Key result
Biallelic PPA2 deficiency causes severe arrhythmogenic cardiomyopathy with ~79% mortality by age 20.
Why the study?
PPA2 deficiency is an emerging recessive cardiac condition causing heart failure and sudden cardiac death in infants and young people, motivating an investigation to define its clinical and molecular spectrum, genotype-phenotype correlations, and predicted prevalence.
Observational (n=63)
Characterizes PPA2 deficiency as a highly lethal pediatric and adolescent arrhythmogenic cardiomyopathy (79% mortality by age 20, prevalence ≥1/135,000 in Europeans) triggered by viral infections or minimal alcohol, supporting its inclusion in newborn genomic screening.
Answers are grounded in this paper and cite their sources.
Supports PPA2 testing in early-onset arrhythmogenic cardiomyopathy; extends the genetic spectrum with prevalence and mortality estimates.
BACKGROUND: PPA2 encodes for inorganic pyrophosphatase 2, a mitochondrial enzyme that hydrolyzes inorganic pyrophosphates into orthophosphate. Biallelic loss-of-function variants cause PPA2 deficiency, an emerging recessive cardiac condition that causes heart failure and sudden cardiac death in infants and young people. METHODS: Using published case reports and large-scale genomics resources, we defined the clinical and molecular spectrum of this disease, classified variants using a customized American College of Medical Genetics and Genomics pipeline, assessed genotype-phenotype correlations, calculated predicted prevalence using the gnomAD GenIE tool, and investigated monoallelic associations in the UK Biobank. RESULTS: A total of 63 cases from 37 families were identified from 12 publications. The natural history of this disease is characterized by clinical heterogeneity and high mortality (79% by 20 years of age), typically presenting as a highly arrhythmogenic cardiomyopathy with 2 distinct risk periods: in infancy, where viral infections can lead to heart failure, and in adolescence, where minimal alcohol exposure can trigger sudden cardiac death. The disease is genetically heterogeneous, with 29 distinct variants described (18 of which were classified as [likely] pathogenic), usually in compound heterozygosity. As complete gene knockout appears to be incompatible with life, PPA2 deficiency is caused by biallelic variants within a particular loss-of-function window, with deficiency mitigated by hypomorphic effects, variants in nonconstitutive exons, and particular compound heterozygous combinations. The spectrum of phenotypic effect extends to monoallelic carriers of pathogenic variants, which demonstrate an apparent mitohormesis-like compensatory protection from heart failure. The disease has an estimated prevalence of at least 1/135 000 in European ancestry populations. CONCLUSIONS: PPA2 deficiency is a genetically complex and clinically severe disease. Given the potential for effective life-saving interventions, PPA2 may warrant inclusion in emerging newborn genomic screening programs.
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Shu et al. (2026) conducted an observational in PPA2 deficiency (arrhythmogenic cardiomyopathy, heart failure, sudden cardiac death) (n=63). Biallelic and monoallelic loss-of-function variants in PPA2 was evaluated on Mortality by 20 years of age. Biallelic PPA2 deficiency causes highly arrhythmogenic cardiomyopathy with 79% mortality by age 20 and an estimated prevalence of at least 1/135,000 in Europeans.
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