首页 > 最新文献

Integrative Medicine Research最新文献

英文 中文
Traditional, complementary and integrative medicine for fatigue post COVID-19 infection: A systematic review of randomized controlled trials 治疗 COVID-19 感染后疲劳的传统、补充和综合疗法:随机对照试验的系统回顾
IF 3.4 4区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-03-22 DOI: 10.1016/j.imr.2024.101039
Xiao-ying Chen , Chun-li Lu , Qian-yun Wang , Xing-ru Pan , Yang-yang Zhang , Jia-le Wang , Jun-Ya Liao , Nai-chong Hu , Chen-yang Wang , Bing-jie Duan , Xue-han Liu , Xin-yan Jin , Jennifer Hunter , Jian-ping Liu

Background

Chronic fatigue is a predominant symptom of post COVID-19 condition, or long COVID. We aimed to evaluate the efficacy and safety of Traditional, Complementary and Integrative Medicine (TCIM) for fatigue post COVID-19 infection.

Methods

Ten English and Chinese language databases and grey literature were searched up to 12 April 2023 for randomized controlled trials (RCTs). Cochrane “Risk of bias” (RoB) tool was applied. Evidence certainty was assessed using Grading of Recommendations Assessment, Development, and Evaluation (GRADE). Effect estimates were presented as risk ratio (RR) or mean difference (MD) with 95% confidence interval (CI).

Results

Thirteen RCTs with 1632 participants were included. One RCT showed that Bufei Huoxue herbal capsules reduced fatigue (n=129, MD -14.90, 95%CI -24.53 to -5.27), one RCT reported that Ludangshen herbal liquid lowered fatigue (n=184, MD -1.90, 95%CI -2.38 to -1.42), and the other one RCT shown that fatigue disappearance rate was higher with Ludangshen herbal liquid (n=184, RR 4.19, 95%CI 2.06 to 8.53). Compared to traditional Chinese medicine rehabilitation (TCM-rahab) alone, one RCT showed that fatigue symptoms were lower following Qingjin Yiqi granules plus TCM-rehab (n=388, MD -0.48, 95%CI -0.50 to -0.46). Due to concerns with RoB and/or imprecision, the certainty in this evidence was low to very low. No serious adverse events was reported.

Conclusions

Limited evidence suggests that various TCIM interventions might reduce post COVID-19 fatigue. Larger, high quality RCTs of longer duration are required to confirm these preliminary findings.

Study Registration

The protocol of this review has been registered at PROSPERO: CRD42022384136.

背景慢性疲劳是COVID-19感染后(或称长COVID)的主要症状。我们的目的是评估传统、补充和整合医学(TCIM)治疗 COVID-19 感染后疲劳的有效性和安全性。方法检索了十个中英文数据库和灰色文献(截至 2023 年 4 月 12 日),以寻找随机对照试验(RCT)。采用 Cochrane "偏倚风险"(RoB)工具。采用建议评估、发展和评价分级法(GRADE)评估证据的确定性。疗效估计值以风险比(RR)或平均差(MD)表示,并附有 95% 的置信区间(CI)。其中一项研究显示,布飞藿香正气胶囊可降低疲劳(n=129,MD -14.90,95%CI -24.53~-5.27);一项研究报告,鲁丹参滴丸可降低疲劳(n=184,MD -1.90,95%CI -2.38~-1.42);另一项研究显示,鲁丹参滴丸的疲劳消失率更高(n=184,RR 4.19,95%CI 2.06~8.53)。与单独使用中药康复治疗相比,一项研究表明,清金益气颗粒加中药康复治疗的疲劳症状较低(n=388,MD -0.48,95%CI -0.50至-0.46)。由于存在RoB和/或不精确的问题,该证据的确定性较低至很低。结论有限的证据表明,各种 TCIM 干预措施可以减轻 COVID-19 后的疲劳。研究注册本综述的方案已在 PROSPERO 注册:CRD42022384136。
{"title":"Traditional, complementary and integrative medicine for fatigue post COVID-19 infection: A systematic review of randomized controlled trials","authors":"Xiao-ying Chen ,&nbsp;Chun-li Lu ,&nbsp;Qian-yun Wang ,&nbsp;Xing-ru Pan ,&nbsp;Yang-yang Zhang ,&nbsp;Jia-le Wang ,&nbsp;Jun-Ya Liao ,&nbsp;Nai-chong Hu ,&nbsp;Chen-yang Wang ,&nbsp;Bing-jie Duan ,&nbsp;Xue-han Liu ,&nbsp;Xin-yan Jin ,&nbsp;Jennifer Hunter ,&nbsp;Jian-ping Liu","doi":"10.1016/j.imr.2024.101039","DOIUrl":"https://doi.org/10.1016/j.imr.2024.101039","url":null,"abstract":"<div><h3>Background</h3><p>Chronic fatigue is a predominant symptom of post COVID-19 condition, or long COVID. We aimed to evaluate the efficacy and safety of Traditional, Complementary and Integrative Medicine (TCIM) for fatigue post COVID-19 infection.</p></div><div><h3>Methods</h3><p>Ten English and Chinese language databases and grey literature were searched up to 12 April 2023 for randomized controlled trials (RCTs). Cochrane “Risk of bias” (RoB) tool was applied. Evidence certainty was assessed using Grading of Recommendations Assessment, Development, and Evaluation (GRADE). Effect estimates were presented as risk ratio (RR) or mean difference (MD) with 95% confidence interval (CI).</p></div><div><h3>Results</h3><p>Thirteen RCTs with 1632 participants were included. One RCT showed that Bufei Huoxue herbal capsules reduced fatigue (n=129, MD -14.90, 95%CI -24.53 to -5.27), one RCT reported that Ludangshen herbal liquid lowered fatigue (n=184, MD -1.90, 95%CI -2.38 to -1.42), and the other one RCT shown that fatigue disappearance rate was higher with Ludangshen herbal liquid (n=184, RR 4.19, 95%CI 2.06 to 8.53). Compared to traditional Chinese medicine rehabilitation (TCM-rahab) alone, one RCT showed that fatigue symptoms were lower following Qingjin Yiqi granules plus TCM-rehab (n=388, MD -0.48, 95%CI -0.50 to -0.46). Due to concerns with RoB and/or imprecision, the certainty in this evidence was low to very low. No serious adverse events was reported.</p></div><div><h3>Conclusions</h3><p>Limited evidence suggests that various TCIM interventions might reduce post COVID-19 fatigue. Larger, high quality RCTs of longer duration are required to confirm these preliminary findings.</p></div><div><h3>Study Registration</h3><p>The protocol of this review has been registered at PROSPERO: CRD42022384136.</p></div>","PeriodicalId":13644,"journal":{"name":"Integrative Medicine Research","volume":"13 2","pages":"Article 101039"},"PeriodicalIF":3.4,"publicationDate":"2024-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2213422024000192/pdfft?md5=bc76ea5e2313a749574bd58c0233f6ff&pid=1-s2.0-S2213422024000192-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140879247","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ameliorative effects of Tagetes erecta Linn. flower against desiccation stress-induced dry eye symptoms in the mice model 万寿菊花对干燥应激引起的小鼠干眼症状的改善作用
IF 3.4 4区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-03-11 DOI: 10.1016/j.imr.2024.101038
Hyesook Lee , Hyun Hwangbo , Jin-Won Hyun , Jung-Hyun Shim , Sun-Hee Leem , Gi-Young Kim , Yung Hyun Choi

Background

Tagetes erecta Linn, popularly known as Marigold, has various pharmacological effects. It is used as a dietary supplement, especially for the posterior segment of the eye. However, the effect of T. erecta Linn on ocular disorders is still unknown. The purpose of this study was to investigate the effect of oral administration of ethanol extract of T. erecta Linn flower (TE) for dry eye syndrome (DED) in a murine model.

