{"title":"NOVAponin(Dolichos lablab Linne Extract Powder)对轻度功能性消化不良的疗效和安全性:一项单中心、随机、双盲、安慰剂对照研究。","authors":"Yonghoon Choi, Nayoung Kim, Dong Ho Lee","doi":"10.5056/jnm23180","DOIUrl":null,"url":null,"abstract":"<p><strong>Background/aims: </strong>NOVAponin, a functional health food derived from <i>Dolichos lablab</i> Linne extract improves gastric mucosal injury and increases regeneration and proliferation. This study aims to investigate the efficacy and safety of NOVAponin in individuals with mild functional dyspepsia (FD).</p><p><strong>Methods: </strong>In this single-center, double-blind, randomized clinical trial, 131 patients with FD meeting the Rome IV criteria were enrolled. Changes in the gastrointestinal symptom rating scale (GSRS), FD-related quality of life (FD-QoL), gastrointestinal symptom (GIS) scores, inflammatory and anti-inflammatory markers, and adverse effects before and after administration were compared.</p><p><strong>Results: </strong>After 12 weeks of administration, GSRS upper abdominal symptom scores were significantly improved in the test group compared to the control group (-5.30 ± 0.60 vs -2.35 ± 0.56, <i>P</i> < 0.001). GSRS upper abdominal symptom scores (-5.13 ± 0.55 vs -1.92 ± 0.44, <i>P</i> < 0.001), GSRS total scores (-7.02 ± 0.91 vs -3.33 ± 0.73, <i>P</i> < 0.001), GIS total scores (-11.21 ± 0.53 vs -6.65 ± 0.70, <i>P</i> < 0.001) after 6 weeks of administration, GSRS total scores (-7.54 ± 0.94 v. -3.31 ± 0.85, <i>P</i> < 0.001), GIS total scores (-11.90 ± 0.52 vs -7.61 ± 0.73, <i>P</i> < 0.001), and FD-QoL total scores (-11.41 ± 1.75 vs -5.55 ± 1.20, <i>P</i> = 0.007) after 12 weeks of administration also showed significant differences between groups. The differences were slightly more pronounced in epigastric pain syndrome subtypes and in females than the others, although more females were assigned to the test group. There were no significant changes in inflammatory and anti-inflammatory markers or adverse reactions.</p><p><strong>Conclusion: </strong>NOVAponin significantly improved mild FD symptoms especially in epigastric pain syndrome subtype and in females, and was found to be safe.</p>","PeriodicalId":16543,"journal":{"name":"Journal of Neurogastroenterology and Motility","volume":"30 4","pages":"468-479"},"PeriodicalIF":3.3000,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11474556/pdf/","citationCount":"0","resultStr":"{\"title\":\"The Efficacy and Safety of NOVAponin (<i>Dolichos lablab</i> Linne Extract Powder) in Mild Functional Dyspepsia: A Single-center, Randomized, Double-Blind, Placebo-controlled Study.\",\"authors\":\"Yonghoon Choi, Nayoung Kim, Dong Ho Lee\",\"doi\":\"10.5056/jnm23180\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background/aims: </strong>NOVAponin, a functional health food derived from <i>Dolichos lablab</i> Linne extract improves gastric mucosal injury and increases regeneration and proliferation. This study aims to investigate the efficacy and safety of NOVAponin in individuals with mild functional dyspepsia (FD).</p><p><strong>Methods: </strong>In this single-center, double-blind, randomized clinical trial, 131 patients with FD meeting the Rome IV criteria were enrolled. Changes in the gastrointestinal symptom rating scale (GSRS), FD-related quality of life (FD-QoL), gastrointestinal symptom (GIS) scores, inflammatory and anti-inflammatory markers, and adverse effects before and after administration were compared.</p><p><strong>Results: </strong>After 12 weeks of administration, GSRS upper abdominal symptom scores were significantly improved in the test group compared to the control group (-5.30 ± 0.60 vs -2.35 ± 0.56, <i>P</i> < 0.001). GSRS upper abdominal symptom scores (-5.13 ± 0.55 vs -1.92 ± 0.44, <i>P</i> < 0.001), GSRS total scores (-7.02 ± 0.91 vs -3.33 ± 0.73, <i>P</i> < 0.001), GIS total scores (-11.21 ± 0.53 vs -6.65 ± 0.70, <i>P</i> < 0.001) after 6 weeks of administration, GSRS total scores (-7.54 ± 0.94 v. -3.31 ± 0.85, <i>P</i> < 0.001), GIS total scores (-11.90 ± 0.52 vs -7.61 ± 0.73, <i>P</i> < 0.001), and FD-QoL total scores (-11.41 ± 1.75 vs -5.55 ± 1.20, <i>P</i> = 0.007) after 12 weeks of administration also showed significant differences between groups. The differences were slightly more pronounced in epigastric pain syndrome subtypes and in females than the others, although more females were assigned to the test group. There were no significant changes in inflammatory and anti-inflammatory markers or adverse reactions.