妇科癌症患者的神经肌肉失调与恶病质的关系

Rizwan Qaisar , Shah Hussain , Asima Karim , Firdos Ahmad
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摘要

目的 人们对神经肌肉接头(NMJ)退化导致癌症患者肌肉萎缩的潜在原因仍然知之甚少。我们招募了患有子宫内膜癌(37 人,56-73 岁)或卵巢癌(40 人,55-72 岁)的女性患者以及年龄匹配的对照组(47 人,55-71 岁),根据是否存在与年龄相关的肌肉损失(称为肌肉疏松症)分为两个亚组。我们测量了血浆 c-端 Agrin-fragment-32(CAF22;NMJ 缺失的生物标志物)、神经丝蛋白轻链(NF-L;神经退行性变的生物标志物)、手握力(HGS)、附着骨骼肌质量指数(AMMI)和短期体能测试(SPPB;体能的标志物)。结果与对照组相比,子宫内膜癌或卵巢癌患者的 HGS、AMMI 和 SPPB 水平较低,血浆 NF-L 水平较高(所有 p 均为 0.05)。我们发现卵巢癌患者的血浆 CAF22 水平略有升高,而子宫内膜癌患者则没有。肌肉疏松症与血浆 NF-L 水平的进一步升高有关,但与 CAF22 水平无关。总而言之,NMJ退化可能对妇科癌症患者的肌肉损失和肌肉疏松症有一定的影响。应对癌症患者肌肉流失的策略可能是针对骨骼肌内与 NMJ 无关的内在变化。
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Association of neuromuscular disjunction with cachexia in patients with gynecological cancers

Purpose

The potential contributions of neuromuscular junction (NMJ) degradation to muscle loss in cancer remain poorly understood. We investigated the biomarkers of NMJ loss to muscle decline in patients with gynecological carcinomas.

Methods

We recruited women with endometrial (n = 37, 56–73 years old) or ovarian (n = 40, 55–72 years old) carcinomas along with age-matched controls (n = 47, 55–71 years old) controls, divided into two subgroups based on the presence of age-associated muscle loss, termed sarcopenia. We measured plasma c-terminal agrin-fragment-32 (CAF22; biomarker of NMJ loss), neurofilament light chain (NF-L; biomarker of neurodegeneration), handgrip strength (HGS), appendicular skeletal muscle mass index (AMMI), and short physical performance battery (SPPB; marker of physical capacity).

Results

Patients with endometrial or ovarian carcinomas exhibits low HGS, AMMI, and SPPB along with higher plasma NF-L levels than in controls (all p < 0.05). We found a modest elevation of plasma CAF22 levels in ovarian but not in endometrial carcinomas. The presence of sarcopenia was associated with further elevation of plasma NF-L but not CAF22 levels. Higher carcinoma stages were associated with higher plasma CAF22 in endometrial carcinoma and higher NF-L levels in both groups of carcinoma patients.

Conclusion

Collectively, NMJ degradation may have a modest contribution to muscle loss and sarcopenia in gynecological carcinomas. The strategies to counter muscle loss in carcinomas may target intrinsic changes within skeletal muscle independent of NMJ.

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