Long-term renal outcome in methylmalonic acidemia in adolescents and adults

Abstract Background Chronic kidney disease (CKD) is one of the main long-term prognosis factors in methylmalonic acidemia (MMA), a rare disease of propionate catabolism. Our objective was to precisely address the clinical and biological characteristics of long-term CKD in MMA adolescent and adult pa...

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Main Authors: Myriam Dao, Jean-Baptiste Arnoux, Frank Bienaimé, Anaïs Brassier, François Brazier, Jean-François Benoist, Clément Pontoizeau, Chris Ottolenghi, Pauline Krug, Olivia Boyer, Pascale de Lonlay, Aude Servais
Format: Article
Language:English
Published: BMC 2021-05-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Online Access:https://doi.org/10.1186/s13023-021-01851-z
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spelling doaj-ac37a157b8d245b5abfc3a9d15a194332021-05-16T11:08:32ZengBMCOrphanet Journal of Rare Diseases1750-11722021-05-0116111010.1186/s13023-021-01851-zLong-term renal outcome in methylmalonic acidemia in adolescents and adultsMyriam Dao0Jean-Baptiste Arnoux1Frank Bienaimé2Anaïs Brassier3François Brazier4Jean-François Benoist5Clément Pontoizeau6Chris Ottolenghi7Pauline Krug8Olivia Boyer9Pascale de Lonlay10Aude Servais11Adult Nephrology and Transplantation Department, Hôpital Necker Enfants Malades, APHPReference Center of Inherited Metabolic Diseases (MAMEA and MetabERN), Hôpital Necker-Enfants Malades, APHPDepartment of Physiology, Hôpital Necker Enfants Malades, APHPReference Center of Inherited Metabolic Diseases (MAMEA and MetabERN), Hôpital Necker-Enfants Malades, APHPDepartment of Physiology, Hôpital Necker Enfants Malades, APHPReference Center of Inherited Metabolic Diseases (MAMEA and MetabERN), Hôpital Necker-Enfants Malades, APHPReference Center of Inherited Metabolic Diseases (MAMEA and MetabERN), Hôpital Necker-Enfants Malades, APHPReference Center of Inherited Metabolic Diseases (MAMEA and MetabERN), Hôpital Necker-Enfants Malades, APHPPediatric Nephrology Department, Hôpital Necker Enfants Malades, APHPPediatric Nephrology Department, Hôpital Necker Enfants Malades, APHPReference Center of Inherited Metabolic Diseases (MAMEA and MetabERN), Hôpital Necker-Enfants Malades, APHPAdult Nephrology and Transplantation Department, Hôpital Necker Enfants Malades, APHPAbstract Background Chronic kidney disease (CKD) is one of the main long-term prognosis factors in methylmalonic acidemia (MMA), a rare disease of propionate catabolism. Our objective was to precisely address the clinical and biological characteristics of long-term CKD in MMA adolescent and adult patients. Patients and methods In this retrospective study, we included MMA patients older than 13 years who had not received kidney and/or liver transplantation. We explored tubular functions, with special attention to proximal tubular function. We measured glomerular filtration rate (mGFR) by iohexol clearance and compared it to estimated glomerular filtration rate (eGFR) by Schwartz formula and CKD-EPI. Results Thirteen patients were included (M/F = 5/8). Median age was 24 years (13 to 32). Median mGFR was 57 mL/min/1.73 m2 (23.3 to 105 mL/min/1.73 m2). Ten out of 13 patients had mGFR below 90 mL/min/1.73 m2. No patient had significant glomerular proteinuria. No patient had complete Fanconi syndrome. Only one patient had biological signs suggestive of incomplete proximal tubulopathy. Four out of 13 patients had isolated potassium loss, related to a non-reabsorbable anion effect of urinary methylmalonate. Both Schwartz formula and CKD-EPI significantly overestimated GFR. Bias were respectively 16 ± 15 mL/min/1.73 m2 and 37 ± 22 mL/min/1.73 m2. Conclusion CKD is a common complication of the MMA. Usual equations overestimate GFR. Therefore, mGFR should be performed to inform therapeutic decisions such as dialysis and/or transplantation. Mild evidence of proximal tubular dysfunction was found in only one patient, suggesting that other mechanisms are involved.https://doi.org/10.1186/s13023-021-01851-zMethylmalonic acidemiaChronic kidney diseaseMeasured glomerular filtration rateEstimated glomerular filtration rateTubulopathy
