Matsubara Yutaka, Matsumoto Takuya, Inoue Kentaro, Matsuda Daisuke, Yoshiga Ryosuke, Yoshiya Keiji, Furuyama Tadashi, Maehara Yoshihiko
Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
J Vasc Surg. 2017 May;65(5):1390-1397. doi: 10.1016/j.jvs.2016.09.030. Epub 2016 Dec 13.
Prognosis is poor for patients with critical limb ischemia (CLI), and the most frequent cause of death is cardiovascular disease. Low grip strength is a risk factor for cardiovascular events, and sarcopenia may be associated as well. Thus, we hypothesized that sarcopenia is a risk factor for cardiovascular events experienced by patients with CLI. If this is true and appropriate therapy becomes available, the prognosis of patients with CLI will improve with appropriate risk management strategies to prevent cardiovascular events. Therefore, the aim of this study was to verify this hypothesis.
We studied 114 patients who underwent revascularization and computed tomography between January 2002 and December 2012 in the Department of Surgery and Sciences at Kyushu University in Japan. Sarcopenia was defined as skeletal muscle area measured by L3-level computed tomography scan <114.0 cm and <89.8 cm for men and women, respectively. Clinical characteristics, cardiovascular event-free survival, <2-year death, causes of death, and effective treatments for sarcopenia were investigated.
We identified 53 (46.5%) patients with sarcopenia. Three-year cardiovascular event-free survival rates were 43.1% and 91.2% for patients with and without sarcopenia, respectively (P < .01). During follow-up, cardiovascular disease caused the deaths of 4 and 15 patients without and with sarcopenia (P < .01), respectively, and in particular, ischemic heart disease caused the deaths of 0 and 5 patients without or with sarcopenia (P < .05), respectively. Single antiplatelet therapy (SAPT; hazard ratio, 0.46; 95% confidence interval, 0.24-0.82; P < .01) and statin therapy (hazard ratio, 0.38; 95% confidence interval, 0.16-0.78; P < .01) were independent factors associated with improved cardiovascular event-free survival. Three-year cardiovascular event-free survival rates for patients with sarcopenia who received SAPT, dual antiplatelet therapies, and no antiplatelet therapy were 75.3%, 21.1%, and 29.5%, respectively (P < .01).
Sarcopenia is a risk factor for worse cardiovascular event-free survival, and SAPT and statin therapy reduced this risk for patients with CLI. Furthermore, SAPT but not dual antiplatelet therapy increased cardiovascular event-free survival in patients with sarcopenia.
严重肢体缺血(CLI)患者预后较差,最常见的死亡原因是心血管疾病。握力低是心血管事件的一个危险因素,肌肉减少症可能也与之相关。因此,我们假设肌肉减少症是CLI患者发生心血管事件的一个危险因素。如果这一假设成立且有合适的治疗方法,那么通过适当的风险管理策略预防心血管事件,CLI患者的预后将会改善。因此,本研究的目的是验证这一假设。
我们研究了2002年1月至2012年12月期间在日本九州大学外科学部接受血管重建术和计算机断层扫描的114例患者。肌肉减少症的定义为:通过L3水平计算机断层扫描测量的骨骼肌面积,男性<114.0平方厘米,女性<89.8平方厘米。研究了患者的临床特征、无心血管事件生存期、2年内死亡情况、死亡原因以及肌肉减少症的有效治疗方法。
我们确定了53例(46.5%)肌肉减少症患者。有和没有肌肉减少症的患者3年无心血管事件生存率分别为43.1%和91.2%(P<.01)。在随访期间,心血管疾病分别导致4例无肌肉减少症患者和15例有肌肉减少症患者死亡(P<.01),特别是缺血性心脏病分别导致0例无肌肉减少症患者和5例有肌肉减少症患者死亡(P<.05)。单一抗血小板治疗(SAPT;风险比,0.46;95%置信区间,0.24 - 0.82;P<.01)和他汀类药物治疗(风险比,0.38;95%置信区间,0.16 - 0.78;P<.01)是与改善无心血管事件生存期相关的独立因素。接受SAPT、双联抗血小板治疗和未接受抗血小板治疗且患有肌肉减少症的患者3年无心血管事件生存率分别为75.3%、21.1%和29.5%(P<.01)。
肌肉减少症是无心血管事件生存期较差的一个危险因素,SAPT和他汀类药物治疗降低了CLI患者的这一风险。此外,SAPT而非双联抗血小板治疗提高了肌肉减少症患者的无心血管事件生存期。