Glycaemic control is positively associated with prevalent fractures but not with bone mineral density in patients with Type 1 diabetes
Diabet. Med. 28, 872–875 (2011) Aim There are conflicting data regarding the risk of osteoporosis in patients with Type 1 diabetes. We investigated an association between diabetes, bone mineral density and prevalent fractures. Methods A single‐centre, cross‐sectional study of men and pre‐menopausa...
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Published in | Diabetic medicine Vol. 28; no. 7; pp. 872 - 875 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.07.2011
Blackwell |
Subjects | |
Online Access | Get full text |
ISSN | 0742-3071 1464-5491 1464-5491 |
DOI | 10.1111/j.1464-5491.2011.03286.x |
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Abstract | Diabet. Med. 28, 872–875 (2011)
Aim There are conflicting data regarding the risk of osteoporosis in patients with Type 1 diabetes. We investigated an association between diabetes, bone mineral density and prevalent fractures.
Methods A single‐centre, cross‐sectional study of men and pre‐menopausal women with Type 1 diabetes (n = 128) and a matched control group (n = 77) was conducted. The primary outcome measure was bone mineral density and secondary measures were markers of bone metabolism and prevalent fractures.
Results Hip and total body bone mineral densities were significantly lower in women with diabetes compared with control subjects. In men, no difference in bone mineral density was found. A multivariate regression analysis in women with diabetes revealed higher BMI as the strongest predictor of higher total hip, femoral neck and total body bone mineral density, whereas previous fractures were inversely associated with total hip bone mineral density and C‐terminal telopeptide of type I collagen with total body bone mineral density. Poor long‐term glycaemic control was not associated with low bone mineral density. Fracture frequency was higher in patients with diabetes compared with control subjects (1.64 vs. 0.62 per 100 patient‐years; P < 0.05). In a multivariable model, long‐term HbA1c control was associated with increased clinical fracture prevalence (OR 1.92; 95% CI 1.09–2.75) in those with diabetes.
Conclusions Type 1 diabetes contributes to low bone mineral density in women. Previous fractures and low BMI were strong predictors of impaired bone mineral density and should therefore be considered in risk estimation. Fractures are more frequent in Type 1 diabetes. Long‐term hyperglycaemia may account for impaired bone strength, independently from bone mineral density. |
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AbstractList | Diabet. Med. 28, 872–875 (2011)
Aim There are conflicting data regarding the risk of osteoporosis in patients with Type 1 diabetes. We investigated an association between diabetes, bone mineral density and prevalent fractures.
Methods A single‐centre, cross‐sectional study of men and pre‐menopausal women with Type 1 diabetes (n = 128) and a matched control group (n = 77) was conducted. The primary outcome measure was bone mineral density and secondary measures were markers of bone metabolism and prevalent fractures.
Results Hip and total body bone mineral densities were significantly lower in women with diabetes compared with control subjects. In men, no difference in bone mineral density was found. A multivariate regression analysis in women with diabetes revealed higher BMI as the strongest predictor of higher total hip, femoral neck and total body bone mineral density, whereas previous fractures were inversely associated with total hip bone mineral density and C‐terminal telopeptide of type I collagen with total body bone mineral density. Poor long‐term glycaemic control was not associated with low bone mineral density. Fracture frequency was higher in patients with diabetes compared with control subjects (1.64 vs. 0.62 per 100 patient‐years; P < 0.05). In a multivariable model, long‐term HbA1c control was associated with increased clinical fracture prevalence (OR 1.92; 95% CI 1.09–2.75) in those with diabetes.
