Butt Nazish, Masood Muhammad, Ali Aamir
Department of Gastroenterology, Jinnah Postgraduate Medical Centre, Karachi, Pakistan.
Euroasian J Hepatogastroenterol. 2023 Jul-Dec;13(2):124-127. doi: 10.5005/jp-journals-10018-1397.
The primary objectives of this study include evaluating changes in lipid profile and liver enzyme levels in nonalcoholic fatty liver disease (NAFLD) patients receiving and choline supplementation (Revolic).
Two-hundred patients were recruited from the hepatology outpatient department of a public hospital between January and June 2023. Patients who had confirmed diagnosis of NAFLD, proven with ultrasound (US) followed by biopsy or US alone with age >18 years were included in this study. The study variables were fasting blood sugar, cholesterol levels, low-density lipoprotein (LDL), triglyceride, alanine aminotransferase (ALT), aspartate aminotransferase (AST) and gamma-glutamyl transferase levels (GGT). All investigations were conducted and compared between baseline, 12 and 24 weeks following treatment.
The mean age of all participants was 40.49 ± 10.59 years with 34 males and 166 females. The mean cholesterol levels were reduced to 179.86 ± 35.63 mg/dL from the mean baseline of 197.57 ± 42.52 mg/dL ( = 0.001). There was also a statistically significant difference found between baseline and posttreatment levels of LDL and triglyceride ( < 0.001). The ATL levels were also reduced from baseline 44.91 ± 32.40 U/L to 44.25 ± 30.66 and 41.06 ± 22.15 U/L between 12 and 24 weeks after treatment respectively. There was a statistically significant reduction in ATL, AST, and GGT levels from baseline with -value < 0.001.
The combination of and choline (Revolic) gives promising results with a significant reduction in lipid profile and liver enzymes.
The combination of and choline can be considered a reliable option for the management of NAFLD due to its efficacy and safety at 24 weeks after treatment as evident in the present study.
Butt N, Masood M, Ali A. Efficacy and Safety of and Choline in Patients with Nonalcoholic Fatty Liver Disease. Euroasian J Hepato-Gastroenterol 2023;13(2):124-127.
本研究的主要目标包括评估接受[具体物质]和胆碱补充剂(Revolic)的非酒精性脂肪性肝病(NAFLD)患者的血脂谱和肝酶水平变化。
2023年1月至6月期间,从一家公立医院的肝病门诊招募了200名患者。本研究纳入了经超声(US)确诊为NAFLD且年龄>18岁的患者,确诊方法为超声检查后活检或仅通过超声检查。研究变量包括空腹血糖、胆固醇水平、低密度脂蛋白(LDL)、甘油三酯、丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)和γ-谷氨酰转移酶水平(GGT)。在治疗后的基线、12周和24周进行了所有检查并进行比较。
所有参与者的平均年龄为40.49±10.59岁,其中男性34名,女性166名。平均胆固醇水平从基线时的197.57±42.52mg/dL降至179.86±35.63mg/dL(P = 0.001)。LDL和甘油三酯的基线水平与治疗后水平之间也存在统计学显著差异(P < 0.001)。治疗后12周和24周时,ALT水平也分别从基线时的44.91±32.40U/L降至44.25±30.66U/L和41.06±22.15U/L。ALT、AST和GGT水平较基线有统计学显著降低,P值<0.001。
[具体物质]和胆碱(Revolic)的组合产生了有前景的结果,血脂谱和肝酶水平显著降低。
鉴于本研究中治疗24周后的疗效和安全性,[具体物质]和胆碱的组合可被视为管理NAFLD的可靠选择。
Butt N, Masood M, Ali A. [具体物质]和胆碱在非酒精性脂肪性肝病患者中的疗效和安全性。《欧亚肝脏胃肠病学杂志》2023;13(2):124 - 127。