Department of Internal Medicine, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
Department of Internal Medicine, All India Institute of Medical Sciences, Bathinda Punjab, India.
Indian J Pharmacol. 2024 Jan 1;56(1):4-9. doi: 10.4103/ijp.ijp_555_23. Epub 2024 Mar 8.
Gastrointestinal neuropathies are frequently found in diabetic patients.
The aim of this study was to find out the safety, adverse reactions, and long-term effectiveness of Pistacia lentiscus plant extract (mastic gum) in diabetic gastroparesis (DG) with respect to sustainable improvement in gastroparesis symptoms (Gastrointestinal Cardinal Symptom Index [GCSI] score) by observational follow-up study of a single-centric double-blind noninferiority randomized control trial.
Thirty-eight individuals were recruited and equally randomized in two study groups based on GCSI score and TC99 radionuclide gastric emptying scintigraphy (GES), i.e. the mastic gum group and the levosulpiride group. After 24 weeks, the GCSI score was recalculated in both the groups, and patients were evaluated for the safety, adverse reactions, and long-term effectiveness of mastic gum and the standard drug levosulpiride.
In the extended study, mean GCSI score changes at 24 weeks were statistically significant (P < 0.001) (t-test) between the two groups. In the mastic gum arm, the change in mean GCSI score at 24 weeks was statistically nonsignificant mean ± (standard deviation [SD]) 16.7± (3.81) compared to the GCSI score at 2-month postintervention mean (SD) 16.35± (2.27) (intragroup P = 0.89) (repeated measures ANOVA). It strongly indicates that mastic gum provided a sustainable improvement in DG symptoms in comparison to levosulpiride, with excellent subjective well-being postintervention, without any obvious significant adverse effects.
Six-month (24-week) interim analysis of patients suggests that mastic gum gives a sustainable improvement in DG symptoms without any obvious adverse effects as compared to levosulpiride.
胃肠道神经病变在糖尿病患者中经常发现。
本研究旨在通过观察性随访单中心双盲非劣效随机对照试验,发现乳香黄连木植物提取物(乳香胶)治疗糖尿病胃轻瘫(DG)的安全性、不良反应和长期疗效,以持续改善胃轻瘫症状(胃肠道主要症状指数[GCSI]评分)。
根据 GCSI 评分和 TC99 放射性核素胃排空闪烁扫描(GES),将 38 名患者招募并平均随机分为两组,即乳香胶组和左旋舒必利组。24 周后,两组均重新计算 GCSI 评分,并评估乳香胶和标准药物左旋舒必利的安全性、不良反应和长期疗效。
在扩展研究中,两组间 24 周时 GCSI 评分的平均变化具有统计学意义(P < 0.001)(t 检验)。在乳香胶组中,24 周时 GCSI 评分的平均变化在统计学上无显著意义,均值±(标准差[SD])为 16.7±(3.81),与干预后 2 个月的 GCSI 评分均值(SD)16.35±(2.27)相比(组内 P = 0.89)(重复测量方差分析)。这强烈表明,与左旋舒必利相比,乳香胶可提供 DG 症状的持续改善,干预后主观幸福感良好,无明显不良反应。
对患者的 6 个月(24 周)中期分析表明,与左旋舒必利相比,乳香胶可持续改善 DG 症状,且无明显不良反应。