Xu Yujing, Liang Yuxin, Kim Jung Eun
Department of Food Science and Technology, National University of Singapore, Singapore 117543, Singapore.
Bezos Centre for Sustainable Protein, National University of Singapore, Singapore 117542, Singapore.
Nutrients. 2025 Aug 31;17(17):2840. doi: 10.3390/nu17172840.
: Arabinoxylan (AX) has shown potential benefits in glycemic control; however, findings remain inconclusive. This systematic review and meta-analysis aimed to assess the impact of AX intake on glycemic control in preclinical and clinical studies. : A database search was conducted in PubMed, Embase, Cochrane Library, and CINAHL. A total of 133 studies were included for systematic review and extracted data from 46 clinical studies and 25 preclinical studies were further analyzed for meta-analysis. : The AX consumption improved overall postprandial glycemic control in clinical studies, as evidenced by reductions in glucose iAUC (SMD: -0.41; 95% CI: [-0.57, -0.25]), insulin iAUC (SMD: -0.28; 95% CI: [-0.44, -0.12]), glucose iPeak (SMD: -0.52; 95% CI: [-0.80, -0.25]), and insulin iPeak (SMD: -0.24; 95% CI: [-0.41, -0.06]) compared to the control. For chronic glycemic control, fasting glucose (Hedges' g: -1.18; 95% CI: [-1.56, -0.80]), insulin (Hedges' g: -1.07; 95% CI: [-1.92, -0.23]), HbA1c (Hedges' g: -2.93; 95% CI: [-5.48, -0.38]), and HOMA-IR (Hedges' g: -2.44; 95% CI: [-3.66, -1.22]) reduced in preclinical studies, while improvements were limited to fasting glucose (MD: -0.10; 95% CI: [-0.16, -0.03]) in clinical studies. Subgroup analyses revealed that AX exerted a greater glycemic-lowering effect in metabolically impaired animals and individuals compared to healthy counterparts. Furthermore, extracted AX was found to be more effective than intrinsic AX in optimizing glycemic control. : The consumption of AX improves glycemic control, particularly in metabolically impaired animals and human participants. Moreover, the benefit appears more pronounced with extract AX interventions.
阿拉伯木聚糖(AX)已显示出在血糖控制方面的潜在益处;然而,研究结果仍无定论。本系统评价和荟萃分析旨在评估临床前和临床研究中AX摄入对血糖控制的影响。:在PubMed、Embase、Cochrane图书馆和CINAHL中进行数据库检索。共纳入133项研究进行系统评价,并从46项临床研究中提取数据,对25项临床前研究的数据进行进一步分析以进行荟萃分析。:在临床研究中,AX的摄入改善了总体餐后血糖控制,与对照组相比,葡萄糖增量曲线下面积(SMD:-0.41;95%CI:[-0.57,-0.25])、胰岛素增量曲线下面积(SMD:-0.28;95%CI:[-0.44,-0.12])、葡萄糖峰值增量(SMD:-0.52;95%CI:[-0.80,-0.25])和胰岛素峰值增量(SMD:-0.24;95%CI:[-0.41,-0.06])均有所降低。对于慢性血糖控制,临床前研究中空腹血糖(Hedges'g:-1.18;95%CI:[-1.56,-0.80])、胰岛素(Hedges'g:-1.07;95%CI:[-1.92,-0.23])、糖化血红蛋白(Hedges'g:-2.93;95%CI:[-5.48,-0.38])和胰岛素抵抗指数(Hedges'g:-2.44;95%CI:[-3.66,-1.22])降低,而临床研究中改善仅限于空腹血糖(MD:-0.10;95%CI:[-0.16,-0.03])。亚组分析显示,与健康动物和个体相比,AX在代谢受损的动物和个体中具有更大的降糖作用。此外,发现提取的AX在优化血糖控制方面比内源性AX更有效。:AX的摄入改善了血糖控制,特别是在代谢受损的动物和人类参与者中。此外,提取物AX干预的益处似乎更为明显。