Comprehensive analysis of pseudoxanthoma elasticum: epidemiological, genetic, and clinical findings from the leading Italian center.


Journal

Italian journal of dermatology and venereology
ISSN: 2784-8450
Titre abrégé: Ital J Dermatol Venerol
Pays: Italy
ID NLM: 101778002

Informations de publication

Date de publication:
Aug 2024
Historique:
medline: 29 7 2024
pubmed: 29 7 2024
entrez: 29 7 2024
Statut: ppublish

Résumé

Pseudoxanthoma elasticum (PXE) is a rare genetic autosomal recessive metabolic disease characterized by progressive mineralization and fragmentation of elastic fibers from soft connective tissues. The objective of our study was to analyze the epidemiological, genetic, cutaneous, and extracutaneous clinical data from the largest Italian monocentric cohort of PXE patients. We included all patients diagnosed with PXE and referred to Neurocutaneous Rare Diseases at Umberto I Polyclinic Hospital (Rome, Italy) between January 1983 and February 2024. A retrospective analysis of their data was performed. We enrolled 86 patients (77.9% women), revealing compound heterozygosity in 19.8% of cases and homozygosity in 5.8%. Missense (34.9%), non-sense (5.8%), splice-site (5.8%), deletion (4.7%), and frameshift (2.3%) mutations were disclosed. Cutaneous alterations were noted in the neck (69.7%), axilla (33.7%), inguinal (17.5%), and cubital folds (11.7%). The most common ocular findings were angioid streaks (64.0%) and choroidal neovascularization (18.6%), with blindness reported in 5.8% of cases. Thicker intima-media was observed around the mid-fifties in the supra-aortic trunks (40.7%), lower limb arteries (32.6%), and renal arteries (4.7%). Regurgitation was more common in atrioventricular valves (48.8%) than in semilunar ones (10.5% and 9.3%). Dyslipidemia (19.8%), hypertension (18.8%), and fatty liver disease (12.8%) were prevalent, with calcifications found in the kidneys (25.6%), liver (15.1%), spleen (11.6%), and testicles (8.1% of males). Autoimmune diseases and depression were observed in 11.6% and 4.7% of cases, respectively. Enhanced understanding of PXE can improve patients' quality of life and facilitate the development of more effective therapeutic strategies.

Sections du résumé

BACKGROUND BACKGROUND
Pseudoxanthoma elasticum (PXE) is a rare genetic autosomal recessive metabolic disease characterized by progressive mineralization and fragmentation of elastic fibers from soft connective tissues. The objective of our study was to analyze the epidemiological, genetic, cutaneous, and extracutaneous clinical data from the largest Italian monocentric cohort of PXE patients.
METHODS METHODS
We included all patients diagnosed with PXE and referred to Neurocutaneous Rare Diseases at Umberto I Polyclinic Hospital (Rome, Italy) between January 1983 and February 2024. A retrospective analysis of their data was performed.
RESULTS RESULTS
We enrolled 86 patients (77.9% women), revealing compound heterozygosity in 19.8% of cases and homozygosity in 5.8%. Missense (34.9%), non-sense (5.8%), splice-site (5.8%), deletion (4.7%), and frameshift (2.3%) mutations were disclosed. Cutaneous alterations were noted in the neck (69.7%), axilla (33.7%), inguinal (17.5%), and cubital folds (11.7%). The most common ocular findings were angioid streaks (64.0%) and choroidal neovascularization (18.6%), with blindness reported in 5.8% of cases. Thicker intima-media was observed around the mid-fifties in the supra-aortic trunks (40.7%), lower limb arteries (32.6%), and renal arteries (4.7%). Regurgitation was more common in atrioventricular valves (48.8%) than in semilunar ones (10.5% and 9.3%). Dyslipidemia (19.8%), hypertension (18.8%), and fatty liver disease (12.8%) were prevalent, with calcifications found in the kidneys (25.6%), liver (15.1%), spleen (11.6%), and testicles (8.1% of males). Autoimmune diseases and depression were observed in 11.6% and 4.7% of cases, respectively.
CONCLUSIONS CONCLUSIONS
Enhanced understanding of PXE can improve patients' quality of life and facilitate the development of more effective therapeutic strategies.

Identifiants

pubmed: 39069841
pii: S2784-8671.24.07949-0
doi: 10.23736/S2784-8671.24.07949-0
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

430-435

Auteurs

Alessandro Laghi (A)

Unit of Dermatology and STDs, Department of Medicine, Celio Military Hospital, Rome, Italy - alessandro.laghi@esercito.difesa.it.
Unit of Dermatology, Department of Internal Medicine and Medical Specialties, Sapienza University, Rome, Italy - alessandro.laghi@esercito.difesa.it.

Victor D Mandel (VD)

Unit of Porphyria and Rare Diseases, IRCCS San Gallicano Dermatological Institute, Rome, Italy.

Ilaria Zubba (I)

Unit of Dermatology, Department of Internal Medicine and Medical Specialties, Sapienza University, Rome, Italy.

Chiara Franceschini (C)

Unit of Porphyria and Rare Diseases, IRCCS San Gallicano Dermatological Institute, Rome, Italy.

Ilaria Demofonte (I)

Unit of Dermatology, Department of Internal Medicine and Medical Specialties, Sapienza University, Rome, Italy.

Camilla Chello (C)

Unit of Dermatology, Department of Internal Medicine and Medical Specialties, Sapienza University, Rome, Italy.

Emanuele Miraglia (E)

Department of Dermatology, San Sebastiano Hospital, Frascati, Rome, Italy.

Marco Ardigò (M)

Unit of Porphyria and Rare Diseases, IRCCS San Gallicano Dermatological Institute, Rome, Italy.
Unit of Dermatology, IRCCS Humanitas Clinic, Rozzano, Milan, Italy.

Sandra Giustini (S)

Unit of Dermatology, Department of Internal Medicine and Medical Specialties, Sapienza University, Rome, Italy.

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Classifications MeSH