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血管紧张素转换酶(ACE)基因的I等位基因与患有麦卡德尔病的女性运动能力的改善有关。

The I allele of the ACE gene is associated with improved exercise capacity in women with McArdle disease.

作者信息

Gómez-Gallego F, Santiago C, Morán M, Pérez M, Maté-Muñoz J L, del Valle M Fernández, Rubio J C, Garcia-Consuegra I, Foster C, Andreu I A L, Martín M A, Arenas J, Lucia A

机构信息

Universidad Europea de Madrid, Madrid, Spain.

出版信息

Br J Sports Med. 2008 Feb;42(2):134-40. doi: 10.1136/bjsm.2007.038992. Epub 2007 Jul 6.

Abstract

BACKGROUND

McArdle disease is an uncommon metabolic disorder usually characterized by marked exercise intolerance although great individual variability exists in its phenotypic manifestation.

OBJECTIVE

The purpose of this study was to determine the association between angiotensin-converting enzyme (ACE) genotypes and indices of exercise capacity (peak oxygen uptake (VO(2)peak), ventilatory threshold (VT) and gross mechanical efficiency (GE)) in patients with McArdle disease. Based on previous research, it was hypothesized that the I allele might favourably influence exercise capacity.

METHODS

Forty-four Spanish patients (23 males, 21 females) and 44 age-matched and gender-matched controls (23 males, 21 females) performed a graded cycle-ergometer test until exhaustion (for VO(2)peak and VT determination) and a 12 min constant-load test at the power output eliciting the VT (for GE determination).

RESULTS

No significant difference (p>0.05) was found in indices of exercise capacity between ID + II genotypes and DD homozygotes in the group of male patients, male controls and female controls. However, in the group of female patients, the ID + II group (n = 11) had a higher VO(2)peak than DD homozygotes (n = 10) (15.8 (SEM 1.6) ml/kg/min versus 11.9 (SEM 0.9) ml/kg/min, respectively; p<0.05).

CONCLUSIONS

The I allele of the ACE gene is associated with a higher functional capacity in female patients, and might partly explain the individual variability in the phenotypic manifestation of McArdle disease.

摘要

背景

麦克尔迪氏病是一种罕见的代谢紊乱疾病,通常表现为明显的运动不耐受,尽管其表型表现存在很大的个体差异。

目的

本研究旨在确定麦克尔迪氏病患者血管紧张素转换酶(ACE)基因型与运动能力指标(峰值摄氧量(VO₂峰值)、通气阈值(VT)和总机械效率(GE))之间的关联。基于先前的研究,推测I等位基因可能对运动能力有有利影响。

方法

44名西班牙患者(23名男性,21名女性)和44名年龄及性别匹配的对照者(23名男性,21名女性)进行了分级自行车测力计测试直至力竭(用于测定VO₂峰值和VT),并在引发VT的功率输出下进行了12分钟的恒定负荷测试(用于测定GE)。

结果

在男性患者组、男性对照组和女性对照组中,ID + II基因型与DD纯合子之间的运动能力指标无显著差异(p>0.05)。然而,在女性患者组中,ID + II组(n = 11)的VO₂峰值高于DD纯合子组(n = 10)(分别为15.8(标准误1.6)ml/kg/min和11.9(标准误0.9)ml/kg/min;p<0.05)。

结论

ACE基因的I等位基因与女性患者较高的功能能力相关,可能部分解释了麦克尔迪氏病表型表现的个体差异。

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