Early Diagnosis of Abnormal Left Ventricular Systolic Functions of Rare Pathogenic Titin Mutation Gene Carriers in FHCM by Three-Dimensional Speckle Tracking Echocardiography Combined with Gene Detection

Objective. This study aimed to explore the early diagnosis of abnormal left ventricular systolic function of rare pathogenic titin (TTN) mutation gene carriers in familial hypertrophic cardiomyopathy (FHCM) by three-dimensional speckle tracking echocardiography (3D-STE) combined with gene detection....

Full description

Saved in:
Bibliographic Details
Main Authors: Xiang-hong Luo, Rui Zhu, Qian Chen, Pei-hong Shi, Li-sha Na
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:International Journal of Clinical Practice
Online Access:http://dx.doi.org/10.1155/2022/3415545
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832567552229769216
author Xiang-hong Luo
Rui Zhu
Qian Chen
Pei-hong Shi
Li-sha Na
author_facet Xiang-hong Luo
Rui Zhu
Qian Chen
Pei-hong Shi
Li-sha Na
author_sort Xiang-hong Luo
collection DOAJ
description Objective. This study aimed to explore the early diagnosis of abnormal left ventricular systolic function of rare pathogenic titin (TTN) mutation gene carriers in familial hypertrophic cardiomyopathy (FHCM) by three-dimensional speckle tracking echocardiography (3D-STE) combined with gene detection. Methods. Eighteen members of a Hui nationality family in Ningxia province of China were enrolled in this study in July 2019. The proband was tested with high-throughput sequencing of gene detection technology to detect the whole exome, and the mutation locus of pathogenic TTN gene was analyzed. According to the result, 16 subjects were divided into two groups: carrier group (n = 4) and noncarrier group (n = 12). Related indicators from 2DE were obtained, and myocardial strain indicators from 3D-STE were analyzed by postprocessing software of Tomtec. Strain indicators included global longitudinal strain (GLS), global circumference strain (GCS), global radial strain (GRS), regional longitudinal strain (RLS), regional circumference strain (RCS), and regional radial strain (RRS). All those indicators were compared between the two groups, and a receiver operating characteristic (ROC) curve was used for further analysis. Results. There were 4 subjects diagnosed as asymptomatic TTN gene carriers with the mutation locus of Val135643Ile. Compared with the noncarrier group, GLS and partial RLS were significantly reduced in the carrier group. The ROC curve shows that GLS has the largest AUC, and its sensitivity was better than LVPWD and specificity was better than IVSD and LVMI obtained from 2DE in the carrier group. Conclusions. There were 4 subjects diagnosed as asymptomatic TTN gene carriers with the mutation locus of Val135643Ile, and their GLS and partial RLS were significantly reduced; GLS had the better sensitivity and specificity than LVPWD, IVSD, and LVMI.
format Article
id doaj-art-dd1bbe5879714f1287ae4ccb3bf91aad
institution Kabale University
issn 1742-1241
language English
publishDate 2022-01-01
publisher Wiley
record_format Article
series International Journal of Clinical Practice
spelling doaj-art-dd1bbe5879714f1287ae4ccb3bf91aad2025-02-03T01:01:19ZengWileyInternational Journal of Clinical Practice1742-12412022-01-01202210.1155/2022/3415545Early Diagnosis of Abnormal Left Ventricular Systolic Functions of Rare Pathogenic Titin Mutation Gene Carriers in FHCM by Three-Dimensional Speckle Tracking Echocardiography Combined with Gene DetectionXiang-hong Luo0Rui Zhu1Qian Chen2Pei-hong Shi3Li-sha Na4Department of CardiologyDepartment of Cardiac Function Examination of Heart CentreEchocardiography and Vascular Ultrasound CenterDepartment of Ultrasonic ImagingDepartment of Cardiac Function Examination of Heart CentreObjective. This study aimed to explore the early diagnosis of abnormal left ventricular systolic function of rare pathogenic titin (TTN) mutation gene carriers in familial hypertrophic cardiomyopathy (FHCM) by three-dimensional speckle tracking echocardiography (3D-STE) combined with gene detection. Methods. Eighteen members of a Hui nationality family in Ningxia province