Department of Emergency Medicine, University of Mississippi Medical Center, Jackson, Mississippi.
Michigan Regional Comprehensive Metabolomics Resource Core (MRC).
Shock. 2018 Apr;49(4):412-419. doi: 10.1097/SHK.0000000000000997.
Sepsis-induced metabolic disturbances include hyperlactatemia, disruption of glycolysis, protein catabolism, and altered fatty acid metabolism. It may also lower serum L-carnitine that supports the use of L-carnitine supplementation as a treatment to ameliorate several of these metabolic consequences.
To further understand the association between L-carnitine-induced changes in serum acylcarnitines, fatty acid metabolism and survival, serum samples from (T0), 12 hfollowing completion (T24) of L-carnitine (n = 16) or placebo (n = 15) administration, and 48 h (T48) after enrollment from patients with septic shock enrolled in a randomized control trial were assayed for acylcarnitines, free fatty acids, and insulin. Data were analyzed comparing 1-year survivors and nonsurvivors within treatment groups.
Mortality was 8 of 16 (50%) and 12 of 15 (80%) at 1 year for L-carnitine and placebo-treated patients, respectively. Free carnitine, C2, C3, and C8 acylcarnitines were higher among nonsurvivors at enrollment. L-Carnitine treatment increased levels of all measured acylcarnitines; an effect that was sustained for at least 36 h following completion of the infusion and was more prominent among nonsurvivors. Several fatty acids followed a similar, though less consistent pattern. Glucose, lactate, and insulin levels did not differ based on survival or treatment arm.
In human patients with septic shock, L-Carnitine supplementation increases a broad range of acylcarnitine concentrations that persist after cessation of infusion, demonstrating both immediate and sustained effects on the serum metabolome. Nonsurvivors demonstrate a distinct metabolic response to L-carnitine compared with survivors, which may indicate preexisting or more profound metabolic derangement that constrains any beneficial response to treatment.
脓毒症引起的代谢紊乱包括高乳酸血症、糖酵解、蛋白质分解和脂肪酸代谢紊乱。它还可能降低血清肉毒碱,支持使用肉毒碱补充剂作为治疗方法来改善其中一些代谢后果。
为了进一步了解血清酰基肉碱、脂肪酸代谢和存活率之间的关联,对接受随机对照试验的脓毒性休克患者在完成肉毒碱(n=16)或安慰剂(n=15)治疗后 12 小时(T24)和入组后 48 小时(T48)的血清样本进行了酰基肉碱、游离脂肪酸和胰岛素的测定。对各组内的 1 年幸存者和非幸存者进行了分析比较。
在接受肉毒碱和安慰剂治疗的患者中,1 年死亡率分别为 16 例中的 8 例(50%)和 15 例中的 12 例(80%)。非幸存者在入组时的游离肉碱、C2、C3 和 C8 酰基肉碱水平较高。肉毒碱治疗增加了所有测量的酰基肉碱的水平;这种作用在输注结束后至少持续 36 小时,在非幸存者中更为明显。几种脂肪酸也呈现出类似的、但不太一致的模式。葡萄糖、乳酸和胰岛素水平不受存活率或治疗组的影响。
在患有脓毒性休克的人类患者中,肉毒碱补充剂增加了广泛的酰基肉碱浓度,在停止输注后仍持续存在,这表明对血清代谢组有立即和持续的影响。与幸存者相比,非幸存者对肉毒碱的代谢反应明显不同,这可能表明存在预先存在的或更严重的代谢紊乱,限制了任何有益的治疗反应。