Correlation between Serum Osteoprotegerin/Soluble Receptor Activator of Nuclear Factor-κβ Ligand Levels and the Left Ventricular Diastolic Dysfunction in Type 2 Diabetes
返回论文页
Clinical Research|更新时间:2024-02-19
|
Correlation between Serum Osteoprotegerin/Soluble Receptor Activator of Nuclear Factor-κβ Ligand Levels and the Left Ventricular Diastolic Dysfunction in Type 2 Diabetes
Journal of Sun Yat-sen University(Medical Sciences)Vol. 44, Issue 6, Pages: 991-998(2023)
ZHENG Ben-rong,TANG Xi-xiang,JIANG Bo-xiong,et al.Correlation between Serum Osteoprotegerin/Soluble Receptor Activator of Nuclear Factor-κβ Ligand Levels and the Left Ventricular Diastolic Dysfunction in Type 2 Diabetes[J].Journal of Sun Yat-sen University(Medical Sciences),2023,44(06):991-998.
ZHENG Ben-rong,TANG Xi-xiang,JIANG Bo-xiong,et al.Correlation between Serum Osteoprotegerin/Soluble Receptor Activator of Nuclear Factor-κβ Ligand Levels and the Left Ventricular Diastolic Dysfunction in Type 2 Diabetes[J].Journal of Sun Yat-sen University(Medical Sciences),2023,44(06):991-998. DOI: 10.13471/j.cnki.j.sun.yat-sen.univ(med.sci).2023.0613.
Correlation between Serum Osteoprotegerin/Soluble Receptor Activator of Nuclear Factor-κβ Ligand Levels and the Left Ventricular Diastolic Dysfunction in Type 2 Diabetes
To study the possible correlation between serum osteoprotegerin (OPG)/soluble receptor activator of the nuclear factor κB ligand (sRANKL) levels and the left ventricular diastolic dysfunction (LADD) in patients with type 2 diabetes mellitus (T2DM).
Methods
2
Totally 68 T2DM patients and 37 healthy controls were selected. Serum OPG and sRANKL were determined by solid-phase enzyme-linked immunosorbent assay (ELISA). The left ventricular diastolic function of T2DM patients was measured by transthoracic echocardiography, where E/A < 1 were regarded as LVDD. T2DM patients were further divided into two subgroups according to E/A ratio (E/A≥1.0 and E/A<1). Spearman correlation analysis, logistic regression and ROC curves were used to assess the possible correlation between serum OPG/sRANKL and LADD in T2DM patients.
Results
2
Compared with the healthy controls, serum OPG level in T2DM patients was higher with statistically significant difference (
P
<
0.01), while serum sRANKL level was lower without statistically significant difference (
P
=0.32). T2DM patients with E/A
<
1 had significantly higher OPG level and lower sRANKL level than those with E/A≥1
(P
<
0.01) in subgroup analysis. Spearman correlation analysis showed serum OPG level was negatively correlated with E/A ratio, while sRANKL was positively related with E/A ratio. In single factor logistic regression analyses, serum OPG [OR (95% CI)=1.068 (1.031, 1.106),
P
<
0.001] and sRANKL [OR (95% CI)=0.976 (0.959, 0.992),
P
=0.003] were significant correlation with LVDD in T2DM patients. ROC curve analysis showed that the sensitivity and specificity of combined OPG and sRANKL in diagnosing T2DM patients LADD were 78.13% and 88.3%, respectively (area under the curve: 0.857; 95% CI=(0.768, 0.946);
P
<
0.001).
Conclusions
2
The elevated OPG and decreased sRANKL levels may be associated with LADD in T2DM patients.
关键词
2型糖尿病左室舒张功能障碍骨保护素NF-κB受体活化因子配体
Keywords
type 2 diabetesleft ventricular diastolic dysfunctionosteoprotegerinreceptor activator of the nuclear factor κB ligand
references
Karwi QG, Ho KL, Pherwani S, et al. Concurrent diabetes and heart failure: interplay and novel therapeutic approaches[J]. Cardiovasc Res, 2022, 118(3):686-715.
Ritchie RH, Abel ED. Basic mechanisms of diabetic heart disease[J]. Circ Res, 2020, 126(11):1501-1525.
Kozakova M, Morizzo C, Fraser AG, et al. Impact of glycemic control on aortic stiffness, left ventricular mass and diastolic longitudinal function in type 2 diabetes mellitus[J]. Cardiovasc Diabetol, 2017,16(1):78.
Dutka M, Bobiński R, Wojakowski W, et al. Osteoprotegerin and RANKL-RANK-OPG-TRAIL signalling axis in heart failure and other cardiovascular diseases[J]. Heart Fail Rev, 2022, 27(4):1395-1411.
Forde H, Davenport C, Harper E, et al. The role of OPG/RANKL in the pathogenesis of diabetic cardiovascular disease[J]. Cardiovasc Endocrinol Metab, 2018, 7(2):28-33.
Loncar G, Bozic B, Cvorovic V, et al. Relationship between RANKL and neuroendocrine activation in elderly males with heart failure[J]. Endocrine, 2010, 37(1):148-56.
Bourron O, Phan F, Diallo MH, et al. Circulating receptor activator of nuclear factor kB ligand and triglycerides are associated with progression of lower limb arterial calcification in type 2 diabetes: a prospective, observational cohort study[J]. Cardiovasc Diabetol, 2020, 19(1):140.
