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Renal cortical abnormalities in siblings of index patients with vesicoureteral reflux
Manuela Hunziker1, Eric Colhoun, Prem Puri
1National Children's Research Centre, Our Lady's Children's Hospital, Dublin, Ireland; and.
Insights
Screening siblings of children with vesicoureteral reflux (VUR) identified significant risks for renal cortical abnormalities. Previous urinary tract infections (UTIs) and high-grade VUR in siblings over one year old are key risk factors.
Area of Science:
- Pediatric Nephrology
- Urology
- Genetics
Background:
- Screening siblings of index patients with vesicoureteral reflux (VUR) aims to detect at-risk children and prevent renal damage.
- The practice of sibling screening for VUR remains a subject of debate within the medical community.
Purpose of the Study:
- To determine the prevalence of VUR and renal cortical abnormalities in siblings of VUR patients.
- To identify independent risk factors for renal cortical abnormalities in this sibling cohort.
Main Methods:
- A cohort of 318 siblings under 6 years old from families with VUR (grades III-V) was studied between 1998 and 2012.
- Siblings were categorized based on a history of urinary tract infection (UTI) or routine VUR screening.
- Logistic regression analysis identified risk factors for renal cortical abnormalities, including age, gender, UTI history, and VUR grade.
Main Results:
- Vesicoureteral reflux (VUR) was detected in 60% of screened siblings and 40% of those with a UTI history.
- Key independent risk factors for renal cortical abnormalities included a prior UTI (OR: 3.38), high-grade VUR (OR: 3.62), and age over 1 year (OR: 2.84).
Conclusions:
- Siblings with a history of UTI, high-grade VUR, or those over one year old face an elevated risk of renal cortical abnormalities.
- Findings aid in counseling families regarding the risks of VUR and reflux nephropathy in familial VUR cases.
Objective:
Screening siblings of index patients with vesicoureteral reflux (VUR) has been proposed to identify children who are at risk for renal damage. However, screening siblings for VUR remains controversial. We investigated the prevalence of VUR and renal cortical abnormalities in the sibling population in a large cohort of families with VUR.
Methods:
Between 1998 and 2012, parents of index patients with grade III to V VUR were asked permission to screen siblings <6 years of age for VUR. Siblings were divided into 2 groups: siblings with a documented history of a previous urinary tract infection (UTI) and siblings who were screened for VUR and never had a UTI. A logistic regression model was used to determine independent risk factors associated with renal cortical abnormalities such as history of presentation, age, gender, and grade of VUR.
Results:
There were 318 siblings in 275 families in the study. VUR was found after screening in 190 (60%) siblings and after a UTI in 128 (40%). Multivariate analysis revealed that siblings who had a previous UTI (odds ratio: 3.38), siblings with high grade reflux (odds ratio: 3.62), and siblings over 1 year of age (odds ratio: 2.84) were the most significant independent risk factors associated with renal cortical abnormalities.
Conclusions:
There is increased risk of renal cortical abnormalities in siblings with a previous UTI, siblings with high-grade VUR, and siblings over age 1 year. This information may help to counsel parents about the risk of VUR and reflux nephropathy in familial VUR.
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