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心肌病基因检测:对人口统计学、咨询及级联筛查的见解

Cardiomyopathy genetic testing: insights into demographics, counseling, and cascade screening.

作者信息

Bui Quan M, Silver Elizabeth, Argiro Alessia, Murray Sarah, Korty Lauren, Silva Enciso Jorge, Urey Marcus A, Chi Neil C, Hong Kimberly N, Adler Eric D

机构信息

Division of Cardiovascular Medicine, University of California, San Diego, CA, USA.

Cardiomyopathy Unit, University of Florence, Florence, Italy.

出版信息

Future Cardiol. 2025 May;21(6):359-364. doi: 10.1080/14796678.2025.2484128. Epub 2025 Apr 9.

Abstract

BACKGROUND

Genetic testing (GT) is clinically indicated for patients with suspected inherited cardiomyopathy (CM) but is underutilized.

METHODS

This single-center study included patients with CM who underwent outpatient GT from 2018 to 2023. Data were collected from the medical record.

RESULTS

A total of 306 patients were included, with a mean age of 62 years and were predominantly male (63%) and White (59%). Heart failure (92%) cardiologists were most likely to order testing, followed by general cardiology (5%) providers at tertiary hospital clinics (89%). The most common phenotypes were hypertrophic (30%), amyloid (29%) and dilated (21%). There were 17% of patients who had a positive test and 53% of patients who had a variant of uncertain significance. Patients with a positive family history had a significantly higher positive yield compared to those without ( < 0.01). Genetic counselors were underutilized (17%). For patients who had a positive test result, only 40% had cascade screening.

CONCLUSIONS

Outpatient GT for CM was primarily ordered by heart failure cardiologists in tertiary hospital clinics. Cascade screening was low, which may reflect the limited use of genetic counselors. Further research is needed to understand implementation barriers to GT.

摘要

背景

基因检测(GT)对疑似遗传性心肌病(CM)患者具有临床指征,但目前未得到充分利用。

方法

这项单中心研究纳入了2018年至2023年接受门诊GT的CM患者。数据从病历中收集。

结果

共纳入306例患者,平均年龄62岁,主要为男性(63%)和白人(59%)。心力衰竭科(92%)的心脏病专家最有可能开具检测医嘱,其次是三级医院门诊(89%)的普通心脏病科(5%)医生。最常见的表型为肥厚型(30%)、淀粉样变型(29%)和扩张型(21%)。检测结果阳性的患者占17%,意义未明变异的患者占53%。有家族史阳性的患者阳性检出率显著高于无家族史者(<0.01)。遗传咨询师的利用不足(17%)。检测结果阳性的患者中,只有40%进行了级联筛查。

结论

三级医院门诊CM患者的门诊GT主要由心力衰竭科心脏病专家开具医嘱。级联筛查率较低,这可能反映了遗传咨询师的使用有限。需要进一步研究以了解GT的实施障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a450/12026082/81ba0f08b23c/IFCA_A_2484128_F0001_B.jpg

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