Effects of risedronate on metabolic bone disease in patients with type 1 diabetes and osteoporosis

  1. María del Mar Campos Pastor
  2. Juan de Dios Luna del Castillo
  3. Fernando Escobar Jiménez
  4. F.J. Gómez Jiménez
  5. M.D. Serrano Pardo
  6. P. López-Ibarra
Revista:
Revista Española de Enfermedades Metabólicas Oseas

ISSN: 1132-8460

Any de publicació: 2008

Volum: 17

Número: 4

Pàgines: 66-70

Tipus: Article

DOI: 10.1016/S1132-8460(08)72481-4 DIALNET GOOGLE SCHOLAR lock_openAccés obert editor

Altres publicacions en: Revista Española de Enfermedades Metabólicas Oseas

Resum

To assess the effect of a antiresorptive on bone mass and remodeling markers in patients with type 1 diabetes mellitus (DM-1) and osteoporosis (OP). Study included 52 patients with DM-1 of 21-36 years duration and OP or osteopenia, aged 29-69 years. OP patients received 30 mg/week risedronate (n=35) and calcium+vitamin D; osteopenic patients and risedronate refusers (n=17) received only calcium+vitamin D. At 12 months, the risedronate group showed significant improvements in tartrate resistant acid phosphatase (p<0.0001), osteocalcin (BGP) (p<0.0001), bone alkaline phosphatase (BAP) (p<0.0001), and hemoglobin A1c (HbA1c) (p<0.0001); bone mineral density (BMD) was increased at 6 and 12 months versus baseline in lumbar spine (LS) (p<0.0001) and femoral neck (FN) (p<0.0001). At 12 months, the conventional group showed a significant improvement in HbA1c (p<0.012) and reduction in BGP (p<0.03) and BAP (p<0.0001). The conventional treatment group showed no significant changes in BMD at LS and FN during the 12-month period. Risedronate treatment improves BMD in long-term DM-1 patients.