of China were enrolled in this study in July 2019. The proband was tested with high-throughput sequencing of gene detection technology to detect the whole exome, and the mutation locus of pathogenic TTN gene was analyzed. According to the result, 16 subjects were divided into two groups: carrier group (n = 4) and noncarrier group (n = 12). Related indicators from 2DE were obtained, and myocardial strain indicators from 3D-STE were analyzed by postprocessing software of Tomtec. Strain indicators included global longitudinal strain (GLS), global circumference strain (GCS), global radial strain (GRS), regional longitudinal strain (RLS), regional circumference strain (RCS), and regional radial strain (RRS). All those indicators were compared between the two groups, and a receiver operating characteristic (ROC) curve was used for further analysis. Results. There were 4 subjects diagnosed as asymptomatic TTN gene carriers with the mutation locus of Val135643Ile. Compared with the noncarrier group, GLS and partial RLS were significantly reduced in the carrier group. The ROC curve shows that GLS has the largest AUC, and its sensitivity was better than LVPWD and specificity was better than IVSD and LVMI obtained from 2DE in the carrier group. Conclusions. There were 4 subjects diagnosed as asymptomatic TTN gene carriers with the mutation locus of Val135643Ile, and their GLS and partial RLS were significantly reduced; GLS had the better sensitivity and specificity than LVPWD, IVSD, and LVMI.http://dx.doi.org/10.1155/2022/3415545
spellingShingle Xiang-hong Luo
Rui Zhu
Qian Chen
Pei-hong Shi
Li-sha Na
Early Diagnosis of Abnormal Left Ventricular Systolic Functions of Rare Pathogenic Titin Mutation Gene Carriers in FHCM by Three-Dimensional Speckle Tracking Echocardiography Combined with Gene Detection
International Journal of Clinical Practice
title Early Diagnosis of Abnormal Left Ventricular Systolic Functions of Rare Pathogenic Titin Mutation Gene Carriers in FHCM by Three-Dimensional Speckle Tracking Echocardiography Combined with Gene Detection
title_full Early Diagnosis of Abnormal Left Ventricular Systolic Functions of Rare Pathogenic Titin Mutation Gene Carriers in FHCM by Three-Dimensional Speckle Tracking Echocardiography Combined with Gene Detection
title_fullStr Early Diagnosis of Abnormal Left Ventricular Systolic Functions of Rare Pathogenic Titin Mutation Gene Carriers in FHCM by Three-Dimensional Speckle Tracking Echocardiography Combined with Gene Detection
title_full_unstemmed Early Diagnosis of Abnormal Left Ventricular Systolic Functions of Rare Pathogenic Titin Mutation Gene Carriers in FHCM by Three-Dimensional Speckle Tracking Echocardiography Combined with Gene Detection
title_short Early Diagnosis of Abnormal Left Ventricular Systolic Functions of Rare Pathogenic Titin Mutation Gene Carriers in FHCM by Three-Dimensional Speckle Tracking Echocardiography Combined with Gene Detection
title_sort early diagnosis of abnormal left ventricular systolic functions of rare pathogenic titin mutation gene carriers in fhcm by three dimensional speckle tracking echocardiography combined with gene detection
url http://dx.doi.org/10.1155/2022/3415545
work_keys_str_mv AT xianghongluo earlydiagnosisofabnormalleftventricularsystolicfunctionsofrarepathogenictitinmutationgenecarriersinfhcmbythreedimensionalspeckletrackingechocardiographycombinedwithgenedetection
AT ruizhu earlydiagnosisofabnormalleftventricularsystolicfunctionsofrarepathogenictitinmutationgenecarriersinfhcmbythreedimensionalspeckletrackingechocardiographycombinedwithgenedetection
AT qianchen earlydiagnosisofabnormalleftventricularsystolicfunctionsofrarepathogenictitinmutationgenecarriersinfhcmbythreedimensionalspeckletrackingechocardiographycombinedwithgenedetection
AT peihongshi earlydiagnosisofabnormalleftventricularsystolicfunctionsofrarepathogenictitinmutationgenecarriersinfhcmbythreedimensionalspeckletrackingechocardiographycombinedwithgenedetection
AT lishana earlydiagnosisofabnormalleftventricularsystolicfunctionsofrarepathogenictitinmutationgenecarriersinfhcmbythreedimensionalspeckletrackingechocardiographycombinedwithgenedetection