Evidence map›Paper›PMID 41050551›Full record

ArticleMolecular genetics and metabolism reports2025

Clinical and biochemical characterization of a patient with prolidase deficiency, a rare disorder of collagen metabolism.

Troy K Coody, Irene De Biase, Julie M Porter, Marzia Pasquali, Brian J Shayota

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Article in Molecular genetics and metabolism reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Troy K CoodyDepartment of Pathology, University of Utah, Salt Lake City, UT 84108, USA.
Irene De BiaseDepartment of Pathology, University of Utah, Salt Lake City, UT 84108, USA.
Julie M PorterDepartment of Pediatrics, Division of Medical Genetics, University of Utah, Salt Lake City, UT 84108, USA.
Marzia PasqualiDepartment of Pathology, University of Utah, Salt Lake City, UT 84108, USA.
Brian J ShayotaDepartment of Pediatrics, Division of Medical Genetics, University of Utah, Salt Lake City, UT 84108, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prolidase deficiency (PD) is an autosomal recessive inborn error of metabolism, with an estimated incidence of 1 per 1.25 million births. Prolidase is critical for the turnover of proline and hydroxyproline-rich proteins, such as collagen. Collagen metabolism is essential for matrix regeneration during cellular proliferation and complex bodily functions such as wound healing and immunological cell differentiation. PD clinical manifestations include persistent skin ulcerations and poor wound healing, hypertelorism, high arched palate, depressed nasal bridge, micrognathia, splenomegaly, intellectual disability, recurring infections, and hematological abnormalities. Biochemically, a diagnosis of PD is supported by increased urinary excretion of glycyl-proline and other proline-containing iminopeptides detected by amino acid analysis. There are no current targeted therapies, but suggested interventions have included topical proline-glycine ointment, manganese supplementation, topical and oral steroids, and immunomodulation with monoclonal antibodies. Here, we describe a 30-year-old patient with PD whose clinical course has been characterized by recurrent skin ulcerations/cysts with secondary scarring, recurrent infections, anemia, thrombocytopenia, lymphopenia, elevated liver enzymes, hirsutism, and seemingly unrelated papillary thyroid cancer. Skin manifestations were particularly severe due to the added complication of a diagnosis of hidradenitis suppurativa. Quantitative analysis of amino acids and related compounds revealed markedly elevated glycyl-proline in urine and plasma. To further characterize the biochemical phenotype, untargeted metabolomic analysis was sent on both plasma and urine. An increase was noted in several metabolites from the prolidase-dependent dipeptide recycling pathways. A better understanding of the pathophysiological mechanisms involved in prolidase deficiency may prove useful as different therapeutic approaches are being considered.

Indexed as

Amino acidsGlycyl-prolineLiquid chromatography-tandem mass spectrometryMetabolomicsProlidase deficiency

Identifiers

PMID41050551
PMCPMC12495286

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