4-Hydroxybenzoic acid rescues multisystemic disease and perinatal lethality in a mouse model of mitochondrial disease
Julia Corral-Sarasa, Juan Manuel Martinez Galvez, Pilar González‐García, Olivia Wendling, Laura Jiménez-Sánchez, Sergio López-Herrador, Catarina M. Quinzii, María Elena Díaz-Casado, Luís C. López
Abstract
<h2>Summary</h2> Coenzyme Q (CoQ) deficiency syndrome is conventionally treated with limited efficacy using exogenous CoQ<sub>10</sub>. Poor outcomes result from low absorption and bioavailability of CoQ<sub>10</sub> and the clinical heterogenicity of the disease. Here, we demonstrate that supplementation with 4-hydroxybenzoic acid (4HB), the precursor of the benzoquinone ring in the CoQ biosynthetic pathway, completely rescues multisystemic disease and perinatal lethality in a mouse model of CoQ deficiency. 4HB stimulates endogenous CoQ biosynthesis in tissues of <i>Coq2</i> mutant mice, normalizing mitochondrial function and rescuing cardiac insufficiency, edema, and neurodevelopmental delay. In contrast, exogenous CoQ<sub>10</sub> supplementation falls short in fully restoring the phenotype. The treatment is translatable to human use, as proven by <i>in vitro</i> studies in skin fibroblasts from patients with pathogenic variants in <i>COQ2</i>. The therapeutic approach extends to other disorders characterized by deficiencies in the production of 4HB and early steps of CoQ biosynthesis and instances of secondary CoQ deficiency.