Determinants of Bone Material Strength and Cortical Porosity in Patients with Type 2 Diabetes Mellitus
Abstract Context Reduced bone material strength index (BMSi) and increased cortical porosity (CtPo) have emerged as potentially contributing to fracture risk in type 2 diabetes mellitus (T2DM) patients. Objective To determine whether BMSi or CtPo are related to other diabetic complications. Design C...
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Published in | The journal of clinical endocrinology and metabolism Vol. 105; no. 10; pp. e3718 - e3729 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
US
Oxford University Press
01.10.2020
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Subjects | |
Online Access | Get full text |
ISSN | 0021-972X 1945-7197 1945-7197 |
DOI | 10.1210/clinem/dgaa388 |
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Abstract | Abstract
Context
Reduced bone material strength index (BMSi) and increased cortical porosity (CtPo) have emerged as potentially contributing to fracture risk in type 2 diabetes mellitus (T2DM) patients.
Objective
To determine whether BMSi or CtPo are related to other diabetic complications.
Design
Cross-sectional observational study.
Setting
Subjects recruited from a random sample of southeast Minnesota residents.
Participants
A total of 171 T2DM patients (mean age, 68.8 years) and 108 age-matched nondiabetic controls (mean age, 67.3 years).
Main Measures
Bone material strength index was measured using microindentation, skin advanced glycation end-products (AGEs) measured using autofluorescence, high-resolution peripheral quantitative computed tomography at the distal radius and tibia, assessment of diabetic microvascular complications including urine microalbuminuria, retinopathy, neuropathy, and vascular disease (ankle brachial index and transcutaneous oxygen tension [TcPO2]). All analyses were adjusted for age, sex, and body mass index.
Results
Skin AGEs were negatively correlated with the BMSi in both T2DM (r = -0.30, P < 0.001) and control (r = -0.23, P = 0.020) subjects. In relating diabetic complications to CtPo, we found that T2DM patients with clinically significant peripheral vascular disease (TcPO2 ≤ 40 mm Hg) had higher (+21.0%, P = 0.031) CtPo at the distal tibia as compared to controls; in these subjects, CtPo was negatively correlated with TcPO2 at both the distal tibia (r = -0.39, P = 0.041) and radius (r = -0.41, P = 0.029).
Conclusions
Our findings demonstrate that bone material properties are related to AGE accumulation regardless of diabetes status, while CtPo in T2DM patients is linked to TcPO2, a measure of microvascular blood flow. |
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AbstractList | Context Reduced bone material strength index (BMSi) and increased cortical porosity (CtPo) have emerged as potentially contributing to fracture risk in type 2 diabetes mellitus (T2DM) patients. Objective To determine whether BMSi or CtPo are related to other diabetic complications. Design Cross-sectional observational study. Setting Subjects recruited from a random sample of southeast Minnesota residents. Participants A total of 171 T2DM patients (mean age, 68.8 years) and 108 age-matched nondiabetic controls (mean age, 67.3 years). Main Measures Bone material strength index was measured using microindentation, skin advanced glycation end-products (AGEs) measured using autofluorescence, high-resolution peripheral quantitative computed tomography at the distal radius and tibia, assessment of diabetic microvascular complications including urine microalbuminuria, retinopathy, neuropathy, and vascular disease (ankle brachial index and transcutaneous oxygen tension [TcPO2]). All analyses were adjusted for age, sex, and body mass index. Results Skin AGEs were negatively correlated with the BMSi in both T2DM (r = -0.30, P < 0.001) and control (r = -0.23, P = 0.020) subjects. In relating diabetic complications to CtPo, we found that T2DM patients with clinically significant peripheral vascular disease (TcPO2 ≤ 40 mm Hg) had higher (+21.0%, P = 0.031) CtPo at the distal tibia as compared to controls; in these subjects, CtPo was negatively correlated with TcPO2 at both the distal tibia (r = -0.39, P = 0.041) and radius (r = -0.41, P = 0.029). Conclusions Our findings demonstrate that bone material properties are related to AGE accumulation regardless of diabetes status, while CtPo in T2DM patients is linked to TcPO2, a measure of microvascular blood flow. Abstract Context Reduced bone material strength index (BMSi) and increased cortical porosity (CtPo) have emerged as potentially contributing to fracture risk in type 2 diabetes mellitus (T2DM) patients. Objective To determine whether BMSi or CtPo are related to other diabetic complications. Design Cross-sectional observational study. Setting Subjects recruited from a random sample of southeast Minnesota residents. Participants A total of 171 T2DM patients (mean age, 68.8 years) and 108 age-matched nondiabetic controls (mean age, 67.3 