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DD2队列中2型糖尿病诊断后的出生体重与慢性肾脏病风险

Birthweight and risk of chronic kidney disease after a type 2 diabetes diagnosis in the DD2 cohort.

作者信息

Hansen Aleksander L, Christiansen Christian F, Brøns Charlotte, Engelhard Leonie M, Hansen Torben, Nielsen Jens S, Vestergaard Peter, Højlund Kurt, Jessen Niels, Olsen Michael H, Sørensen Henrik T, Rossing Peter, Thomsen Reimar W, Vaag Allan

机构信息

Steno Diabetes Center Copenhagen, Herlev, Denmark.

Department of Clinical Epidemiology, Aarhus University Hospital, and Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.

出版信息

Diabetologia. 2025 Apr;68(4):778-791. doi: 10.1007/s00125-024-06357-4. Epub 2025 Feb 1.

Abstract

AIMS/HYPOTHESIS: Low birthweight (LBW) is associated with younger age, less obesity and more hypertension among people recently diagnosed with type 2 diabetes, as well as increased cardiovascular morbidity and mortality risk. It is not known whether LBW is associated with an increased risk of incident chronic kidney disease (CKD) among people with a type 2 diabetes diagnosis.

METHODS

Original midwife records were retrieved for 5982 participants with recently diagnosed type 2 diabetes enrolled in the Danish Center for Strategic Research in Type 2 Diabetes (DD2) cohort between 2010 and 2024. They were followed until first incident CKD diagnosis, defined as either two eGFR measurements <60 ml/min per 1.73m or two urine albumin/creatinine ratio (UACR) measurements >3 mg/mmol, each 90-365 days apart. Confounder-standardised 10 year risks of CKD were estimated, with death considered as a competing risk. Adjusted hazard ratios (aHRs) for CKD were computed using Cox and spline regression analyses. All analyses were controlled for differences in sex, age at enrolment, calendar year at birth, family history of diabetes and born-at-term status. Mixed-effects models were used to examine the trajectories of eGFR and UACR following enrolment.

RESULTS

A total of 1501 incident CKD endpoints occurred, corresponding to an incidence rate of 42.4 per 1000 person-years over a median follow-up time of 8.3 years. Spline models with birthweight as a continuous measure showed progressively increasing aHRs for CKD with decreasing birthweight. The 10-year standardised risk of CKD was 36.0% in people with LBW (<2500 g) and 30.6% in people with a normal birthweight (2500-4000 g), yielding a risk difference (RD) of 5.5% (95% CI -0.5%, 11.8%) and an aHR of 1.23 (95% CI 0.98, 1.55). People with type 2 diabetes and high birthweight (>4000 g) had a similar 10-year standardised CKD risk compared with normal birthweight (33.1% and 30.6%, respectively). This yielded an RD of 2.5% (95% CI -1.6%, 6.7%) and an aHR of 1.10 (95% CI 0.93, 1.29). In mixed-effects models examining eGFR and UACR trajectories, each 1 kg decrease in birthweight was associated with a 6.6% (95% CI 1.9, 11.1) increase in UACR, whereas no association was found for eGFR.

CONCLUSIONS/INTERPRETATION: A history of LBW was associated with elevated risk of CKD among people with a recent type 2 diabetes diagnosis, although the precision of risk estimates was limited.

摘要

目的/假设:低出生体重(LBW)与近期诊断为2型糖尿病的人群年龄较轻、肥胖程度较低、高血压较多有关,同时也与心血管疾病发病率和死亡率风险增加有关。目前尚不清楚低出生体重是否与2型糖尿病诊断人群发生慢性肾脏病(CKD)的风险增加有关。

方法

检索了2010年至2024年期间纳入丹麦2型糖尿病战略研究中心(DD2)队列的5982名近期诊断为2型糖尿病参与者的原始助产士记录。对他们进行随访,直至首次诊断为CKD,定义为两次估算肾小球滤过率(eGFR)测量值<60 ml/(min·1.73m²)或两次尿白蛋白/肌酐比值(UACR)测量值>3 mg/mmol,每次间隔90 - 365天。估计了经过混杂因素标准化的10年CKD风险,并将死亡视为竞争风险。使用Cox回归和样条回归分析计算CKD的调整后风险比(aHRs)。所有分析均对性别、入组年龄、出生年份、糖尿病家族史和足月出生状态的差异进行了控制。使用混合效应模型来研究入组后eGFR和UACR的变化轨迹。

结果

共发生1501例CKD终点事件,在中位随访时间8.3年期间,发病率为每1000人年42.4例。以出生体重作为连续变量的样条模型显示,随着出生体重降低,CKD的aHRs逐渐增加。低出生体重(<2500 g)人群的10年标准化CKD风险为36.0%,正常出生体重(2500 - 4000 g)人群为30.6%,风险差异(RD)为5.5%(95% CI -0.5%,11.8%),aHR为1.23(95% CI 0.98,1.55)。2型糖尿病且出生体重高(>4000 g)的人群与正常出生体重人群的10年标准化CKD风险相似(分别为33.1%和30.6%)。这产生的RD为2.5%(95% CI -1.6%,6.7%),aHR为1.10(95% CI 0.93,1.29)。在研究eGFR和UACR变化轨迹的混合效应模型中,出生体重每降低1 kg,UACR增加6.6%(95% CI 1.9,11.1),而未发现与eGFR有关联。

结论/解读:近期诊断为2型糖尿病的人群中,低出生体重史与CKD风险升高有关,尽管风险估计的精确性有限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e662/11950141/9b0580745da5/125_2024_6357_Fig1_HTML.jpg

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