Survival and psychomotor development with early betaine treatment in patients with severe methylenetetrahydrofolate reductase deficiency

Research output: Contribution to journalArticle

Abstract

IMPORTANCE: The impact of betaine treatment on outcome in patients with severe methylenetetrahydrofolate reductase (MTHFR) deficiency is presently unclear. OBJECTIVE: To investigate the effect of betaine treatment on development and survival in patients with severe MTHFR deficiency. DATA SOURCES: MEDLINE, EMBASE, and Cochrane databases between January 1960 and December 2012. STUDY SELECTION: Studies that described patients with severe MTHFR deficiency who received betaine treatment. DATA EXTRACTION AND SYNTHESIS: We identified 15 case reports and case series, totaling 36 patients. Data included the following: (1) families with 2 or more patients with severe MTHFR deficiency, of whom at least 1 received betaine, or (2) single patients with severe MTHFR deficiency treated with betaine. To define severe MTHFR deficiency, methionine, homocysteine, MTHFR enzyme activity in fibroblasts, or mutations (in the MTHFR gene) had to be described as well as the effect of treatment (survival and/or psychomotor development). We compared the outcome in treated vs untreated patients and early-vs late-treated patients. Sensitivity analysis was performed to address definition of early treatment. To further assess the impact of treatment on mortality, we performed a subanalysis in families with at least 1 untreated deceased patient. MAINOUTCOMES ANDMEASURES: Survival and psychomotor development. RESULTS: Eleven of 36 patients (31%) died. All deaths occurred in patients who did not receive treatment or in patients in whom treatment was delayed. In contrast, all 5 early-treated patients survived. Subgroup analysis of patients with deceased siblings-their genotypically identical controls-revealed that betaine treatment prevented mortality (P =.002). In addition, psychomotor development in surviving patients treated with betaine was normal in all 5 early-treated patients but in none of the 19 surviving patients with delayed treatment (P <.001). CONCLUSIONS AND RELEVANCE: Early betaine treatment prevents mortality and allows normal psychomotor development in patients with severe MTHFR deficiency, highlighting the importance of timely recognition through newborn screening.

Details

Authors
  • Eugene F. Diekman
  • Tom J. De Koning
  • Nanda M. Verhoeven-Duif
  • Maroeska M. Rovers
  • Peter M. Van Hasselt
External organisations
  • Wilhelmina Children’s Hospital
  • University Medical Center Groningen
  • University Medical Center Utrecht
  • Radboud University Medical Center
Research areas and keywords

Subject classification (UKÄ) – MANDATORY

  • Neurology
Original languageEnglish
Pages (from-to)188-194
Number of pages7
JournalJAMA Neurology
Volume71
Issue number2
Publication statusPublished - 2014 Jan 1
Publication categoryResearch
Peer-reviewedYes
Externally publishedYes