Department of Veterans Affairs, Birmingham/Atlanta Geriatric Research, Education, and Clinical Center, Birmingham, AL, and Atlanta, GA; Department of Medicine, The University of Alabama at Birmingham, Birmingham, AL.
Department of Veterans Affairs, Birmingham/Atlanta Geriatric Research, Education, and Clinical Center, Birmingham, AL, and Atlanta, GA; Atlanta Veterans Affairs Medical Center, Department of Medicine, Emory University School of Medicine, Atlanta, GA.
Am J Obstet Gynecol. 2022 Apr;226(4):535.e1-535.e12. doi: 10.1016/j.ajog.2021.10.017. Epub 2021 Oct 19.
Observational studies among older women have associated vitamin D insufficiency with a greater prevalence and incidence of urinary incontinence. However, little is known about the effect of vitamin D supplementation in reducing urinary incontinence.
This study aimed to evaluate the effects of vitamin D supplementation in reducing the frequency of urinary incontinence in older women.
We conducted an ancillary study of women aged ≥55 years in the Vitamin D and Omega-3 Trial, a randomized trial with a 2×2 factorial design. Recruitment of participants started from 2011 to 2014 across 50 US states, and the follow-up of participants ended in January 2018. Randomized treatments in the parent study included (1) vitamin D (cholecalciferol) at a dosage of 2000 IU/d, (2) marine omega-3 fatty acids at a dosage of 1 g/d, and (3) matching placebo. Here, we analyzed women according to their randomization to vitamin D supplementation or placebo, regardless of treatment with omega-3 fatty acid supplementation. Validated frequency of urinary incontinence questions were added in year 2 of the study and were used again in year 5 at the end of trial. Prespecified ancillary outcomes included the prevalence of urinary incontinence at years 2 and 5, along with incident incontinence and progression of incontinence (from lower to higher frequency) from year 2 to year 5. Preplanned subgroup analyses examined the following outcomes: prerandomization of low serum levels of vitamin D (serum 25-hydroxyvitamin D<20 ng/mL), incontinence types, weight categories, and African American race.
Among the randomized women who provided urinary incontinence data, 11,646 women at year 2 and 10,527 women at year 5, the mean age was 70 years at year 2, with 29% racial and ethnic minorities. The prevalence of urinary incontinence that occurred at least weekly was 29% at year 2 and increased to 37% at year 5. Vitamin D supplementation compared to with placebo was not associated with lower odds of urinary incontinence occurring at least weekly at year 2 (odds ratio, 1.08; 95% confidence interval, 0.99-1.19) or year 5 (odds ratio, 1.04; 95% confidence interval, 0.94-1.15). Vitamin D supplementation compared to placebo was not associated with lower incidence or progression of urinary incontinence from year 2 to year 5: incidence (odds ratio, 1.06; 95% confidence interval, 0.83-1.35) or progression (odds ratio, 0.94; 95% confidence interval, 0.82-1.08). Women with prerandomization of low serum levels of vitamin D (n=836) did not have lower odds of the prevalence, incidence, or progression of urinary incontinence. The findings were null in subgroups according to incontinence type, women with obesity, and African American women. Only women with healthy weight randomized to vitamin D had lower odds of progression of urinary incontinence (odds ratio, 0.78; 95% confidence interval, 0.63-0.95; P=.01).
Vitamin D supplementation compared to placebo for 2 to 5 years was not associated with differences in the prevalence, incidence, or progression of urinary incontinence in older women with and without adequate serum vitamin D levels, with inconsistent differences among subgroups. The findings showed that the broad use of moderate doses of vitamin D supplementation did not reduce urinary incontinence in older women.
在老年女性中进行的观察性研究表明,维生素 D 不足与尿失禁的患病率和发生率增加有关。然而,关于维生素 D 补充剂在减少尿失禁方面的作用知之甚少。
本研究旨在评估维生素 D 补充剂在减少老年女性尿失禁频率方面的效果。
我们对维生素 D 和 ω-3 试验中的年龄≥55 岁的女性进行了一项辅助研究,该试验采用 2×2 析因设计进行。参与者的招募工作从 2011 年至 2014 年在美国 50 个州进行,参与者的随访于 2018 年 1 月结束。母研究中的随机治疗包括(1)每天 2000IU 的胆钙化醇维生素 D,(2)每天 1 克的海洋 ω-3 脂肪酸,和(3)匹配的安慰剂。在这里,我们根据随机分配到维生素 D 补充剂或安慰剂的情况对女性进行了分析,而不考虑 ω-3 脂肪酸补充剂的治疗情况。在研究的第 2 年添加了经过验证的尿失禁频率问题,并在试验结束时的第 5 年再次使用。预先指定的辅助结果包括第 2 年和第 5 年尿失禁的患病率,以及从第 2 年到第 5 年的新发尿失禁和尿失禁进展(从较低频率到较高频率)。预先计划的亚组分析检查了以下结果:随机分组前血清维生素 D 水平较低(血清 25-羟维生素 D<20ng/mL)、尿失禁类型、体重类别和非裔美国人种族。
在提供尿失禁数据的随机女性中,有 11646 名女性在第 2 年,10527 名女性在第 5 年,平均年龄为第 2 年的 70 岁,其中 29%为少数族裔和少数民族。至少每周发生一次尿失禁的患病率在第 2 年为 29%,在第 5 年增加到 37%。与安慰剂相比,维生素 D 补充剂与至少每周发生尿失禁的可能性较低无关,第 2 年(比值比,1.08;95%置信区间,0.99-1.19)或第 5 年(比值比,1.04;95%置信区间,0.94-1.15)。与安慰剂相比,维生素 D 补充剂与第 2 年至第 5 年尿失禁的发生率或进展无关:发生率(比值比,1.06;95%置信区间,0.83-1.35)或进展(比值比,0.94;95%置信区间,0.82-1.08)。随机分组前血清维生素 D 水平较低的女性(n=836)发生尿失禁的患病率、发生率或进展的可能性没有降低。根据尿失禁类型、肥胖女性和非裔美国女性的亚组,这些发现均为无效。只有体重健康的女性随机接受维生素 D 治疗,其尿失禁进展的可能性降低(比值比,0.78;95%置信区间,0.63-0.95;P=.01)。
与安慰剂相比,在 2 至 5 年内补充维生素 D 与有和没有足够血清维生素 D 水平的老年女性的尿失禁患病率、发生率或进展无差异,亚组之间存在不一致的差异。研究结果表明,广泛使用中等剂量的维生素 D 补充剂并不能减少老年女性的尿失禁。