Division of Research, Kaiser Permanente Northern California, Oakland.
Division of Preventive Medicine, School of Medicine, University of Alabama at Birmingham, Birmingham.
JAMA Intern Med. 2018 Mar 1;178(3):328-337. doi: 10.1001/jamainternmed.2017.7978.
Lactation duration has shown weak protective associations with incident diabetes (3%-15% lower incidence per year of lactation) in older women based solely on self-report of diabetes, studies initiated beyond the reproductive period are vulnerable to unmeasured confounding or reverse causation from antecedent biochemical risk status, perinatal outcomes, and behaviors across the childbearing years.
To evaluate the association between lactation and progression to diabetes using biochemical testing both before and after pregnancy and accounting for prepregnancy cardiometabolic measures, gestational diabetes (GD), and lifestyle behaviors.
DESIGN, SETTING, AND PARTICIPANTS: For this US multicenter, community-based 30-year prospective cohort study, there were 1238 women from the Coronary Artery Risk Development in Young Adults (CARDIA) study of young black and white women ages 18 to 30 years without diabetes at baseline (1985-1986) who had 1 or more live births after baseline, reported lactation duration, and were screened for diabetes up to 7 times during 30 years after baseline (1986-2016).
Time-dependent lactation duration categories (none, >0 to 6 months, >6 to <12 months, and ≥12 months) across all births since baseline through 30 years.
Diabetes incidence rates per 1000 person-years and adjusted relative hazards (RH) with corresponding 95% CIs, as well as proportional hazards regression models adjusted for biochemical, sociodemographic, and reproductive risk factors, as well as family history of diabetes, lifestyle, and weight change during follow-up.
Overall 1238 women were included in this analysis (mean [SD] age, 24.2 [3.7] years; 615 black women). There were 182 incident diabetes cases during 27 598 person-years for an overall incidence rate of 6.6 cases per 1000 person-years (95% CI, 5.6-7.6); and rates for women with GD and without GD were 18.0 (95% CI, 13.3-22.8) and 5.1 (95% CI, 4.2-6.0), respectively (P for difference < .001). Lactation duration showed a strong, graded inverse association with diabetes incidence: adjusted RH for more than 0 to 6 months, 0.75 (95% CI, 0.51-1.09); more than 6 months to less than 12 months, 0.52 (95% CI, 0.31-0.87), and 12 months or more 0.53 (0.29-0.98) vs none (0 days) (P for trend = .01). There was no evidence of effect modification by race, GD, or parity.
This study provides longitudinal biochemical evidence that lactation duration is independently associated with lower incidence of diabetes. Further investigation is required to elucidate mechanisms that may explain this relationship.
基于自我报告的糖尿病,哺乳期时间与新发糖尿病呈弱保护相关性(每年哺乳增加 3%-15%的发病率降低),但仅基于自我报告的糖尿病的研究,容易受到未测量的混杂因素或来自妊娠前生化风险状况、围产期结局以及整个生育期行为的反向因果关系的影响。
使用妊娠前后的生化检测来评估哺乳与糖尿病进展之间的关系,并考虑到妊娠前的心血管代谢指标、妊娠糖尿病(GD)和生活方式行为。
设计、地点和参与者:这是一项美国多中心、基于社区的 30 年前瞻性队列研究,纳入了来自冠状动脉风险发展在年轻人(CARDIA)研究的 1238 名年龄在 18 至 30 岁之间的年轻黑人和白人女性,这些女性在基线时(1985-1986 年)没有糖尿病,在基线后有 1 次或多次活产,报告了哺乳时间,并在基线后 30 年期间最多进行了 7 次糖尿病筛查(1986-2016 年)。
在基线后通过所有分娩,跨所有出生的时间依赖性哺乳时间类别(无、>0 至 6 个月、>6 至<12 个月和≥12 个月)。
每 1000 人年的糖尿病发病率和调整后的相对危险度(RH)及其相应的 95%置信区间(CI),以及调整了生化、社会人口学和生殖风险因素、糖尿病家族史、生活方式和随访期间体重变化的比例风险回归模型。
共有 1238 名女性纳入了本分析(平均[标准差]年龄为 24.2[3.7]岁;615 名黑人女性)。在 27598 人年的随访期间,有 182 例新发糖尿病,总发病率为 6.6 例/1000 人年(95%CI,5.6-7.6);GD 和非 GD 女性的发病率分别为 18.0(95%CI,13.3-22.8)和 5.1(95%CI,4.2-6.0)(差异 P<.001)。哺乳时间与糖尿病发病率呈强烈、分级负相关:调整后,超过 0 至 6 个月的 RH 为 0.75(95%CI,0.51-1.09);超过 6 个月至小于 12 个月的 RH 为 0.52(95%CI,0.31-0.87),12 个月或更长时间的 RH 为 0.53(0.29-0.98),与无哺乳(0 天)相比(趋势 P=.01)。未发现种族、GD 或产次存在效应修饰。
本研究提供了纵向生化证据,表明哺乳时间与糖尿病发病率的降低独立相关。需要进一步研究来阐明可能解释这种关系的机制。