Open Access
Denosumab versus zoledronic acid for patients with beta-thalassemia major-induced osteoporosis
Author(s) -
Mohamed A Yassin,
Mohamed Osman Abdel Rahman,
Anas Hamad,
Abdul Razzakh Poil,
Mohamed Abdelrazek,
Radwa M Hussein,
Nancy Kassem,
Afraa M. Fadul,
Sarah A. Elkourashy,
Abdulqadir J. Nashwan
Publication year - 2020
Publication title -
medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.59
H-Index - 148
eISSN - 1536-5964
pISSN - 0025-7974
DOI - 10.1097/md.0000000000023637
Subject(s) - medicine , denosumab , zoledronic acid , osteoporosis , n terminal telopeptide , thalassemia , outpatient clinic , densitometry , bone remodeling , frax , alkaline phosphatase , pediatrics , bone mineral , osteocalcin , biochemistry , chemistry , osteoporotic fracture , enzyme
Abstract The main aim of this study is to compare the 2 medications denosumab and zoledronic acid for patients with beta-thalassemia major induced osteoporosis. Patients with B-thalassemia major induced osteoporosis will undergo baseline assessment of the bone densitometry by bone density (DEXA) scan as a standard of care by the radiology department, then a blood test for bone-specific alkaline phosphatase and type-1 collagen telopeptide will be measured by the chemistry laboratory. Patients with B-thalassemia major induced osteoporosis, who are 18 years of age or more and willing to participate in the study will be enrolled after consenting by the primary investigator in hematology outpatient clinics. Patients with osteoporosis will receive 1 of the 2 medications; at the end of the year, DEXA scan will be done to compare the response of the 2 medications. The potential risks include drug-related side effects. The outcome will be measured biochemically by measuring bone-specific alkaline phosphatase and type 1 collagen carboxy telopeptide and radiologically by DEXA scan at baseline and 1 year using Z score.