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Incidence of vertebral fractures in calcium and vitamin D-supplemented postmenopausal Brazilian women with osteopenia or osteoporosis: data from Arzoxifene Generations Trial
Arantes, Henrique Pierotti; Gimeno, Suely Godoy Agostinho; Chiang, Alan Y.; Bilezikian, John P.; Lazaretti-Castro, Marise.
  • Arantes, Henrique Pierotti; Universidade Federal de São Paulo. Departamento de Endocrinologia. Unidade de Metabolismo Ósseo e Mineral. São Paulo. BR
  • Gimeno, Suely Godoy Agostinho; Universidade Federal de São Paulo. Departamento de Endocrinologia. Unidade de Metabolismo Ósseo e Mineral. São Paulo. BR
  • Chiang, Alan Y.; Universidade Federal de São Paulo. Departamento de Endocrinologia. Unidade de Metabolismo Ósseo e Mineral. São Paulo. BR
  • Bilezikian, John P.; Universidade Federal de São Paulo. Departamento de Endocrinologia. Unidade de Metabolismo Ósseo e Mineral. São Paulo. BR
  • Lazaretti-Castro, Marise; Universidade Federal de São Paulo. Departamento de Endocrinologia. Unidade de Metabolismo Ósseo e Mineral. São Paulo. BR
Arch. endocrinol. metab. (Online) ; 60(1): 54-59, Feb. 2016. tab, graf
Article in English | LILACS | ID: lil-774619
ABSTRACT
ABSTRACT Objective Vertebral fracture is the most common osteoporotic fracture, affecting quality of life and increasing mortality. Epidemiological data on incidence of vertebral fracture are scarce in Brazil and throughout Latin America. Our aim was to determine vertebral fracture incidence and risk factors in a female Brazilian population. Subjects and methods Postmenopausal women with low bone mass were studied from the Brazilian placebo group of Arzoxifene Generations Trial (n = 974), followed for up to 5 years. The primary endpoint was new vertebral fractures, detected by X-Ray. Experimental design defined two strata A. Osteoporosis or previous vertebral fracture with osteopenia; B. Osteopenia without previous fracture. Previous fracture, T-score, ionized calcium, alkaline phosphatase, creatinine and glucose were analyzed at baseline. Crude and adjusted incidence rates of vertebral fractures were estimated and Poisson regression model was used. Results Incidence rate was 7.7 (95% CI of 5.4 to 10.9) per 1,000 person-years (PY), increasing as a function of age. Women with new vertebral fractures had higher prevalence of previous nonvertebral fracture after menopause, were older and had lower lumbar spine (LS) T-score. Fracture risk increased by 46% for each unit reduction in LS T-score. Variables correlated with new vertebral fracture were age (p = 0.034), LS T-score, stratum A (p = 0.001 for both) and previous nonvertebral fracture after menopause (p = 0.019). In the final model, LS T-score was the strongest predictor. Conclusions Incidence rate of vertebral fracture of 7.7 per 1,000 PY. Age and previous fractures were associated with new vertebral fracture, but LS T-score was the most important predictor.
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Full text: Available Index: LILACS (Americas) Main subject: Bone Diseases, Metabolic / Spinal Fractures / Postmenopause Type of study: Controlled clinical trial / Etiology study / Incidence study / Observational study / Prognostic study / Risk factors Limits: Aged / Aged80 / Female / Humans Country/Region as subject: South America / Brazil Language: English Journal: Arch. endocrinol. metab. (Online) Journal subject: Endocrinology / Metabolism Year: 2016 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal de São Paulo/BR

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Full text: Available Index: LILACS (Americas) Main subject: Bone Diseases, Metabolic / Spinal Fractures / Postmenopause Type of study: Controlled clinical trial / Etiology study / Incidence study / Observational study / Prognostic study / Risk factors Limits: Aged / Aged80 / Female / Humans Country/Region as subject: South America / Brazil Language: English Journal: Arch. endocrinol. metab. (Online) Journal subject: Endocrinology / Metabolism Year: 2016 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal de São Paulo/BR