Ectopic Ocular Surface Calcification in Patients With Hypophosphatasia Treated With Asfotase Alfa.
Adolescent
Adult
Aged
Alkaline Phosphatase
/ adverse effects
Calcinosis
/ chemically induced
Conjunctival Diseases
/ chemically induced
Enzyme Replacement Therapy
/ adverse effects
Female
Humans
Hypophosphatasia
/ drug therapy
Immunoglobulin G
/ adverse effects
Male
Middle Aged
Recombinant Fusion Proteins
/ adverse effects
Young Adult
Journal
Cornea
ISSN: 1536-4798
Titre abrégé: Cornea
Pays: United States
ID NLM: 8216186
Informations de publication
Date de publication:
Jul 2019
Jul 2019
Historique:
pubmed:
11
4
2019
medline:
27
6
2019
entrez:
11
4
2019
Statut:
ppublish
Résumé
To assess for ectopic ocular calcification in a series of patients with hypophosphatasia (HPP) treated with asfotase alfa, a recombinant tissue-nonspecific alkaline phosphatase. This is a retrospective analysis of subjects enrolled at Duke University Medical Center in ENB-009-10 (ClinicalTrials.gov: NCT01163149), a randomized controlled trial of asfotase alfa in adolescents and adults with HPP. Seven patients between the ages of 45 and 66 years diagnosed with HPP based on clinical features and low serum alkaline phosphatase levels were enrolled at our site. Subjects were randomized to receive either daily subcutaneous injections of asfotase alfa or no treatment. After 24 weeks, during the open-label extension phase, all subjects received treatment for at least 4 years. All subjects underwent comprehensive eye examinations at baseline and at 24-week intervals throughout the study to assess for development of ocular calcifications. By week 120, all 7 subjects developed asymptomatic white refractile deposits in the interpalpebral perilimbal conjunctiva. Biopsy of the conjunctival lesions in 2 subjects revealed elastosis with subepithelial calcification. The lesions were nonprogressive and in 5 subjects exhibited some degree of regression. Asfotase alfa was invariably associated with development of mild focal conjunctival calcification, likely through disinhibition of hydroxyapatite crystal propagation. The calcifications were not symptomatic or vision-threatening and should not preclude enzyme replacement therapy for patients with this rare and often debilitating disease.
Identifiants
pubmed: 30969260
doi: 10.1097/ICO.0000000000001947
doi:
Substances chimiques
Immunoglobulin G
0
Recombinant Fusion Proteins
0
Alkaline Phosphatase
EC 3.1.3.1
asfotase alfa
Z633861EIM
Banques de données
ClinicalTrials.gov
['NCT01163149']
Types de publication
Journal Article
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM