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[Role of m6A methylation modification in photoaging and ultraviolet-induced skin cancers]. [m6A甲基化修饰在光老化和紫外线诱导皮肤癌中的作用]。
Q3 Medicine Pub Date : 2025-11-28 DOI: 10.11817/j.issn.1672-7347.2025.250199
Yanni Hou, Xiaoqing Zhang, Jun Liu, Jingdong Wu

Ultraviolet (UV) radiation, one of the critical environmental carcinogenic factors, promotes skin photoaging and carcinogenesis by inducing DNA damage, oxidative stress, and chronic inflammatory cascades. N6-methyladenosine (m6A)-modifying enzymes (writers, erasers, and readers) play bidirectional regulatory roles in UV-mediated skin pathology. In photoaging, the reactive oxygen species (ROS)-m6A axis accelerates collagen degradation and epithelial-mesenchymal transition (EMT) through modulation of matrix metalloproteinases (MMPs), inflammatory mediators, DNA damage repair, apoptosis, and collagen metabolism. In skin cancers, m6A regulators promote tumor progression by influencing oncogenic signaling, proliferation, invasion, metastasis, and immune evasion. Bioactive monomeric compounds derived from traditional Chinese medicine, including polyphenols, saponins, and alkaloids, can regulate the activity of m6A enzymes to interfere with photoaging and UV-induced skin carcinogenesis. This study integrates current evidence to establish an m6A-targeted epigenetic intervention framework for UV-induced skin injury and highlights the potential of synergistic multi-component m6A-modulating therapeutic strategies as a future research priority.

紫外线(UV)辐射是重要的环境致癌因素之一,通过诱导DNA损伤、氧化应激和慢性炎症级联反应,促进皮肤光老化和致癌。n6 -甲基腺苷(m6A)修饰酶(写入酶、擦除酶和读取酶)在紫外线介导的皮肤病理中起双向调节作用。在光老化过程中,活性氧(ROS)-m6A轴通过调节基质金属蛋白酶(MMPs)、炎症介质、DNA损伤修复、细胞凋亡和胶原代谢,加速胶原降解和上皮-间质转化(EMT)。在皮肤癌中,m6A调节因子通过影响致癌信号、增殖、侵袭、转移和免疫逃避来促进肿瘤进展。来自中药的生物活性单体化合物,包括多酚、皂苷和生物碱,可以调节m6A酶的活性,从而干扰光老化和紫外线诱导的皮肤癌。本研究整合了目前的证据,建立了针对m6a的紫外线诱导皮肤损伤的表观遗传干预框架,并强调了协同多组分m6a调节治疗策略的潜力,作为未来的研究重点。
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引用次数: 0
Toxic epidermal necrolysis associated with immune checkpoint inhibitors for bladder cancer: A case report. 膀胱癌中毒性表皮坏死松解与免疫检查点抑制剂相关:1例报告。
Q3 Medicine Pub Date : 2025-11-28 DOI: 10.11817/j.issn.1672-7347.2025.250313
Yangyang Wang, Lihua Liu, Meiyun Li

Immune checkpoint inhibitors (ICIs) play a significant role in tumor treatment, but the immune-related adverse events (irAEs), which brings about have also attracted much attention. Among them, toxic epidermal necrolysis (TEN) is one of the most severe skin toxic reactions. This article reports a case of a bladder cancer patient who developed TEN after receiving ICIs treatment. The male patient was diagnosed with bladder cancer in November 2023. On April 29, 2024, he was admitted to the Third Hospital of Changsha for antitumor treatment. In May 2024, he developed immune-related myocarditis after treatment with toripalimab. On July 6, 2024, the patient switched to envafolimab treatment, and on July 16, he developed rashes and eventually progressed to TEN. After treatment with glucocorticoids and related symptomatic measures, the patient improved. TEN is a rare but serious irAE in ICIs treatment. Suspected patients should be intervened early, and patients who have already developed it should be actively treated, in order to enhance the understanding and management of TEN caused by ICIs treatment.

免疫检查点抑制剂(Immune checkpoint inhibitors, ICIs)在肿瘤治疗中发挥着重要作用,但其带来的免疫相关不良事件(Immune -related adverse events, irAEs)也备受关注。其中,毒性表皮坏死松解(TEN)是最严重的皮肤毒性反应之一。本文报告一例膀胱癌患者在接受ICIs治疗后发生TEN。这名男性患者于2023年11月被诊断出患有膀胱癌。2024年4月29日,在长沙市第三医院接受抗肿瘤治疗。2024年5月,他在接受托帕里单抗治疗后出现免疫相关性心肌炎。2024年7月6日,患者改用依那福利单抗治疗,7月16日,患者出现皮疹,最终进展为TEN。经糖皮质激素治疗及相关对症治疗后,患者病情好转。在ICIs治疗中,10是一种罕见但严重的irAE。疑似患者应及早干预,已发生的患者应积极治疗,以提高对ICIs治疗所致TEN的认识和管理。
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引用次数: 0
LOX-1 gene knockout improves metabolic dysfunction-associated steatohepatitis in mice. 敲除LOX-1基因可改善小鼠代谢功能障碍相关的脂肪性肝炎。
Q3 Medicine Pub Date : 2025-11-28 DOI: 10.11817/j.issn.1672-7347.2025.250194
Ruihua Huang, Yongyu Yang, Shuhan Zhou, Xiaoyun Zhu, Changping Hu
<p><strong>Objectives: </strong>Metabolic dysfunction-associated steatohepatitis (MASH), a progressive subtype of metabolic dysfunction-associated steatotic liver disease (MASLD), is characterized by hepatic steatosis, lobular inflammation, and hepatocyte ballooning, and may further progress to liver fibrosis and cirrhosis. Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1), a member of the scavenger receptor family, recognizes and binds oxidized low-density lipoprotein. This study aims to investigate the role of LOX-1 in MASH progression.</p><p><strong>Methods: </strong>LOX-1 expression in MASLD mouse liver was analyzed using Gene Expression Omnibus (GEO) datasets. Immunofluorescence staining was performed to detect LOX-1 and alpha-smooth muscle actin (α-SMA) levels and co-localization in fibrotic liver tissues and LX-2 cells. <i>LOX-1</i> knockout (<i>Lox-1</i><sup>-/-</sup>) mice were generated using CRISPR/caspase-9 (Cas9) and genotyped by PCR and Sanger sequencing. Wild-type (WT) and <i>Lox-1</i><sup>-/-</sup> mice were randomized into control and Western diet model groups. Serum and liver samples were collected for alanine aminotransferase (ALT) and aspartate aminotransferase (AST) measurement by biochemical kits, liver structure evaluation by hematoxylin and eosin (HE) staining, collagen deposition by Masson staining, lipid accumulation by Oil Red O staining, and fibrotic marker gene expression by real-time quantitative PCR (RT-qPCR). Network pharmacology and search tool for the retrieval of interacting genes/proteins (STRING)-based protein-protein interaction (PPI) with Gene Ontology (GO) enrichment were used to predict downstream targets and pathways.</p><p><strong>Results: </strong>The results from the GEO datasets GSE30552 and GSE40041 indicated <i>LOX-1</i> mRNA was upregulated in high fat diet (HFD) and bile duct ligation (BDL) mouse models (both <i>P</i><0.001). LOX-1 and α-SMA levels were elevated in fibrotic liver tissues. <i>Lox-1</i><sup>-/-</sup> mice were successfully established. Biochemical tests showed that serum AST and ALT levels were significantly elevated in WT mice fed a Western diet (both <i>P</i><0.001), and these levels decreased after <i>LOX-1</i> knockout (both <i>P</i><0.05). HE staining revealed that WT mice on the Western diet exhibited marked hepatocellular ballooning degeneration, steatosis, inflammatory cell infiltration, and