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Published in: Orphanet Journal of Rare Diseases 1/2019

Open Access 01-12-2019 | Cardiomyopathy | Review

Evaluation of earlier versus later dietary management in long-chain 3-hydroxyacyl-CoA dehydrogenase or mitochondrial trifunctional protein deficiency: a systematic review

Authors: Hannah Fraser, Julia Geppert, Rebecca Johnson, Samantha Johnson, Martin Connock, Aileen Clarke, Sian Taylor-Phillips, Chris Stinton

Published in: Orphanet Journal of Rare Diseases | Issue 1/2019

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Abstract

Background

Mitochondrial trifunctional protein (MTP) and long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiencies are rare fatty acid β-oxidation disorders. Without dietary management the conditions are life-threatening. We conducted a systematic review to investigate whether pre-symptomatic dietary management following newborn screening provides better outcomes than treatment following symptomatic detection.

Methods

We searched Web of Science, Medline, Pre-Medline, Embase and the Cochrane Library up to 23rd April 2018. Two reviewers independently screened titles, abstracts and full texts for eligibility and quality appraised the studies. Data extraction was performed by one reviewer and checked by another.

Results

We included 13 articles out of 7483 unique records. The 13 articles reported on 11 patient groups, including 174 people with LCHAD deficiency, 18 people with MTP deficiency and 12 people with undifferentiated LCHAD/MTP deficiency. Study quality was moderate to weak in all studies. Included studies suggested fewer heart and liver problems in screen-detected patients, but inconsistent results for mortality. Follow up analyses compared long-term outcomes of (1) pre-symptomatically versus symptomatically treated patients, (2) screened versus unscreened patients, and (3) asymptomatic screen-detected, symptomatic screen-detected, and clinically diagnosed patients in each study. For follow up analyses 1 and 2, we found few statistically significant differences in the long-term outcomes. For follow up analysis 3 we found a significant difference for only one comparison, in the incidence of cardiomyopathy between the three groups.

