肥胖妇女的心血管自律神经和外周感觉神经病变

Nóra Keller, János Zádori, Balázs Lippai, Dalma Szöllősi, Virág Márton, Károly Wellinger, Szilvia Lada, Mónika Szűcs, Adrienn Menyhárt, P. Kempler, István Baczkó, Tamás T. Várkonyi, Cs Lengyel, Anna Vágvölgyi
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引用次数: 0

摘要

肥胖症患者的神经功能障碍发生率较高。我们确定了肥胖女性神经病变的发病率,并评估了这些病变与人体测量和实验室参数之间的潜在联系。在横断面研究中,我们招募了肥胖症女性患者和未接受肥胖症治疗的糖尿病患者。在这项横断面研究中,我们招募了肥胖症女性患者和未接受肥胖症治疗的糖尿病女性患者,并以身体质量指数(BMI)正常的女性受试者作为对照组。自律神经功能通过尤因心血管反射测试进行评估,而外周神经病理性综合评估则通过 Neurometer®、Tiptherm®、Monofilament® 和 Rydel-Seiffer 音叉测试进行。须弥运动功能通过 Neuropad® 测试进行评估。71 名患者(平均值 ± SD;年龄:36.1 ± 8.3 岁;体重指数:40.2 ± 8.5 kg/m2)和 36 名对照组患者(年龄:36.4 ± 13.3 岁;体重指数:21.6 ± 2.1 kg/m2)参加了身体成分检测。与对照组相比,患者的收缩压(患者对对照组;137.5 ± 16.9 对 114.6 ± 14.8 mmHg,p<0.001)和舒张压(83.0 ± 11.7 对 69.8 ± 11.2 mmHg,p<0.001)明显较高。在自律神经测试中,只有对瓦尔萨尔瓦手法的心率反应(瓦尔萨尔瓦比值)显示患者的自律神经功能明显受损(1.4 ± 0.2 vs. 1.7 ± 0.4,p<0.001)。正中神经的 Neurometer® 显示,在所有刺激频率下,患者的电流感知阈值(CPT)均有所提高(2000 Hz 时的 CPT 值为 204.6 ± 70.9,而 2000 Hz 时的 CPT 值为 204.6 ± 70.9):204.6 ± 70.9 vs. 168.1 ± 66.9,p=0.013;250 Hz:84.4 ± 38.9 vs. 56.5 ± 34.8,p<0.001;5 Hz 时的 CPT:58.5 ± 31.2 vs. 56.5 ± 34.8,p<0.001:58.5 ± 31.2 vs 36.9 ± 29.1,p<0.001)。Rydel-Seiffer音叉测试显示,患者下肢的振动感应能力明显受损(右侧拇指:6.8 ± 0.9 vs. 7.4 ± 0.8,p=0.030;左侧拇指:6.9 ± 0.8 vs. 7.3 ± 0.9,p=0.029)。Neuropad® 测试表明,肥胖女性的臀部运动功能明显受损。肥胖症患者的体重指数与 25- 羟基-D3/D2-维生素水平呈负相关(r=-0.41,p=0.00126),体重指数与静息收缩压呈正相关(r=0.26,p=0.0325)。这些患者的瓦尔萨尔瓦比率也显示出心血管自律神经功能失调,表明存在副交感神经功能障碍。体重指数与 25- 羟基-D3/D2-维生素之间的负相关突出表明,肥胖症患者可能缺乏维生素 D。
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Cardiovascular autonomic and peripheral sensory neuropathy in women with obesity
A higher incidence of neural dysfunction in people with obesity has been described. We determined the prevalence of neuropathic lesions in obese women and evaluated their potential association with anthropometric and laboratory parameters.In our cross-sectional study, we enrolled female patients with obesity and without diabetes before obesity treatment. Voluntary female subjects were controls with a normal body mass index (BMI). Autonomic function was assessed by Ewing’s cardiovascular reflex tests, while comprehensive peripheral neuropathic assessments were conducted utilizing the Neurometer®, Tiptherm®, Monofilament®, and Rydel-Seiffer tuning fork tests. Sudomotor function was assessed by the Neuropad®-test. Body composition was examined using the InBody 770.71 patients (mean ± SD; age: 36.1 ± 8.3 years; BMI: 40.2 ± 8.5 kg/m2) and 36 controls (age: 36.4 ± 13.3 years; BMI: 21.6 ± 2.1 kg/m2) were enrolled. Patients had significantly higher systolic (patients vs. controls; 137.5 ± 16.9 vs. 114.6 ± 14.8 mmHg, p<0.001) and diastolic (83.0 ± 11.7 vs.69.8 ± 11.2 mmHg, p<0.001) blood pressure compared to controls. Among autonomic tests, only the heart rate response to Valsalva maneuver (Valsalva-ratio) revealed significant impairment in patients (1.4 ± 0.2 vs. 1.7 ± 0.4, p<0.001). Neurometer® at the median nerve revealed increased current perception threshold (CPT) values at all stimulating frequencies in patients (CPT at 2000 Hz: 204.6 ± 70.9 vs. 168.1 ± 66.9, p=0.013; 250 Hz: 84.4 ± 38.9 vs. 56.5 ± 34.8, p<0.001; CPT at 5 Hz: 58.5 ± 31.2 vs 36.9 ± 29.1, p<0.001). The Rydel-Seiffer tuning fork test has revealed a significant impairment of vibrational sensing on the lower limb in patients (right hallux: 6.8 ± 0.9 vs. 7.4 ± 0.8, p=0.030; left hallux: 6.9 ± 0.8 vs. 7.3 ± 0.9, p=0.029). The Neuropad® testing showed a significant impairment of sudomotor function in women with obesity. A negative correlation was found in patients between BMI and the 25-hydroxy-D3/D2-vitamin levels (r=-0.41, p=0.00126) and a positive correlation between the BMI and resting systolic blood pressure (r=0.26, p=0.0325).Peripheral sensory neuronal and sudomotor function impairments were detected in female patients with obesity compared to the controls with normal BMI. Cardiovascular autonomic dysfunction was also revealed by the Valsalva-ratio in these patients, suggesting the presence of parasympathetic dysfunction. The negative correlation between BMI and the 25-hydroxy-D3/D2-vitamin highlights the potential deficiency of vitamin D in the population affected by obesity.
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