years). Main Measures Bone material strength index was measured using microindentation, skin advanced glycation end-products (AGEs) measured using autofluorescence, high-resolution peripheral quantitative computed tomography at the distal radius and tibia, assessment of diabetic microvascular complications including urine microalbuminuria, retinopathy, neuropathy, and vascular disease (ankle brachial index and transcutaneous oxygen tension [TcPO2]). All analyses were adjusted for age, sex, and body mass index. Results Skin AGEs were negatively correlated with the BMSi in both T2DM (r = -0.30, P < 0.001) and control (r = -0.23, P = 0.020) subjects. In relating diabetic complications to CtPo, we found that T2DM patients with clinically significant peripheral vascular disease (TcPO2 ≤ 40 mm Hg) had higher (+21.0%, P = 0.031) CtPo at the distal tibia as compared to controls; in these subjects, CtPo was negatively correlated with TcPO2 at both the distal tibia (r = -0.39, P = 0.041) and radius (r = -0.41, P = 0.029). Conclusions Our findings demonstrate that bone material properties are related to AGE accumulation regardless of diabetes status, while CtPo in T2DM patients is linked to TcPO2, a measure of microvascular blood flow. Main Measures: Bone material strength index was measured using microindentation, skin advanced glycation end-products (AGEs) measured using autofluorescence, high-resolution peripheral quantitative computed tomography at the distal radius and tibia, assessment of diabetic microvascular complications including urine microalbuminuria, retinopathy, neuropathy, and vascular disease (ankle brachial index and transcutaneous oxygen tension [TcP[O.sub.2]]). All analyses were adjusted for age, sex, and body mass index. Context: Reduced bone material strength index (BMSi) and increased cortical porosity (CtPo) have emerged as potentially contributing to fracture risk in type 2 diabetes mellitus (T2DM) patients. Objective: To determine whether BMSi or CtPo are related to other diabetic complications. Design: Cross-sectional observational study. Setting: Subjects recruited from a random sample of southeast Minnesota residents. Participants: A total of 171 T2DM patients (mean age, 68.8 years) and 108 age-matched nondiabetic controls (mean age, 67.3 years). Main Measures: Bone material strength index was measured using microindentation, skin advanced glycation end-products (AGEs) measured using autofluorescence, high-resolution peripheral quantitative computed tomography at the distal radius and tibia, assessment of diabetic microvascular complications including urine microalbuminuria, retinopathy, neuropathy, and vascular disease (ankle brachial index and transcutaneous oxygen tension [TcP[O.sub.2]]). All analyses were adjusted for age, sex, and body mass index. Results: Skin AGEs were negatively correlated with the BMSi in both T2DM (r = -0.30, P < 0.001) and control (r = -0.23, P = 0.020) subjects. In relating diabetic complications to CtPo, we found that T2DM patients with clinically significant peripheral vascular disease (TcP[O.sub.2] [less than or equal to] 40 mm Hg) had higher (+21.0%, P = 0.031) CtPo at the distal tibia as compared to controls; in these subjects, CtPo was negatively correlated with TcP[O.sub.2] at both the distal tibia (r = -0.39, P = 0.041) and radius (r = -0.41, P = 0.029). Conclusions: Our findings demonstrate that bone material properties are related to AGE accumulation regardless of diabetes status, while CtPo in T2DM patients is linked to TcP[O.sub.2], a measure of microvascular blood flow. (J Clin Endocrinol Metab 105: 1-12, 2020) Key Words: bone, osteoporosis, diabetes, vascular disease, AGEs Reduced bone material strength index (BMSi) and increased cortical porosity (CtPo) have emerged as potentially contributing to fracture risk in type 2 diabetes mellitus (T2DM) patients. To determine whether BMSi or CtPo are related to other diabetic complications. Cross-sectional observational study. Subjects recruited from a random sample of southeast Minnesota residents. A total of 171 T2DM patients (mean age, 68.8 years) and 108 age-matched nondiabetic controls (mean age, 67.3 years). Bone material strength index was measured using microindentation, skin advanced glycation end-products (AGEs) measured using autofluorescence, high-resolution peripheral quantitative computed tomography at the distal radius and tibia, assessment of diabetic microvascular complications including urine microalbuminuria, retinopathy, neuropathy, and vascular disease (ankle brachial index and transcutaneous oxygen tension [TcPO2]). All analyses were adjusted for age, sex, and body mass index. Skin AGEs were negatively correlated with the BMSi in both T2DM (r = -0.30, P < 0.001) and control (r = -0.23, P = 0.020) subjects. In relating diabetic complications to CtPo, we found that T2DM patients with clinically significant peripheral vascular disease (TcPO2 ≤ 40 mm Hg) had higher (+21.0%, P = 0.031) CtPo at the distal tibia as compared to controls; in these