Is the prognosis of congenital single functioning kidney benign? A population-based study
- PMID: 33619660
- DOI: 10.1007/s00467-021-04980-6
Is the prognosis of congenital single functioning kidney benign? A population-based study
Abstract
Background: We investigated the risk of kidney injury among adolescents with and without a congenital single functioning kidney (SFK).
Methods: This retrospective study is based on a medical evaluation database of 17-year-old Israeli conscripts, born during 1989-1999. Those with congenital SFK diagnosis, verified by a pediatric nephrologist's review of the original military medical committee classifications, were compared to the rest of the cohort. Kidney injury (KI) was defined as proteinuria, high blood pressure (BP), or estimated glomerular filtration rate (eGFR) < 90 ml/min/1.73 m2 prior to army recruitment. Risk factors for KI were examined using logistic regression.
Results: Of 979,630 screened candidates, 353 were diagnosed with SFK. The yearly incidence of SFK gradually increased in the first years of the study, reaching a plateau in 1995 (5.5 ± 1.2/10,000 births/year). The male to female ratio was 2.7:1. Concomitant genital malformations were documented in 5.5% of those with SFK. KI was more prevalent in the SFK than the control group (42.2% vs. 23.5%, p < 0.001). All three components of KI were more common in the SFK than the control group: high BP (31.7% vs. 23.1%, p < 0.001), proteinuria (18.2% vs. 0.4%, p < 0.001), and eGFR <90 ml/min/1.73m2 (12.0% vs 0.1%, p < 0.001). Multivariate analysis of the SFK group revealed associations of higher mean BMI, male sex, and smaller ultrasonographic kidney length with KI.
Conclusions: This large population-based study documents a significant risk for KI among adolescents with SFK. Obesity represents a major modifiable risk factor for KI, implicating the need for closer follow-up in this group during childhood.
Keywords: Hypertension; Kidney failure; Kidney injury; Proteinuria; Single kidney; Solitary kidney.
© 2021. IPNA.
References
-
- Loane M, Dolk H, Kelly A, Teljeur C, Greenlees R, Densem J, EUROCAT Working Group (2011) Paper 4: EUROCAT statistical monitoring: identification and investigation of ten year trends of congenital anomalies in Europe. Birth Defects Res A Clin Mol Teratol 91(Suppl 1):S31–S43. https://doi.org/10.1002/bdra.20778 - DOI - PubMed
-
- Wühl E, van Stralen KJ, Verrina E, Bjerre A, Wanner C, Heaf JG, Zurriaga O, Hoitsma A, Niaudet P, Palsson R, Ravani P, Jager KJ, Schaefer F (2013) Timing and outcome of renal replacement therapy in patients with congenital malformations of the kidney and urinary tract. Clin J Am Soc Nephrol 8:67–74. https://doi.org/10.2215/CJN.03310412 - DOI - PubMed
-
- Westland R, Schreuder MF, Ket JCF, Van Wijk JAE (2013) Unilateral renal agenesis: a systematic review on associated anomalies and renal injury. Nephrol Dial Transplant 28:1844–1855. https://doi.org/10.1093/ndt/gft012 - DOI - PubMed
-
- Hiraoka M, Tsukahara H, Ohshima Y, Kasuga K, Ishihara Y, Mayumi M (2002) Renal aplasia is the predominant cause of congenital solitary kidneys. Kidney Int 61:1840–1844. https://doi.org/10.1046/j.1523-1755.2002.00322.x - DOI - PubMed
-
- Schreuder MF (2011) Unilateral anomalies of kidney development: why is left not right. Kidney Int 80:740–745. https://doi.org/10.1038/ki.2011.204 - DOI - PubMed
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous