» Articles » PMID: 30563371

Degenerative Aortic Valve Disease and Diabetes: Implications for a Link Between Proteoglycans and Diabetic Disorders in the Aortic Valve

Overview
Publisher Sage Publications
Date 2018 Dec 20
PMID 30563371
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Degenerative aortic valve disease in combination with diabetes is an increasing burden worldwide. There is growing evidence that particularly small leucine-rich proteoglycans are involved in the development of degenerative aortic valve disease. Nevertheless, the role of these molecules in this disease in the course of diabetes has not been elucidated in detail and previous studies remain controversial. Therefore, the aim of this study is to broaden the knowledge about small leucine-rich proteoglycans in degenerative aortic valve disease and the influence of diabetes and hyperglycaemia on aortic valves and valvular interstitial cells is examined. Analyses were performed using reverse-transcription polymerase chain reaction, Western blot, enzyme-linked immunosorbent assay, (immuno)histology and colorimetric assays. We could show that biglycan, but not decorin and lumican, is upregulated in degenerated human aortic valve cusps. Subgroup analysis reveals that upregulation of biglycan is stage-dependent. In vivo, loss of biglycan leads to stage-dependent calcification and also to migratory effects on interstitial cells within the extracellular matrix. In late stages of degenerative aortic valve disease, diabetes increases the expression of biglycan in aortic valves. In vitro, the combinations of hyperglycaemic with pro-degenerative conditions lead to an upregulation of biglycan. In conclusion, biglycan represents a potential link between degenerative aortic valve disease and diabetes.

Citing Articles

Aortic regurgitation is associated with African American and Asian race, smoking, renal disease, and numerous autoimmune diseases in addition to traditional cardiovascular risk factors but has lower risk with alcohol intake.

Timmerman B, Hashemzadeh M, Movahed M Clin Res Cardiol. 2024; .

PMID: 38478089 DOI: 10.1007/s00392-024-02424-3.


Molecular cues for immune cells from small leucine-rich repeat proteoglycans in their extracellular matrix-associated and free forms.

Maiti G, Ashworth S, Choi T, Chakravarti S Matrix Biol. 2023; 123:48-58.

PMID: 37793508 PMC: 10841460. DOI: 10.1016/j.matbio.2023.10.001.


[Bioinformatics Analysis of Hub Genes of Diabetic Foot Ulcer and Their Biofunctions].

Xu F, Rui S, Luo P, Chen Y, Ma Y, Deng W Sichuan Da Xue Xue Bao Yi Xue Ban. 2022; 53(6):961-968.

PMID: 36443035 PMC: 10408990. DOI: 10.12182/20220860106.


Interactive contribution of hyperinsulinemia, hyperglycemia, and mammalian target of rapamycin signaling to valvular interstitial cell differentiation and matrix remodeling.

Selig J, Krug H, Kuppers C, Ouwens D, Kraft F, Adler E Front Cardiovasc Med. 2022; 9:942430.

PMID: 36386326 PMC: 9661395. DOI: 10.3389/fcvm.2022.942430.


Proteoglycans in Toll-like receptor responses and innate immunity.

Garantziotis S, Savani R Am J Physiol Cell Physiol. 2022; 323(1):C202-C214.

PMID: 35675639 PMC: 9273283. DOI: 10.1152/ajpcell.00088.2022.