Methods

Twenty-four mice were subjected to desiccation stress (DS) to induce DED and subcutaneous injection of scopolamine hydrobromide was administered 4 times a day for 21 days. TE and cyclosporine A (CsA) were administered for an additional 14 days under DS conditions. Mice were randomly divided into four groups: control, TE200, TE400, and CsA. Changes in tear production and corneal fluorescein staining were measured at baseline, after 7 days of DS, and after treatment for 7 and 14 days.

Results

DS significantly decreased tear production and increased corneal fluorescein score; the parameters were significantly reversed in the TE400 (oral administration of 400 mg TE/kg body weight) group. TE markedly improved DS-induced changes including corneal epithelial detachment and lacrimal gland inflammation. The anti-inflammatory effect of TE 400 supplementation was similar to that of CsA.

Conclusions

Our findings suggest that oral administration of TE may protect against DS-induced DED via stabilization of the tear film and suppression of inflammation. This study provides an experimental basis for further studies on the potential clinical use of TE in preventing DED.

Tagetes erecta Linn 俗称万寿菊,具有多种药理作用。它被用作天然食品着色剂、家禽饲料添加剂和营养补充剂,尤其是对眼球后段的作用。然而,直立金盏花对眼部疾病的影响尚不清楚。为了研究口服麟花乙醇提取物(TE)对小鼠干眼症(DED)模型的影响,我们对小鼠进行了干燥应激(DS)实验,并给小鼠皮下注射氢溴酸东莨菪碱,每天四次,连续 21 天。在干燥应激条件下,再注射 14 天 TE 和环孢素 A (CsA)。分别在基线、DS 7 天后以及治疗 7 天和 14 天后测量泪液分泌量和角膜荧光素染色的变化。DS明显降低了泪液分泌量,增加了角膜荧光素评分;TE400(口服400毫克TE/千克体重)组明显逆转了这些参数。TE 明显改善了 DS 引起的变化,包括角膜上皮脱落和泪腺炎症。补充 TE 400 的抗炎效果与 CsA 相似。我们的研究结果表明,口服 TE 可保护泪膜稳定和抑制炎症,防止 DS 引起的 DED。这项研究为进一步研究 TE 在预防 DED 方面的潜在临床应用提供了实验基础。
{"title":"Ameliorative effects of Tagetes erecta Linn. flower against desiccation stress-induced dry eye symptoms in the mice model","authors":"Hyesook Lee ,&nbsp;Hyun Hwangbo ,&nbsp;Jin-Won Hyun ,&nbsp;Jung-Hyun Shim ,&nbsp;Sun-Hee Leem ,&nbsp;Gi-Young Kim ,&nbsp;Yung Hyun Choi","doi":"10.1016/j.imr.2024.101038","DOIUrl":"10.1016/j.imr.2024.101038","url":null,"abstract":"<div><h3>Background</h3><p>Tagetes erecta Linn, popularly known as Marigold, has various pharmacological effects. It is used as a dietary supplement, especially for the posterior segment of the eye. However, the effect of T. erecta Linn on ocular disorders is still unknown. The purpose of this study was to investigate the effect of oral administration of ethanol extract of <em>T. erecta</em> Linn flower (TE) for dry eye syndrome (DED) in a murine model.</p></div><div><h3>Methods</h3><p>Twenty-four mice were subjected to desiccation stress (DS) to induce DED and subcutaneous injection of scopolamine hydrobromide was administered 4 times a day for 21 days. TE and cyclosporine A (CsA) were administered for an additional 14 days under DS conditions. Mice were randomly divided into four groups: control, TE200, TE400, and CsA. Changes in tear production and corneal fluorescein staining were measured at baseline, after 7 days of DS, and after treatment for 7 and 14 days.</p></div><div><h3>Results</h3><p>DS significantly decreased tear production and increased corneal fluorescein score; the parameters were significantly reversed in the TE400 (oral administration of 400 mg TE/kg body weight) group. TE markedly improved DS-induced changes including corneal epithelial detachment and lacrimal gland inflammation. The anti-inflammatory effect of TE 400 supplementation was similar to that of CsA.</p></div><div><h3>Conclusions</h3><p>Our findings suggest that oral administration of TE may protect against DS-induced DED <em>via</em> stabilization of the tear film and suppression of inflammation. This study provides an experimental basis for further studies on the potential clinical use of TE in preventing DED.</p></div>","PeriodicalId":13644,"journal":{"name":"Integrative Medicine Research","volume":"13 2","pages":"Article 101038"},"PeriodicalIF":3.4,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2213422024000180/pdfft?md5=0c1067b98ff7ae394de01323ba6a8e26&pid=1-s2.0-S2213422024000180-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140150903","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Using the right design controls for acupuncture trials: Methodological rigor and validity in research 在针灸试验中使用正确的设计控制:研究方法的严谨性和有效性
IF 3.4 4区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-02-17 DOI: 10.1016/j.imr.2024.101026
Younbyoung Chae , Jun-Hwan Lee , Myeong Soo Lee

Acupuncture treatment can be defined as a medical procedure with an acupuncture needle at acupoints. Establishing suitable control settings is essential, based on the target elements of the acupuncture therapy. In order to properly design a clinical trial or an experiment, a control group must be established. Here, we overview the significance of the control group and its limitations in acupuncture research. Clinical trials have employed a variety of study designs and controls for acupuncture treatment in order to compare the effects of actual treatments with control groups that include no treatment or treatment as usual, sham acupuncture at true acupoints, real acupuncture at non-acupoints, and sham acupuncture at non-acupoints. In order to determine the point-specificity of acupuncture, real acupuncture at non-acupoints should be taken into consideration, whereas sham acupuncture at the same true acupoints should be used to determine the needling-specific effect of acupuncture. It is crucial to choose the optimum control for acupuncture treatments depending on the study's main goal and to interpret the results in accordance with the research design.

