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Updated: Oct 3, 2025

Technique of Minimally Invasive Transverse Aortic Constriction in Mice for Induction of Left Ventricular Hypertrophy
Published on: September 25, 2017
Comprehensive bioinformatics analysis identifies LAPTM5 as a potential blood biomarker for hypertensive patients with
Tiegang Li1, Weiqi Wang1, Wenqiang Gan1
1State Key Laboratory of Bioactive Substances and Function of Natural Medicine, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
Insights
Researchers identified lysosomal associated transmembrane protein 5 (LAPTM5) as a potential blood biomarker for diagnosing left ventricular hypertrophy (LVH) in hypertension patients. This finding offers new insights into hypertensive heart disease.
Area of Science:
- Biochemistry
- Molecular Biology
- Cardiovascular Research
Background:
- Left ventricular hypertrophy (LVH) is a key indicator of hypertensive organ damage and elevates cardiovascular risk.
- Current diagnostic biomarkers for early detection of LVH in hypertension (HT) patients are insufficient.
Purpose of the Study:
- To identify novel blood biomarkers for diagnosing hypertensive LVH using bioinformatics and experimental validation.
- To investigate the potential of LAPTM5 as a diagnostic marker for hypertensive LVH.
Main Methods:
- Analysis of GSE74144 mRNA expression profiles from the GEO database.
- Application of Weighted Gene Co-expression Network Analysis (WGCNA), LASSO regression, and SVM-RFE algorithms.
- Experimental verification in an animal model using RT-PCR and cardiac magnetic resonance imaging (CMRI).
Main Results:
- 142 hub genes related to ATP metabolism, oxidative phosphorylation, and mitochondrial function were identified.
- Lysosomal associated transmembrane protein 5 (LAPTM5) emerged as a potential diagnostic marker.
- Elevated LAPTM5 expression correlated with LVH, increased reactive oxygen species (ROS), and altered autophagy, and showed associations with cardiac structure and ECG parameters.
Conclusions:
- LAPTM5 shows promise as a diagnostic biomarker for LVH in hypertensive patients.
- LAPTM5 may offer new avenues for understanding the mechanisms of hypertensive LVH.
Abstract:
Left ventricular hypertrophy (LVH) is a pivotal manifestation of hypertensive organ damage associated with an increased cardiovascular risk. However, early diagnostic biomarkers for assessing LVH in patients with hypertension (HT) remain indefinite. Here, multiple bioinformatics tools combined with an experimental verification strategy were used to identify blood biomarkers for hypertensive LVH. GSE74144 mRNA expression profiles were downloaded from the Gene Expression Omnibus (GEO) database to screen candidate biomarkers, which were used to perform weighted gene co-expression network analysis (WGCNA) and establish the least absolute shrinkage and selection operator (LASSO) regression model, combined with support vector machine-recursive feature elimination (SVM-RFE) algorithms. Finally, the potential blood biomarkers were verified in an animal model. A total of 142 hub genes in peripheral blood leukocytes were identified between HT with LVH and HT without LVH, which were mainly involved in the ATP metabolic process, oxidative phosphorylation, and mitochondrial structure and function. Notably, lysosomal associated transmembrane protein 5 (LAPTM5) was identified as the potential diagnostic marker of hypertensive LVH, which showed strong correlations with diverse marker sets of reactive oxygen species (ROS) and autophagy. RT-PCR validation of blood samples and cardiac magnetic resonance imaging (CMRI) showed that the expression of LAPTM5 was significantly higher in the HT with LVH model than in normal controls, LAPTM5 demonstrated a positive association with the left ventricle wall thickness as well as electrocardiogram (ECG) parameters widths of the QRS complex and QTc interval. In conclusion, LAPTM5 may be a potential biomarker for the diagnosis of LVH in patients with HT, and it can provide new insights for future studies on the occurrence and the molecular mechanisms of hypertensive LVH.
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