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Secondhand smoke exposure is associated with proteinuria in children with chronic kidney disease
Abiodun Omoloja1, Judith Jerry-Fluker, Derek K Ng
1Department of Pediatrics, Wright State University, One Children's Plaza, Dayton, OH 45404, USA. omolojaa@childrensdayton.org
Insights
Secondhand smoke (SHS) exposure is common in children with chronic kidney disease (CKD). SHS exposure was linked to an increased risk of nephrotic range proteinuria, suggesting it may impact CKD progression.
Area of Science:
- Pediatric Nephrology
- Environmental Health
- Chronic Kidney Disease Research
Background:
- Cigarette smoking increases CKD progression risk in adults.
- Secondhand smoke (SHS) exposure is linked to elevated blood pressure in children.
- No prior studies investigated SHS prevalence or effects in pediatric CKD.
Purpose of the Study:
- To determine the prevalence of SHS exposure in children with CKD.
- To assess the association between SHS exposure and proteinuria in pediatric CKD patients.
Main Methods:
- 366 children (aged 1-16) with CKD from the CKiD Study were analyzed.
- SHS exposure assessed via questionnaire and confirmed by urine cotinine (Ucot) levels.
- Cross-sectional analysis of SHS exposure and proteinuria.
Main Results:
- 22% of children with CKD showed evidence of SHS exposure via Ucot.
- SHS exposure associated with lower maternal education, African American race, and higher prevalence of nephrotic range proteinuria and left ventricular hypertrophy.
- Multivariate analysis revealed SHS-exposed children had 2.64 times higher odds of nephrotic range proteinuria.
Conclusions:
- SHS exposure is prevalent (22%) in children with CKD.
- SHS exposure is independently associated with nephrotic range proteinuria in this cohort.
- SHS exposure may be a significant factor influencing CKD progression in children.
Background:
In adults with chronic kidney disease (CKD), cigarette smoking is associated with an increased risk for CKD progression and transplant failure. In children, secondhand smoke (SHS) exposure has been associated with elevated blood pressure. There are no studies on the prevalence and effect of SHS exposure in CKD.
Methods:
Subjects were enrolled in the Chronic Kidney Disease in Children (CKiD) Study, an observational cohort of 366 children aged 1 to 16 years with CKD. Secondhand smoke exposure was obtained via questionnaire. SHS exposure was also determined based on urine cotinine (Ucot) measurements (1 ng/mL ≤ Ucot < 75 ng/mL). The cross-sectional association of SHS exposure with proteinuria was assessed.
Results:
Using Ucot, 22 % of subjects were exposed to SHS. SHS exposure was significantly associated with lower maternal education and African American race, and a greater prevalence of nephrotic range proteinuria and left ventricular hypertrophy. In a multivariate model (including sex, age, race, maternal education, income level, private insurance status, abnormal birth history and CKD diagnosis), the prevalence odds of nephrotic range proteinuria was 2.64, (95 % confidence interval 1.08, 6.42) higher in children exposed to SHS compared to those unexposed.
Conclusions:
In our cohort of children with CKD, SHS exposure was common (22 %) and independently associated with nephrotic range proteinuria. Exposure to SHS may be an important factor to consider in CKD progression.
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