针灸治疗可定义为在穴位上使用针灸针的医疗过程。根据针灸疗法的目标要素,建立合适的对照组是至关重要的。为了正确设计临床试验或实验,必须设立对照组。在此,我们将概述对照组在针灸研究中的意义及其局限性。临床试验采用了多种研究设计和针灸治疗对照,以比较实际治疗与对照组的效果,对照组包括不治疗或照常治疗、真穴假针、非穴真针和非穴假针。为了确定针刺的穴位特异性,应考虑在非穴位上进行真针刺,而在相同的真穴上进行假针刺,以确定针刺的针刺效应。根据研究的主要目标选择针灸治疗的最佳对照,并根据研究设计解释结果至关重要。
{"title":"Using the right design controls for acupuncture trials: Methodological rigor and validity in research","authors":"Younbyoung Chae ,&nbsp;Jun-Hwan Lee ,&nbsp;Myeong Soo Lee","doi":"10.1016/j.imr.2024.101026","DOIUrl":"https://doi.org/10.1016/j.imr.2024.101026","url":null,"abstract":"<div><p>Acupuncture treatment can be defined as a medical procedure with an acupuncture needle at acupoints. Establishing suitable control settings is essential, based on the target elements of the acupuncture therapy. In order to properly design a clinical trial or an experiment, a control group must be established. Here, we overview the significance of the control group and its limitations in acupuncture research. Clinical trials have employed a variety of study designs and controls for acupuncture treatment in order to compare the effects of actual treatments with control groups that include no treatment or treatment as usual, sham acupuncture at true acupoints, real acupuncture at non-acupoints, and sham acupuncture at non-acupoints. In order to determine the point-specificity of acupuncture, real acupuncture at non-acupoints should be taken into consideration, whereas sham acupuncture at the same true acupoints should be used to determine the needling-specific effect of acupuncture. It is crucial to choose the optimum control for acupuncture treatments depending on the study's main goal and to interpret the results in accordance with the research design.</p></div>","PeriodicalId":13644,"journal":{"name":"Integrative Medicine Research","volume":"13 1","pages":"Article 101026"},"PeriodicalIF":3.4,"publicationDate":"2024-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2213422024000064/pdfft?md5=f9cce0036e86b6ddf4f91f1598c56b9f&pid=1-s2.0-S2213422024000064-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139942456","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Efficacy and safety of herbal medicine Gongjin-Dan and Ssanghwa-Tang in patients with chronic fatigue: A randomized, double-blind, placebo-controlled, clinical trial 宫金丹和双黄连对慢性疲劳患者的疗效和安全性:随机、双盲、安慰剂对照临床试验
IF 3.4 4区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-02-16 DOI: 10.1016/j.imr.2024.101025
Jun-Yong Choi , Bom Choi , Ojin Kwon , Chang-Seob Seo , Ae-Ran Kim , Hyeun-kyoo Shin , Kibong Kim

Background

Gongjin-dan (GJD, also known as Gongchen-dan) and Ssanghwa-tang (SHT, also known as Shuanghe-tang or Souwa-to) are herbal medicines that are widely used in Korea for treating fatigue. However, few studies have evaluated the efficacy and safety of GJD and SHT in the treatment of chronic fatigue.

Methods

In this randomized, double-blind, placebo-controlled clinical trial, 90 individuals with persistent (≥6 months) chronic fatigue of unknown cause and a Fatigue Severity Scale (FSS) score of ≥4 were randomly assigned to GJD group, SHT group, and control group in a 1:1:1 ratio. Outcomes were the changes in the self-reported fatigue questionnaire scores, levels of fatigue-related biomarkers and safety assessment.

Results

Out of 103 patients recruited, 90 were included in the analysis. A significant improvement in the Social Functioning (SF) score of Short-Form 36 Health Survey (SF-36) at week 4 was observed in the GJD group; similarly, a significant improvement compared with that in the Control group was observed in the Role Emotional (RE) score of SF-36 at weeks 4 and 6 and the Physical Functioning (PF) score of SF-36 at week 6 in the SHT group. Laboratory tests revealed no abnormalities, and serious intervention-related adverse events were not reported.

Conclusions

It is suggested that SHT can effectively treat chronic mental and physical fatigue, whereas GJD can effectively treat chronic mental and social fatigue. Furthermore, this study presents evidence supporting the safety of the long-term use of GJD and SHT (up to 4 weeks).

Trial registration

This study was registered at Clinical Research Information Service (CRIS) of Korea with the registration number KCT0007515.

背景公瑾丹(GJD,又称拱辰丹)和双和汤(SHT,又称双和汤或苏和汤)是韩国广泛用于治疗疲劳的草药。在这项随机、双盲、安慰剂对照临床试验中,90 名不明原因的持续性(≥6 个月)慢性疲劳且疲劳严重程度量表(FSS)评分≥4 分的患者按 1:1:1 的比例被随机分配到 GJD 组、SHT 组和对照组。研究结果包括自我报告的疲劳问卷得分变化、疲劳相关生物标志物水平和安全性评估。GJD组在第4周时的短表36健康调查(SF-36)社会功能(SF)评分有明显改善;同样,SHT组在第4周和第6周时的SF-36角色情感(RE)评分和第6周时的SF-36身体功能(PF)评分与对照组相比也有明显改善。结论 本研究表明,SHT 可有效治疗慢性精神和身体疲劳,而 GJD 可有效治疗慢性精神和社交疲劳。此外,本研究还提供了支持长期使用 GJD 和 SHT(长达 4 周)安全性的证据。试验注册本研究已在韩国临床研究信息服务机构(CRIS)注册,注册号为 KCT0007515。
{"title":"Efficacy and safety of herbal medicine Gongjin-Dan and Ssanghwa-Tang in patients with chronic fatigue: A randomized, double-blind, placebo-controlled, clinical trial","authors":"Jun-Yong Choi ,&nbsp;Bom Choi ,&nbsp;Ojin Kwon ,&nbsp;Chang-Seob Seo ,&nbsp;Ae-Ran Kim ,&nbsp;Hyeun-kyoo Shin ,&nbsp;Kibong Kim","doi":"10.1016/j.imr.2024.101025","DOIUrl":"10.1016/j.imr.2024.101025","url":null,"abstract":"<div><h3>Background</h3><p>Gongjin-dan (GJD, also known as Gongchen-dan) and Ssanghwa-tang (SHT, also known as Shuanghe-tang or Souwa-to) are herbal medicines that are widely used in Korea for treating fatigue. However, few studies have evaluated the efficacy and safety of GJD and SHT in the treatment of chronic fatigue.</p></div><div><h3>Methods</h3><p>In this randomized, double-blind, placebo-controlled clinical trial, 90 individuals with persistent (≥6 months) chronic fatigue of unknown cause and a Fatigue Severity Scale (FSS) score of ≥4 were randomly assigned to GJD group, SHT group, and control group in a 1:1:1 ratio. Outcomes were the changes in the self-reported fatigue questionnaire scores, levels of fatigue-related biomarkers and safety assessment.</p></div><div><h3>Results</h3><p>Out of 103 patients recruited, 90 were included in the analysis. A significant improvement in the Social Functioning (SF) score of Short-Form 36 Health Survey (SF-36) at week 4 was observed in the GJD group; similarly, a significant improvement compared with that in the Control group was observed in the Role Emotional (RE) score of SF-36 at weeks 4 and 6 and the Physical Functioning (PF) score of SF-36 at week 6 in the SHT group. Laboratory tests revealed no abnormalities, and serious intervention-related adverse events were not reported.</p></div><div><h3>Conclusions</h3><p>It is suggested that SHT can effectively treat chronic mental and physical fatigue, whereas GJD can effectively treat chronic mental and social fatigue. Furthermore, this study presents evidence supporting the safety of the long-term use of GJD and SHT (up to 4 weeks).</p></div><div><h3>Trial registration</h3><p>This study was registered at Clinical Research Information Service (CRIS) of Korea with the registration number KCT0007515.</p></div>","PeriodicalId":13644,"journal":{"name":"Integrative Medicine Research","volume":"13 1","pages":"Article 101025"},"PeriodicalIF":3.4,"publicationDate":"2024-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2213422024000052/pdfft?md5=0180e2aec9ae7d2e2114f8bded2ad2bb&pid=1-s2.0-S2213422024000052-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139927571","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Traditional, complementary, and integrative medicine and artificial intelligence: Novel opportunities in healthcare 传统医学、补充医学和综合医学与人工智能:医疗保健领域的新机遇
IF 3.4 4区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-02-09 DOI: 10.1016/j.imr.2024.101024
Jeremy Y. Ng , Holger Cramer , Myeong Soo Lee , David Moher

