Methylmalonic acidemia/propionic acidemia - The biochemical presentation and comparing the outcome between liver transplantation versus non-liver transplantation groups
Journal
Orphanet Journal of Rare Diseases
Journal Volume
14
Journal Issue
1
Date Issued
2019
Author(s)
Chu T.-H.
Lin H.-Y.
Liao H.-C.
Ho H.-J.
Lai C.-J.
Chiang C.-C.
Lin N.-C.
Yang C.-F.
Lin S.-P.
Liu C.-S.
Niu D.-M.
Abstract
Background: Most patients with isolated methylmalonic acidemia (MMA) /propionic acidemia (PA) presenting during the neonatal period with acute metabolic distress are at risk for death and significant neurodevelopmental disability. The nationwide newborn screening for MMA/PA has been in place in Taiwan from January, 2000 and data was collected until December, 2016. Results: During the study period, 3,155,263 newborns were screened. The overall incidence of MMA mutase type cases was 1/121,356 (n = 26), 1 cobalamin B was detected and that for PA cases (n = 4) was 1/788,816. The time of referral is 8.8 days for MMA patients, and 7.5 days for PA patients. The MMA mutase type patients have higher AST, ALT, and NH 3 values as well as a lower pH value (p < 0.05). The mean age for liver transplantation (LT) is 402 days (range from 0.6-6.7 yr) with 16 out of 20 cases (80.0%) using living donors. The mean admission length shortened from 90.6 days/year (pre-LT) to 5.3 days/year (at 3rd year post-LT) (p < 0.0005). Similarly, the tube feeding ratio decreased from 67.8 to 0.50% (p < 0.00005). The anxiety level of the caregiver was reduced from 33.4 to 27.2 after LT (p = 0.001) and the DQ/IQ performance of the patients was improved after LT from 50 to 60.1 (p = 0.07). Conclusion: MMA/PA patients with LT do survive and have reduced admission time, reduced tube feeding and the caregiver is less anxious. ? 2019 The Author(s).
SDGs
Other Subjects
acetylcarnitine; alanine aminotransferase; ammonia; aspartate aminotransferase; cobalamin; cobalamin B; methylmalonyl coenzyme A mutase; propionylcarnitine; unclassified drug; alanine aminotransferase blood level; anxiety; Article; aspartate aminotransferase blood level; biochemical analysis; caregiver burden; child; clinical article; comparative study; controlled study; development; developmental quotient; enteric feeding; female; functional assessment; human; infant; intelligence quotient; length of stay; liver transplantation; living donor; male; methylmalonic acidemia; newborn; newborn screening; outcome assessment; patient referral; pH; propionic acidemia; school child; survival rate; Taiwan; caregiver; disorders of amino acid and protein metabolism; genetics; hospitalization; liver transplantation; mortality; mutation; pathophysiology; propionic acidemia; psychology; treatment outcome; Amino Acid Metabolism, Inborn Errors; Caregivers; Enteral Nutrition; Female; Hospitalization; Humans; Infant, Newborn; Liver Transplantation; Male; Mutation; Neonatal Screening; Propionic Acidemia; Taiwan; Treatment Outcome
Publisher
BioMed Central Ltd.
Type
journal article