCA(平均值±标准差)为 20%±10%,第二次访问时为 18%±10%,第三次访问时为 30±3 天每天服用奥美拉唑后为 23%±10%(p=0.07,方差分析)。多元线性回归显示,年龄、胃 pH 值、血清奥美拉唑水平、奥美拉唑的依从性和 25-羟维生素 D 水平与研究访问 2 和 3 之间 FCA 的变化无关。第二次访问时 1,25-二羟维生素 D(3)水平是唯一与访问 2 和 3 之间 FCA 变化相关的变量(p=0.049)。PPIs 相关的低胃酸在连续使用 30 天后不会降低 FCA。未来的研究应集中于确定 PPI 增加骨质疏松性骨折风险的机制。