Conclusions

There is some evidence that dietary management following screen-detection might be associated with a lower incidence of some LCHAD and MTP deficiency-related complications. However, the evidence base is limited by small study sizes, quality issues and risk of confounding. An internationally collaborative research effort is needed to fully examine the risks and the benefits to pre-emptive dietary management with particular attention paid to disease severity and treatment group.
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Literature
1.
go back to reference Moorthie S, et al. Systematic review and meta-analysis to estimate the birth prevalence of five inherited metabolic diseases. J Inherit Metab Dis. 2014;37:889–98.CrossRef Moorthie S, et al. Systematic review and meta-analysis to estimate the birth prevalence of five inherited metabolic diseases. J Inherit Metab Dis. 2014;37:889–98.CrossRef
2.
go back to reference Wanders RJA, et al. Long-chain 3-HYDROXYACYL-COA dehydrogenase-deficiency - identification of a new inborn error of mitochondrial fatty-acid BETA-oxidation. J Inherit Metab Dis. 1990;13(3):311–4.CrossRef Wanders RJA, et al. Long-chain 3-HYDROXYACYL-COA dehydrogenase-deficiency - identification of a new inborn error of mitochondrial fatty-acid BETA-oxidation. J Inherit Metab Dis. 1990;13(3):311–4.CrossRef
3.
go back to reference Wanders R, et al. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acidβ-oxidation. J Inherit Metab Dis. 1990;13(3):311–4.CrossRef Wanders R, et al. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acidβ-oxidation. J Inherit Metab Dis. 1990;13(3):311–4.CrossRef
4.
go back to reference Yang Z, et al. Fetal genotypes and pregnancy outcomes in 35 families with mitochondrial trifunctional protein mutations. Am J Obstet Gynecol. 2002;187(3):715–20.CrossRef Yang Z, et al. Fetal genotypes and pregnancy outcomes in 35 families with mitochondrial trifunctional protein mutations. Am J Obstet Gynecol. 2002;187(3):715–20.CrossRef
5.
go back to reference Spiekerkoetter U, et al. Current issues regarding treatment of mitochondrial fatty acid oxidation disorders. J Inherit Metab Dis. 2010;33(5):555–61.CrossRef Spiekerkoetter U, et al. Current issues regarding treatment of mitochondrial fatty acid oxidation disorders. J Inherit Metab Dis. 2010;33(5):555–61.CrossRef
6.
go back to reference Spiekerkoetter U, et al. Management and outcome in 75 individuals with long-chain fatty acid oxidation defects: results from a workshop. J Inherit Metab Dis. 2009;32(4):488–97.CrossRef Spiekerkoetter U, et al. Management and outcome in 75 individuals with long-chain fatty acid oxidation defects: results from a workshop. J Inherit Metab Dis. 2009;32(4):488–97.CrossRef
7.
go back to reference Bo R, et al. Clinical and molecular investigation of 14 Japanese patients with complete TFP deficiency: a comparison with Caucasian cases. J Hum Genet. 2017;62(9):809–14.CrossRef Bo R, et al. Clinical and molecular investigation of 14 Japanese patients with complete TFP deficiency: a comparison with Caucasian cases. J Hum Genet. 2017;62(9):809–14.CrossRef
8.
go back to reference Sander J, et al. Neonatal screening for defects of the mitochondrial trifunctional protein. Mol Genet Metab. 2005;85(2):108–14.CrossRef Sander J, et al. Neonatal screening for defects of the mitochondrial trifunctional protein. Mol Genet Metab. 2005;85(2):108–14.CrossRef
9.
go back to reference Sperk A, Mueller M, Spiekerkoetter U. Outcome in six patients with mitochondrial trifunctional protein disorders identified by newborn screening. Mol Genet Metab. 2010;101(2–3):205–7.CrossRef Sperk A, Mueller M, Spiekerkoetter U. Outcome in six patients with mitochondrial trifunctional protein disorders identified by newborn screening. Mol Genet Metab. 2010;101(2–3):205–7.CrossRef
10.
go back to reference Boutron, A., et al., Comprehensive cDNA study and quantitative analysis of mutant HADHA and HADHB transcripts in a French cohort of 52 patients with mitochondrial trifunctional protein deficiency. Molecular Genetics and Metabolism. 2011;103(4):341–348.CrossRef Boutron, A., et al., Comprehensive cDNA study and quantitative analysis of mutant HADHA and HADHB transcripts in a French cohort of 52 patients with mitochondrial trifunctional protein deficiency. Molecular Genetics and Metabolism. 2011;103(4):341–348.CrossRef
11.
go back to reference den Boer ME, et al. Mitochondrial trifunctional protein deficiency: a severe fatty acid oxidation disorder with cardiac and neurologic involvement. J Pediatr. 2003;142(6):684–9.CrossRef den Boer ME, et al. Mitochondrial trifunctional protein deficiency: a severe fatty acid oxidation disorder with cardiac and neurologic involvement. J Pediatr. 2003;142(6):684–9.CrossRef
12.
go back to reference den Boer ME, et al. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients. Pediatrics. 2002;109(1):99–104.CrossRef den Boer ME, et al. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients. Pediatrics. 2002;109(1):99–104.CrossRef
13.
go back to reference Karall D, et al. Clinical outcome, biochemical and therapeutic follow-up in 14 Austrian patients with long-chain 3-Hydroxy acyl CoA dehydrogenase deficiency (LCHADD). Orphanet J Rare Dis. 2015;10:21.CrossRef Karall D, et al. Clinical outcome, biochemical and therapeutic follow-up in 14 Austrian patients with long-chain 3-Hydroxy acyl CoA dehydrogenase deficiency (LCHADD). Orphanet J Rare Dis. 2015;10:21.CrossRef
14.
go back to reference Lindner M, et al. Efficacy and outcome of expanded newborn screening for metabolic diseases-report of 10 years from south-West Germany. Orphanet J Rare Dis. 2011;6(1):44.CrossRef Lindner M, et al. Efficacy and outcome of expanded newborn screening for metabolic diseases-report of 10 years from south-West Germany. Orphanet J Rare Dis. 2011;6(1):44.CrossRef
15.
