HMG-CoA reductase inhibitors increase BMD in type 2 diabetes mellitus patients

被引:137
作者
Chung, YS
Lee, MD
Lee, SK
Kim, HM
Fitzpatrick, LA
机构
[1] Mayo Clin & Mayo Fdn, Endocrine Res Unit, Dept Internal Med, Div Endocrinol Metab & Nutr, Rochester, MN 55905 USA
[2] Ajou Univ, Sch Med, Dept Endocrinol & Metab, Suwon 442721, South Korea
关键词
D O I
10.1210/jc.85.3.1137
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recently, it was reported that 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors increased bone mineral density (BMD) in mice. We studied the effect of HMG-CoA reductase inhibitors on BMD of type 2 diabetes mellitus by a retrospective review of medical records. Sixty-nine type 2 diabetic patients were included. The control group (n = 33) did not take HMG-CoA reductase inhibitors. The treatment group (n = 36) was administered either lovastatin, pravastatin, or simvastatin. BMD of the spine, femoral neck, femoral trochanter, and total hip were measured by dual-energy X-ray absorptiometry. There were no significant differences between control and treatment groups in age, sex, body mass index, glycemic control, and serum insulin levels. In the control group, BMD of the spine significantly decreased (from 1.116 +/- 0.165 to 1.081 +/- 0.178 g/cm(2)) after 14 months. In the treatment group, BMD of the femoral neck significantly increased (from 0.853 +/- 0.139 to 0.878 +/- 0.147 g/cm(2)) after 15 months. In male subjects treated with HMG-CoA reductase inhibitors, there was a significant increase in BMD of the femoral neck and femoral trochanter (from 0.899 +/- 0.139 to 0.934 +/- 0.139 and from 0.801 +/- 0.145 to 0.833 +/- 0.167 g/cm(2), respectively), but in female subjects, only BMD of the femoral neck increased (from 0.819 +/- 0.132 to 0.834 +/- 0.143 g/cm(2)). Percentage increments of MD of the femoral neck, femoral wards triangle, femoral trochanter, and total hip in the treatment group were significantly higher than in the control group (2.32% vs. -0.99, 1.77% vs. -1.25%, 1.40% vs. -1.21%, 0.88% us. -1.03%, respectively). The proportion of subjects who had an increase in BMD of the spine and total hip more than two percentages was significantly larger in the treatment group than in the control group (30.6% us. 15.2% and 30.6% vs. 9.1%, respectively). The increased increment in BMD of the treatment group was significantly greater than those in the control group after adjustment for age and body mass index (P < 0.05). These results suggest that HMG-CoA reductase inhibitors may increase BMD of the femur in male patients with type 2 diabetes mellitus.
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页码:1137 / 1142
页数:6
相关论文
共 23 条
  • [1] AARON JE, 1987, CLIN ORTHOP RELAT R, P260
  • [2] Bauer DC, 1999, J BONE MINER RES, V14, pS179
  • [3] BRAGA V, 1998, BONE S, V23, pS405
  • [4] EFFECT OF HORMONES AND GROWTH-FACTORS ON ALKALINE-PHOSPHATASE ACTIVITY AND COLLAGEN-SYNTHESIS IN CULTURED RAT CALVARIAE
    CANALIS, E
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 1983, 32 (01): : 14 - 20
  • [5] ERICSSON J, 1993, J BIOL CHEM, V268, P832
  • [6] Alendronate mechanism of action:: geranylgeraniol, an intermediate in the mevalonate pathway, prevents inhibition of osteoclast formation, bone resorption, and kinase activation in vitro
    Fisher, JE
    Rogers, MJ
    Halasy, JM
    Luckman, SP
    Hughes, DE
    Masarachia, PJ
    Wesolowski, G
    Russell, RGG
    Rodan, GA
    Reszka, AA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (01) : 133 - 138
  • [7] FISHER JE, 1998, BONE S, V23, pS399
  • [8] EFFECTS OF DIETARY CARBOHYDRATES ON METABOLISM OF CALCIUM AND OTHER MINERALS IN NORMAL SUBJECTS AND PATIENTS WITH NONINSULIN-DEPENDENT DIABETES-MELLITUS
    GARG, A
    BONANOME, A
    GRUNDY, SM
    UNGER, RH
    BRESLAU, NA
    PAK, CYC
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1990, 70 (04) : 1007 - 1013
  • [9] HUGHES DE, 1995, J BONE MINER RES, V10, P1478
  • [10] DIABETIC OSTEOPENIA AND CIRCULATING LEVELS OF VITAMIN-D METABOLITES IN TYPE-2 (NONINSULIN-DEPENDENT) DIABETES
    ISHIDA, H
    SEINO, Y
    MATSUKURA, S
    IKEDA, M
    YAWATA, M
    YAMASHITA, G
    ISHIZUKA, S
    IMURA, H
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 1985, 34 (09): : 797 - 801