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Meta-Analysis
. 2019 Feb 13;14(1):40.
doi: 10.1186/s13023-018-0987-z.

Systematic literature review and meta-analysis on the epidemiology of propionic acidemia

Affiliations
Meta-Analysis

Systematic literature review and meta-analysis on the epidemiology of propionic acidemia

Tímea Almási et al. Orphanet J Rare Dis. .

Abstract

Propionic acidemia (PA, OMIM #606054) is a serious, life-threatening, inherited, metabolic disorder caused by the deficiency of the mitochondrial enzyme propionyl-coenzyme A (CoA) carboxylase (EC 6.4.1.3). The primary objective of this study was to conduct a systematic literature review and meta-analysis on the epidemiology of PA. The literature search was performed covering Medline, Embase, Cochrane Database of Systematic Reviews, CRD Database, Academic Search Complete, CINAHL and PROSPERO databases. Websites of rare disease organizations were also searched for eligible studies. Of the 2338 identified records, 188 articles were assessed for eligibility in full text, 43 articles reported on disease epidemiology, and 31 studies were included into the quantitative synthesis. Due to the rarity of PA, broadly targeted population-based prevalence studies are not available. Nonetheless, implementation of newborn screening programs has allowed the estimation of the birth prevalence data of PA across multiple geographic regions. The pooled point estimates indicated detection rates of 0.29; 0.33; 0.33 and 4.24 in the Asia-Pacific, Europe, North America and the Middle East and North Africa (MENA) regions, respectively. Our systematic literature review and meta-analysis confirm that PA is an ultra-rare disorder, with similar detection rates across all regions with the exception of the MENA region where the disease, similar to other inherited metabolic disorders, is more frequent.

Keywords: Epidemiology; Inherited metabolic disorder; Meta-analysis; Newborn screening; Propionic acidemia; Systematic literature review.

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Conflict of interest statement

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

Tímea Almási, Tamás Zelei, Kata Csetneki, and Zoltán Vokó are employees of Syreon Research Institute and performed contracted research for Moderna, Inc. Lin T. Guey and Christine Lukacs are employees of Moderna, Inc. and receive salary and stock options as compensation for their employment. Nonetheless, the content of this paper, as well as the views and opinions expressed therein are those of the Authors and not the organizations that employ them.

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Figures

Fig. 1
Fig. 1
Flow of information diagram
Fig. 2
Fig. 2
Estimates of birth prevalence of propionic acidemia in the different countries and geographical regions

References

    1. Gilksman FJ. Propionic Acidemia. 2018.
    1. Wongkittichote P, Mew NA, Chapman KA. Propionyl-CoA carboxylase–a review. Mol Genet Metab. 2017. - PMC - PubMed
    1. Kölker S, Cazorla AG, Valayannopoulos V, Lund AM, Burlina AB, Sykut-Cegielska J, et al. The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation. J Inherit Metab Dis. 2015;38(6):1041–1057. doi: 10.1007/s10545-015-9839-3. - DOI - PubMed
    1. Shchelochkov OA, Carrillo N, Venditti C. Propionic acidemia. 2018.
    1. De Baulny HO, Benoist J, Rigal O, Touati G, Rabier D, Saudubray J. Methylmalonic and propionic acidaemias: management and outcome. J Inherit Metab Dis. 2005;28(3):415–423. doi: 10.1007/s10545-005-7056-1. - DOI - PubMed

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