Conclusions Type 1 diabetes contributes to low bone mineral density in women. Previous fractures and low BMI were strong predictors of impaired bone mineral density and should therefore be considered in risk estimation. Fractures are more frequent in Type 1 diabetes. Long‐term hyperglycaemia may account for impaired bone strength, independently from bone mineral density. There are conflicting data regarding the risk of osteoporosis in patients with Type 1 diabetes. We investigated an association between diabetes, bone mineral density and prevalent fractures.AIMThere are conflicting data regarding the risk of osteoporosis in patients with Type 1 diabetes. We investigated an association between diabetes, bone mineral density and prevalent fractures.A single-centre, cross-sectional study of men and pre-menopausal women with Type 1 diabetes (n = 128) and a matched control group (n = 77) was conducted. The primary outcome measure was bone mineral density and secondary measures were markers of bone metabolism and prevalent fractures.METHODSA single-centre, cross-sectional study of men and pre-menopausal women with Type 1 diabetes (n = 128) and a matched control group (n = 77) was conducted. The primary outcome measure was bone mineral density and secondary measures were markers of bone metabolism and prevalent fractures.Hip and total body bone mineral densities were significantly lower in women with diabetes compared with control subjects. In men, no difference in bone mineral density was found. A multivariate regression analysis in women with diabetes revealed higher BMI as the strongest predictor of higher total hip, femoral neck and total body bone mineral density, whereas previous fractures were inversely associated with total hip bone mineral density and C-terminal telopeptide of type I collagen with total body bone mineral density. Poor long-term glycaemic control was not associated with low bone mineral density. Fracture frequency was higher in patients with diabetes compared with control subjects (1.64 vs. 0.62 per 100 patient-years; P < 0.05). In a multivariable model, long-term HbA(1c) control was associated with increased clinical fracture prevalence (OR 1.92; 95% CI 1.09-2.75) in those with diabetes.RESULTSHip and total body bone mineral densities were significantly lower in women with diabetes compared with control subjects. In men, no difference in bone mineral density was found. A multivariate regression analysis in women with diabetes revealed higher BMI as the strongest predictor of higher total hip, femoral neck and total body bone mineral density, whereas previous fractures were inversely associated with total hip bone mineral density and C-terminal telopeptide of type I collagen with total body bone mineral density. Poor long-term glycaemic control was not associated with low bone mineral density. Fracture frequency was higher in patients with diabetes compared with control subjects (1.64 vs. 0.62 per 100 patient-years; P < 0.05). In a multivariable model, long-term HbA(1c) control was associated with increased clinical fracture prevalence (OR 1.92; 95% CI 1.09-2.75) in those with diabetes.Type 1 diabetes contributes to low bone mineral density in women. Previous fractures and low BMI were strong predictors of impaired bone mineral density and should therefore be considered in risk estimation. Fractures are more frequent in Type 1 diabetes. Long-term hyperglycaemia may account for impaired bone strength, independently from bone mineral density.CONCLUSIONSType 1 diabetes contributes to low bone mineral density in women. Previous fractures and low BMI were strong predictors of impaired bone mineral density and should therefore be considered in risk estimation. Fractures are more frequent in Type 1 diabetes. Long-term hyperglycaemia may account for impaired bone strength, independently from bone mineral density. There are conflicting data regarding the risk of osteoporosis in patients with Type 1 diabetes. We investigated an association between diabetes, bone mineral density and prevalent fractures. A single-centre, cross-sectional study of men and pre-menopausal women with Type 1 diabetes (n = 128) and a matched control group (n = 77) was conducted. The primary outcome measure was bone mineral density and secondary measures were markers of bone metabolism and prevalent fractures. Hip and total body bone mineral densities were significantly lower in women with diabetes compared with control subjects. In men, no difference in bone mineral density was found. A multivariate regression analysis in women with diabetes revealed higher BMI as the strongest predictor of higher total hip, femoral neck and total body bone mineral density, whereas previous fractures were inversely associated with total hip bone mineral density and C-terminal telopeptide of type I collagen with total body bone mineral density. Poor long-term glycaemic control was not associated with low bone mineral density. Fracture frequency was higher in patients with diabetes compared with control subjects (1.64 vs. 0.62 per 100 patient-years; P < 0.05). In a multivariable model, long-term HbA(1c) control was associated with increased clinical fracture prevalence (OR 1.92; 95% CI 1.09-2.75) in those with diabetes. Type 1 diabetes contributes to low bone mineral density in women. Previous fractures and low BMI were strong predictors of impaired bone mineral density and should therefore be considered in risk estimation. Fractures are more frequent in Type 1 diabetes. Long-term hyperglycaemia may account for impaired bone strength, independently from bone mineral density. |
