Volume 85, Issue 1 pp. 65-67

Vitamin D deficiency does not alter biochemical markers of bone metabolism before or after autograft in patients with multiple myeloma

Michel Laroche

Michel Laroche

Rheumatology Department, Purpan University Hospital, Toulouse, France

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Olivia Lemaire

Olivia Lemaire

Rheumatology Department, Purpan University Hospital, Toulouse, France

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Michel Attal

Michel Attal

Haematology Department, Purpan University Hospital, Toulouse, France

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First published: 15 June 2010
Citations: 12
Prof Michel Laroche, Centre de Rhumatologie, CHU Purpan, 1 place du Dr Baylac, 31059 Toulouse Cedex 9, France. Tel: 0033561776976, Fax: 0033561777375; e-mail : [email protected]

Abstract

So far, only one study has demonstrated a high incidence of vitamin D deficiency in patients with multiple myeloma. Vitamin D deficiency may alter bone remodelling in myeloma. In this study, we aimed to determine the prevalence of vitamin D deficiency and to assess its impact on bone remodelling and bone mineral density before and after autologous stem cell transplantation (ASCT). Patients and methods: In 39 consecutive patients receiving high-dose chemotherapy (melphalan 200 mg/m2) followed by ASCT for multiple myeloma, we measured before (T0) and 12 months after ASCT (T12) serum calcium, 25-OH-D, PTH 1-84, bone alkaline phosphatase (bALP), serum C-terminal cross-linking telopeptide and lumbar spine bone mineral density (BMD). Results: Mean vitamin D levels were low: 15 ± 5 ng/mL (9–18) at T0 and 16 ± 5 ng/mL (14–22) at T12. Twenty-six patients (68%) had vitamin D deficiency (25-OH-D < 20 ng/mL) at T0 and 58% at T12. Patients in the vitamin D-deficient group had higher serum PTH levels than those in the vitamin D-sufficient group : 71 ± 24 pg/mL vs. 52 ± 18 pg/mL (P = 0.04). Biochemical bone markers were identical in both groups at T0 and T12. Z-score values did not significantly differ between the two groups at T0 and T12. There were no correlations between 25-OH-D and BMD or bone marker levels. Conclusion: Vitamin D deficiency does not impair biochemical markers of bone metabolism in patients with multiple myeloma, before or after ASCT.

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