Familial Factors, Low Birth Weight, and Development of ESRD: A Nationwide Registry Study

详细信息    查看全文

• 作者：Paschal Ruggajo ; MD¹ ; ² ; ^{prugajo@yahoo.com" class="auth_mail" title="E-mail the corresponding author} ; Rannveig Skrunes ; MD² ; ³ ; Einar Svarstad ; MD ; PhD² ; ³ ; Rolv Skjæ ; rven ; PhD⁴ ; ⁵ ; Anna Varberg Reisæ ; ther ; MD ; PhD⁶ ; Bjø ; rn Egil Vikse ; MD ; PhD² ; ⁷
• 关键词：Low birth weight (LBW) ; end-stage renal disease (ESRD) ; index ; sibling ; genetic factors ; small for gestational age (SGA) ; placental insufficiency ; intrauterine growth restriction ; early determinants of disease ; prenatal exposure delayed effects
• 刊名：American Journal of Kidney Diseases
• 出版年：2016
• 出版时间：April 2016
• 年：2016
• 卷：67
• 期：4
• 页码：601-608
• 全文大小：581 K

文摘

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.

Study Design

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.

Predictor

LBW in the participant and/or LBW in at least 1 sibling.

Outcome

ESRD.

Results

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.

Limitations

Follow-up only until 42 years of age.

Conclusions

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.