Endocrine, metabolic & immune disorders drug targets最新文献

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Highlights from the Top 100 Most Influential Articles Regarding the Nuclear Receptor PPAR-γ: A Bibliometric Analysis 关于核受体 PPAR-γ 的最具影响力的 100 篇文章集锦:文献计量分析
IF 1.9 4区 医学
Endocrine, metabolic & immune disorders drug targets Pub Date : 2024-02-03 DOI: 10.2174/0118715303265935231114073638
Si Wu, Haijiao Dai, Xianxiang Bai, Zhen Wu, Xianglei Wang, Bin Xiao
{"title":"Highlights from the Top 100 Most Influential Articles Regarding the Nuclear Receptor PPAR-γ: A Bibliometric Analysis","authors":"Si Wu, Haijiao Dai, Xianxiang Bai, Zhen Wu, Xianglei Wang, Bin Xiao","doi":"10.2174/0118715303265935231114073638","DOIUrl":"https://doi.org/10.2174/0118715303265935231114073638","url":null,"abstract":"Background: PPAR-γ is one of three members of the PPAR group of the nuclear receptor superfamily and plays an important regulatory role as a ligand-dependent transcription factor. Objective: This study aimed to identify the top 100 most influential articles in the field of PPAR-γ. We hypothesized that a bibliometric and scientometric analysis of the PPAR-γ research field could render trends that provide researchers and funding agencies valuable insight into the history of the field, and potential future directions. Methods: A literature search of publications was carried out using the Web of Science (WOS) and Scopus database based on specific subject words on September 11, 2023. Articles were listed in descending order of the number of citations. Statistical analysis was performed on the data of the top 100 cited articles in terms of year of publication, journal, research direction, institution, author, and country. Meanwhile, co-authorship networks and co-citation networks were constructed by using VOSviewer software, and keywords were analyzed for cooccurrence. Results: A total of 9,456 articles regarding PPAR-γ were identified and analyzed based on the WOS database, and the top 100 cited articles in the field of PPAR-γ were ranked by citation. The most cited article was published in 1998, with 2,571 citations and a density of 102.80 citations/ year. Of the 100 articles, Harvard University was the institution with the highest number of articles published. Spiegelman, B. M. was the author with the highest number of articles published. Using the VOSviewer software, we found that the most used keywords were geneexpression, activated receptor-gamma, and adipocyte differentiation. PPAR-γ, one of the most widely studied transcription factors, is an important drug target for many diseases. Therefore, screening for small molecule compounds targeting PPAR-γ remains of great value. Conclusion: The present study identified the top 100 most influential articles in the field of PPAR-γ, which help global researchers to better understand research perspectives and develop future research directions of PPAR-γ.","PeriodicalId":11614,"journal":{"name":"Endocrine, metabolic & immune disorders drug targets","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139677765","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comorbidity, Eating Behaviors and Smartphone Addiction in Italian Nurses’ Characteristics 意大利护士的共病、饮食行为和智能手机成瘾特征
IF 1.9 4区 医学
Endocrine, metabolic & immune disorders drug targets Pub Date : 2024-02-03 DOI: 10.2174/0118715303271067231129103920
Elsa Vitale, Rocco Mea
{"title":"Comorbidity, Eating Behaviors and Smartphone Addiction in Italian Nurses’ Characteristics","authors":"Elsa Vitale, Rocco Mea","doi":"10.2174/0118715303271067231129103920","DOIUrl":"https://doi.org/10.2174/0118715303271067231129103920","url":null,"abstract":"Background: Evidence suggested how nurses experienced worse lifestyles than the general population by recording deterioration rates in healthy conditions. Aim: To assess differences between comorbidity, eating behavior, and smartphone addiction according to sex, Body Mass Index (BMI), age, work experience, shift, alcohol assumption, and physical activity in Italian nurses. Methods: An online questionnaire was spread through some professional internet pages. Data included demographic characteristics, the