Evidence map›Paper›PMID 40935900›Full record

ArticleEuropean journal of pediatrics2025

Descriptive cohort study of transient isolated tubular acidosis in early childhood: experience from a rare kidney disease expert center.

Hajer Charfi, Aurelia Bertholet-Thomas, Justine Bacchetta, Sacha Flammier, Laurence Derain Dubourg, Aurélie De Mul

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Article in European journal of pediatrics, 2025. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Hajer CharfiCentre de Référence Des Maladies Rénales Rares, Centre de Référence Des Maladies Rares du Calcium Et du Phosphore, Filières Maladies Rares ORKiD, OSCAR Et ERKNet, Hôpital Femme Mère Enfant, 69677, Bron, France.
Aurelia Bertholet-Thomas *Centre de Référence Des Maladies Rénales Rares, Centre de Référence Des Maladies Rares du Calcium Et du Phosphore, Filières Maladies Rares ORKiD, OSCAR Et ERKNet, Hôpital Femme Mère Enfant, 69677, Bron, France.
Justine BacchettaCentre de Référence Des Maladies Rénales Rares, Centre de Référence Des Maladies Rares du Calcium Et du Phosphore, Filières Maladies Rares ORKiD, OSCAR Et ERKNet, Hôpital Femme Mère Enfant, 69677, Bron, France.
Sacha FlammierCentre de Référence Des Maladies Rénales Rares, Centre de Référence Des Maladies Rares du Calcium Et du Phosphore, Filières Maladies Rares ORKiD, OSCAR Et ERKNet, Hôpital Femme Mère Enfant, 69677, Bron, France.
Laurence Derain DubourgCentre de Référence Des Maladies Rénales Rares, Centre de Référence Des Maladies Rares du Calcium Et du Phosphore, Filières Maladies Rares ORKiD, OSCAR Et ERKNet, Hôpital Femme Mère Enfant, 69677, Bron, France.
Aurélie De Mul *Centre de Référence Des Maladies Rénales Rares, Centre de Référence Des Maladies Rares du Calcium Et du Phosphore, Filières Maladies Rares ORKiD, OSCAR Et ERKNet, Hôpital Femme Mère Enfant, 69677, Bron, France. aurelie.de-mul@chu-lyon.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Growth faltering and/or failure to thrive in children often prompts metabolic assessment, sometimes revealing metabolic acidosis and leading to referral to pediatric nephrology. Renal tubular acidosis (RTA), causing hyperchloremic metabolic acidosis due to impaired renal acidification, includes transient isolated RTA, a relatively frequent but poorly described condition. We reviewed pediatric patients referred to the Lyon Rare Kidney Disease Center (MAREGE) between March 2023 and March 2024 for linear growth faltering and/or failure to thrive associated with isolated metabolic acidosis, after excluding systemic, endocrine, and gastrointestinal causes. Patients with suspected secondary, genetic forms, or distal RTA were excluded. Follow-up was analyzed from the initial nephrology consultation to the last visit before March 2025. Data are presented as medians [IQR] and compared using non-parametric tests. Thirty-five patients were included. At diagnosis, age was 15.3 [13.1-25.6] months, with weight and height standard deviation (SD) scores of - 1.5 [- 2.5; - 1.0] and - 1.0 [- 2.0; 0.0], respectively. Tubular assessments showed low plasma bicarbonate (19 [18-20] mmol/L), non-adapted bicarbonaturia (8.0 [2.8-18.6] mmol/L), and elevated urinary pH (7.0 [6.4-7.4]). After a follow-up of 2.2 [1.4-3.1] years at an of age 3.4 [1.9-4.1] years, weight SD scores increased significantly (- 1.0 [- 1.9; - 0.4], p = 0.04). Height SD scores also increased (- 0.5 [- 1.5; 0.0]), though not significantly (p = 0.41). Catch-up growth in weight, height, or both was achieved in 77% of patients. Bicarbonate supplementation, initiated at 1.2 [0.7-1.6] mmol/kg/day, was discontinued in 54% of cases; for others, dosing remained stable (1.3 [0.9-2.0] mmol/kg/day, p = 0.16).

conclusionTransient isolated RTA is observed in infants and young children with mild metabolic acidosis, isolated bicarbonaturia, and moderate failure to thrive and/or growth faltering. It resolves spontaneously within a few years, usually requiring only low-dose alkalizing therapy. WHAT IS KNOWN: • Renal tubular acidosis (RTA) is a hyperchloremic, normal anion gap metabolic acidosis due to impaired renal acidification. In children, it is a recognized cause of growth faltering or failure to thrive and is usually a genetic disease (either proximal or distal acidosis). WHAT IS NEW: • In cases of mild metabolic acidosis associated with moderate growth delay, without other tubular or extrarenal abnormalities, the possibility of transient isolated renal tubular acidosis should be considered. This condition warrants parental reassurance, as most patients show catch-up growth with minimal bicarbonate supplementation, which can usually be discontinued over time.

Indexed as

Acidosis, Renal TubularGrowth DisordersBicarbonatesChild, PreschoolFailure to ThriveFemaleFollow-Up StudiesHumansInfantMaleRare DiseasesRetrospective StudiesBicarbonatesBicarbonateFailure to thriveLinear growth falteringSodium bicarbonate supplementationTubular acidosis

Identifiers

PMID40935900
PMCPMC12426147

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