Department of Internal Medicine, MUHAS, Dar es Salaam, Tanzania; Department of Clinical Medicine, University of Bergen, Bergen, Norway.
Department of Clinical Medicine, University of Bergen, Bergen, Norway; Department of Medicine, Haukeland University Hospital, Bergen, Norway.
Am J Kidney Dis. 2016 Apr;67(4):601-8. doi: 10.1053/j.ajkd.2015.11.015. Epub 2015 Dec 31.
Previous studies have demonstrated that low birth weight (LBW) is associated with higher risk for end-stage renal disease (ESRD). However, both LBW and ESRD cluster in families. The present study investigates whether familial factors explain the association between LBW and ESRD.
Retrospective registry-based cohort study.
SETTING & PARTICIPANTS: Since 1967, the Medical Birth Registry of Norway has recorded medical data for all births in the country. Sibling data are available through the Norwegian Population Registry. Since 1980, all patients with ESRD in Norway have been registered in the Norwegian Renal Registry. Individuals registered in the Medical Birth Registry with at least 1 registered sibling were included.
LBW in the participant and/or LBW in at least 1 sibling.
ESRD.
Of 1,852,080 included individuals, 527 developed ESRD. Compared with individuals without LBW and with no siblings with LBW, individuals without LBW but with a sibling with LBW had an HR for ESRD of 1.20 (95% CI, 0.91-1.59), individuals with LBW but no siblings with LBW had an HR of 1.59 (95% CI, 1.18-2.14), and individuals with LBW and a sibling with LBW had an HR of 1.78 (95% CI, 1.26-2.53). Similar results were observed for individuals who were small for gestational age (SGA). Separate analyses for the association of age 18 to 42 years and noncongenital ESRD showed stronger associations for SGA than for LBW, and the associations were not statistically significant for age 18 to 42 years for LBW.
Follow-up only until 42 years of age.
LBW and SGA are associated with higher risk for ESRD during the first 40 years of life, and the associations were not explained by familial factors. Our results support the hypothesis that impaired intrauterine nephron development may be a causal risk factor for progressive kidney disease.
先前的研究表明,低出生体重(LBW)与终末期肾病(ESRD)的风险增加有关。然而,LBW 和 ESRD 都在家族中聚集。本研究旨在探讨家族因素是否能解释 LBW 与 ESRD 之间的关联。
回顾性基于登记的队列研究。
自 1967 年以来,挪威医学出生登记处记录了该国所有出生的医疗数据。通过挪威人口登记处可获得兄弟姐妹的数据。自 1980 年以来,挪威所有 ESRD 患者都在挪威肾脏登记处登记。在医学出生登记处登记并有至少 1 名登记兄弟姐妹的个人被纳入研究。
参与者的 LBW 和/或至少 1 名兄弟姐妹的 LBW。
ESRD。
在纳入的 1852080 名个体中,有 527 人发展为 ESRD。与无 LBW 且无 LBW 兄弟姐妹的个体相比,无 LBW 但有 LBW 兄弟姐妹的个体发生 ESRD 的 HR 为 1.20(95%CI,0.91-1.59),有 LBW 但无 LBW 兄弟姐妹的个体发生 ESRD 的 HR 为 1.59(95%CI,1.18-2.14),有 LBW 和 LBW 兄弟姐妹的个体发生 ESRD 的 HR 为 1.78(95%CI,1.26-2.53)。对于小于胎龄儿(SGA),也观察到了类似的结果。对于 18 至 42 岁年龄组和非先天性 ESRD 的关联进行单独分析,发现 SGA 与 ESRD 的关联比 LBW 更强,而 LBW 与 18 至 42 岁年龄组的关联在统计学上无显著意义。
仅随访至 42 岁。
LBW 和 SGA 与生命最初 40 年期间 ESRD 的风险增加相关,家族因素并不能解释这种关联。我们的结果支持这样一种假说,即宫内肾单位发育受损可能是进行性肾脏疾病的一个因果风险因素。