Evidence map›Paper›PMID 41116885›Full record

ArticleIndian journal of orthopaedics2025

Assessment of Bone Density in Osteogenesis Imperfecta in Pediatric and Adolescent Age Group: Can the Metacarpal Index Play a Role?

Vrisha Madhuri, Madhavi Kandagaddala, Ashis Kumar, Jemimah Jane

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Article in Indian journal of orthopaedics, 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

4 authors.

Vrisha MadhuriDepartment of Paediatric Orthopaedic, Christian Medical College, Ida Scudder Road, Vellore, Tamil Nadu India.ORCID 0000-0003-4494-222X
Madhavi KandagaddalaDepartment of Radiology, Christian Medical College, Ida Scudder Road, Vellore, Tamil Nadu India.
Ashis KumarDepartment of Paediatric Orthopaedic, Christian Medical College, Ida Scudder Road, Vellore, Tamil Nadu India.
Jemimah JaneDepartment of Paediatric Orthopaedic, Christian Medical College, Ida Scudder Road, Vellore, Tamil Nadu India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objective: Osteogenesis Imperfecta (OI), an inherited genetic disorder affecting 1 in 20,000 people worldwide, is currently treated with bisphosphonates for moderate and severe forms. Dual-energy X-ray absorptiometry (DXA) is the standard method for assessing the improvement in bone quality in OI but due to the unavailability of DXA in some places, hand radiographs can be used to calculate the second metacarpal index (MCI) to assess the bone quality in many osteoporotic disorders. In this study we evaluated the feasibility of using metacarpal index to assess the bone quality in OI in children. Methods: We evaluated the MCI values in 37 children aged 1-18 years at baseline (before intervention), and following pamidronate treatment in 18 children with type III or type IV OI. Results: A decrease in MCI was noted with ageing as anticipated in the OI population, and we also observed an increase in MCI among the younger cohort (under 8 years) receiving pamidronate compared to the older cohort (above 8 years). The change in MCI after pamidronate therapy was monitored, and those who were initiated on pamidronate at a younger age showed more improvement in MCI than those who were started at a later age. Conclusions: Our study suggests that when DXA measurements are not feasible, MCI can be a potential tool to assess bone quality and evaluate bisphosphonate therapy in the OI population.

Indexed as

Bone qualityMetacarpal indexOsteogenesis imperfectaPamidronate

Identifiers

PMID41116885
PMCPMC12535557

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