Effects of allogeneic bone marrow transplantation on recipient bone mineral density: A prospective study

Biol Blood Marrow Transplant. 2000;6(3A):344-51. doi: 10.1016/s1083-8791(00)70061-9.

Abstract

Allogeneic bone marrow transplant (BMT) recipients have many known risk factors for developing decreased bone mineral density (BMD) after transplantation. We performed a prospective sequential evaluation of BMD in the lumbar spine and nondominant hip using dual-energy x-ray absorptiometry (DEXA) in a cohort of 47 adult patients (median age, 43 years) who were undergoing radiation-based BMT for hematologic malignancies. Baseline DEXA studies were performed before BMT and repeated at 3 to 4 months, 6 to 8 months, and 12 to 14 months after BMT. The majority of patients (60%) had been minimally treated with combination cytotoxic chemotherapy, having received no more than 1 treatment regimen before BMT. Graft-versus-host disease prophylaxis consisted of cyclosporine in combination with either methotrexate or prednisone, or both. Mean lumbar spine and hip BMD were normal before BMT (spine: 1.01 g/cm2, z score = 96%; hip: 0.86 g/cm2, z score = 100%) and gradually decreased (spine: 0.98 g/cm2, z score = 94%; hip: 0.76 g/cm2, z score = 91%) at 12 to 14 months. These declines were statistically significant (P < .006 and < .002 for lumbar spine; P < .001 and < .001 for hip). In addition, the sharpest decline occurred during the first 6 months after BMT and was more marked in the hip than the lumbar spine. These data suggest that BMT adversely affects BMD in this patient population.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Absorptiometry, Photon
  • Adult
  • Antineoplastic Agents / adverse effects
  • Bone Density*
  • Bone Diseases, Metabolic / etiology*
  • Bone Marrow Transplantation / adverse effects*
  • Bone and Bones / chemistry
  • Cohort Studies
  • Combined Modality Therapy
  • Female
  • Hematologic Neoplasms / drug therapy
  • Hematologic Neoplasms / therapy
  • Hip Joint / pathology
  • Humans
  • Lumbar Vertebrae / pathology
  • Male
  • Middle Aged
  • Minerals / analysis
  • Myelodysplastic Syndromes / drug therapy
  • Myelodysplastic Syndromes / therapy
  • Myeloproliferative Disorders / drug therapy
  • Myeloproliferative Disorders / therapy
  • Osteoporosis / epidemiology
  • Osteoporosis / etiology*
  • Prospective Studies
  • Racial Groups
  • Risk Factors
  • Transplantation, Homologous / adverse effects*

Substances

  • Antineoplastic Agents
  • Minerals