Charlson Comorbidity Index (CCI), the Italian Version of the Dutch Eating Behavior Questionnaire, and the Smartphone Addiction Scale (SASSV). Results: A total of 456 nurses were recruited. Significant differences were registered in the smartphone addiction score (p=0.030) and BMI scores and work experience (p=0.001), as underweight participants reported higher scores in the smartphone addiction attitude (2.4714 ± 1.25812) than the other subjects and also participants with the highest number of years in work experience also reported higher smartphone addiction scores (2.8074 ± 1.2022). Significant difference was reported in the CCI scores according to age (p< 0.001): subjects aged over 61 years recorded higher scores in the CCI (1.67 ± 1.528) and also according to work experience and CCI scores (p< 0.001), as participants employed between 21 and 30 years reported higher scores in the CCI (1.27 ± 1.382) and also to night shift (p=0.037), as participants who worked during the night shift also reported higher scores in the CCI. A significant difference was reported only for restrained eating attitude (p=0.034), as participants who declared to assume alcohol 2-3 times per month recorded higher levels in this eating attitude aspect (32.32 ± 7.181). Conclusion: Female nurses, overweight and obese nurses with low physical activity practice, seemed to spend more time with their smartphones. Healthcare organizations should consider findings to prevent unhealthy lifestyles among nurses, which could negatively influence the whole healthcare system.","PeriodicalId":11614,"journal":{"name":"Endocrine, metabolic & immune disorders drug targets","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139677776","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Yiqi Jiedu Xiaoying Decoction Improves Experimental Autoimmune Thyroiditis in Rats by Regulating Th17/Treg Cell Balance 益气解毒汤通过调节 Th17/Treg 细胞平衡改善大鼠的实验性自身免疫性甲状腺炎
IF 1.9 4区 医学
Endocrine, metabolic & immune disorders drug targets Pub Date : 2024-02-03 DOI: 10.2174/0118715303256311231122094516
Hui Zhu, Shumin Mu, Shiyin Liu, Yang Cui, Jianyu Ren, Enquan Yang, Lining Wang, Xiaoke Cui, Ailing Ren
{"title":"Yiqi Jiedu Xiaoying Decoction Improves Experimental Autoimmune Thyroiditis in Rats by Regulating Th17/Treg Cell Balance","authors":"Hui Zhu, Shumin Mu, Shiyin Liu, Yang Cui, Jianyu Ren, Enquan Yang, Lining Wang, Xiaoke Cui, Ailing Ren","doi":"10.2174/0118715303256311231122094516","DOIUrl":"https://doi.org/10.2174/0118715303256311231122094516","url":null,"abstract":"Background: Experimental autoimmune thyroiditis (EAT) is a widely used animal model to study the pathogenesis and treatment of autoimmune thyroid diseases. Yiqi Jiedu Xiaoying Decoction (YJXD) is a traditional Chinese medicine formula with potential immunomodulatory effects. In this study, we investigated the therapeutic effects of YJXD on EAT in rats and explored its underlying mechanisms. background: The study created a rat model of experimental autoimmune thyroiditis (EAT) to explore the mechanism of Yiqi Jiedu Xiaoying Decoction (YJXD) in the treatment of Hashimoto's thyroiditis (HT). Methods: Female Wistar rats were induced to develop EAT by immunization with thyroglobulin (Tg) and taken sodium iodide water (0.05%) and then treated with YJXD or sodium selenite. HE staining was used to observe the pathological changes of thyroid tissue in EAT rats. Th17 and Treg cell frequencies were analyzed by flow cytometry, and the expression levels of Th17- and Treg-related cytokines and thyroid autoantibody were determined by enzyme-linked immunosorbent assay (ELISA). The expression of Th17- and Treg-related transcriptional factors was detected by real-time polymerase chain reaction (RT-PCR) and Immunohistochemistry (IHC). objective: No Results: Our results demonstrated that treatment with YJXD significantly attenuated the severity of EAT, as evidenced by reduced thyroid gland inflammatory infiltration and decreased serum thyroglobulin autoantibody levels. Importantly, YJXD treatment effectively modulated the Th17/Treg cell balance by suppressing Th17 cell differentiation and promoting Treg cell expansion. Moreover, YJXD