Objective To investigate whether women with systemic sclerosis (SSc) have an increased risk of osteoporosis (OP) and related fractures compared to a high-risk population with rheumatoid arthritis (RA) and also healthy controls, and to determine putative specific OP and fracture risk factors. Methods We performed a cross-sectional study with successive inclusion of age-matched healthy women and women with SSc and RA. Risk factors for OP and fracture were collected for all patients. Bone mineral density (BMD) was systematically measured at the lumbar spine and total hip region with dual x-ray absorptiometry. Results We included 71 women with SSc, 139 women with RA, and 227 healthy women. The prevalence of OP and fracture was similar in SSc and RA, and was for both diseases higher than in healthy controls (OP: 30% in SSc, 32% in RA, and 11% in controls; fracture: 35% in SSc, 33% in RA, and 10% in controls). Multivariate analysis identified age as a risk factor of OP in SSc. Age and low 25-hydroxyvitamin D (25[OH]D) levels were recognized as risk factors of fracture in SSc. In comparison, age and corticosteroid treatment were associated with OP in RA. Multivariate analysis confirmed age, OP, and low 25(OH)D levels as independent risk factors of fractures in RA. Conclusion The prevalence of OP and fracture in SSc was increased compared to healthy women and reached the high prevalence associated with RA. Age and vitamin D deficiency were identified as risk factors of fracture in SSc. Therefore, increasing the awareness and performance of BMD measurements together with the vitamin D supply in patients with SSc is warranted.
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Univ Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Univ Paris 05, Hop Cochin, INSERM, U1016, F-75014 Paris, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Coustet, B.
Dieude, P.
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Univ Paris 07, Hop Bichat, Paris, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Dieude, P.
Wipff, J.
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Univ Paris 05, Hop Cochin, INSERM, U1016, F-75014 Paris, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Wipff, J.
Avouac, J.
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Univ Paris 05, Hop Cochin, INSERM, U1016, F-75014 Paris, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Avouac, J.
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Hachulla, E.
Diot, E.
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CHU Bretonneau, INSERM EMI U 00 10, F-37044 Tours, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Diot, E.
Cracowski, J. L.
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CHU Grenoble, INSERM CIC3, Grenoble, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Cracowski, J. L.
Tiev, K.
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Univ Paris 06, Hop St Antoine, Paris, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Tiev, K.
Sibilia, J.
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Univ Strasbourg, Hop Hautepierre, Strasbourg, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Sibilia, J.
Mouthon, L.
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机构:Univ Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Mouthon, L.
Frances, C.
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Univ Paris 06, Hop Tenon, Paris, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Frances, C.
Amoura, Z.
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Univ Paris 06, Paris, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Amoura, Z.
Carpentier, P.
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CHU Grenoble, Clin Univ Med Vasc, F-38043 Grenoble, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Carpentier, P.
Meyer, O.
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Univ Paris 07, Hop Bichat, Paris, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Meyer, O.
Kahan, A.
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机构:Univ Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Kahan, A.
Boileau, C.
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Univ Versailles St Quentin Yvelines, Hop Ambroise Pare, AP HP, Lab Biochim Hormonale & Genet, Boulogne, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France
Boileau, C.
Allanore, Y.
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Univ Paris 05, Hop Cochin, INSERM, U1016, F-75014 Paris, FranceUniv Paris 05, Hop Cochin, APHP, Serv Rhumatol A, F-75014 Paris, France