collection DOAJ
language English
format Article
sources DOAJ
author Myriam Dao
Jean-Baptiste Arnoux
Frank Bienaimé
Anaïs Brassier
François Brazier
Jean-François Benoist
Clément Pontoizeau
Chris Ottolenghi
Pauline Krug
Olivia Boyer
Pascale de Lonlay
Aude Servais
spellingShingle Myriam Dao
Jean-Baptiste Arnoux
Frank Bienaimé
Anaïs Brassier
François Brazier
Jean-François Benoist
Clément Pontoizeau
Chris Ottolenghi
Pauline Krug
Olivia Boyer
Pascale de Lonlay
Aude Servais
Long-term renal outcome in methylmalonic acidemia in adolescents and adults
Orphanet Journal of Rare Diseases
Methylmalonic acidemia
Chronic kidney disease
Measured glomerular filtration rate
Estimated glomerular filtration rate
Tubulopathy
author_facet Myriam Dao
Jean-Baptiste Arnoux
Frank Bienaimé
Anaïs Brassier
François Brazier
Jean-François Benoist
Clément Pontoizeau
Chris Ottolenghi
Pauline Krug
Olivia Boyer
Pascale de Lonlay
Aude Servais
author_sort Myriam Dao
title Long-term renal outcome in methylmalonic acidemia in adolescents and adults
title_short Long-term renal outcome in methylmalonic acidemia in adolescents and adults
title_full Long-term renal outcome in methylmalonic acidemia in adolescents and adults
title_fullStr Long-term renal outcome in methylmalonic acidemia in adolescents and adults
title_full_unstemmed Long-term renal outcome in methylmalonic acidemia in adolescents and adults
title_sort long-term renal outcome in methylmalonic acidemia in adolescents and adults
publisher BMC
series Orphanet Journal of Rare Diseases
issn 1750-1172
publishDate 2021-05-01
description Abstract Background Chronic kidney disease (CKD) is one of the main long-term prognosis factors in methylmalonic acidemia (MMA), a rare disease of propionate catabolism. Our objective was to precisely address the clinical and biological characteristics of long-term CKD in MMA adolescent and adult patients. Patients and methods In this retrospective study, we included MMA patients older than 13 years who had not received kidney and/or liver transplantation. We explored tubular functions, with special attention to proximal tubular function. We measured glomerular filtration rate (mGFR) by iohexol clearance and compared it to estimated glomerular filtration rate (eGFR) by Schwartz formula and CKD-EPI. Results Thirteen patients were included (M/F = 5/8). Median age was 24 years (13 to 32). Median mGFR was 57 mL/min/1.73 m2 (23.3 to 105 mL/min/1.73 m2). Ten out of 13 patients had mGFR below 90 mL/min/1.73 m2. No patient had significant glomerular proteinuria. No patient had complete Fanconi syndrome. Only one patient had biological signs suggestive of incomplete proximal tubulopathy. Four out of 13 patients had isolated potassium loss, related to a non-reabsorbable anion effect of urinary methylmalonate. Both Schwartz formula and CKD-EPI significantly overestimated GFR. Bias were respectively 16 ± 15 mL/min/1.73 m2 and 37 ± 22 mL/min/1.73 m2. Conclusion CKD is a common complication of the MMA. Usual equations overestimate GFR. Therefore, mGFR should be performed to inform therapeutic decisions such as dialysis and/or transplantation. Mild evidence of proximal tubular dysfunction was found in only one patient, suggesting that other mechanisms are involved.
topic Methylmalonic acidemia
Chronic kidney disease
Measured glomerular filtration rate
Estimated glomerular filtration rate
Tubulopathy
url https://doi.org/10.1186/s13023-021-01851-z
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