was also found to regulate the expression levels of Th17- and Tregrelated cytokines and transcriptional factors, further supporting its immunomodulatory effects in EAT. method: The rat model of EAT was established by subcutaneous injection of porcine thyroglobulin(pTg) combined with high iodine water, and was treated with YJXD and sodium selenite. HE staining was used to observe the pathological changes of thyroid tissue in rats. ELISA were used to detect levels of serum TPOAb, TGAb, interleukin (IL)-17, interleukin (IL)-6, transforming growth factor-β (TGF-β) and interleukin (IL)-10. The percentage of T helper cells 17 (Th17) and regulatory T cells (Treg) of rat spleen mononuclear cells were detected by flow cytometry. The expression of forkhead box P3 (FOXP3), RAR-related orphan receptor gamma T (RORγt) in thyroid tissues of rats were detected by immunohistochemistry. The mRNA expression of Signal Transducer and Activator of Transcription 3 (STAT3), RORγt, FOXP3 and Signal Transducer and Activator of Transcription 5 (STAT5) in spleen was detected by quantitative real-time polymerase chain reaction (qRT-PCR). Conclusion: YJXD exerted therapeutic effects on EAT by regulating the Th17/Treg cell balance, modulating the production of Th17- and Treg-related cytokines and the expression of transcriptional factors. result: In traditional Chin","PeriodicalId":11614,"journal":{"name":"Endocrine, metabolic & immune disorders drug targets","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139677771","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Review on the Role of Inflammation in Coronavirus Disease 炎症在冠状病毒疾病中的作用综述
IF 1.9 4区 医学
Endocrine, metabolic & immune disorders drug targets Pub Date : 2024-02-02 DOI: 10.2174/0118715303265274231204075802
Arezoo Lotfi, Pouran Hajian, Laleh Abbasi, Morad Kohandel Gargari, Najmeh Nameh Goshay Fard, Delaram Naderi
{"title":"A Review on the Role of Inflammation in Coronavirus Disease","authors":"Arezoo Lotfi, Pouran Hajian, Laleh Abbasi, Morad Kohandel Gargari, Najmeh Nameh Goshay Fard, Delaram Naderi","doi":"10.2174/0118715303265274231204075802","DOIUrl":"https://doi.org/10.2174/0118715303265274231204075802","url":null,"abstract":": The respiratory illness known as COVID-19 is caused by the novel coronavirus, SARS-CoV-2. While the precise pathogenic mechanism of COVID-19 remains unclear, the occurrence of a cytokine storm subsequent to viral infection plays a pivotal role in the initiation and advancement of the disease. The infection of SARS-CoV-2 induces a state of immune system hyperactivity, leading to an excessive production of inflammatory cytokines. Consequently, the identification of the various signaling pathways implicated in the inflammation induced by COVID-19 will enable researchers to investigate new targets for therapeutic intervention.","PeriodicalId":11614,"journal":{"name":"Endocrine, metabolic & immune disorders drug targets","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139668742","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Organelle Targeted Drug Delivery: Key Challenges, Recent Advancements and Therapeutic Implications 细胞器靶向给药:关键挑战、最新进展和治疗意义
IF 1.9 4区 医学
Endocrine, metabolic & immune disorders drug targets Pub Date : 2024-02-02 DOI: 10.2174/0118715303282573240112104035
Dilpreet Singh
{"title":"Organelle Targeted Drug Delivery: Key Challenges, Recent Advancements and Therapeutic Implications","authors":"Dilpreet Singh","doi":"10.2174/0118715303282573240112104035","DOIUrl":"https://doi.org/10.2174/0118715303282573240112104035","url":null,"abstract":": Organelle-specific targeted drug delivery has emerged as a promising approach in the field of drug delivery and therapeutics. This innovative strategy involves the precise delivery of therapeutic agents to specific organelles within cells, such as the nucleus, mitochondria, endoplasmic reticulum, or lysosomes, with the aim of enhancing drug efficacy while minimizing offtarget effects. Despite its tremendous potential, organelle-specific drug delivery faces several key challenges. One major challenge is the development of delivery systems that can accurately navigate the complex intracellular