Environmental lead exposure is associated with neurocognitive dysfunction in children with chronic kidney disease.

Background: Environmental lead exposure is associated with cognitive impairment in healthy children, with deficits seen in intelligence quotient (IQ), attention, and behavior. Neurocognitive dysfunction is also a well-described complication among children with chronic kidney disease (CKD). The objec...

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Published in:Pediatric Nephrology Vol. 34; no. 11; pp. 2371 - 2380
Main Authors: Ruebner, Rebecca L., Hooper, Stephen R., Parrish, Carisa, Furth, Susan L., Fadrowski, Jeffrey J.
Format: research tables/charts Journal Article
Published: Springer Nature Nov2019
Online Access:View this record in EBSCOhost
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      dt: Nov2019
      vid: 34
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      pub: Springer Nature
      place: New York, New York
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        10.1007/s00467-019-04306-7
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        atl: Environmental lead exposure is associated with neurocognitive dysfunction in children with chronic kidney disease.
      aug:
        au:
          Ruebner, Rebecca L.
          Hooper, Stephen R.
          Parrish, Carisa
          Furth, Susan L.
          Fadrowski, Jeffrey J.
        affil: Division of Pediatric Nephrology, Johns Hopkins University School of Medicine, 200 N Wolfe St, Room 3055, 21287, Baltimore, MD, USA
      sug:
        subj:
          Renal Insufficiency, Chronic Complications
          Lead Poisoning Complications
          Environmental Exposure Adverse Effects
          Cognition Disorders Risk Factors
          Lead Blood
          Cognition Evaluation
          Risk Assessment
          Child Health
          Adolescent Health
          Human
          Prospective Studies
          Cross Sectional Studies
          Multicenter Studies
          Child
          Adolescence
          Severity of Illness
          Intelligence Tests
          Executive Function Evaluation
          Attention Evaluation
          Child Behavior Evaluation
          Multiple Linear Regression
          Glomerular Filtration Rate Evaluation
          Scales
          Cognition Disorders Diagnosis
          Child: 6-12 years
          Adolescent: 13-18 years
      ab: Background: Environmental lead exposure is associated with cognitive impairment in healthy children, with deficits seen in intelligence quotient (IQ), attention, and behavior. Neurocognitive dysfunction is also a well-described complication among children with chronic kidney disease (CKD). The objective was to evaluate the association between blood lead levels (BLL) and performance on neurocognitive assessments in a cohort of children with CKD. Methods: Cross-sectional study of children with mild to moderate CKD from the Chronic Kidney Disease in Children (CKiD) multicenter prospective cohort study. The primary exposure was BLL. The primary outcome was performance on age-specific neurocognitive assessments evaluating IQ, executive functioning, attention, hyperactivity, and behavior. Multivariable linear regression was used to evaluate the association between BLL and neurocognitive performance, adjusted for key sociodemographic and clinical variables. Results: A total of 412 subjects were included with median age 15.4 years, median estimated GFR 39 mL/min/1.732, median BLL 1.2 mcg/dL, and median IQ score 99. In multivariable linear regression, higher BLL was associated with significantly lower IQ score (− 2.1 IQ points for every 1-mcg/dL increase in BLL, p = 0.029). Higher BLL was associated with worse scores on the Conners' Continuous Performance Test II Variability T-Score, a measure of inattention (+ 1.8 T-Score points for every 1-mcg/dL increase in BLL, p = 0.033). Conclusions: Low-level lead exposure is associated with significantly lower IQ and more inattention in children with CKD, a population already at high risk for neurocognitive dysfunction. Universal screening for elevated BLL should be considered for all children with CKD at age 12–24 months.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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