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 inThe journal of clinical endocrinology and metabolism Vol. 105; no. 10; pp. e3718 - e3729
Main Authors Samakkarnthai, Parinya, Sfeir, Jad G, Atkinson, Elizabeth J, Achenbach, Sara J, Wennberg, Paul W, Dyck, Peter J, Tweed, Amanda J, Volkman, Tammie L, Amin, Shreyasee, Farr, Joshua N, Vella, Adrian, Drake, Matthew T, Khosla, Sundeep
Format Journal Article
LanguageEnglish
Published US Oxford University Press 01.10.2020
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Online AccessGet full text
ISSN0021-972X
1945-7197
1945-7197
DOI10.1210/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.
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
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  organization: Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/32556277$$D View this record in MEDLINE/PubMed
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Issue 10
Keywords bone
AGEs
vascular disease
osteoporosis
diabetes
Language English
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Snippet Abstract Context 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
URI https://www.ncbi.nlm.nih.gov/pubmed/32556277
https://www.proquest.com/docview/2471030408
https://www.proquest.com/docview/2415287078
https://pubmed.ncbi.nlm.nih.gov/PMC7458544
Volume 105
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