The convergence of traditional, complementary, and integrative medicine (TCIM) with artificial intelligence (AI) is a promising frontier in healthcare. TCIM is a patient-centric approach that combines conventional medicine with complementary therapies, emphasizing holistic well-being. AI can revolutionize healthcare through data-driven decision-making and personalized treatment plans. This article explores how AI technologies can complement and enhance TCIM, aligning with the shared objectives of researchers from both fields in improving patient outcomes, enhancing care quality, and promoting holistic wellness. This integration of TCIM and AI introduces exciting opportunities but also noteworthy challenges. AI may augment TCIM by assisting in early disease detection, providing personalized treatment plans, predicting health trends, and enhancing patient engagement. Challenges at the intersection of AI and TCIM include data privacy and security, regulatory complexities, maintaining the human touch in patient-provider relationships, and mitigating bias in AI algorithms. Patients' trust, informed consent, and legal accountability are all essential considerations. Future directions in AI-enhanced TCIM include advanced personalized medicine, understanding the efficacy of herbal remedies, and studying patient-provider interactions. Research on bias mitigation, patient acceptance, and trust in AI-driven TCIM healthcare is crucial. In this article, we outlined that the merging of TCIM and AI holds great promise in enhancing healthcare delivery, personalizing treatment plans, preventive care, and patient engagement. Addressing challenges and fostering collaboration between AI experts, TCIM practitioners, and policymakers, however, is vital to harnessing the full potential of this integration.

传统医学、补充医学和综合医学(TCIM)与人工智能(AI)的融合是医疗保健领域前景广阔的前沿领域。传统医学、补充医学和综合医学是一种以病人为中心的方法,它将传统医学与补充疗法相结合,强调整体健康。人工智能可以通过数据驱动决策和个性化治疗方案彻底改变医疗保健。本文探讨了人工智能技术如何与 TCIM 相辅相成、相得益彰,并与这两个领域的研究人员在改善患者预后、提高护理质量和促进整体健康方面的共同目标保持一致。TCIM 与人工智能的融合带来了令人兴奋的机遇,同时也带来了值得注意的挑战。人工智能可以通过协助早期疾病检测、提供个性化治疗方案、预测健康趋势和提高患者参与度来增强 TCIM。人工智能与 TCIM 的交叉点面临的挑战包括数据隐私与安全、监管的复杂性、在患者与医疗服务提供者的关系中保持人情味,以及减少人工智能算法中的偏见。患者的信任、知情同意和法律责任都是必须考虑的因素。人工智能增强 TCIM 的未来发展方向包括先进的个性化医疗、了解草药疗法的疗效以及研究患者与医疗服务提供者之间的互动。在人工智能驱动的TCIM医疗保健中,有关减少偏见、患者接受度和信任度的研究至关重要。在这篇文章中,我们概述了 TCIM 与人工智能的融合在加强医疗服务、个性化治疗计划、预防性护理和患者参与方面的巨大前景。然而,应对挑战并促进人工智能专家、TCIM 从业人员和政策制定者之间的合作,对于充分发挥这种融合的潜力至关重要。
{"title":"Traditional, complementary, and integrative medicine and artificial intelligence: Novel opportunities in healthcare","authors":"Jeremy Y. Ng ,&nbsp;Holger Cramer ,&nbsp;Myeong Soo Lee ,&nbsp;David Moher","doi":"10.1016/j.imr.2024.101024","DOIUrl":"https://doi.org/10.1016/j.imr.2024.101024","url":null,"abstract":"<div><p>The convergence of traditional, complementary, and integrative medicine (TCIM) with artificial intelligence (AI) is a promising frontier in healthcare. TCIM is a patient-centric approach that combines conventional medicine with complementary therapies, emphasizing holistic well-being. AI can revolutionize healthcare through data-driven decision-making and personalized treatment plans. This article explores how AI technologies can complement and enhance TCIM, aligning with the shared objectives of researchers from both fields in improving patient outcomes, enhancing care quality, and promoting holistic wellness. This integration of TCIM and AI introduces exciting opportunities but also noteworthy challenges. AI may augment TCIM by assisting in early disease detection, providing personalized treatment plans, predicting health trends, and enhancing patient engagement. Challenges at the intersection of AI and TCIM include data privacy and security, regulatory complexities, maintaining the human touch in patient-provider relationships, and mitigating bias in AI algorithms. Patients' trust, informed consent, and legal accountability are all essential considerations. Future directions in AI-enhanced TCIM include advanced personalized medicine, understanding the efficacy of herbal remedies, and studying patient-provider interactions. Research on bias mitigation, patient acceptance, and trust in AI-driven TCIM healthcare is crucial. In this article, we outlined that the merging of TCIM and AI holds great promise in enhancing healthcare delivery, personalizing treatment plans, preventive care, and patient engagement. Addressing challenges and fostering collaboration between AI experts, TCIM practitioners, and policymakers, however, is vital to harnessing the full potential of this integration.</p></div>","PeriodicalId":13644,"journal":{"name":"Integrative Medicine Research","volume":"13 1","pages":"Article 101024"},"PeriodicalIF":3.4,"publicationDate":"2024-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2213422024000040/pdfft?md5=b8cbf1adb83572dbee54fa4b37730fde&pid=1-s2.0-S2213422024000040-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139743281","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Recommendations and guidelines of integrative medicine for COVID-19 care: The APEC project outcome 针对 COVID-19 护理的综合医学建议和指南:亚太经合组织项目成果
IF 3.4 4区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-02-07 DOI: 10.1016/j.imr.2024.101022
Libin Jia , Michelle Beidelschies , Joel M. Evans , Richard C. Niemtzow , Songxuan Zhou Niemtzow , Jeffery A. Dusek , Yufang Lin , Charles Wu , Yi-Chang Su , C. Jason Wang , Chien-Yu Lin , Peristiwan Ridha Widhi Astana , Danang Ardiyanto , Rusmiyati Hardjoutomo , Khwanchai Visithanon , Jagravudh Puagkong , Julalak Chokpaisarn , Martha Villar Lopez , Hiroshi Yotsuyanagi , Myeong Soo Lee , Cecilia C. Maramba-Lazarte

This article - Recommendations and Guidelines of Integrative Medicine (IM) for COVID-19 Care - was one of the outcomes from an Asia-Pacific Economic Cooperation (APEC) Project (Integrative Medicine (IM) and COVID -19 Care) during the time between May 2022 and March 2023. With the efforts from care providers, researchers, health policy makers and healthcare administrative leaders among APEC economies, the purpose of this file was to provide comprehensive IM systems for COVID-19 care as recommendations and suggestive guidelines including care methods, tools, procedures, symptom conditions and targets selections, and points need to be considered during care applications. All cited COVID-19 care practices have confirmed their efficacy and usefulness either used alone or combined with conventional medicine. This article provides current useful medical information on IM for COVID-19 care which could benefit APEC economies and world health communities on their healthcare system.