environment and deliver drugs exclusively to the desired organelles. Achieving this level of precision demands advanced nanotechnology and biomaterials engineering. Furthermore, ensuring the safety and biocompatibility of these delivery systems is paramount. Recent advancements in this field include the development of nanocarriers, such as liposomes, nanoparticles, and dendrimers, designed to target specific organelles through ligandreceptor interactions or pH-responsive mechanisms. Additionally, advancements in molecular biology and genetic engineering have enabled the design of genetically encoded organellespecific drug delivery systems. The therapeutic implications of organelle-specific drug delivery are vast. This approach has the potential to revolutionize the treatment of diseases with organelle- specific pathologies, such as neurodegenerative disorders, cancer, and mitochondrial diseases. By precisely targeting the organelles involved in disease progression, the efficacy of therapies can be significantly improved while minimizing collateral damage to healthy tissues.","PeriodicalId":11614,"journal":{"name":"Endocrine, metabolic & immune disorders drug targets","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139668507","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
CD163 as a Potential Biomarker-associated Immune Inflammation in Diabetes Mellitus: A Systematic Review and Bioinformatics Analysis. CD163 作为糖尿病相关免疫炎症的潜在生物标记物:系统综述和生物信息学分析
IF 1.9 4区 医学
Endocrine, metabolic & immune disorders drug targets Pub Date : 2024-01-01 DOI: 10.2174/1871530323666230714162324
Yang Cao, Ning Liang, Kaili Kong, Xiaomei Qiao, Ting Liu, Jing-Ai Fang, Xiaodong Zhang
{"title":"CD163 as a Potential Biomarker-associated Immune Inflammation in Diabetes Mellitus: A Systematic Review and Bioinformatics Analysis.","authors":"Yang Cao, Ning Liang, Kaili Kong, Xiaomei Qiao, Ting Liu, Jing-Ai Fang, Xiaodong Zhang","doi":"10.2174/1871530323666230714162324","DOIUrl":"10.2174/1871530323666230714162324","url":null,"abstract":"<p><strong>Background: </strong>Several studies have identified CD163 as a potential mediator of diabetes mellitus through an immune-inflammation. Further study is necessary to identify its specific mechanism.</p><p><strong>Objectives: </strong>In this study, we aimed to investigate CD163 as a potential biomarker associated with immune inflammation in diabetes mellitus through a systematic review and bioinformatics analysis.</p><p><strong>Methods: </strong>We searched PubMed, Web of Science, the Cochrane Library, and Embase databases with a time limit of September 2, 2022. Furthermore, we conducted a systematic search and review based on PRISMA guidelines. Additionally, diabetic gene expression microarray datasets GSE29221, GSE30528, GSE30529, and GSE20966 were downloaded from the GEO database (http://www.ncbi.nlm.nih.gov/geo) for bioinformatics analysis. The PROSPERO number for this study is CRD420222347160.</p><p><strong>Results: </strong>Following the inclusion and exclusion criteria, seven articles included 1607 patients, comprising 912 diabetic patients and 695 non-diabetic patients. This systematic review found significantly higher levels of CD163 in diabetic patients compared to non-diabetic patients. People with diabetes had higher levels of CRP expression compared to the control group. Similarly, two of the three papers that used TNF- α as an outcome indicator showed higher expression levels in diabetic patients. Furthermore, IL-6 expression levels were higher in diabetic patients than in the control group. A total of 62 samples were analyzed by bioinformatics (33 case controls and 29 experimental groups), and 85 differential genes were identified containing CD163. According to the immune cell correlation analysis, CD163 was associated with macrophage M2, γδ T lymphocytes, macrophage M1, and other immune cells. Furthermore, to evaluate the diagnostic performance of CD163, we validated it using the GSE20966 dataset. In the validation set, CD163 showed high diagnostic accuracy.</p><p><strong>Conclusion: </strong>This study suggests CD163 participates in the inflammatory immune response associated with diabetes mellitus and its complications by involving several immune cells. Furthermore, the results suggest CD163 may be a potential biomarker reflecting immune inflammation in diabetic mellitus.</p>","PeriodicalId":11614,"journal":{"name":"Endocrine, metabolic & immune disorders drug targets","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9771240","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Mini-review on Helicobacter pylori with Gastric Cancer and Available Treatments. 幽门螺杆菌与胃癌及现有治疗方法微型综述。
