Aleksander L. Hansen, Christian F. Christiansen, Charlotte Brøns, Leonie M. Engelhard, Torben Hansen, Jens S. Nielsen, Peter Vestergaard, Kurt Højlund, Niels Jessen, Michael H. Olsen, Henrik T. Sørensen, Peter Rossing, Reimar W. Thomsen, Allan Vaag
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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.</p><h3 data-test=\"abstract-sub-heading\">Methods</h3><p>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<sup>2</sup> 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. 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引用次数: 0
摘要
目的/假设在新近诊断为2型糖尿病的人群中,低出生体重(LBW)与年龄更小、肥胖更少、高血压更多以及心血管发病率和死亡风险增加有关。目前尚不清楚LBW是否与诊断为2型糖尿病的患者发生慢性肾脏疾病(CKD)的风险增加有关。方法检索2010年至2024年丹麦2型糖尿病战略研究中心(DD2)队列中5982名新近诊断为2型糖尿病的参与者的原始助产士记录。随访至首次CKD诊断,定义为两次eGFR测量(每1.73m2 60 ml/min)或两次尿白蛋白/肌酐比(UACR)测量(每1.73m2 3 mg/mmol),每次间隔90-365天。估计混杂标准化的CKD 10年风险,死亡被认为是一个竞争风险。采用Cox和样条回归分析计算CKD的校正风险比(aHRs)。所有的分析都控制了性别、入组年龄、出生年份、糖尿病家族史和足月出生状况的差异。使用混合效应模型来检查入组后eGFR和UACR的轨迹。结果:在8.3年的中位随访时间内,总共发生了1501个CKD终点,对应于每1000人年42.4个发病率。以出生体重为连续指标的样条模型显示,随着出生体重的降低,慢性肾病患者的ahr逐渐增加。低体重人群(2500克)10年CKD标准化风险为36.0%,正常出生体重人群(2500 - 4000克)10年CKD标准化风险为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型糖尿病和高出生体重(4000克)的人与正常出生体重的人相比,10年标准化CKD风险相似(分别为33.1%和30.6%)。RD为2.5% (95% CI - 1.6%, 6.7%), aHR为1.10 (95% CI 0.93, 1.29)。在检查eGFR和UACR轨迹的混合效应模型中,出生体重每减少1公斤,UACR增加6.6% (95% CI 1.9, 11.1),而eGFR没有关联。结论/解释:在近期诊断为2型糖尿病的人群中,LBW病史与CKD风险升高相关,尽管风险估计的准确性有限。图形抽象
Birthweight and risk of chronic kidney disease after a type 2 diabetes diagnosis in the DD2 cohort
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 1.73m2 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.
期刊介绍:
Diabetologia, the authoritative journal dedicated to diabetes research, holds high visibility through society membership, libraries, and social media. As the official journal of the European Association for the Study of Diabetes, it is ranked in the top quartile of the 2019 JCR Impact Factors in the Endocrinology & Metabolism category. The journal boasts dedicated and expert editorial teams committed to supporting authors throughout the peer review process.