本文--COVID-19 护理的整合医学(IM)建议和指南--是亚太经济合作组织(APEC)项目(整合医学(IM)和 COVID -19 护理)在 2022 年 5 月至 2023 年 3 月期间的成果之一。在亚太经合组织各经济体的护理提供者、研究人员、卫生政策制定者和卫生保健行政领导的努力下,本文件旨在为 COVID-19 护理提供全面的 IM 系统,作为建议和提示性指南,包括护理方法、工具、程序、症状条件和目标选择,以及护理应用过程中需要考虑的要点。所有引用的 COVID-19 护理实践都证实了其单独使用或与传统医学结合使用的有效性和实用性。本文提供了有关 COVID-19 护理的 IM 的最新有用医学信息,可使亚太经合组织经济体和世界卫生界在其医疗保健系统中受益。
{"title":"Recommendations and guidelines of integrative medicine for COVID-19 care: The APEC project outcome","authors":"Libin Jia ,&nbsp;Michelle Beidelschies ,&nbsp;Joel M. Evans ,&nbsp;Richard C. Niemtzow ,&nbsp;Songxuan Zhou Niemtzow ,&nbsp;Jeffery A. Dusek ,&nbsp;Yufang Lin ,&nbsp;Charles Wu ,&nbsp;Yi-Chang Su ,&nbsp;C. Jason Wang ,&nbsp;Chien-Yu Lin ,&nbsp;Peristiwan Ridha Widhi Astana ,&nbsp;Danang Ardiyanto ,&nbsp;Rusmiyati Hardjoutomo ,&nbsp;Khwanchai Visithanon ,&nbsp;Jagravudh Puagkong ,&nbsp;Julalak Chokpaisarn ,&nbsp;Martha Villar Lopez ,&nbsp;Hiroshi Yotsuyanagi ,&nbsp;Myeong Soo Lee ,&nbsp;Cecilia C. Maramba-Lazarte","doi":"10.1016/j.imr.2024.101022","DOIUrl":"https://doi.org/10.1016/j.imr.2024.101022","url":null,"abstract":"<div><p>This article - Recommendations and Guidelines of Integrative Medicine (IM) for COVID-19 Care - was one of the outcomes from an Asia-Pacific Economic Cooperation (APEC) Project (Integrative Medicine (IM) and COVID -19 Care) during the time between May 2022 and March 2023. With the efforts from care providers, researchers, health policy makers and healthcare administrative leaders among APEC economies, the purpose of this file was to provide comprehensive IM systems for COVID-19 care as recommendations and suggestive guidelines including care methods, tools, procedures, symptom conditions and targets selections, and points need to be considered during care applications. All cited COVID-19 care practices have confirmed their efficacy and usefulness either used alone or combined with conventional medicine. This article provides current useful medical information on IM for COVID-19 care which could benefit APEC economies and world health communities on their healthcare system.</p></div>","PeriodicalId":13644,"journal":{"name":"Integrative Medicine Research","volume":"13 1","pages":"Article 101022"},"PeriodicalIF":3.4,"publicationDate":"2024-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2213422024000027/pdfft?md5=810297852db3200d2ed65099f89cf9a7&pid=1-s2.0-S2213422024000027-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139975972","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acupuncture treatment for Hashimoto's thyroiditis: An exploratory randomized controlled trial 针灸治疗桥本氏甲状腺炎:一项探索性随机对照试验
IF 3.4 4区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-02-06 DOI: 10.1016/j.imr.2024.101023
Shanze Wang , Chao Yang , Weimei Zeng , Hongfang Tian , Shihao Du , Jiping Zhao

Background

Hashimoto's thyroiditis (HT) has a high incidence rate and unresolved clinical symptoms. Although Hand Yangming Meridian Penetrating Acupuncture has been used to treat thyroid diseases in China, there is no randomized controlled trial (RCT) on HT.

Methods

This exploratory RCT aims to preliminarily evaluate the efficacy, safety, and feasibility of Hand Yangming Meridian Penetrating Acupuncture in the treatment of HT. Included subjects were randomly assigned to the acupuncture group and the waiting treatment group at a ratio of 1:1. Subjects in the acupuncture group received 16 weeks of acupuncture treatment, followed by a 16-week follow-up observation phase. Subjects in the waiting group received thyroxine supplementation for 16 weeks, followed by 16 weeks of compensation treatment. Serum thyroid peroxidase antibody (TPOab) and thyroglobulin antibody (TGab) levels were the main indicators, and Thyroid-Related Patient-Reported Outcome short form (ThyPRO-39), MOS Item Short Form Health Survey (SF-36), and Hospital Anxiety and Depression Scale (HADS) scores were also recorded.

Results

In total, 58 subjects were included. After 16 weeks of treatment, there was no statistical difference in the changes in TPOab levels between the two groups, but the TGab level in the acupuncture group was significantly lower than in the waiting group (difference: −141.97 [95 % CI: −222.4 to −61.5], P = 0.011). Moreover, the total ThyPRO-39 and SF-36 scores were statistically different between the two groups (PThyPRO-39 < 0.001, PSF-36 = 0.005). There was no statistical difference in HADS between the two groups.

Conclusions

Hand Yangming Meridian Penetrating Acupuncture may be safe and feasible for HT hypothyroidism to improve symptoms and reduce TGab levels.

Trial registration number

This trial was registered at Acupuncture-Moxibustion Clinical Trial Registry: AMCTR-IOR-19000308 (ChiCTR1900026830, https://www.chictr.org.cn/searchprojEN.html).

