Abbaszadeh Fatemeh, Azizi Samaneh, Mobasseri Majid, Ebrahimi-Mameghani Mehrangiz
Student Research Committee, School of Nutrition and Food Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.
Endocrine Research Center, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Diabetol Metab Syndr. 2021 May 5;13(1):52. doi: 10.1186/s13098-021-00669-w.
This study aimed to examine the effects of L-citrulline (l-CIT) on low-grade inflammation (meta-inflammation) and insulin sensitivity in type 2 diabetes (T2D) patients since it has exhibited hypoglycemic and anti-inflammatory effects in most animal studies.
In this double-blind, placebo-controlled randomized clinical trial, 54 patients with T2D referred to specialized clinics of Tabriz University of Medical Sciences were assigned to L-CIT group (receiving orally one 3 g sachet of L-CIT daily before breakfast) or placebo group (receiving orally one 3 g sachet of microcrystalline cellulose daily before breakfast) for eight weeks. Serum levels of fasting blood glucose, hemoglobin A1c (HbA1c), CIT, monocyte chemoattractant protein 1 (MCP-1), interleukin-6 (IL-6), and toll-like receptor 4 (TLR-4) were determined. The quantitative insulin sensitivity check index (QUICKI) and homeostatic model assessment of β-cell function (HOMA-B) index were estimated at the baseline and post-intervention.
No significant difference was observed between the studied parameters at the baseline. L-CIT supplementation significantly reduced not only serum concentrations of fasting blood glucose but also HbA1c, serum IL-6 and TLR-4 levels in the L-CIT group (p < 0.05). Additionally, at the end of the study serum levels of CIT increased significantly in L-CIT group compared to the baseline and placebo group. Fasting blood glucose concentrations and HbA1c significantly decreased after the intervention compared to the placebo. There was no significant difference in serum IL-6, TLR-4, MCP-1 levels, as well as QUICKI and HOMA-B index between the two groups, even after adjusting for baseline variables and confounders.
Our findings revealed that, although L-CIT supplementation significantly reduced fasting blood glucose concentrations, HbA1c and increased serum levels of CIT. It seems it could not significantly improve insulin sensitivity and meta-inflammation biomarkers. Additional studies with longer duration and different doses of L-CIT are required. Trial registration The protocol of this clinical trial is registered at the Iranian Registry of Clinical Trials (registration no: IRCT20100209003320N16 at www.irct.ir ).
本研究旨在探讨L-瓜氨酸(L-CIT)对2型糖尿病(T2D)患者低度炎症(亚炎症)和胰岛素敏感性的影响,因为在大多数动物研究中它已显示出降血糖和抗炎作用。
在这项双盲、安慰剂对照的随机临床试验中,54名转诊至大不里士医科大学专科诊所的T2D患者被分为L-CIT组(早餐前每天口服1袋3克L-CIT)或安慰剂组(早餐前每天口服1袋3克微晶纤维素),为期8周。测定空腹血糖、糖化血红蛋白(HbA1c)、瓜氨酸(CIT)、单核细胞趋化蛋白1(MCP-1)、白细胞介素-6(IL-6)和Toll样受体4(TLR-4)的血清水平。在基线和干预后评估定量胰岛素敏感性检查指数(QUICKI)和β细胞功能的稳态模型评估(HOMA-B)指数。
在基线时,所研究的参数之间未观察到显著差异。补充L-CIT不仅显著降低了L-CIT组的空腹血糖血清浓度,还降低了HbA1c、血清IL-6和TLR-4水平(p < 0.05)。此外,在研究结束时,与基线和安慰剂组相比,L-CIT组的CIT血清水平显著升高。与安慰剂相比,干预后空腹血糖浓度和HbA1c显著降低。即使在调整基线变量和混杂因素后,两组之间的血清IL-6、TLR-4、MCP-1水平以及QUICKI和HOMA-B指数也没有显著差异。
我们的研究结果表明,虽然补充L-CIT显著降低了空腹血糖浓度、HbA1c并提高了CIT血清水平。但似乎它不能显著改善胰岛素敏感性和亚炎症生物标志物。需要进行更长时间和不同剂量L-CIT的进一步研究。试验注册 本临床试验方案已在伊朗临床试验注册中心注册(注册号:www.irct.ir上的IRCT20100209003320N16)。