Suppr超能文献

弗里德赖希共济失调患者心脏的形态学和功能特征

Morphologic and functional characteristics of the heart in Friedreich's ataxia.

作者信息

Unverferth D V, Schmidt W R, Baker P B, Wooley C F

出版信息

Am J Med. 1987 Jan;82(1):5-10. doi: 10.1016/0002-9343(87)90369-x.

Abstract

The purpose of this study was to characterize the heart in patients with Friedreich's ataxia by two-dimensional echocardiography, systolic time intervals, and heart biopsy. Ten patients with Friedreich's ataxia (seven females and three males, age 15 +/- 7 years) were compared with 10 age-matched normal subjects (five males and five females, age 16 +/- 7 years). The mean systolic blood pressure in the patients with Friedreich's ataxia was lower (114 +/- 9 mm Hg) than that in the control subjects (122 +/- 8 mm Hg; p less than 0.05); diastolic blood pressures were the same. The heart rate in the patients with Friedreich's ataxia (102 +/- 17 beats/minute) was greater than that in the control subjects (76 +/- 12 beats/minute; p less than 0.001). The interventricular septal wall thickness was much greater in Friedreich's ataxia (13 +/- 2 versus 8 +/- 1 mm, p less than 0.001) as was the posterior wall thickness (13 +/- 3 versus 8 +/- 1 mm, p less than 0.001). The left ventricular end-diastolic diameter was smaller in Friedreich's ataxia (35 +/- 6 mm versus 47 +/- 6 mm; p less than 0.01), and the fractional change of the left ventricular minor axis with systole was greater in Friedreich's ataxia (40 +/- 9 percent versus 33 +/- 5 percent; p less than 0.05). An 11th patient with Friedreich's ataxia (age 33) had clinical heart failure, but his course was complicated by alcohol abuse. Heart biopsy in three patients with Friedreich's ataxia demonstrated myocyte hypertrophy (21.5 +/- 2.0 microns diameter; normal, 14 to 17 microns) and increased fibrosis (16 +/- 9 percent; normal, less than 5 percent). Thus, heart disease in Friedreich's ataxia is characterized by myocyte hypertrophy, interstitial fibrosis, increased left ventricular wall thickness, decreased left ventricular cavity size, sinus tachycardia, and normal systolic function. Further biochemical analysis of tissues may lead to the link of the neurologic and cardiac diseases and eventually to more effective therapy of this condition.

摘要

本研究的目的是通过二维超声心动图、收缩期时间间期和心脏活检来描述弗里德赖希共济失调患者的心脏特征。将10例弗里德赖希共济失调患者(7例女性和3例男性,年龄15±7岁)与10例年龄匹配的正常受试者(5例男性和5例女性,年龄16±7岁)进行比较。弗里德赖希共济失调患者的平均收缩压(114±9mmHg)低于对照组(122±8mmHg;p<0.05);舒张压相同。弗里德赖希共济失调患者的心率(102±17次/分钟)高于对照组(76±12次/分钟;p<0.001)。弗里德赖希共济失调患者的室间隔厚度(13±2对8±1mm,p<0.001)和后壁厚度(13±3对8±1mm,p<0.001)也明显更大。弗里德赖希共济失调患者的左心室舒张末期直径较小(35±6mm对47±6mm;p<0.01),且左心室短轴在收缩期的分数变化在弗里德赖希共济失调患者中更大(40±9%对33±5%;p<0.05)。第11例弗里德赖希共济失调患者(33岁)患有临床心力衰竭,但其病程因酒精滥用而复杂化。3例弗里德赖希共济失调患者的心脏活检显示心肌细胞肥大(直径21.5±2.0微米;正常为14至17微米)和纤维化增加(16±9%;正常小于5%)。因此,弗里德赖希共济失调的心脏病特征为心肌细胞肥大、间质纤维化、左心室壁厚度增加、左心室腔大小减小、窦性心动过速和收缩功能正常。对组织进行进一步的生化分析可能会揭示神经疾病和心脏疾病之间的联系,并最终实现对这种疾病更有效的治疗。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验