A case of hepatitis C-associated osteosclerosis: accelerated bone turnover controlled by pulse steroid therapy

Nobuhiro Miyamura1, Shuhei Nishida1, Mina Itasaka1

  • 1Departments of Diabetes and Endocrinology.

Insights

Hepatitis C-associated osteosclerosis (HCAO) is a rare bone disorder linked to Hepatitis C virus (HCV). Corticosteroid therapy effectively reduced bone pain and markers in the 19th reported case, suggesting an immune basis for HCAO.

Area of Science:

  • Bone Metabolism
  • Hepatology
  • Immunology

Background:

  • Hepatitis C-associated osteosclerosis (HCAO) is a rare disorder characterized by rapid bone turnover and osteosclerosis, linked to chronic Hepatitis C virus (HCV) infection.
  • Pathogenesis remains unknown, but patients experience severe bone pain due to hyper-bone-formation and hyper-bone-resorption.

Purpose of the Study:

  • To report the 19th case of HCAO, detailing diagnostic confirmation and treatment outcomes.
  • To investigate potential therapeutic strategies and elucidate the underlying pathogenesis of HCAO.

Main Methods:

  • Diagnosis confirmed via bone biopsy.
  • Treatment initiated with bisphosphonates, followed by corticosteroids (intravenous methylprednisolone pulse and oral prednisolone).
  • Direct-acting antivirals (DAA: sofosbuvir and ribavirin) administered for HCV infection post-steroid therapy.

Main Results:

  • Bisphosphonate therapy showed no improvement in symptoms or bone markers.
  • Corticosteroid therapy significantly ameliorated bone pain and reduced elevated bone markers.
  • DAA therapy achieved sustained virological response for HCV but did not further impact HCAO symptoms.
  • Bone mineral density increased by 14% over four months.

Conclusions:

  • Corticosteroid therapy represents the first successful treatment for HCAO, suggesting an immunological basis for the condition.
  • Understanding HCAO pathogenesis may offer new therapeutic approaches for osteoporosis.
  • HCAO highlights a unique interplay between viral infection, immune response, and bone metabolism.

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