Bone mineral density and fracture risk in type-2 diabetes mellitus: the Rotterdam Study
The aim of this study was to determine the association between type-2 diabetes mellitus (DM), BMD and fractures in 6,655 men and women aged 55 years and over from the Rotterdam Study. We compared subjects with type-2 DM to subjects without DM. Additionally, subset analyses were performed, dividing s...
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Published in | Osteoporosis international Vol. 16; no. 12; pp. 1713 - 1720 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Springer
01.12.2005
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Abstract | The aim of this study was to determine the association between type-2 diabetes mellitus (DM), BMD and fractures in 6,655 men and women aged 55 years and over from the Rotterdam Study. We compared subjects with type-2 DM to subjects without DM. Additionally, subset analyses were performed, dividing subjects on the basis of the glucose tolerance test into already treated DM, newly diagnosed DM, impaired glucose tolerance (IGT) and normal glucose tolerance (NGT, reference). Femoral neck and lumbar spine BMD were measured using DEXA. Nonvertebral fracture ascertainment was performed using an automated record system involving GPs and local hospitals. Although subjects with DM had higher BMD, they had an increased nonvertebral fracture risk: hazard ratio (HR) 1.33 (1.00-1.77). In subset analysis, the increased fracture risk appeared restricted to treated DM subjects only: HR 1.69 (1.16-2.46). Subjects with IGT had a higher BMD, but contrary to treated DM, they had a lower fracture risk: HR 0.80 (0.63-1.00). In conclusion, subjects with type-2 DM and IGT both have a higher BMD. Whereas, subjects with IGT have a decreased fracture risk, subjects with DM (primarily those with already established and treated DM) had an increased fracture risk, probably due to long-term complications associated with DM. |
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AbstractList | The aim of this study was to determine the association between type-2 diabetes mellitus (DM), BMD and fractures in 6,655 men and women aged 55 years and over from the Rotterdam Study. We compared subjects with type-2 DM to subjects without DM. Additionally, subset analyses were performed, dividing subjects on the basis of the glucose tolerance test into already treated DM, newly diagnosed DM, impaired glucose tolerance (IGT) and normal glucose tolerance (NGT, reference). Femoral neck and lumbar spine BMD were measured using DEXA. Nonvertebral fracture ascertainment was performed using an automated record system involving GPs and local hospitals. Although subjects with DM had higher BMD, they had an increased nonvertebral fracture risk: hazard ratio (HR) 1.33 (1.00-1.77). In subset analysis, the increased fracture risk appeared restricted to treated DM subjects only: HR 1.69 (1.16-2.46). Subjects with IGT had a higher BMD, but contrary to treated DM, they had a lower fracture risk: HR 0.80 (0.63-1.00). In conclusion, subjects with type-2 DM and IGT both have a higher BMD. Whereas, subjects with IGT have a decreased fracture risk, subjects with DM (primarily those with already established and treated DM) had an increased fracture risk, probably due to long-term complications associated with DM.The aim of this study was to determine the association between type-2 diabetes mellitus (DM), BMD and fractures in 6,655 men and women aged 55 years and over from the Rotterdam Study. We compared subjects with type-2 DM to subjects without DM. Additionally, subset analyses were performed, dividing subjects on the basis of the glucose tolerance test into already treated DM, newly diagnosed DM, impaired glucose tolerance (IGT) and normal glucose tolerance (NGT, reference). Femoral neck and lumbar spine BMD were measured using DEXA. Nonvertebral fracture ascertainment was performed using an automated record system involving GPs and local hospitals. Although subjects with DM had higher BMD, they had an increased nonvertebral fracture risk: hazard ratio (HR) 1.33 (1.00-1.77). In subset analysis, the increased fracture risk appeared restricted to treated DM subjects only: HR 1.69 (1.16-2.46). Subjects with IGT had a higher BMD, but contrary to treated DM, they had a lower fracture risk: HR 0.80 (0.63-1.00). In conclusion, subjects with type-2 DM and IGT both have a higher BMD. Whereas, subjects with IGT have a decreased fracture risk, subjects with DM (primarily those with already established and treated DM) had an increased fracture risk, probably due to long-term complications associated with DM. The aim of this study was to determine the association between type-2 diabetes mellitus (DM), BMD and fractures in 6,655 men and women aged 55 years and over from the Rotterdam Study. We compared subjects with type-2 DM to subjects without DM. Additionally, subset analyses were performed, dividing subjects on the basis of the glucose tolerance test into already treated DM, newly diagnosed DM, impaired glucose tolerance (IGT) and normal glucose tolerance (NGT, reference). Femoral neck and lumbar spine BMD were measured using DEXA. Nonvertebral fracture ascertainment was performed using an automated record system involving GPs and local hospitals. Although subjects with DM had higher BMD, they had an increased nonvertebral fracture risk: hazard ratio (HR) 1.33 (1.00-1.77). In subset analysis, the increased fracture risk appeared restricted to treated DM subjects only: HR 1.69 (1.16-2.46). Subjects with IGT had a higher BMD, but contrary to treated DM, they had a lower fracture risk: HR 0.80 (0.63-1.00). In conclusion, subjects with type-2 DM and IGT both have a higher BMD. Whereas, subjects with IGT have a decreased fracture risk, subjects with DM (primarily those with already established and treated DM) had an increased fracture risk, probably due to long-term complications associated with DM. |
Author | de Liefde, I. I. de Laet, C. E. D. H. van Daele, P. L. A. Pols, H. A. P. van der Klift, M. Hofman, A. |
Author_xml | – sequence: 1 givenname: I. I. surname: de Liefde fullname: de Liefde, I. I. – sequence: 2 givenname: M. surname: van der Klift fullname: van der Klift, M. – sequence: 3 givenname: C. E. D. H. surname: de Laet fullname: de Laet, C. E. D. H. – sequence: 4 givenname: P. L. A. surname: van Daele fullname: van Daele, P. L. A. – sequence: 5 givenname: A. surname: Hofman fullname: Hofman, A. – sequence: 6 givenname: H. A. P. surname: Pols fullname: Pols, H. A. P. |
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Snippet | The aim of this study was to determine the association between type-2 diabetes mellitus (DM), BMD and fractures in 6,655 men and women aged 55 years and over... |
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SubjectTerms | Absorptiometry, Photon - methods Aged Biological and medical sciences Bone density Bone Density - physiology Cohort analysis Diabetes Diabetes Mellitus, Type 2 - complications Diabetes Mellitus, Type 2 - drug therapy Diabetes Mellitus, Type 2 - physiopathology Diseases of the osteoarticular system Female Femur Neck Fractures Fractures, Bone - etiology Fractures, Bone - physiopathology Glucose Glucose Tolerance Test Hip Fractures - etiology Hip Fractures - physiopathology Humans Hypoglycemic Agents - therapeutic use Injuries of the limb. Injuries of the spine Insulin resistance Insulin Resistance - physiology Investigative techniques, diagnostic techniques (general aspects) Lumbar Vertebrae Male Medical sciences Metabolism Middle Aged Osteoarticular system. Muscles Osteoporosis Osteoporosis. Osteomalacia. Paget disease Population Surveillance - methods Prospective Studies Questionnaires Radiodiagnosis. Nmr imagery. Nmr spectrometry Risk Factors Traumas. Diseases due to physical agents Visual acuity Women Wrist Injuries - etiology Wrist Injuries - physiopathology |
Title | Bone mineral density and fracture risk in type-2 diabetes mellitus: the Rotterdam Study |
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