Department of Neurology, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Department of Clinical Pharmacology, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Sci Rep. 2023 Nov 21;13(1):20405. doi: 10.1038/s41598-023-47232-3.
Critical illness polyneuropathy (CIP) is a frequent and underdiagnosed phenomenon among intensive care unit patients. The lipophilic nature of neuronal synapses may result in the association of low serum cholesterol levels with a higher rate of CIP development. We aimed to investigate this issue in critically ill patients. All cases diagnosed with CIP in our tertiary care hospital between 2013 and 2017 were 1:1 matched with controls without the condition by age, sex, and ICD diagnoses. The main risk factors examined were the differences in change between initial and minimum serum total cholesterol levels, and minimum serum total cholesterol levels between matched pairs. Other predictors were serum markers of acute inflammation. We included 67 cases and 67 controls (134 critically ill patients, 49% female, 46% medical). Serum total cholesterol levels decreased more profoundly in cases than controls (median: -74 (IQR -115 to -24) vs. -39 (IQR -82 to -4), median difference: -28, 95% CI [-51, -5]), mg/dl). Minimum serum total cholesterol levels were lower in the cases (median difference: -24, 95% CI [-39, -9], mg/dl). We found significant median differences across matched pairs in maximum serum C-reactive protein (8.9, 95% CI [4.6, 13.2], mg/dl), minimum albumin (-4.2, 95% CI [-6.7, -1.7], g/l), decrease in albumin (-3.9, 95% CI [-7.6, -0.2], g/l), and lowest cholinesterase levels (-0.72, 95% CI [-1.05, -0.39], U/l). Subsequently, more pronounced decreases in serum total cholesterol levels and lower minimum total cholesterol levels during critical care unit hospitalizations may be a risk factor for CIP.
危重病性多发性神经病(CIP)是重症监护病房患者中一种常见且未被充分诊断的现象。神经元突触的亲脂性可能导致血清胆固醇水平较低与 CIP 发展率较高相关。我们旨在调查重症患者中的这一问题。我们医院 2013 年至 2017 年间诊断为 CIP 的所有病例均按年龄、性别和 ICD 诊断与无该疾病的对照组进行 1:1 匹配。检查的主要危险因素是初始和最低血清总胆固醇水平之间变化的差异,以及配对之间的最低血清总胆固醇水平。其他预测因素是急性炎症的血清标志物。我们纳入了 67 例病例和 67 例对照(134 例重症患者,49%为女性,46%为内科)。病例的血清总胆固醇水平下降幅度比对照组更明显(中位数:-74(IQR-115 至-24)vs. -39(IQR-82 至-4),中位数差值:-28,95%CI[-51,-5],mg/dl)。病例的最低血清总胆固醇水平更低(中位数差值:-24,95%CI[-39,-9],mg/dl)。我们发现配对之间最大血清 C 反应蛋白(8.9,95%CI[4.6,13.2],mg/dl)、最低白蛋白(-4.2,95%CI[-6.7,-1.7],g/l)、白蛋白下降(-3.9,95%CI[-7.6,-0.2],g/l)和最低胆碱酯酶水平(-0.72,95%CI[-1.05,-0.39],U/l)均有显著的中位数差异。随后,重症监护病房住院期间血清总胆固醇水平下降更明显且最低总胆固醇水平更低可能是 CIP 的危险因素。