subjects, CtPo was negatively correlated with TcPO2 at both the distal tibia (r = -0.39, P = 0.041) and radius (r = -0.41, P = 0.029). Our findings demonstrate that bone material properties are related to AGE accumulation regardless of diabetes status, while CtPo in T2DM patients is linked to TcPO2, a measure of microvascular blood flow. Reduced bone material strength index (BMSi) and increased cortical porosity (CtPo) have emerged as potentially contributing to fracture risk in type 2 diabetes mellitus (T2DM) patients.CONTEXTReduced bone material strength index (BMSi) and increased cortical porosity (CtPo) have emerged as potentially contributing to fracture risk in type 2 diabetes mellitus (T2DM) patients.To determine whether BMSi or CtPo are related to other diabetic complications.OBJECTIVETo determine whether BMSi or CtPo are related to other diabetic complications.Cross-sectional observational study.DESIGNCross-sectional observational study.Subjects recruited from a random sample of southeast Minnesota residents.SETTINGSubjects recruited from a random sample of southeast Minnesota residents.A total of 171 T2DM patients (mean age, 68.8 years) and 108 age-matched nondiabetic controls (mean age, 67.3 years).PARTICIPANTSA total of 171 T2DM patients (mean age, 68.8 years) and 108 age-matched nondiabetic controls (mean age, 67.3 years).Bone material strength index was measured using microindentation, skin advanced glycation end-products (AGEs) measured using autofluorescence, high-resolution peripheral quantitative computed tomography at the distal radius and tibia, assessment of diabetic microvascular complications including urine microalbuminuria, retinopathy, neuropathy, and vascular disease (ankle brachial index and transcutaneous oxygen tension [TcPO2]). All analyses were adjusted for age, sex, and body mass index.MAIN MEASURESBone material strength index was measured using microindentation, skin advanced glycation end-products (AGEs) measured using autofluorescence, high-resolution peripheral quantitative computed tomography at the distal radius and tibia, assessment of diabetic microvascular complications including urine microalbuminuria, retinopathy, neuropathy, and vascular disease (ankle brachial index and transcutaneous oxygen tension [TcPO2]). All analyses were adjusted for age, sex, and body mass index.Skin AGEs were negatively correlated with the BMSi in both T2DM (r = -0.30, P < 0.001) and control (r = -0.23, P = 0.020) subjects. In relating diabetic complications to CtPo, we found that T2DM patients with clinically significant peripheral vascular disease (TcPO2 ≤ 40 mm Hg) had higher (+21.0%, P = 0.031) CtPo at the distal tibia as compared to controls; in these subjects, CtPo was negatively correlated with TcPO2 at both the distal tibia (r = -0.39, P = 0.041) and radius (r = -0.41, P = 0.029).RESULTSSkin AGEs were negatively correlated with the BMSi in both T2DM (r = -0.30, P < 0.001) and control (r = -0.23, P = 0.020) subjects. In relating diabetic complications to CtPo, we found that T2DM patients with clinically significant peripheral vascular disease (TcPO2 ≤ 40 mm Hg) had higher (+21.0%, P = 0.031) CtPo at the distal tibia as compared to controls; in these subjects, CtPo was negatively correlated with TcPO2 at both the distal tibia (r = -0.39, P = 0.041) and radius (r = -0.41, P = 0.029).Our findings demonstrate that bone material properties are related to AGE accumulation regardless of diabetes status, while CtPo in T2DM patients is linked to TcPO2, a measure of microvascular blood flow.CONCLUSIONSOur findings demonstrate that bone material properties are related to AGE accumulation regardless of diabetes status, while CtPo in T2DM patients is linked to TcPO2, a measure of microvascular blood flow. |
Audience | Academic |
Author | Farr, Joshua N Atkinson, Elizabeth J Dyck, Peter J Amin, Shreyasee Tweed, Amanda J Khosla, Sundeep Achenbach, Sara J Samakkarnthai, Parinya Vella, Adrian Sfeir, Jad G Drake, Matthew T Wennberg, Paul W Volkman, Tammie L |
AuthorAffiliation | 6 Division of Rheumatology, Mayo Clinic , Rochester, Minnesota 1 Robert and Arlene Kogod Center on Aging and Division of Endocrinology, Mayo Clinic College of Medicine and Science , Rochester, Minnesota 5 Department of Neurology, Mayo Clinic , Rochester, Minnesota 4 Department of Cardiovascular Diseases and Gonda Vascular Center, Mayo Clinic , Rochester, Minnesota 2 Division of Endocrinology, Phramongkutklao Hospital and College of Medicine , Bangkok, Thailand 3 Department of Health Sciences Research, Mayo Clinic , Rochester, Minnesota |
AuthorAffiliation_xml | – name: 2 Division of Endocrinology, Phramongkutklao Hospital and College of Medicine , Bangkok, Thailand – name: 6 Division of Rheumatology, Mayo Clinic , Rochester, Minnesota – name: 3 Department of Health Sciences Research, Mayo Clinic , Rochester, Minnesota – name: 4 Department of Cardiovascular Diseases and Gonda Vascular Center, Mayo Clinic , Rochester, Minnesota – name: 1 Robert and Arlene Kogod Center on Aging and Division of Endocrinology, Mayo Clinic College of Medicine and Science , Rochester, Minnesota – name: 5 Department of Neurology, Mayo Clinic , Rochester, Minnesota |
