ACE I/D and AGT Met235Thr Polymorphisms Distinctly Affect Biomarker Levels and Risk of AKI and Exertional Rhabdomyolysis After Intense Exercise.

IF 1.1 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Military Medicine Pub Date : 2025-09-01 DOI:10.1093/milmed/usaf041
Ayexa Cruz, Diego Gomes, Cintia Verdan, Jessica Branquinho, Michele Xavier, Gianna Kirsztajn, Caleb Guedes Miranda Dos Santos, João Bosco Pesquero, Andreia Carneiro
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Abstract

Introduction: Exertional rhabdomyolysis (ER) is one of the severe complications attributable to prolonged and repeated muscle exercises and is most commonly seen in military personnel and elite athletes. In military personnel, ER usually results from the long and strenuous nature of military training and may sometimes result in severe outcomes, such as acute kidney injury (AKI) and cardiac arrhythmias. Besides, muscle tissue injuries impair physical function, decreasing strength and flexibility and delaying muscle soreness and inflammation. The existing literature has studied genetic polymorphisms related to the renin-angiotensin-aldosterone system, such as AGT*Met235Thr (rs699) and ACE I/D (rs1799752), and clinical chemistry-related markers about their influence on athletic performance and injury prevention from exercise-induced trauma. The present study aimed to evaluate the association between the ACE (rs1799752) and AGT (rs699) gene polymorphisms and the increased susceptibility to exertional rhabdomyolysis risk (ERR) and AKI induced by strenuous exercise in military personnel.

Materials and methods: Sixty-four male volunteers from the Brazilian Marine Corps who were sent on the Sandstorm mission in 2017, 2018, 2019, and 2022 were enrolled in the study. Blood and urine samples were collected from the participants before and immediately after the mission.

Results: After physical exercise, 54 of 64 individuals (84%) were positive for ER. Of these, 13 participants (24%) were positive for AKI, representing 20% of the whole group. AKI was more frequent in T allele carriers, as 13 of 14 positive findings belonged to the MT + TT group, while only one case occurred in MM (approaching significance at P = .063). A significant postexercise increase in serum creatinine (CRE) levels was observed for carriers of I (II + ID) and T (MT + TT) alleles (P = .008 and P = .028, respectively), with a significantly higher ΔCRE in the (II + ID) group compared to the DD group (P = .001).

Conclusion: These findings suggest that the ACE I/D and AGT M235T polymorphisms might be related to an increased risk for AKI following intensive, mixed-type exercise in military personnel.

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ACE I/D和AGT Met235Thr多态性明显影响高强度运动后AKI和劳损性横纹肌溶解的生物标志物水平和风险。
简介:劳损性横纹肌溶解(ER)是由于长时间和反复的肌肉锻炼引起的严重并发症之一,最常见于军事人员和优秀运动员。在军事人员中,ER通常是由于长期和艰苦的军事训练造成的,有时可能导致严重的后果,如急性肾损伤(AKI)和心律失常。此外,肌肉组织损伤会损害身体功能,降低力量和柔韧性,延缓肌肉酸痛和炎症。已有文献研究了肾素-血管紧张素-醛固酮系统相关的遗传多态性,如AGT*Met235Thr (rs699)和ACE I/D (rs1799752),以及临床化学相关标志物对运动表现和运动损伤预防的影响。本研究旨在评估ACE (rs1799752)和AGT (rs699)基因多态性与军事人员剧烈运动诱导的劳损性横纹肌溶解风险(ERR)和AKI易感性增加之间的关系。材料和方法:来自巴西海军陆战队的64名男性志愿者参加了这项研究,他们分别于2017年、2018年、2019年和2022年被派往沙尘暴任务。在执行任务之前和之后,从参与者身上收集了血液和尿液样本。结果:体育锻炼后,64例患者中有54例(84%)ER阳性。其中,13名参与者(24%)为AKI阳性,占整个组的20%。AKI在T等位基因携带者中更为常见,因为14例阳性结果中有13例属于MT + TT组,而MM仅发生1例(P = 0.063接近显著性)。I (II + ID)和T (MT + TT)等位基因携带者运动后血清肌酐(CRE)水平显著升高(P =。008, P =。(II + ID)组的ΔCRE明显高于DD组(P = .001)。结论:这些研究结果表明,ACE I/D和AGT M235T多态性可能与军事人员密集、混合类型运动后AKI风险增加有关。
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来源期刊
Military Medicine
Military Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
2.20
自引率
8.30%
发文量
393
审稿时长
4-8 weeks
期刊介绍: Military Medicine is the official international journal of AMSUS. Articles published in the journal are peer-reviewed scientific papers, case reports, and editorials. The journal also publishes letters to the editor. The objective of the journal is to promote awareness of federal medicine by providing a forum for responsible discussion of common ideas and problems relevant to federal healthcare. Its mission is: To increase healthcare education by providing scientific and other information to its readers; to facilitate communication; and to offer a prestige publication for members’ writings.
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