Author | Sämann, A. Kästner, B. Lehmann, T. Müller, U. A. Neumann, T. Hein, G. Hemmelmann, C. Kiehntopf, M. Franke, S. Wolf, G. Lodes, S. |
Author_xml | – sequence: 1 givenname: T. surname: Neumann fullname: Neumann, T. – sequence: 2 givenname: A. surname: Sämann fullname: Sämann, A. – sequence: 3 givenname: S. surname: Lodes fullname: Lodes, S. organization: Department of Medicine III – sequence: 4 givenname: B. surname: Kästner fullname: Kästner, B. organization: Department of Medicine III – sequence: 5 givenname: S. surname: Franke fullname: Franke, S. organization: Department of Medicine III – sequence: 6 givenname: M. surname: Kiehntopf fullname: Kiehntopf, M. organization: Institute of Clinical Chemistry and Laboratory Diagnostics – sequence: 7 givenname: C. surname: Hemmelmann fullname: Hemmelmann, C. organization: Institute of Medical Statistics, Computer Sciences and Documentation, University-Hospital Jena, Jena, Germany – sequence: 8 givenname: T. surname: Lehmann fullname: Lehmann, T. organization: Institute of Medical Statistics, Computer Sciences and Documentation, University-Hospital Jena, Jena, Germany – sequence: 9 givenname: U. A. surname: Müller fullname: Müller, U. A. organization: Department of Medicine III – sequence: 10 givenname: G. surname: Hein fullname: Hein, G. organization: Department of Medicine III – sequence: 11 givenname: G. surname: Wolf fullname: Wolf, G. organization: Department of Medicine III |
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Keywords | Endocrinopathy Human Immunopathology Obesity Prevalence Nutrition HbA Diseases of the osteoarticular system Nutrition disorder Patient Autoimmune disease Metabolic diseases Fracture Hemoglobin A1 Trauma Association Surveillance Type 1 diabetes Hemoglobin A1c Bone mineral density Endocrinology Nutritional status Glycemia |
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References_xml | – reference: Kanis JA, Brazier JE, Stevenson M, Calvert NW, Lloyd Jones M. Treatment of established osteoporosis: a systematic review and cost-utility analysis. Health Technol Assess 2002; 6: 1-146. – reference: Marshall D, Johnell O, Wedel H. Meta-analysis of how well measures of bone mineral density predict occurrence of osteoporotic fractures. Br Med J 1996; 312: 1254-1259. – reference: Ingberg CM, Palmer M, Aman J, Arvidsson B, Schvarcz E, Berne C. Body composition and bone mineral density in long-standing type 1 diabetes. J Intern Med 2004; 255: 392-398. – reference: Silverman SL. Quality-of-life issues in osteoporosis. Curr Rheumatol Rep 2005; 7: 39-45. – reference: Valerio G, del Puente A, Esposito-del Puente A, Buono P, Mozzillo E, Franzese A. The lumbar bone mineral density is affected by long-term poor metabolic control in adolescents with type 1 diabetes mellitus. 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Snippet | Diabet. Med. 28, 872–875 (2011)
Aim There are conflicting data regarding the risk of osteoporosis in patients with Type 1 diabetes. We investigated an... There are conflicting data regarding the risk of osteoporosis in patients with Type 1 diabetes. We investigated an association between diabetes, bone mineral... |
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SubjectTerms | Biological and medical sciences Biomarkers - metabolism Bone Density - drug effects Bone Density - physiology bone mineral density Case-Control Studies Cross-Sectional Studies Diabetes Mellitus, Type 1 - complications Diabetes Mellitus, Type 1 - drug therapy Diabetes Mellitus, Type 1 - physiopathology Diabetes. Impaired glucose tolerance Endocrine pancreas. Apud cells (diseases) Endocrinopathies Etiopathogenesis. Screening. Investigations. Target tissue resistance Feeding. Feeding behavior Female fracture Fractures, Bone - diagnostic imaging Fractures, Bone - metabolism Fractures, Bone - physiopathology Fundamental and applied biological sciences. Psychology Glycated Hemoglobin A - metabolism HbA1c Humans Lumbar Vertebrae - diagnostic imaging Lumbar Vertebrae - metabolism Lumbar Vertebrae - physiopathology Male Medical sciences Middle Aged Osteoporosis - chemically induced Osteoporosis - metabolism Osteoporosis - physiopathology Prevalence Radiography Risk Factors Type 1 diabetes Vertebrates: anatomy and physiology, studies on body, several organs or systems Vertebrates: endocrinology |
Title | Glycaemic control is positively associated with prevalent fractures but not with bone mineral density in patients with Type 1 diabetes |
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