背景桥本氏甲状腺炎(HT)发病率高,临床症状难以缓解。本研究旨在初步评估手阳明经针刺治疗桥本氏甲状腺炎的疗效、安全性和可行性。58名受试者按1:1的比例随机分配到针灸组和等待治疗组。针灸组受试者接受16周的针灸治疗,然后进行16周的随访观察。等待治疗组的受试者先接受16周的甲状腺素补充治疗,然后再接受16周的补偿治疗。主要指标为血清甲状腺过氧化物酶抗体(TPOab)和甲状腺球蛋白抗体(TGab)水平,同时记录甲状腺相关患者报告结果简表(ThyPRO-39)、MOS项目健康调查简表(SF-36)和医院焦虑抑郁量表(HADS)评分。结果治疗16周后,两组的TPOab水平变化无统计学差异,但针刺组的TGab水平显著低于等待组(差异:-141.97 [95% CI:-222.4 至 -61.5],P = 0.011)。此外,两组的 ThyPRO-39 和 SF-36 总分也存在统计学差异(PThyPRO-39 < 0.001,PSF-36 = 0.005)。试验注册号:AMCTR-IOR-19000308,ChiCTR1900026830(注册名称:手阳明经穴针刺治疗桥本氏甲状腺炎临床随机对照试验。注册网站:https://www.chictr.org.cn/searchprojEN.html)
{"title":"Acupuncture treatment for Hashimoto's thyroiditis: An exploratory randomized controlled trial","authors":"Shanze Wang ,&nbsp;Chao Yang ,&nbsp;Weimei Zeng ,&nbsp;Hongfang Tian ,&nbsp;Shihao Du ,&nbsp;Jiping Zhao","doi":"10.1016/j.imr.2024.101023","DOIUrl":"10.1016/j.imr.2024.101023","url":null,"abstract":"<div><h3>Background</h3><p>Hashimoto's thyroiditis (HT) has a high incidence rate and unresolved clinical symptoms. Although Hand Yangming Meridian Penetrating Acupuncture has been used to treat thyroid diseases in China, there is no randomized controlled trial (RCT) on HT.</p></div><div><h3>Methods</h3><p>This exploratory RCT aims to preliminarily evaluate the efficacy, safety, and feasibility of Hand Yangming Meridian Penetrating Acupuncture in the treatment of HT. Included subjects were randomly assigned to the acupuncture group and the waiting treatment group at a ratio of 1:1. Subjects in the acupuncture group received 16 weeks of acupuncture treatment, followed by a 16-week follow-up observation phase. Subjects in the waiting group received thyroxine supplementation for 16 weeks, followed by 16 weeks of compensation treatment. Serum thyroid peroxidase antibody (TPOab) and thyroglobulin antibody (TGab) levels were the main indicators, and Thyroid-Related Patient-Reported Outcome short form (ThyPRO-39), MOS Item Short Form Health Survey (SF-36), and Hospital Anxiety and Depression Scale (HADS) scores were also recorded.</p></div><div><h3>Results</h3><p>In total, 58 subjects were included. After 16 weeks of treatment, there was no statistical difference in the changes in TPOab levels between the two groups, but the TGab level in the acupuncture group was significantly lower than in the waiting group (difference: −141.97 [95 % CI: −222.4 to −61.5]<em>, P</em> = 0.011). Moreover, the total ThyPRO-39 and SF-36 scores were statistically different between the two groups (<em>P</em><sub>ThyPRO-39</sub> &lt; 0.001, <em>P</em><sub>SF-36</sub> = 0.005). There was no statistical difference in HADS between the two groups.</p></div><div><h3>Conclusions</h3><p>Hand Yangming Meridian Penetrating Acupuncture may be safe and feasible for HT hypothyroidism to improve symptoms and reduce TGab levels.</p></div><div><h3>Trial registration number</h3><p>This trial was registered at Acupuncture-Moxibustion Clinical Trial Registry: AMCTR-IOR-19000308 (ChiCTR1900026830, <span>https://www.chictr.org.cn/searchprojEN.html</span><svg><path></path></svg>).</p></div>","PeriodicalId":13644,"journal":{"name":"Integrative Medicine Research","volume":"13 1","pages":"Article 101023"},"PeriodicalIF":3.4,"publicationDate":"2024-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2213422024000039/pdfft?md5=46d85862d2dae13130ef55fe03b3b5ba&pid=1-s2.0-S2213422024000039-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139754365","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acupuncture for response and complete pain relief time of acute renal colic: Secondary analysis of a randomized controlled trial 针灸治疗急性肾绞痛的反应和完全止痛时间:随机对照试验的二次分析
IF 3.4 4区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-01-20 DOI: 10.1016/j.imr.2024.101021
Xue-Zhou Wang , Cun-Zhi Liu , Li-Qiong Wang , Zhi-Cheng Qu , Ying Cao , Shi-Yan Yan , Jing-Wen Yang , Jian-Feng Tu

Background

The integration of acupuncture with intramuscular injection of diclofenac sodium can expedite the onset of analgesia in treating acute renal colic caused by urolithiasis. However, it remains unclear whether acupuncture can accelerate pain relief constantly until complete remission. This study aimed to explore the extent to which acupuncture can expedite the onset time of response or complete pain relief in treating acute renal colic, and the predictive value of patient characteristics for treatment efficacy.

Methods

This secondary analysis utilized data from a prior randomized controlled trial. Eighty patients with acute renal colic were randomly assigned 1:1 to the acupuncture group or the sham acupuncture group. After intramuscular injection of diclofenac sodium, acupuncture or sham acupuncture was delivered to patients. The outcomes included time to response (at least a 50 % reduction in pain) and complete pain relief. Between-group comparison under the 2 events was estimated by Kaplan-Meier methodology. Subgroup analysis was performed utilizing the Cox proportional hazards model.

Results

The median response time and complete pain relief time in the acupuncture group were lower than those in the sham acupuncture group (5 vs 30 min, Log Rank P < 0.001; 20 min vs not observed, Log Rank P < 0.001, respectively). Hazard Ratios (HRs) for response across all subgroups favored the acupuncture group. All HRs for complete pain relief favored acupuncture, expect large stone and moderate pain at baseline. No interaction was found in either event.

Conclusion

Acupuncture can accelerate the response time and complete pain relief time for patients with acute renal colic, with the efficacy universally.

Trial registration

This study has been registered at Chinese Clinical Trial Registry: ChiCTR1900025202.

