Evidence map›Paper›PMID 40560272›Full record

ArticlePediatric nephrology (Berlin, Germany)2025

Risk profile of promoters and inhibitors of kidney stone formation in paediatric inflammatory bowel disease.

Britta Zobel, Burkhard Rodeck, Michael van Husen

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Article in Pediatric nephrology (Berlin, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Britta ZobelChristliches Kinderhospital Osnabrück, Academic Teaching Hospital of Hannover Medical School, Osnabrück, Germany. b.zobel@ckos.de.ORCID 0009-0000-4546-0682
Burkhard RodeckDepartment of Paediatric Gastroenterology, Christliches Kinderhospital Osnabrück, Academic Teaching Hospital of Hannover Medical School, Osnabrück, Germany.
Michael van HusenDepartment of Paediatric Nephrology, Christliches Kinderhospital Osnabrück, Academic Teaching Hospital of Hannover Medical School, Osnabrück, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNephrolithiasis is a well-known extraintestinal complication of adult inflammatory bowel disease (IBD), mainly attributed to hyperoxaluria. In contrast, data for paediatric IBD are limited. The objective of this study was to evaluate renal stone risk in children and adolescents with IBD by analysing urine composition concerning stone promoters and inhibitors and their possible influencing factors.

methodsIn this cross-sectional study, the 24-h urine composition of 107 children and adolescents with surgically untreated IBD compared to 27 healthy controls was analysed regarding the risk of kidney stone development, including an evaluation using the CMC index [(citrate × magnesium)/calcium]. Disease activity, as assessed by the Paediatric Crohn Disease Activity Index (PCDAI), Paediatric Ulcerative Colitis Activity Index (PUCAI), and faecal calprotectin (FC) was investigated as influencing factor.

resultsStone inhibitors were lower in active IBD than in remission (citrate, P = 0.001; magnesium, P = 0.004). The CMC index was also decreased in active disease (P = 0.001), indicating increased urinary lithogenicity in these children. PCDAI and PUCAI were predictors of the CMC index. This proved relevant in the groups IBD, IBD with active disease (B = - 0.072, P = 0.029, adjusted R

conclusionsMonitoring urine for lithogenic alterations and calculating CMC index in paediatric active IBD could contribute to identifying at-risk patients for later nephrolithiasis early, although childhood stone prevalence is low.

Indexed as

Colitis, UlcerativeCrohn DiseaseInflammatory Bowel DiseasesKidney CalculiAdolescentCalciumCase-Control StudiesChildCitric AcidCross-Sectional StudiesFecesFemaleHumansLeukocyte L1 Antigen ComplexMagnesiumMaleCalciumCitric AcidLeukocyte L1 Antigen ComplexMagnesiumChildrenHypocitraturiaHypomagnesuriaInflammatory bowel diseaseKidney stonesLithogenic risk

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.