go back to reference Lund AM, et al. Biochemical screening of 504,049 newborns in Denmark, the Faroe Islands and Greenland--experience and development of a routine program for expanded newborn screening. Mol Genetics Metab. 2012;107(3):281–93.CrossRef Lund AM, et al. Biochemical screening of 504,049 newborns in Denmark, the Faroe Islands and Greenland--experience and development of a routine program for expanded newborn screening. Mol Genetics Metab. 2012;107(3):281–93.CrossRef
16.
go back to reference Frazier DM, et al. The tandem mass spectrometry newborn screening experience in North Carolina: 1997-2005. J Inherit Metab Dis. 2006;29(1):76–85.CrossRef Frazier DM, et al. The tandem mass spectrometry newborn screening experience in North Carolina: 1997-2005. J Inherit Metab Dis. 2006;29(1):76–85.CrossRef
17.
go back to reference Zytkovicz TH, et al. Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England newborn screening program. Clin Chem. 2001;47(11):1945–55.PubMed Zytkovicz TH, et al. Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England newborn screening program. Clin Chem. 2001;47(11):1945–55.PubMed
18.
go back to reference Thomas B, et al. A process for systematically reviewing the literature: providing the research evidence for public health nursing interventions. Worldviews Evid-Based Nurs. 2004;1(3):176–84.CrossRef Thomas B, et al. A process for systematically reviewing the literature: providing the research evidence for public health nursing interventions. Worldviews Evid-Based Nurs. 2004;1(3):176–84.CrossRef
20.
go back to reference Nyaga V.N., M. Arbyn, and M.J.A.o.P.H. Aerts, Metaprop: a Stata command to perform meta-analysis of binomial data. Archives of Public Health. 2014;72(1):39. Nyaga V.N., M. Arbyn, and M.J.A.o.P.H. Aerts, Metaprop: a Stata command to perform meta-analysis of binomial data. Archives of Public Health. 2014;72(1):39.
21.
go back to reference Fahnehjelm KT, et al. Ocular characteristics in 10 children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a cross-sectional study with long-term follow-up. Acta Ophthalmol. 2008;86(3):329–37.CrossRef Fahnehjelm KT, et al. Ocular characteristics in 10 children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a cross-sectional study with long-term follow-up. Acta Ophthalmol. 2008;86(3):329–37.CrossRef
22.
go back to reference Fahnehjelm KT, et al. Most patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency develop pathological or subnormal retinal function. Acta Paediatr. 2016;105(12):1451–60.CrossRef Fahnehjelm KT, et al. Most patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency develop pathological or subnormal retinal function. Acta Paediatr. 2016;105(12):1451–60.CrossRef
23.
go back to reference Haglind CB, et al. Growth in long-chain 3-Hydroxyacyl-CoA dehydrogenase deficiency. Jimd Reports. 2013;8:81–90.CrossRef Haglind CB, et al. Growth in long-chain 3-Hydroxyacyl-CoA dehydrogenase deficiency. Jimd Reports. 2013;8:81–90.CrossRef
24.
go back to reference Immonen T, et al. Earlier diagnosis and strict diets improve the survival rate and clinical course of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Acta Paediatr. 2016;105(5):549–54.CrossRef Immonen T, et al. Earlier diagnosis and strict diets improve the survival rate and clinical course of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Acta Paediatr. 2016;105(5):549–54.CrossRef
25.
go back to reference Boese EA, et al. Characterization of Chorioretinopathy associated with mitochondrial Trifunctional protein disorders: long-term follow-up of 21 cases. Ophthalmology. 2016;123(10):2183–95.CrossRef Boese EA, et al. Characterization of Chorioretinopathy associated with mitochondrial Trifunctional protein disorders: long-term follow-up of 21 cases. Ophthalmology. 2016;123(10):2183–95.CrossRef
26.
go back to reference De Biase I, et al. Diagnosis, treatment, and clinical outcome of patients with mitochondrial Trifunctional protein/long-chain 3-Hydroxy acyl-CoA dehydrogenase deficiency. Jimd Reports. 2017;31:63–71.CrossRef De Biase I, et al. Diagnosis, treatment, and clinical outcome of patients with mitochondrial Trifunctional protein/long-chain 3-Hydroxy acyl-CoA dehydrogenase deficiency. Jimd Reports. 2017;31:63–71.CrossRef
27.
go back to reference Gillingham MB, et al. Triheptanoin versus trioctanoin for long-chain fatty acid oxidation disorders: a double blinded, randomized controlled trial. J Inherit Metab Dis. 2017;40(6):831–43.CrossRef Gillingham MB, et al. Triheptanoin versus trioctanoin for long-chain fatty acid oxidation disorders: a double blinded, randomized controlled trial. J Inherit Metab Dis. 2017;40(6):831–43.CrossRef
28.
go back to reference Kang E, et al. Clinical and genetic characteristics of patients with fatty acid oxidation disorders identified by newborn screening. BMC Pediatr. 2018;18(1):103.CrossRef Kang E, et al. Clinical and genetic characteristics of patients with fatty acid oxidation disorders identified by newborn screening. BMC Pediatr. 2018;18(1):103.CrossRef
29.
go back to reference Sykut-Cegielska J, et al. Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening. J Inherit Metab Dis. 2011;34(1):185–95.CrossRef Sykut-Cegielska J, et al. Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening. J Inherit Metab Dis. 2011;34(1):185–95.CrossRef
Metadata
Title
Evaluation of earlier versus later dietary management in long-chain 3-hydroxyacyl-CoA dehydrogenase or mitochondrial trifunctional protein deficiency: a systematic review
Authors
Hannah Fraser
Julia Geppert
Rebecca Johnson
Samantha Johnson
Martin Connock
Aileen Clarke
Sian Taylor-Phillips
Chris Stinton
Publication date
01-12-2019
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue 1/2019
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/s13023-019-1226-y

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