背景 在治疗由尿路结石引起的急性肾绞痛时,针灸与肌肉注射双氯芬酸钠的结合可加快镇痛的开始。然而,针灸是否能持续加速疼痛缓解直至完全缓解仍不清楚。本研究旨在探讨针灸在治疗急性肾绞痛时能在多大程度上加快起效时间或完全缓解疼痛,以及患者特征对疗效的预测价值。80 名急性肾绞痛患者按 1:1 随机分配到针灸组或假针灸组。肌肉注射双氯芬酸钠后,对患者进行针灸或假针灸。结果包括反应时间(疼痛至少减轻 50%)和疼痛完全缓解。采用 Kaplan-Meier 方法估算 2 个事件下的组间比较。结果针灸组的反应时间和疼痛完全缓解时间低于假针灸组(分别为 5 分钟 vs 30 分钟,Log Rank P < 0.001;20 分钟 vs 未观察到,Log Rank P < 0.001)。所有分组的反应危险比(HRs)均倾向于针灸组。所有完全缓解疼痛的危险比都倾向于针灸组,预计大结石和基线中度疼痛。结论针灸可加快急性肾绞痛患者的反应时间和完全缓解疼痛的时间,疗效普遍。
{"title":"Acupuncture for response and complete pain relief time of acute renal colic: Secondary analysis of a randomized controlled trial","authors":"Xue-Zhou Wang ,&nbsp;Cun-Zhi Liu ,&nbsp;Li-Qiong Wang ,&nbsp;Zhi-Cheng Qu ,&nbsp;Ying Cao ,&nbsp;Shi-Yan Yan ,&nbsp;Jing-Wen Yang ,&nbsp;Jian-Feng Tu","doi":"10.1016/j.imr.2024.101021","DOIUrl":"10.1016/j.imr.2024.101021","url":null,"abstract":"<div><h3>Background</h3><p>The integration of acupuncture with intramuscular injection of diclofenac sodium can expedite the onset of analgesia in treating acute renal colic caused by urolithiasis. However, it remains unclear whether acupuncture can accelerate pain relief constantly until complete remission. This study aimed to explore the extent to which acupuncture can expedite the onset time of response or complete pain relief in treating acute renal colic, and the predictive value of patient characteristics for treatment efficacy.</p></div><div><h3>Methods</h3><p>This secondary analysis utilized data from a prior randomized controlled trial. Eighty patients with acute renal colic were randomly assigned 1:1 to the acupuncture group or the sham acupuncture group. After intramuscular injection of diclofenac sodium, acupuncture or sham acupuncture was delivered to patients. The outcomes included time to response (at least a 50 % reduction in pain) and complete pain relief. Between-group comparison under the 2 events was estimated by Kaplan-Meier methodology. Subgroup analysis was performed utilizing the Cox proportional hazards model.</p></div><div><h3>Results</h3><p>The median response time and complete pain relief time in the acupuncture group were lower than those in the sham acupuncture group (5 vs 30 min, Log Rank <em>P</em> &lt; 0.001; 20 min vs not observed, Log Rank <em>P</em> &lt; 0.001, respectively). Hazard Ratios (HRs) for response across all subgroups favored the acupuncture group. All HRs for complete pain relief favored acupuncture, expect large stone and moderate pain at baseline. No interaction was found in either event.</p></div><div><h3>Conclusion</h3><p>Acupuncture can accelerate the response time and complete pain relief time for patients with acute renal colic, with the efficacy universally.</p></div><div><h3>Trial registration</h3><p>This study has been registered at Chinese Clinical Trial Registry: ChiCTR1900025202.</p></div>","PeriodicalId":13644,"journal":{"name":"Integrative Medicine Research","volume":"13 1","pages":"Article 101021"},"PeriodicalIF":3.4,"publicationDate":"2024-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2213422024000015/pdfft?md5=ee00c056134e72095dbd3da8043d8b0c&pid=1-s2.0-S2213422024000015-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139507269","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Curcuma xanthorrhiza extract and xanthorrhizol ameliorate cancer-induced adipose wasting in CT26-bearing mice by regulating lipid metabolism and adipose tissue browning 莪术提取物和黄柏酚通过调节脂质代谢和脂肪组织褐变,改善癌症诱发的 CT26 小鼠脂肪消耗
IF 3.4 4区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-12-24 DOI: 10.1016/j.imr.2023.101020
Haeun Kim , Dong-Woo Lee , Jae-Kwan Hwang

Background

Cancer cachexia—characterized by anorexia, body weight loss, skeletal muscle atrophy, and fat loss—affects nearly 80% of cancer patients and accounts for 20% of cancer deaths. Curcuma xanthorrhiza, known as Java turmeric, and its active compound xanthorrhizol (XAN) exhibit anticancer, anti-inflammatory, and antioxidant properties. However, the ameliorative effects of C. xanthorrhiza extract (CXE) and XAN on cancer-associated adipose atrophy remain unexplored. This study aimed to evaluate the therapeutic effects of CXE and XAN on cancer cachexia-induced adipose tissue wasting in CT26 tumor-bearing mice.

Methods

CT26 cells were injected subcutaneously into the right flank of BALB/c mice to establish a cancer cachexia model. To evaluate the inhibitory effects of CXE and XAN on cancer cachexia, 50 and 100 mg/kg CXE and 15 mg/kg XAN were administered orally every day for 1 week.

Results

CXE and XAN administration significantly attenuated the loss of body weight and epidydimal fat mass by cancer cachexia. In epididymal adipose tissues, administration of CXE or XAN inhibited white adipose tissue browning by repressing expression of the thermogenic genes. Simultaneously, CXE or XAN attenuated fat catabolism through the downregulation of lipolytic genes. The administration of CXE or XAN induced the expression of genes associated with adipogenesis and lipogenesis-related genes. Moreover, CXE or XAN treatment was associated with maintaining metabolic homeostasis; regulating the expression of adipokines and AMP-activated protein kinase (AMPK).

Conclusions

CXE and XAN mitigate cancer-induced adipose tissue atrophy, primarily by modulating lipid metabolism and WAT browning, indicating their therapeutic potential for cachectic cancer patients.

背景癌症恶病质以厌食、体重下降、骨骼肌萎缩和脂肪减少为特征,影响着近 80% 的癌症患者,占癌症死亡人数的 20%。莪术(又名爪哇姜黄)及其活性化合物黄皮酚(XAN)具有抗癌、抗炎和抗氧化特性。然而,黄柏提取物(CXE)和黄柏酚(XAN)对癌症相关性脂肪萎缩的改善作用仍有待探索。本研究旨在评估 CXE 和 XAN 对 CT26 肿瘤小鼠因癌症恶病质引起的脂肪组织萎缩的治疗作用。为了评估 CXE 和 XAN 对癌症恶病质的抑制作用,小鼠每天口服 50 和 100 mg/kg CXE 和 15 mg/kg XAN,持续 1 周。在附睾脂肪组织中,服用 CXE 或 XAN 可抑制生热基因的表达,从而抑制白色脂肪组织的褐变。同时,CXE 或 XAN 通过下调脂肪分解基因,抑制脂肪分解。服用 CXE 或 XAN 会诱导脂肪生成相关基因和脂肪生成相关基因的表达。结论CXE和XAN主要通过调节脂质代谢和WAT棕色化来缓解癌症诱导的脂肪组织萎缩,这表明它们对恶性肿瘤患者具有治疗潜力。
{"title":"Curcuma xanthorrhiza extract and xanthorrhizol ameliorate cancer-induced adipose wasting in CT26-bearing mice by regulating lipid metabolism and adipose tissue browning","authors":"Haeun Kim ,&nbsp;Dong-Woo Lee ,&nbsp;Jae-Kwan Hwang","doi":"10.1016/j.imr.2023.101020","DOIUrl":"10.1016/j.imr.2023.101020","url":null,"abstract":"<div><h3>Background</h3><p>Cancer cachexia—characterized by anorexia, body weight loss, skeletal muscle atrophy, and fat loss—affects nearly 80% of cancer patients and accounts for 20% of cancer deaths. <em>Curcuma xanthorrhiza</em>, known as Java turmeric, and its active compound xanthorrhizol (XAN) exhibit anticancer, anti-inflammatory, and antioxidant properties. However, the ameliorative effects of <em>C. xanthorrhiza</em> extract (CXE) and XAN on cancer-associated adipose atrophy remain unexplored. This study aimed to evaluate the therapeutic effects of CXE and XAN on cancer cachexia-induced adipose tissue wasting in CT26 tumor-bearing mice.</p></div><div><h3>Methods</h3><p>CT26 cells were injected subcutaneously into the right flank of BALB/c mice to establish a cancer cachexia model. To evaluate the inhibitory effects of CXE and XAN on cancer cachexia, 50 and 100 mg/kg CXE and 15 mg/kg XAN were administered orally every day for 1 week.</p></div><div><h3>Results</h3><p>CXE and XAN administration significantly attenuated the loss of body weight and epidydimal fat mass by cancer cachexia. In epididymal adipose tissues, administration of CXE or XAN inhibited white adipose tissue browning by repressing expression of the thermogenic genes. Simultaneously, CXE or XAN attenuated fat catabolism through the downregulation of lipolytic genes. The administration of CXE or XAN induced the expression of genes associated with adipogenesis and lipogenesis-related genes. Moreover, CXE or XAN treatment was associated with maintaining metabolic homeostasis; regulating the expression of adipokines and AMP-activated protein kinase (AMPK).</p></div><div><h3>Conclusions</h3><p>CXE and XAN mitigate cancer-induced adipose tissue atrophy, primarily by modulating lipid metabolism and WAT browning, indicating their therapeutic potential for cachectic cancer patients.</p></div>","PeriodicalId":13644,"journal":{"name":"Integrative Medicine Research","volume":"13 1","pages":"Article 101020"},"PeriodicalIF":3.4,"publicationDate":"2023-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2213422023000999/pdfft?md5=45e7aae2ce23721f60bbb95812194cda&pid=1-s2.0-S2213422023000999-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139036846","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Traditional Chinese medicine diagnostic prediction model for holistic syndrome differentiation based on deep learning 基于深度学习的中医综合症诊断预测模型
IF 3.4 4区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-12-19 DOI: 10.1016/j.imr.2023.101019
Zhe Chen , Dong Zhang , Chunxiang Liu , Hui Wang , Xinyao Jin , Fengwen Yang , Junhua Zhang

