Lower microhardness along with less heterogeneous mineralization in the femoral neck of individuals with type 2 diabetes mellitus indicates higher fracture risk

Author:

Cirovic Aleksandar12,Schmidt Felix N345,Vujacic Marko6,Sihota Praveer34,Petrovic Bojan6,Zivkovic Vladimir127,Bascarevic Zoran6,Nikolic Slobodan127,Djonic Danijela12,Djuric Marija12,Busse Björn345,Milovanovic Petar12

Affiliation:

1. Center of Bone Biology , Institute of Anatomy, , 11000 Belgrade , Serbia

2. University of Belgrade - Faculty of Medicine , Institute of Anatomy, , 11000 Belgrade , Serbia

3. Department of Osteology and Biomechanics , , 22529 Hamburg , Germany

4. University Medical Center Hamburg-Eppendorf , , 22529 Hamburg , Germany

5. Interdisciplinary Competence Center for Interface Research (ICCIR) , 20246 Hamburg , Germany

6. University of Belgrade - Faculty of Medicine Institute for Orthopedic Surgery “Banjica”; , 11000 Belgrade , Serbia

7. Institute of Forensic Medicine, University of Belgrade - Faculty of Medicine , 11000 Belgrade , Serbia

Abstract

Abstract There is still limited understanding of the microstructural reasons for the higher susceptibility to fractures in individuals with type 2 diabetes mellitus (T2DM). In this study, we examined bone mineralization, osteocyte lacunar parameters, and microhardness of the femoral neck trabeculae in 18 individuals with T2DM who sustained low-energy fracture (T2DMFx: 78 ± 7 years, 15 women and 3 men) and 20 controls (74 ± 7 years, 16 women and 4 men). Femoral necks of the T2DMFx subjects were obtained at a tertiary orthopedic hospital, while those of the controls were collected at autopsy. T2DMFx individuals had lower trabecular microhardness (P = .023) and mineralization heterogeneity (P = .001), and a tendency to a lower bone area with mineralization above 95th percentile (P = .058) than the controls. There were no significant intergroup differences in the numbers of osteocyte lacunae per bone area, mineralized lacunae per bone area, and total lacunae per bone area (each P > .05). After dividing the T2DMFx group based on the presence of vascular complications (VD) to T2DMFxVD (VD present) and T2DMFxNVD (VD absent), we observed that microhardness was particularly reduced in the T2DMFxVD group (vs. control group, P = .02), while mineralization heterogeneity was significantly reduced in both T2DMFx subgroups (T2DMFxNVD vs. control, P = .002; T2DMFxVD vs. control, P = .038). The observed changes in mineralization and microhardness may contribute to the increased hip fracture susceptibility in individuals with T2DM.

Funder

Science Fund of the Republic of Serbia

BoFraM

DiaBoNet

Ministry of Science of the Republic of Serbia

Alexander von Humboldt Foundation

German Research Foundation

DFG

Publisher

Oxford University Press (OUP)

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