Author_xml | – sequence: 1 givenname: Parinya surname: Samakkarnthai fullname: Samakkarnthai, Parinya organization: Robert and Arlene Kogod Center on Aging and Division of Endocrinology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota – sequence: 2 givenname: Jad G surname: Sfeir fullname: Sfeir, Jad G organization: Robert and Arlene Kogod Center on Aging and Division of Endocrinology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota – sequence: 3 givenname: Elizabeth J surname: Atkinson fullname: Atkinson, Elizabeth J organization: Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota – sequence: 4 givenname: Sara J surname: Achenbach fullname: Achenbach, Sara J organization: Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota – sequence: 5 givenname: Paul W surname: Wennberg fullname: Wennberg, Paul W organization: Department of Cardiovascular Diseases and Gonda Vascular Center, Mayo Clinic, Rochester, Minnesota – sequence: 6 givenname: Peter J surname: Dyck fullname: Dyck, Peter J organization: Department of Neurology, Mayo Clinic, Rochester, Minnesota – sequence: 7 givenname: Amanda J surname: Tweed fullname: Tweed, Amanda J organization: Robert and Arlene Kogod Center on Aging and Division of Endocrinology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota – sequence: 8 givenname: Tammie L surname: Volkman fullname: Volkman, Tammie L organization: Robert and Arlene Kogod Center on Aging and Division of Endocrinology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota – sequence: 9 givenname: Shreyasee surname: Amin fullname: Amin, Shreyasee organization: Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota – sequence: 10 givenname: Joshua N surname: Farr fullname: Farr, Joshua N organization: Robert and Arlene Kogod Center on Aging and Division of Endocrinology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota – sequence: 11 givenname: Adrian surname: Vella fullname: Vella, Adrian organization: Robert and Arlene Kogod Center on Aging and Division of Endocrinology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota – sequence: 12 givenname: Matthew T surname: Drake fullname: Drake, Matthew T organization: Robert and Arlene Kogod Center on Aging and Division of Endocrinology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota – sequence: 13 givenname: Sundeep surname: Khosla fullname: Khosla, Sundeep email: khosla.sundeep@mayo.edu organization: Robert and Arlene Kogod Center on Aging and Division of Endocrinology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32556277$$D View this record in MEDLINE/PubMed |
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Keywords | bone AGEs vascular disease osteoporosis diabetes |
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Reduced bone material strength index (BMSi) and increased cortical porosity (CtPo) have emerged as potentially contributing to fracture risk... Reduced bone material strength index (BMSi) and increased cortical porosity (CtPo) have emerged as potentially contributing to fracture risk in type 2 diabetes... Context: Reduced bone material strength index (BMSi) and increased cortical porosity (CtPo) have emerged as potentially contributing to fracture risk in type 2... Main Measures: Bone material strength index was measured using microindentation, skin advanced glycation end-products (AGEs) measured using autofluorescence,... Context Reduced bone material strength index (BMSi) and increased cortical porosity (CtPo) have emerged as potentially contributing to fracture risk in type 2... |
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SubjectTerms | Advanced glycation end products Advanced glycosylation end products Age Aged Ankle Ankle Brachial Index Blood flow Body mass index Bone Density - physiology Bones Complications and side effects Computed tomography Cortical bone Cross-Sectional Studies Density Diabetes Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - complications Diabetes Mellitus, Type 2 - metabolism Diabetes Mellitus, Type 2 - physiopathology Diabetic Angiopathies - diagnosis Diabetic Angiopathies - epidemiology Diabetic Angiopathies - physiopathology Diabetic neuropathy Female Fractures Glycation End Products, Advanced - analysis Glycation End Products, Advanced - metabolism Glycosylation Health aspects Humans Male Microvasculature Middle Aged Online Only Osteoporosis Osteoporotic Fractures - epidemiology Osteoporotic Fractures - physiopathology Oxygen tension Porosity Radius Radius - diagnostic imaging Radius - physiopathology Retinopathy Risk Factors Skin - chemistry Skin - metabolism Tibia Tibia - diagnostic imaging Tibia - physiopathology Tomography, X-Ray Computed Type 2 diabetes Vascular diseases |
Title | Determinants of Bone Material Strength and Cortical Porosity in Patients with Type 2 Diabetes Mellitus |
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