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Changes in bone mineral density after allogenic stem cell transplantation - 21/09/22

Doi : 10.1016/j.jbspin.2022.105373 
Diane Leguy a, , Leonardo Magro b, Adeline Pierache c, Valérie Coiteux b, Ibrahim Yakoub Agha b, Bernard Cortet a, Isabelle Legroux-Gerot a
a Department of Rheumatology, Lille University Hospital, 59000 Lille, France 
b Department of Hematology, Lille University Hospital, 59000 Lille, France 
c University of Lille, CHU Lille, ULR 2694–METRICS: évaluation des technologies de santé et des pratiques médicales, 59000 Lille, France 

Corresponding author. Department of Rheumatology, Lille University Hospital, Rue Emile Laine, 59037 Lille, France.Department of Rheumatology, Lille University HospitalRue Emile LaineLille59037France

Highlights

Bone fragility occurred in pre- and post-allogenic stem cell transplantation.
The highest bone loss occurred during the first months.
Bone loss is predominant at the hip, where recovery is slower compared to lumbar spine.
Corticosteroid treatment, progressive disease before allogenic stem cell transplantation and bone marrow stem cells are the main factors explaining bone loss.

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Abstract

Objective

Osteoporosis is a complication after allogenic stem cell transplantation (alloSCT). The purpose of this study was to assess changes in bone mineral density (BMD) 6 months and 3 years after alloSCT, as well as predictors of bone loss.

Methods

A longitudinal, prospective, single-center study was conducted at Lille University Hospital between 2005 and 2016. Clinical, biological, radiologic (thoracic and lumbar spine) and densitometric (DXA) assessments were carried out at baseline (pre-transplant), 6 months and 3 years. Patients with myeloma were not included.

Results

Two hundred and fifty-eight patients were included (144 men). Among them, 60.1% had leukemia and 65.8% of them, acute myeloid leukemia. At baseline, 6 months and 3 years, DXA-confirmed that osteoporosis was observed in 17%, 22.8% and 17.5% of the patients, respectively, mainly at the femoral neck. At baseline, 6 months and 3 years, 9 (8.5%), 53 (21.5%) and 38 (16.7%) patients, respectively, were receiving anti-osteoporotic treatment. From baseline to 6-month follow-up, BMD decreased significantly (p<0.001) at the lumbar spine (−36 [95%CI; −51 to −20] mg/cm2 of hydroxyapatite), femoral neck (−43 [95%CI; −57 to −29] mg/cm2 of hydroxyapatite) and total hip (−53 [95%CI; −68 to −39] mg/cm2 of hydroxyapatite). From 6-month to 3-year follow-up, a significant increase in BMD was observed at the lumbar spine only (+31 [95%CI; 20 to 42] mg/cm2 of hydroxyapatite, p<0.001). At all 3 sites, changes in BMD did not differ between patients treated or untreated by anti-osteoporotic treatment from 6-month to 3 year follow-up. Incident fractures were found in 4.1% and 5.7% of the patients at 6 months and 3 years, respectively. Between baseline and 6 months, bone loss at all 3 sites was associated with corticosteroid intake. At the total hip, 23.3% of the decrease in BMD from baseline to 6 months was due to an active hematological disease (p<0.05), a bone marrow stem cells (p<0.01) and a corticosteroid intake (p<0.01).

Conclusion

Our study found evidence of bone fragility in alloSCT patients. Low BMD persisted at the hip 3 years after transplantation due to slower improvement at this site.

Il testo completo di questo articolo è disponibile in PDF.

Keywords : Osteoporosis, Allogenic stem cells transplantation, Fracture, Bone mineral density


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