Background

With the development of traditional Chinese medicine (TCM) syndrome knowledge accumulation and artificial intelligence (AI), this study proposes a holistic TCM syndrome differentiation model for the classification prediction of multiple TCM syndromes based on deep learning and accelerates the construction of modern foundational TCM equipment.

Methods

We searched publicly available TCM guidelines and textbooks for expert knowledge and validated these sources using ten-fold cross-validation. Based on the BERT and CNN models, with the classification constraints from TCM holistic syndrome differentiation, the TCM-BERT-CNN model was constructed, which completes the end-to-end TCM holistic syndrome text classification task through symptom input and syndrome output. We assessed the performance of the model using precision, recall, and F1 scores as evaluation metrics.

Results

The TCM-BERT-CNN model had a higher precision (0.926), recall (0.9238), and F1 score (0.9247) than the BERT, TextCNN, LSTM RNN, and LSTM ATTENTION models and achieved superior results in model performance and predictive classification of most TCM syndromes. Symptom feature visualization demonstrated that the TCM-BERT-CNN model can effectively identify the correlation and characteristics of symptoms in different syndromes with a strong correlation, which conforms to the diagnostic characteristics of TCM syndromes.

Conclusions

The TCM-BERT-CNN model proposed in this study is in accordance with the TCM diagnostic characteristics of holistic syndrome differentiation and can effectively complete diagnostic prediction tasks for various TCM syndromes. The results of this study provide new insights into the development of deep learning models for holistic syndrome differentiation in TCM.

背景随着中医证候知识积累和人工智能(AI)的发展,本研究提出了一种基于深度学习的中医证候整体分型模型,用于多种中医证候的分类预测,加快了现代中医基础装备的建设。方法我们搜索了公开的中医指南和教科书中的专家知识,并使用十倍交叉验证对这些来源进行了验证。在 BERT 和 CNN 模型的基础上,结合中医整体证候分型的分类约束,构建了中医-BERT-CNN 模型,该模型通过症状输入和证候输出完成端到端的中医整体证候文本分类任务。结果 TCM-BERT-CNN 模型的精确度(0.926)、召回率(0.9238)和 F1 得分(0.9247)均高于 BERT、TextCNN、LSTM RNN 和 LSTM ATTENTION 模型,并在模型性能和大多数中医证候的预测分类方面取得了优异的成绩。症状特征可视化表明,TCM-BERT-CNN 模型能有效识别不同综合征中症状的相关性和特征,具有较强的相关性,符合中医综合征的诊断特点。 结论本研究提出的 TCM-BERT-CNN 模型符合中医整体辨证的诊断特点,能有效完成各种中医综合征的诊断预测任务。本研究的结果为开发中医整体证候分型的深度学习模型提供了新的思路。
{"title":"Traditional Chinese medicine diagnostic prediction model for holistic syndrome differentiation based on deep learning","authors":"Zhe Chen ,&nbsp;Dong Zhang ,&nbsp;Chunxiang Liu ,&nbsp;Hui Wang ,&nbsp;Xinyao Jin ,&nbsp;Fengwen Yang ,&nbsp;Junhua Zhang","doi":"10.1016/j.imr.2023.101019","DOIUrl":"10.1016/j.imr.2023.101019","url":null,"abstract":"<div><h3>Background</h3><p>With the development of traditional Chinese medicine (TCM) syndrome knowledge accumulation and artificial intelligence (AI), this study proposes a holistic TCM syndrome differentiation model for the classification prediction of multiple TCM syndromes based on deep learning and accelerates the construction of modern foundational TCM equipment.</p></div><div><h3>Methods</h3><p>We searched publicly available TCM guidelines and textbooks for expert knowledge and validated these sources using ten-fold cross-validation. Based on the BERT and CNN models, with the classification constraints from TCM holistic syndrome differentiation, the TCM-BERT-CNN model was constructed, which completes the end-to-end TCM holistic syndrome text classification task through symptom input and syndrome output. We assessed the performance of the model using precision, recall, and F1 scores as evaluation metrics.</p></div><div><h3>Results</h3><p>The TCM-BERT-CNN model had a higher precision (0.926), recall (0.9238), and F1 score (0.9247) than the BERT, TextCNN, LSTM RNN, and LSTM ATTENTION models and achieved superior results in model performance and predictive classification of most TCM syndromes. Symptom feature visualization demonstrated that the TCM-BERT-CNN model can effectively identify the correlation and characteristics of symptoms in different syndromes with a strong correlation, which conforms to the diagnostic characteristics of TCM syndromes.</p></div><div><h3>Conclusions</h3><p>The TCM-BERT-CNN model proposed in this study is in accordance with the TCM diagnostic characteristics of holistic syndrome differentiation and can effectively complete diagnostic prediction tasks for various TCM syndromes. The results of this study provide new insights into the development of deep learning models for holistic syndrome differentiation in TCM.</p></div>","PeriodicalId":13644,"journal":{"name":"Integrative Medicine Research","volume":"13 1","pages":"Article 101019"},"PeriodicalIF":3.4,"publicationDate":"2023-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2213422023000987/pdfft?md5=99cd836599379ae327efed4c3301b406&pid=1-s2.0-S2213422023000987-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138745678","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Integrative Medicine Research
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1