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Published on: February 20, 2017
Correlations of circulating miR-26b level with left ventricular hypertrophy and cardiac function in elderly patients
Jian Fu1, Fang Lin2, Zhengxia Pan3
1Jian Fu, Department of Cardiac Surgery, Children's Hospital of Chongqing Medical University, National International Science and Technology Cooperation Base for Children's Developmental Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing 400014, P.R. China.
Insights
Lower levels of miR-26b are linked to left ventricular hypertrophy (LVH) and impaired cardiac function in elderly hypertensive patients. Elevated miR-26b may protect against LVH and diastolic dysfunction.
Area of Science:
- Cardiology
- Molecular Biology
- Biomarkers
Background:
- Hypertension is a major risk factor for cardiovascular diseases, including left ventricular hypertrophy (LVH).
- LVH is associated with impaired cardiac function and increased risk of heart failure.
- MicroRNAs (miRNAs) are emerging as key regulators in cardiovascular pathophysiology.
Purpose of the Study:
- To investigate the association between circulating miR-26b levels and LVH in elderly hypertensive patients.
- To evaluate the correlation of miR-26b with cardiac function parameters.
- To determine the diagnostic potential of miR-26b for LVH.
Main Methods:
- 132 elderly hypertensive patients were categorized into low and high miR-26b groups.
- Echocardiographic parameters (IVST, LVPWT, LVMI, E/A) and clinical data were analyzed.
- Pearson correlation, logistic regression, and ROC curve analyses were employed.
Main Results:
- Low miR-26b levels were significantly associated with increased interventricular septal thickness (IVST), left ventricular posterior wall thickness (LVPWT), left ventricular mass index (LVMI), and reduced E/A ratio.
- Circulating miR-26b showed negative correlations with IVST, LVPWT, LVMI, and positive correlation with E/A.
- Elevated miR-26b was identified as a protective factor against LVH, with an AUC of 0.836 for diagnosis.
Conclusions:
- Circulating miR-26b levels are inversely correlated with LVH and positively correlated with diastolic function in elderly hypertensive patients.
- miR-26b may serve as a protective factor against LVH and diastolic dysfunction.
- miR-26b demonstrates potential as a diagnostic biomarker for LVH in this population.
Objectives:
To study the correlations of circulating miR-26b level with left ventricular hypertrophy (LVH) and cardiac function in elderly patients with hypertension.
Methods:
A total of 132 eligible patients were divided into low and high miR-26b level groups. Their baseline clinical data and biochemical indices were compared. The correlations between miR-26b level and echocardiographic parameters were studied by Pearson's analysis. Factors affecting LVH were explored by multivariate logistic regression analysis. The role of miR-26b in diagnosing LVH was predicted by receiver operating characteristic curve.
Results:
The relative expression level of miR-26b was 4.56-16.93, with a median of 7.62. The two groups had similar baseline clinical data and biochemical indices (P>0.05). Compared with high miR-26b level group, interventricular septal thickness (IVST), left ventricular posterior wall thickness (LVPWT), left ventricular mass index (LVMI) and number of LVH cases in low miR-26b level group significantly increased (P<0.05), and mitral ratio of peak early to late diastolic filling velocity (E/A) decreased (P<0.05). Circulating miR-26b level was negatively correlated with IVST, LVPWT and LVMI (P<0.0001), and positively correlated with E/A (P<0.0001). The proportion of cardiac hypofunction cases in low miR-26b level group significantly exceeded that of high miR-26b level group (P<0.05). Age and increased IVST, LVPWT and LVMI were independent risk factors for LVH (P<0.05), and elevated miR-26b level was a protective factor (P<0.05). AUC was 0.836, and the optimal cutoff value was 8.83, with high sensitivity and specificity.
Conclusions:
MiR-26b level is negatively correlated with LVH and positively correlated with left ventricular diastolic function in elderly hypertensive patients. It is a protective factor for LVH complicated with diastolic dysfunction and a potential biomarker for diagnosis.
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