• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Sex Differences in the Phenotype of Transthyretin Cardiac Amyloidosis Due to Val122Ile Mutation: Insights from Noninvasive Pressure-Volume Analysis.由于 Val122lle 突变导致转甲状腺素蛋白心脏淀粉样变的表型存在性别差异:来自无创压力-容积分析的见解。
J Card Fail. 2021 Jan;27(1):67-74. doi: 10.1016/j.cardfail.2020.08.007. Epub 2020 Aug 20.
2
Racial Differences in Val122Ile-Associated Transthyretin Cardiac Amyloidosis.载脂蛋白 AI 米兰变体与心血管淀粉样变性的相关性研究
J Card Fail. 2022 Jun;28(6):950-959. doi: 10.1016/j.cardfail.2021.12.016. Epub 2021 Dec 30.
3
Relation of Body Mass Index to Transthyretin Cardiac Amyloidosis Particularly in Black and Hispanic Patients (from the SCAN-MP Study).体重指数与转甲状腺素蛋白心脏淀粉样变的关系,特别是在黑人和西班牙裔患者中(来自 SCAN-MP 研究)。
Am J Cardiol. 2022 Aug 15;177:116-120. doi: 10.1016/j.amjcard.2022.05.003. Epub 2022 Jun 12.
4
Genotype and Phenotype of Transthyretin Cardiac Amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey).转甲状腺素蛋白心脏淀粉样变性的基因型与表型:THAOS(转甲状腺素蛋白淀粉样变性结局调查)
J Am Coll Cardiol. 2016 Jul 12;68(2):161-72. doi: 10.1016/j.jacc.2016.03.596.
5
Pressure-volume relationships in patients with transthyretin (ATTR) cardiac amyloidosis secondary to V122I mutations and wild-type transthyretin: Transthyretin Cardiac Amyloid Study (TRACS).转甲状腺素蛋白(ATTR)心脏淀粉样变性继发于 V122I 突变和野生型转甲状腺素蛋白的患者的压力-容积关系:转甲状腺素蛋白心脏淀粉样变性研究(TRACS)。
Circ Heart Fail. 2011 Mar;4(2):121-8. doi: 10.1161/CIRCHEARTFAILURE.109.910455. Epub 2010 Dec 29.
6
Sex differences in transthyretin cardiac amyloidosis.转甲状腺素蛋白心脏淀粉样变性的性别差异。
Heart Fail Rev. 2024 Mar;29(2):321-330. doi: 10.1007/s10741-023-10339-w. Epub 2023 Aug 11.
7
A case of cardiac amyloidosis in an elderly Japanese patient with amyloidogenic transthyretin Val122Ile variant.一名患有淀粉样前体蛋白缬氨酸122异亮氨酸变异体的老年日本心脏淀粉样变性患者的病例。
J Cardiol Cases. 2020 Jul 29;22(5):221-225. doi: 10.1016/j.jccase.2020.07.010. eCollection 2020 Nov.
8
Clinical features and predictors of atrial fibrillation in patients with light-chain or transthyretin cardiac amyloidosis.轻链或转甲状腺素蛋白心脏淀粉样变患者心房颤动的临床特征和预测因素。
ESC Heart Fail. 2022 Jun;9(3):1740-1748. doi: 10.1002/ehf2.13851. Epub 2022 Feb 17.
9
Practical recommendations for the diagnosis and management of transthyretin cardiac amyloidosis.转甲状腺素蛋白心脏淀粉样变性诊断与管理的实用建议。
Heart Fail Rev. 2021 Jul;26(4):861-879. doi: 10.1007/s10741-020-10062-w. Epub 2021 Jan 15.
10
Stabilization of Cardiac Function With Diflunisal in Transthyretin (ATTR) Cardiac Amyloidosis.双氯芬酸对转甲状腺素蛋白(ATTR)心脏淀粉样变性患者心脏功能的稳定作用
J Card Fail. 2020 Sep;26(9):753-759. doi: 10.1016/j.cardfail.2019.11.024. Epub 2019 Dec 2.