Maddaloni E, Coraggio L, Amendolara R, et al. Association of osteocalcin, osteoprotegerin, and osteopontin with cardiovascular disease and retinopathy in type 2 diabetes[J]. Diabetes Metab Res Rev, 2023, 39(5):e3632.
Moh AMC, Pek SLT, Liu J, et al. Plasma osteoprotegerin as a biomarker of poor glycaemic control that predicts progression of albuminuria in type 2 diabetes mellitus: A 3-year longitudinal cohort study[J]. Diabetes Res Clin Pract, 2020, 161:107992.
Vachliotis ID, Polyzos SA. Osteoprotegerin/receptor activator of nuclear factor-kappa B ligand/receptor activator of nuclear factor-kappa B axis in obesity, type 2 diabetes mellitus, and nonalcoholic fatty liver disease[J]. Curr Obes Rep, 2023, 12(2):147-162.
Pezhman L, Sheikhzadeh Hesari F, Ghiasi R, et al. The impact of forced swimming on expression of RANKL and OPG in a type 2 diabetes mellitus rat model[J]. Arch Physiol Biochem, 2019, 125(3):195-200.
Browner WS, Lui LY, Cummings SR. Associations of serum osteoprotegerin levels with diabetes, stroke, bone density, fractures, and mortality in elderly women[J]. J Clin Endocrinol Metab, 2001, 86(2):631-637.
Yaturu S, Rains J, Jain SK. Relationship of elevated osteoprotegerin with insulin resistance, CRP, and TNF-alpha levels in men with type 2 diabetes[J]. Cytokine, 2008, 168-171.
Kiechl S, Wittmann J, Giaccari A, et al. Blockade of receptor activator of nuclear factor-κB (RANKL) signaling improves hepatic insulin resistance and prevents development of diabetes mellitus[J]. Nat Med, 2013, 19(3):358-363.
Xiang GD, Sun HL, Zhao LS, et al. Changes of osteoprotegerin before and after insulin therapy in type 1 diabetic patients[J]. Natl Med J Chin, 2007, 87(18): 1234-1237.
Toffoli B, Pickering RJ, Tsorotes D, et al. Osteoprotegerin promotes vascular fibrosis via a TGF-β1 autocrine loop[J]. Atherosclerosis, 2011, 218(1):61-68.
Eschler DC, Kulina G, Garcia-Ocana A, et al. Circulating levels of bone and inflammatory markers in gestational diabetes mellitus[J]. Biores Open Access, 2018, 7(1):123-130.
O'Sullivan EP, Ashley DT, Davenport C, et al. Osteoprotegerin and biomarkers of vascular inflammation in type 2 diabetes[J]. Diabetes Metab Res Rev, 2010, 26(6):496-502.
Grigorescu ED, Lacatusu CM, Floria M, et al. Left ventricular diastolic dysfunction in type 2 diabetes-progress and perspectives[J]. Diagnostics (Basel), 2019, 9(3):121.
Zampetti S, Lucantoni F, Pacifico L, et al. Association of OPG-RANKL ratio with left ventricular hypertrophy and geometric remodeling in male overweight/obese youths[J]. J Endocrinol Invest, 2019, 42(4):427-434.
Liu W, Feng W, Wang F, et al. Osteoprotegerin/RANK/RANKL axis in cardiac remodeling due to immuno-inflammatory myocardial disease[J]. Exp Mol Pathol, 2008, 84(3):213-217.
Wang X, Liu J, Yang Y, et al. An update on the potential role of advanced glycation end products in glycolipid metabolism[J]. Life Sci, 2020, 245:117344.
Ndip A, Wilkinson FL, Jude EB, et al. RANKL-OPG and RAGE modulation in vascular calcification and diabetes: novel targets for therapy[J]. Diabetologia, 2014, 57(11):2251-2260.
Galeone A, Grano M, Brunetti G. Tumor necrosis factor family members and myocardial ischemia-reperfusion injury: State of the art and therapeutic implications[J]. Int J Mol Sci, 2023, 24(5):4606.
Marcadet L, Bouredji Z, Argaw A, et al. The roles of RANK/RANKL/OPG in cardiac, skeletal, and smooth muscles in health and disease[J]. Front Cell Dev Biol, 2022, 10:903657.
Development and Validation of a Predictive Risk Model for Vision-threatening Diabetic Retinopathy in Patients with Type 2 Diabetes
Clinical Effects of Chinese Medicine Fasting Therapy in Overweight/Obese Type 2 Diabetes Patients
Decreased Caveolin-1 Expression of Peripheral Blood Mononuclear Cells in Newly Diagnosed Type 2 Diabetic Patients and Its Relationship with Insulin Resistance
Association of Polymorphisms in CAV1/CAV2 Locus with Type 2 Diabetes in Chinese Han
Population
Related Author
HUANG Sheng-song
LIU Jia-hui
CHEN Shu-hui
CHEN Min-yu
ZHANG Jian
LI Yu-ting
HUANG Wen-yong
LUO Jin
Related Institution
State Key Laboratory of Ophthalmology//Zhongshan Ophthalmic Center, Sun Yat-sen University//Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science
The Tenth Affiliated Hospital of Southern Medical University (Dongguan People's Hospital)
Department of Traditional Chinese Medicine, The Seventh Affiliated Hospital, Sun Yat-sen University