IF 1.9 4区 医学
Endocrine, metabolic & immune disorders drug targets Pub Date : 2024-01-01 DOI: 10.2174/1871530323666230824161901
Teresa V Jacob, Gaurav M Doshi
{"title":"A Mini-review on <i>Helicobacter pylori</i> with Gastric Cancer and Available Treatments.","authors":"Teresa V Jacob, Gaurav M Doshi","doi":"10.2174/1871530323666230824161901","DOIUrl":"10.2174/1871530323666230824161901","url":null,"abstract":"<p><p><i>Helicobacter pylori (H. pylori)</i> is the most thoroughly researched etiological component for stomach inflammation and malignancies. Even though there are conventional recommendations and treatment regimens for eradicating <i>H. pylori</i>, failure rates continue to climb. Antibiotic resistance contributes significantly to misdiagnoses, false positive results, and clinical failures, all of which raise the chance of infection recurrence. This review aims to explore the molecular mechanisms underlying drug resistance in <i>H. pylori</i> and discuss novel approaches for detecting genotypic resistance. Modulation of drug uptake/ efflux, biofilm, and coccoid development. Newer genome sequencing approaches capable of detecting <i>H. pylori</i> genotypic resistance are presented. Prolonged infection in the stomach causes major problems such as gastric cancer. The review discusses how <i>H. pylori</i> causes stomach cancer, recent biomarkers such as miRNAs, molecular pathways in the development of gastric cancer, and diagnostic methods and clinical trials for the disease. Efforts have been made to summarize the recent advancements made toward early diagnosis and novel therapeutic approaches for <i>H. pylori</i>-induced gastric cancer.</p>","PeriodicalId":11614,"journal":{"name":"Endocrine, metabolic & immune disorders drug targets","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10124098","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Investigation of Pancreatic-beta Cells Role in the Biological Process of Ageing. 研究胰腺-β细胞在生物老化过程中的作用
IF 1.9 4区 医学
Endocrine, metabolic & immune disorders drug targets Pub Date : 2024-01-01 DOI: 10.2174/1871530323666230822095932
Rishabh Chaudhary, Janvi Khanna, Manni Rohilla, Sumeet Gupta, Seema Bansal
{"title":"Investigation of Pancreatic-beta Cells Role in the Biological Process of Ageing.","authors":"Rishabh Chaudhary, Janvi Khanna, Manni Rohilla, Sumeet Gupta, Seema Bansal","doi":"10.2174/1871530323666230822095932","DOIUrl":"10.2174/1871530323666230822095932","url":null,"abstract":"<p><strong>Background: </strong>Cellular senescence is associated with the formation and progression of a range of illnesses, including ageing and metabolic disorders such as diabetes mellitus and pancreatic beta cell dysfunction. Ageing and reduced glucose tolerance are interconnected. Often, Diabetes is becoming more common, which is concerning since it raises the risk of a variety of age-dependent disorders such as cardiovascular disease, cancer, Parkinson's disease, stroke, and Alzheimer's disease.</p><p><strong>Objectives: </strong>The objectives of this study are to find out the most recent research on how ageing affects the functions of pancreatic beta cells, beta cell mass, beta cell senescence, mitochondrial dysfunction, and hormonal imbalance.</p><p><strong>Methods: </strong>Various research and review manuscripts are gathered from various records such as Google Scholar, PubMed, Mendeley, Scopus, Science Open, the Directory of Open Access Journals, and the Education Resources Information Centre, using different terms like \"Diabetes, cellular senescence, beta cells, ageing, insulin, glucose\".