引用本文的文献

1
Race, Genetics, and Social Determinants of Health in Transthyretin Cardiac Amyloidosis: A Literature Review and Call to Action.转甲状腺素蛋白心脏淀粉样变中的种族、遗传学与健康的社会决定因素:文献综述与行动呼吁
Curr Cardiol Rep. 2025 Mar 5;27(1):66. doi: 10.1007/s11886-025-02220-z.
2
Hereditary Transthyretin Amyloidosis in Patients Referred to a Genetic Testing Program.转诊至基因检测项目的患者中的遗传性转甲状腺素蛋白淀粉样变性
J Am Heart Assoc. 2024 Dec 3;13(23):e033770. doi: 10.1161/JAHA.123.033770. Epub 2024 Nov 22.
3
Hereditary transthyretin amyloidosis: a myriad of factors that influence phenotypic variability.遗传性转甲状腺素蛋白淀粉样变性:影响表型变异性的众多因素。
J Neurol. 2024 Sep;271(9):5746-5761. doi: 10.1007/s00415-024-12509-8. Epub 2024 Jun 22.
4
Sex Differences in Transthyretin Cardiac Amyloidosis: Unraveling the Complexities in Epidemiology, Pathophysiology, Diagnosis, and Treatment.转甲状腺素蛋白心脏淀粉样变中的性别差异:揭示流行病学、病理生理学、诊断和治疗中的复杂性。
Curr Heart Fail Rep. 2024 Aug;21(4):344-353. doi: 10.1007/s11897-024-00667-9. Epub 2024 May 22.
5
Disease features and management of cardiomyopathies in women.女性心肌病的疾病特征与管理
Heart Fail Rev. 2024 May;29(3):663-674. doi: 10.1007/s10741-024-10386-x. Epub 2024 Feb 3.
6
A 15-year consolidated overview of data in over 6000 patients from the Transthyretin Amyloidosis Outcomes Survey (THAOS).一项针对超过 6000 名转甲状腺素蛋白淀粉样变性患者数据的长达 15 年的综合回顾:转甲状腺素蛋白淀粉样变性结局调查(THAOS)。
Orphanet J Rare Dis. 2023 Nov 10;18(1):350. doi: 10.1186/s13023-023-02962-5.
7
Sex differences in transthyretin cardiac amyloidosis.转甲状腺素蛋白心脏淀粉样变性的性别差异。
Heart Fail Rev. 2024 Mar;29(2):321-330. doi: 10.1007/s10741-023-10339-w. Epub 2023 Aug 11.
8
Sex Differences in Heart Failure: What Do We Know?心力衰竭中的性别差异:我们了解什么?
J Cardiovasc Dev Dis. 2023 Jun 29;10(7):277. doi: 10.3390/jcdd10070277.
9
Sex differences among patients with transthyretin amyloid cardiomyopathy - from diagnosis to prognosis.转甲状腺素蛋白淀粉样变性心肌病患者的性别差异——从诊断到预后。
Eur J Heart Fail. 2022 Dec;24(12):2355-2363. doi: 10.1002/ejhf.2646. Epub 2022 Aug 16.
10
Clinical Profile and Prognosis of Hereditary Transthyretin Amyloid Cardiomyopathy: A Single-Center Study in South China.遗传性转甲状腺素蛋白淀粉样变心肌病的临床特征与预后:中国南方单中心研究
Front Cardiovasc Med. 2022 Jun 27;9:900313. doi: 10.3389/fcvm.2022.900313. eCollection 2022.

本文引用的文献

1
Clinicopathological correlations of sural nerve biopsies in Val30Met familial amyloid polyneuropathy.缬氨酸30蛋氨酸型家族性淀粉样多神经病腓肠神经活检的临床病理相关性
Brain Commun. 2019 Nov 4;1(1):fcz032. doi: 10.1093/braincomms/fcz032. eCollection 2019.
2
Cardiac Amyloidosis: Evolving Diagnosis and Management: A Scientific Statement From the American Heart Association.心脏淀粉样变性:不断发展的诊断和治疗——美国心脏协会的科学声明。
Circulation. 2020 Jul 7;142(1):e7-e22. doi: 10.1161/CIR.0000000000000792. Epub 2020 Jun 1.
3
Sex differences in heart failure.心力衰竭中的性别差异。
Eur Heart J. 2019 Dec 14;40(47):3859-3868c. doi: 10.1093/eurheartj/ehz835.
4
Transthyretin Amyloid Cardiomyopathy: JACC State-of-the-Art Review.转甲状腺素蛋白淀粉样心肌病:美国心脏病学会最新临床综述
J Am Coll Cardiol. 2019 Jun 11;73(22):2872-2891. doi: 10.1016/j.jacc.2019.04.003.
5
Natural History, Quality of Life, and Outcome in Cardiac Transthyretin Amyloidosis.心脏转甲状腺素蛋白淀粉样变性的自然病史、生活质量和结局。
Circulation. 2019 Jul 2;140(1):16-26. doi: 10.1161/CIRCULATIONAHA.118.038169. Epub 2019 May 21.
6
Sex Dimorphism in the Myocardial Response to Aortic Stenosis.主动脉狭窄心肌反应的性别二态性。
JACC Cardiovasc Imaging. 2018 Jul;11(7):962-973. doi: 10.1016/j.jcmg.2017.08.025. Epub 2017 Nov 15.
7
Relation of the Myocardial Contraction Fraction, as Calculated from M-Mode Echocardiography, With Incident Heart Failure, Atherosclerotic Cardiovascular Disease and Mortality (Results from the Cardiovascular Health Study).基于M型超声心动图计算的心肌收缩分数与新发心力衰竭、动脉粥样硬化性心血管疾病及死亡率的关系(心血管健康研究结果)
Am J Cardiol. 2017 Mar 15;119(6):923-928. doi: 10.1016/j.amjcard.2016.11.048. Epub 2016 Dec 18.
8
Multicenter Study of Planar Technetium 99m Pyrophosphate Cardiac Imaging: Predicting Survival for Patients With ATTR Cardiac Amyloidosis.多中心研究 99mTc 焦磷酸盐平面心肌显像术:预测ATTR 心脏淀粉样变性患者的生存率。
JAMA Cardiol. 2016 Nov 1;1(8):880-889. doi: 10.1001/jamacardio.2016.2839.
9
Genotype and Phenotype of Transthyretin Cardiac Amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey).转甲状腺素蛋白心脏淀粉样变性的基因型与表型:THAOS(转甲状腺素蛋白淀粉样变性结局调查)
J Am Coll Cardiol. 2016 Jul 12;68(2):161-72. doi: 10.1016/j.jacc.2016.03.596.
10
Nonbiopsy Diagnosis of Cardiac Transthyretin Amyloidosis.非活检诊断心脏转甲状腺素淀粉样变性。
Circulation. 2016 Jun 14;133(24):2404-12. doi: 10.1161/CIRCULATIONAHA.116.021612. Epub 2016 Apr 22.

