Diagnostic Performances of Urinary Methylmalonic Acid/Creatinine Ratio in Vitamin B12 Deficiency

Sole measurement of plasma vitamin B12 is no longer enough to identify vitamin B12 (B12) deficiency. When plasma vitamin B12 is in the low-normal range, especially between 201 and 350 ng/L, B12 deficiency should be assessed by measurements of plasma homocysteine and/or plasma methylmalonic acid (MMA...

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Main Authors: Sopak Supakul, Floris Chabrun, Steve Genebrier, Maximilien N’Guyen, Guillaume Valarche, Arthur Derieppe, Adeline Villoteau, Valentin Lacombe, Geoffrey Urbanski
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Journal of Clinical Medicine
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Online Access:https://www.mdpi.com/2077-0383/9/8/2335
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author Sopak Supakul
Floris Chabrun
Steve Genebrier
Maximilien N’Guyen
Guillaume Valarche
Arthur Derieppe
Adeline Villoteau
Valentin Lacombe
Geoffrey Urbanski
author_facet Sopak Supakul
Floris Chabrun
Steve Genebrier
Maximilien N’Guyen
Guillaume Valarche
Arthur Derieppe
Adeline Villoteau
Valentin Lacombe
Geoffrey Urbanski
author_sort Sopak Supakul
collection DOAJ
description Sole measurement of plasma vitamin B12 is no longer enough to identify vitamin B12 (B12) deficiency. When plasma vitamin B12 is in the low-normal range, especially between 201 and 350 ng/L, B12 deficiency should be assessed by measurements of plasma homocysteine and/or plasma methylmalonic acid (MMA). However, these biomarkers also accumulate during renal impairment, leading to a decreased specificity for B12 deficiency. In such cases, urinary methylmalonic acid/creatinine ratio (uMMA/C) could be of interest, due to the stable urinary excretion of MMA. The objectives were to evaluate the influence of renal impairment on uMMA/C compared to plasma homocysteine and plasma methylmalonic acid, and to determine the diagnostic performances of uMMA/C in the diagnosis of B12 deficiency. We prospectively studied 127 patients with a plasma B12 between 201 and 350 ng/L. We noticed that uMMA/C was not dependent on renal function (<i>p</i> = 0.34), contrary to plasma homocysteine and plasma methylmalonic acid. uMMA/C showed a perspective diagnostic performance (AUC 0.71 [95% CI: 0.62–0.80]) and the threshold of 1.45 umol/mmol presented a high degree of specificity (87.9% [95% CI: 72.0–98.9]). In conclusion, uMMA/C is a promising biomarker to assess vitamin B12 status in doubtful cases, notably during renal impairment.
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spelling doaj.art-1073f4fe5e59496cab3e1ea175200c342023-11-20T07:34:43ZengMDPI AGJournal of Clinical Medicine2077-03832020-07-0198233510.3390/jcm9082335Diagnostic Performances of Urinary Methylmalonic Acid/Creatinine Ratio in Vitamin B12 DeficiencySopak Supakul0Floris Chabrun1Steve Genebrier2Maximilien N’Guyen3Guillaume Valarche4Arthur Derieppe5Adeline Villoteau6Valentin Lacombe7Geoffrey Urbanski8Department of Internal Medicine, University Hospital, 49000 Angers, FranceDepartment of Biochemistry, University Hospital, 49000 Angers, FranceDepartment of Biochemistry, University Hospital, 49000 Angers, FranceDepartment of Internal Medicine, University Hospital, 49000 Angers, FranceDepartment of Internal Medicine, University Hospital, 49000 Angers, FranceDepartment of Internal Medicine, University Hospital, 49000 Angers, FranceDepartment of Internal Medicine, University Hospital, 49000 Angers, FranceDepartment of Internal Medicine, University Hospital, 49000 Angers, FranceDepartment of Internal Medicine, University Hospital, 49000 Angers, FranceSole measurement of plasma vitamin B12 is no longer enough to identify vitamin B12 (B12) deficiency. When plasma vitamin B12 is in the low-normal range, especially between 201 and 350 ng/L, B12 deficiency should be assessed by measurements of plasma homocysteine and/or plasma methylmalonic acid (MMA). However, these biomarkers also accumulate during renal impairment, leading to a decreased specificity for B12 deficiency. In such cases, urinary methylmalonic acid/creatinine ratio (uMMA/C) could be of interest, due to the stable urinary excretion of MMA. The objectives were to evaluate the influence of renal impairment on uMMA/C compared to plasma homocysteine and plasma methylmalonic acid, and to determine the diagnostic performances of uMMA/C in the diagnosis of B12 deficiency. We prospectively studied 127 patients with a plasma B12 between 201 and 350 ng/L. We noticed that uMMA/C was not dependent on renal function (<i>p</i> = 0.34), contrary to plasma homocysteine and plasma methylmalonic acid. uMMA/C showed a perspective diagnostic performance (AUC 0.71 [95% CI: 0.62–0.80]) and the threshold of 1.45 umol/mmol presented a high degree of specificity (87.9% [95% CI: 72.0–98.9]). In conclusion, uMMA/C is a promising biomarker to assess vitamin B12 status in doubtful cases, notably during renal impairment.https://www.mdpi.com/2077-0383/9/8/2335vitamin B12 deficiencyplasma homocysteineplasma methylmalonic acidurinary methylmalonic acidbiomarkerrenal impairment
spellingShingle Sopak Supakul
Floris Chabrun
Steve Genebrier
Maximilien N’Guyen
Guillaume Valarche
Arthur Derieppe
Adeline Villoteau
Valentin Lacombe
Geoffrey Urbanski
Diagnostic Performances of Urinary Methylmalonic Acid/Creatinine Ratio in Vitamin B12 Deficiency
Journal of Clinical Medicine
vitamin B12 deficiency
plasma homocysteine
plasma methylmalonic acid
urinary methylmalonic acid
biomarker
renal impairment
title Diagnostic Performances of Urinary Methylmalonic Acid/Creatinine Ratio in Vitamin B12 Deficiency
title_full Diagnostic Performances of Urinary Methylmalonic Acid/Creatinine Ratio in Vitamin B12 Deficiency
title_fullStr Diagnostic Performances of Urinary Methylmalonic Acid/Creatinine Ratio in Vitamin B12 Deficiency
title_full_unstemmed Diagnostic Performances of Urinary Methylmalonic Acid/Creatinine Ratio in Vitamin B12 Deficiency
title_short Diagnostic Performances of Urinary Methylmalonic Acid/Creatinine Ratio in Vitamin B12 Deficiency
title_sort diagnostic performances of urinary methylmalonic acid creatinine ratio in vitamin b12 deficiency
topic vitamin B12 deficiency
plasma homocysteine
plasma methylmalonic acid
urinary methylmalonic acid
biomarker
renal impairment
url https://www.mdpi.com/2077-0383/9/8/2335
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