</p><p><strong>Conclusion: </strong>NOVAponin significantly improved mild FD symptoms especially in epigastric pain syndrome subtype and in females, and was found to be safe.</p>\",\"PeriodicalId\":16543,\"journal\":{\"name\":\"Journal of Neurogastroenterology and Motility\",\"volume\":\"30 4\",\"pages\":\"468-479\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2024-10-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11474556/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Neurogastroenterology and Motility\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.5056/jnm23180\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neurogastroenterology and Motility","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.5056/jnm23180","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
背景/目的:NOVAponin是从马褂木林提取物中提取的一种功能性保健食品,它能改善胃黏膜损伤,促进胃黏膜的再生和增殖。本研究旨在调查 NOVAponin 对轻度功能性消化不良(FD)患者的疗效和安全性:在这项单中心、双盲、随机临床试验中,共招募了 131 名符合罗马 IV 标准的功能性消化不良患者。比较了用药前后胃肠道症状评分量表(GSRS)、FD相关生活质量(FD-QoL)、胃肠道症状(GIS)评分、炎症和抗炎标志物以及不良反应的变化:用药 12 周后,与对照组相比,试验组的 GSRS 上腹部症状评分明显改善(-5.30 ± 0.60 vs -2.35 ± 0.56,P < 0.001)。用药 6 周后,GSRS 上腹部症状评分(-5.13 ± 0.55 vs -1.92 ± 0.44,P < 0.001)、GSRS 总评分(-7.02 ± 0.91 vs -3.33±0.73,P < 0.001)、GIS 总评分(-11.21 ± 0.53 vs -6.65±0.70,P < 0.001)、GSRS 总评分(-7.用药 12 周后,GSRS 总分(-7.54±0.94 vs -3.31±0.85,P<0.001)、GIS 总分(-11.90±0.52 vs -7.61±0.73,P<0.001)和 FD-QoL 总分(-11.41±1.75 vs -5.55±1.20,P=0.007)在组间也显示出显著差异。上腹痛综合征亚型和女性的差异比其他组稍明显,尽管更多女性被分配到试验组。炎症和抗炎标志物以及不良反应均无明显变化:结论:NOVAponin 能明显改善轻度 FD 症状,尤其是上腹痛综合征亚型和女性患者的症状,而且是安全的。
The Efficacy and Safety of NOVAponin (Dolichos lablab Linne Extract Powder) in Mild Functional Dyspepsia: A Single-center, Randomized, Double-Blind, Placebo-controlled Study.
Background/aims: NOVAponin, a functional health food derived from Dolichos lablab Linne extract improves gastric mucosal injury and increases regeneration and proliferation. This study aims to investigate the efficacy and safety of NOVAponin in individuals with mild functional dyspepsia (FD).
Methods: In this single-center, double-blind, randomized clinical trial, 131 patients with FD meeting the Rome IV criteria were enrolled. Changes in the gastrointestinal symptom rating scale (GSRS), FD-related quality of life (FD-QoL), gastrointestinal symptom (GIS) scores, inflammatory and anti-inflammatory markers, and adverse effects before and after administration were compared.
Results: After 12 weeks of administration, GSRS upper abdominal symptom scores were significantly improved in the test group compared to the control group (-5.30 ± 0.60 vs -2.35 ± 0.56, P < 0.001). GSRS upper abdominal symptom scores (-5.13 ± 0.55 vs -1.92 ± 0.44, P < 0.001), GSRS total scores (-7.02 ± 0.91 vs -3.33 ± 0.73, P < 0.001), GIS total scores (-11.21 ± 0.53 vs -6.65 ± 0.70, P < 0.001) after 6 weeks of administration, GSRS total scores (-7.54 ± 0.94 v. -3.31 ± 0.85, P < 0.001), GIS total scores (-11.90 ± 0.52 vs -7.61 ± 0.73, P < 0.001), and FD-QoL total scores (-11.41 ± 1.75 vs -5.55 ± 1.20, P = 0.007) after 12 weeks of administration also showed significant differences between groups. The differences were slightly more pronounced in epigastric pain syndrome subtypes and in females than the others, although more females were assigned to the test group. There were no significant changes in inflammatory and anti-inflammatory markers or adverse reactions.
Conclusion: NOVAponin significantly improved mild FD symptoms especially in epigastric pain syndrome subtype and in females, and was found to be safe.
期刊介绍:
Journal of Neurogastroenterology and Motility (J Neurogastroenterol Motil) is a joint official journal of the Korean Society of Neurogastroenterology and Motility, the Thai Neurogastroenterology and Motility Society, the Japanese Society of Neurogastroenterology and Motility, the Indian Motility and Functional Disease Association, the Chinese Society of Gastrointestinal Motility, the South East Asia Gastro-Neuro Motility Association, the Taiwan Neurogastroenterology and Motility Society and the Asian Neurogastroenterology and Motility Association, launched in January 2010 after the title change from the Korean Journal of Neurogastroenterology and Motility, published from 1994 to 2009.