由于 Val122lle 突变导致转甲状腺素蛋白心脏淀粉样变的表型存在性别差异:来自无创压力-容积分析的见解。

Sex Differences in the Phenotype of Transthyretin Cardiac Amyloidosis Due to Val122Ile Mutation: Insights from Noninvasive Pressure-Volume Analysis.

机构信息

Division of Cardiology, Department of Medicine, Columbia University College of Physicians and Surgeons, 630 W 168th St, New York, NY 10032.

Cardiovascular Research Foundation, 1700 Broadway, New York, NY 10019.

出版信息

J Card Fail. 2021 Jan;27(1):67-74. doi: 10.1016/j.cardfail.2020.08.007. Epub 2020 Aug 20.

DOI:10.1016/j.cardfail.2020.08.007
PMID:32829019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7869136/
Abstract

BACKGROUND

Transthyretin cardiac amyloidosis (ATTR-CA) is an under-recognized cause of heart failure with preserved ejection fraction. In the United States, the valine-to-isoleucine substitution (Val122Ile) is the most common inherited variant. Data on sex differences in presentation and outcomes of Val122Ile associated ATTR-CA are lacking.

METHODS AND RESULTS

In a retrospective, single-center study of 73 patients diagnosed with Val122Ile associated ATTR-CA between 2001 and 2018, sex differences in clinical and echocardiographic data at the time of diagnosis were evaluated. Pressure-volume analysis using noninvasive single beat techniques was used to compare chamber performance. Compared with men (n = 46), women (n = 27) were significantly older at diagnosis, 76 years vs 69 years; P < .001. The end-systolic pressure-volume relationship, 5.1 mm Hgm/mL vs 4.3 mm Hgm/mL; P = .27, arterial elastance, 5.5 mm Hgm/mL vs 5.7 mm Hgm/mL; P = .62, and left ventricular capacitance were similar between sexes as was pressure-volume areas indexed to a left ventricular end-diastolic pressure of 30 mm Hg, a measure of overall pump function. The 3-year mortality rates were also similar, 34% vs 43%; P = .64.

CONCLUSIONS

Despite being significantly older at time of diagnosis with Val122Ile associated ATTR-CA, women have similar overall cardiac chamber function and rates of mortality to men, suggesting a less aggressive disease trajectory. These findings should be confirmed with longitudinal studies.

摘要

背景

转甲状腺素蛋白心脏淀粉样变(ATTR-CA)是射血分数保留型心力衰竭的一种未被充分认识的病因。在美国,缬氨酸到异亮氨酸的取代(Val122Ile)是最常见的遗传性变异。关于 Val122Ile 相关 ATTR-CA 患者的临床表现和结局的性别差异的数据尚缺乏。

方法和结果

在一项回顾性、单中心研究中,对 2001 年至 2018 年间诊断为 Val122Ile 相关 ATTR-CA 的 73 例患者进行了研究,评估了诊断时临床和超声心动图数据的性别差异。使用非侵入性单次搏动技术进行压力-容积分析,以比较心室功能。与男性(n=46)相比,女性(n=27)的诊断年龄明显更大,分别为 76 岁和 69 岁;P<0.001。女性的收缩末期压力-容积关系为 5.1mmHg·m/mL,男性为 4.3mmHg·m/mL;P=0.27。动脉弹性为 5.5mmHg·m/mL,男性为 5.7mmHg·m/mL;P=0.62。左心室顺应性在性别间相似,左心室舒张末期压力为 30mmHg 时的压力-容积面积也相似,这是整体泵功能的指标。3 年死亡率也相似,分别为 34%和 43%;P=0.64。

结论

尽管 Val122Ile 相关 ATTR-CA 患者在诊断时年龄明显更大,但女性的整体心脏腔室功能和死亡率与男性相似,提示疾病进程较为缓和。这些发现需要通过纵向研究来证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d89/7869136/cb81746da23c/nihms-1623234-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d89/7869136/1de19613976f/nihms-1623234-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d89/7869136/187906e01b76/nihms-1623234-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d89/7869136/cb81746da23c/nihms-1623234-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d89/7869136/1de19613976f/nihms-1623234-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d89/7869136/187906e01b76/nihms-1623234-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d89/7869136/cb81746da23c/nihms-1623234-f0003.jpg