TY - JOUR
T1 - Vertebral Fracture Risk in Diabetic Elderly Men
T2 - The MrOS Study
AU - for the Osteoporotic Fractures in Men (MrOS) Study Research Group
AU - Napoli, Nicola
AU - Schwartz, Ann V.
AU - Schafer, Anne L.
AU - Vittinghoff, Eric
AU - Cawthon, Peggy M.
AU - Parimi, Neeta
AU - Orwoll, Eric
AU - Strotmeyer, Elsa S.
AU - Hoffman, Andrew R.
AU - Barrett-Connor, Elizabeth
AU - Black, Dennis M.
N1 - Funding Information:
The Osteoporotic Fractures in Men (MrOS) Study is supported by National Institutes of Health funding. The following institutes provide support: the National Institute on Aging (NIA), the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), the National Center for Advancing Translational Sciences (NCATS), and NIH Roadmap for Medical Research under the following grant numbers: U01 AR45580, U01 AR45614, U01 AR45632, U01AR45647, U01 AR45654, U01 AR45583, U01 AG18197, U01, AG027810, and UL1 TR000128. The American Diabetes Association provided funding for ESS's grant “Longitudinal Changes in BMD with Diabetes Mellitus” (1-04-JF-46, ESS). ALS received support from a VA Clinical Science Research and Development Career Development Award, Project number 5IK2CX000549-05. Authors’ roles: NN: concept and design, data interpretation-Writing the MS-Final approval of the MS. AVS, DMB: Substantial contributions to conception and design, interpretation of data- Revising the article critically for important intellectual content-Final approval of the MS. ALS, PG, EO, ESS, ARH, EBC: acquisition/interpretation of data-Critical review for important intellectual content- Final approval of the MS. NP and EV: data acquisition and analysis-Revising the article-Final approval of the MS.
Funding Information:
The Osteoporotic Fractures in Men (MrOS) Study is supported by National Institutes of Health funding. The following institutes provide support: the National Institute on Aging (NIA), the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), the National Center for Advancing Translational Sciences (NCATS), and NIH Roadmap for Medical Research under the following grant numbers: U01 AR45580, U01 AR45614, U01 AR45632, U01AR45647, U01 AR45654, U01 AR45583, U01 AG18197, U01, AG027810, and UL1 TR000128. The American Diabetes Association provided funding for ESS’s grant “Longitudinal Changes in BMD with Diabetes Mellitus” (1-04-JF-46, ESS). ALS received support from a VA Clinical Science Research and Development Career Development Award, Project number 5IK2CX000549-05.
Publisher Copyright:
© 2017 American Society for Bone and Mineral Research
PY - 2018/1
Y1 - 2018/1
N2 - Type 2 diabetes (T2DM) is associated with a significant increase in risk of nonvertebral fractures, but information on risk of vertebral fractures (VFs) in subjects with T2DM, particularly among men, is lacking. Furthermore, it is not known whether spine bone mineral density (BMD) can predict the risk of VF in T2DM. We sought to examine the effect of diabetes status on prevalent and incident vertebral fracture, and to estimate the effect of lumbar spine BMD (areal and volumetric) as a risk factor for prevalent and incident morphometric vertebral fracture in T2DM (n = 875) and nondiabetic men (n = 4679). We used data from the Osteoporotic Fractures in Men (MrOS) Study, which enrolled men aged ≥65 years. Lumbar spine areal BMD (aBMD) was measured with dual-energy X-ray absorptiometry (DXA), and volumetric BMD (vBMD) by quantitative computed tomography (QCT). Prevalence (7.0% versus 7.7%) and incidence (4.4% versus 4.5%) of VFs were not higher in T2DM versus nondiabetic men. The risk of prevalent (OR, 1.05; 95% CI, 0.78 to 1.40) or incident vertebral-fracture (OR, 1.28; 95% CI, 0.81 to 2.00) was not higher in T2DM versus nondiabetic men in models adjusted for age, clinic site, race, BMI, and aBMD. Higher spine aBMD was associated with lower risk of prevalent VF in T2DM (OR, 0.55; 95% CI, 0.48 to 0.63) and nondiabetic men (OR, 0.66; 95% CI, 0.5 to 0.88) (p for interaction = 0.24) and of incident VF in T2DM (OR, 0.50; 95% CI, 0.41 to 0.60) and nondiabetic men (OR, 0.54; 95% CI, 0.33 to 0.88) (p for interaction = 0.77). Results were similar for vBMD. In conclusion, T2DM was not associated with higher prevalent or incident VF in older men, even after adjustment for BMI and BMD. Higher spine aBMD and vBMD are associated with lower prevalence and incidence of VF in T2DM as well as nondiabetic men.
AB - Type 2 diabetes (T2DM) is associated with a significant increase in risk of nonvertebral fractures, but information on risk of vertebral fractures (VFs) in subjects with T2DM, particularly among men, is lacking. Furthermore, it is not known whether spine bone mineral density (BMD) can predict the risk of VF in T2DM. We sought to examine the effect of diabetes status on prevalent and incident vertebral fracture, and to estimate the effect of lumbar spine BMD (areal and volumetric) as a risk factor for prevalent and incident morphometric vertebral fracture in T2DM (n = 875) and nondiabetic men (n = 4679). We used data from the Osteoporotic Fractures in Men (MrOS) Study, which enrolled men aged ≥65 years. Lumbar spine areal BMD (aBMD) was measured with dual-energy X-ray absorptiometry (DXA), and volumetric BMD (vBMD) by quantitative computed tomography (QCT). Prevalence (7.0% versus 7.7%) and incidence (4.4% versus 4.5%) of VFs were not higher in T2DM versus nondiabetic men. The risk of prevalent (OR, 1.05; 95% CI, 0.78 to 1.40) or incident vertebral-fracture (OR, 1.28; 95% CI, 0.81 to 2.00) was not higher in T2DM versus nondiabetic men in models adjusted for age, clinic site, race, BMI, and aBMD. Higher spine aBMD was associated with lower risk of prevalent VF in T2DM (OR, 0.55; 95% CI, 0.48 to 0.63) and nondiabetic men (OR, 0.66; 95% CI, 0.5 to 0.88) (p for interaction = 0.24) and of incident VF in T2DM (OR, 0.50; 95% CI, 0.41 to 0.60) and nondiabetic men (OR, 0.54; 95% CI, 0.33 to 0.88) (p for interaction = 0.77). Results were similar for vBMD. In conclusion, T2DM was not associated with higher prevalent or incident VF in older men, even after adjustment for BMI and BMD. Higher spine aBMD and vBMD are associated with lower prevalence and incidence of VF in T2DM as well as nondiabetic men.
KW - BONE QCT
KW - DIABETES
KW - FRACTURE RISK ASSESSMENT
KW - VERTEBRAL FRACTURES
KW - VOLUMETRIC BMD
UR - http://www.scopus.com/inward/record.url?scp=85039152154&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85039152154&partnerID=8YFLogxK
U2 - 10.1002/jbmr.3287
DO - 10.1002/jbmr.3287
M3 - Article
C2 - 28861910
AN - SCOPUS:85039152154
SN - 0884-0431
VL - 33
SP - 63
EP - 69
JO - Journal of Bone and Mineral Research
JF - Journal of Bone and Mineral Research
IS - 1
ER -