Evidence map›Paper›PMID 26959481›Full record

ArticlePediatric research2016

Influence of common genetic variants on childhood kidney outcomes.

Kozeta Miliku, Suzanne Vogelezang, Oscar H Franco, Albert Hofman, Vincent W V Jaddoe, Janine F Felix

Abstract read
In one paragraph

Article in Pediatric research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Kozeta MilikuThe Generation R Study Group, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.ORCID 0000-0002-9614-7191
Suzanne VogelezangThe Generation R Study Group, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Oscar H FrancoDepartment of Epidemiology, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Albert HofmanDepartment of Epidemiology, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Vincent W V JaddoeThe Generation R Study Group, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Janine F FelixThe Generation R Study Group, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.

Funding

European Research Council 648916
6 · The paper itself

Abstract

backgroundKidney measures in early life are associated with kidney disease in later life. We hypothesized that these associations are partly explained by common genetic variants that lead to both smaller kidneys with lower kidney function in early childhood and kidney disease in adulthood.

methodsWe examined in a population-based prospective cohort study among 4,119 children the associations of a weighted genetic risk score combining 20 previously identified common genetic variants related to adult eGFRcreat with kidney outcomes in children aged 6.0 years (95% range 5.7-7.8). Childhood kidney outcomes included combined kidney volume, glomerular filtration rate (eGFR) based on creatinine levels, and microalbuminuria based on albumin and creatinine urine levels.

resultsWe observed that the genetic risk score based on variants related to impaired kidney function in adults was associated with a smaller combined kidney volume (P value 3.0 × 10(-3)) and with a lower eGFR (P value 4.0 × 10(-4)) in children. The genetic risk score was not associated with microalbuminuria.

conclusionCommon genetic variants related to impaired kidney function in adults already lead to subclinical changes in childhood kidney outcomes. The well-known associations of kidney measures in early life with kidney disease in later life may at least be partly explained by common genetic variants.

Indexed as

AlbuminuriaAllelesChildChild, PreschoolCreatinineEthnicityFemaleGenetic VariationGenome-Wide Association StudyGlomerular Filtration RateHumansKidneyKidney DiseasesMalePolymorphism, Single NucleotideProspective StudiesCreatinine

Identifiers

PMID26959481
PMCPMC5496666

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