</p><p><strong>Results: </strong>In this review, we research novel targets in order to discover new strategies to treat diabetes. Abnormal glucose homeostasis and type 2 diabetes mellitus in the elderly may aid in the development of novel medicines to delay or prevent diabetes onset, improve quality of life, and, finally, increase life duration.</p><p><strong>Conclusion: </strong>Aging accelerates beta cell senescence by generating premature cell senescence, which is mostly mediated by high glucose levels. Despite higher plasma glucose levels, hepatic gluconeogenesis accelerates and adipose tissue lipolysis rises, resulting in an increase in free fatty acid levels in the blood and worsening insulin resistance throughout the body.</p>","PeriodicalId":11614,"journal":{"name":"Endocrine, metabolic & immune disorders drug targets","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10407786","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Association of Obesity based on Different Metabolic Status with Risk of Gout Occurrence in Patients: A National Study. 基于不同代谢状态的肥胖与痛风患者发病风险的关系:一项全国性研究。
IF 1.9 4区 医学
Endocrine, metabolic & immune disorders drug targets Pub Date : 2024-01-01 DOI: 10.2174/1871530323666230911140635
Yanyan Wang, Luna Liu, Shizhan Ma, Junming Han, Zhixiang Wang, Xiude Fan, Xu Hou
{"title":"Association of Obesity based on Different Metabolic Status with Risk of Gout Occurrence in Patients: A National Study.","authors":"Yanyan Wang, Luna Liu, Shizhan Ma, Junming Han, Zhixiang Wang, Xiude Fan, Xu Hou","doi":"10.2174/1871530323666230911140635","DOIUrl":"10.2174/1871530323666230911140635","url":null,"abstract":"<p><strong>Background: </strong>Obesity often co-exists with metabolic abnormalities, but the results of studies on the relationship between obesity, metabolic abnormalities and the risk of gout are inconsistent.</p><p><strong>Objectives: </strong>We aimed to study whether there was a mutual regulation between obesity, metabolic abnormalities and the risk of gout.</p><p><strong>Methods: </strong>We conducted a cross-sectional study to expound the association between obesity based on different metabolic statuses and the risk of gout. Patients were derived from Nationwide Readmission Database (2018 sample).</p><p><strong>Results: </strong>A total of 9,668,330 records were recruited for analysis from January to December. The risk of gout in the obesity group, metabolic abnormalities group and obesity combined with metabolic abnormalities group was 1.67 times (OR = 1.67, 95%CI 1.64-1.70), 3.12 times (OR = 3.12, 95%CI 3.09-3.15) and 4.27 times (OR = 4.27, 95%CI 4.22-4.32) higher than that in the normal control group. For different metabolic components, OR value was highest in hypertension group (OR = 2.65, 95%CI 2.60-2.70 and OR = 4.85, 95%CI 4.73-4.97), followed by dyslipidemia group (OR = 2.23, 95%CI 2.16-2.30 and OR = 3.74, 95%CI 3.55-3.95) and in hyperglycemia group (OR = 1.73, 95%CI 1.66-1.80 and OR = 2.94, 95%CI 2.78-3.11). Fewer components of metabolic syndrome were associated with a lower risk of gout in both nonobese and obese patients.</p><p><strong>Conclusion: </strong>When metabolic abnormalities were present, obesity induced a higher risk of gout. Different components of metabolic abnormalities had different effects on the risk of gout occurrence, and the number of metabolic abnormalities was closely related to the risk of gout occurrence. Follow-up and intervention methods targeting obesity and metabolic abnormalities should be considered for patients with gout.</p>","PeriodicalId":11614,"journal":{"name":"Endocrine, metabolic & immune disorders drug targets","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10590717","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Boswellic Acids: A Critical Appraisal of Their Therapeutic and Nutritional Benefits in Chronic Inflammatory Diseases. 乳香酸:对其在慢性炎症性疾病中的治疗和营养作用的批判性评估。
IF 1.9 4区 医学
Endocrine, metabolic & immune disorders drug targets Pub Date : 2024-01-01 DOI: 10.2174/1871530323666230512154634
Neeta Solanki, Gaurav Gupta, Dinesh Kumar Chellappan, Sachin Kumar Singh, Monica Gulati, Keshav Raj Paudel, Philip M Hansbro, Kamal Dua, Suraj Bhan, Manisha Saini, Harish Dureja
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