periportal fibroplasia, which were significantly ameliorated by <i>LOX-1</i> knockout. Masson staining demonstrated increased blue-stained collagen fibers in the liver tissues of WT mice fed the Western diet compared with control-diet mice, and <i>LOX-1</i> knockout inhibited collagen fiber deposition (all <i>P</i><0.05). RT‑qPCR results showed that hepatic mRNA levels of <i>Acta2</i>, <i>Col1a1</i>, and <i>Timp1</i> were significantly increased in Western diet-fed mice, and <i>LOX-1</i> knockout reduced the expression of these fibrogenic marker genes. Oil Red O staining in
目的:代谢功能障碍相关脂肪性肝炎(MASH)是代谢功能障碍相关脂肪性肝病(MASLD)的一种进行性亚型,以肝脂肪变性、小叶炎症和肝细胞球囊化为特征,并可能进一步发展为肝纤维化和肝硬化。凝集素样氧化低密度脂蛋白受体-1 (LOX-1)是清道夫受体家族的一员,可识别并结合氧化低密度脂蛋白。本研究旨在探讨LOX-1在MASH进展中的作用。方法:采用基因表达综合数据库(Gene expression Omnibus, GEO)分析MASLD小鼠肝脏中LOX-1的表达。免疫荧光染色检测肝纤维化组织和LX-2细胞中LOX-1和α-平滑肌肌动蛋白(α-SMA)水平及共定位。采用CRISPR/caspase-9 (Cas9)技术构建LOX-1基因敲除(LOX-1 -/-)小鼠,采用PCR和Sanger测序进行基因分型。野生型(WT)和Lox-1-/-小鼠随机分为对照组和西粮模型组。采集血清和肝脏标本,采用生化试剂盒检测谷丙转氨酶(ALT)和天冬氨酸转氨酶(AST),苏木精和伊红(HE)染色评估肝脏结构,Masson染色评估胶原沉积,Oil Red O染色评估脂质积累,实时定量PCR (RT-qPCR)检测纤维化标志物基因表达。利用网络药理学和检索相互作用基因/蛋白质(STRING)的搜索工具(基于基因本体(GO)富集的蛋白质-蛋白质相互作用(PPI))来预测下游靶点和途径。结果:GEO数据集GSE30552和GSE40041的结果表明,高脂饮食(HFD)和胆管结扎(BDL)小鼠模型(两种PLox-1-/-小鼠均成功建立)中LOX-1 mRNA表达上调。生化试验显示,饲喂Western diet(均敲除PLOX-1)的WT小鼠血清AST和ALT水平显著升高。Masson染色显示,与对照组小鼠相比,饲喂西方饮食的WT小鼠肝组织中蓝色胶原纤维增加,并且敲除LOX-1抑制胶原纤维沉积(Western饮食小鼠的PActa2、Col1a1和Timp1均显著增加,敲除LOX-1降低了这些纤维化标记基因的表达。油红O染色显示,喂食西方饮食的WT小鼠肝细胞明显增大,表现为大泡性脂肪变性,并呈现弥散分布的红色脂滴,而敲除LOX-1可减轻肝脏脂质积累(PLOX-1均降低LX - 2细胞中Acta2、Col1a1和Timp1 mRNA水平)(所有PLOX-1沉默均抑制α - SMA表达。网络药理学提示LOX-1可能通过脂质和胆固醇代谢网络促进MASH。结论:敲除LOX-1基因可改善西方饮食诱导的小鼠MASH,可能是一个潜在的治疗靶点。
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引用次数: 0
[Influencing factors of cognitive function decline in elderly patients with type 2 diabetes mellitus]. 老年2型糖尿病患者认知功能下降的影响因素
Q3 Medicine Pub Date : 2025-11-28 DOI: 10.11817/j.issn.1672-7347.2025.250081
Hui Zeng, Guanxiu Tang, Qian Liu, Yue He, Hongmei Zhou, Pingping Yan

Objectives: The global prevalence of type 2 diabetes mellitus (T2DM) continues to rise, and cognitive impairment caused by T2DM is particularly common among elderly patients. This study aims to explore the influencing factors of cognitive function decline in elderly patients with T2DM, so as to provide references for the prevention of cognitive impairment in elderly patients with T2DM.

Methods: A total of 376 patients aged over 60 years with T2DM without cognitive impairment who visited the Department of Geriatrics and Endocrinology of Third Xiangya Hospital for the first time from June 2019 to December 2020 were selected. General information, lifestyle behaviors, laboratory-related indicators, activities of daily living, and depression scores were collected. One year after discharge, cognitive function was reassessed. According to the reassessment scores, patients were divided into a cognitive function maintenance group and a cognitive function decline group. Logistic regression analysis was used to explore the risk factors for cognitive function decline in elderly patients with T2DM.

Results: The incidence of cognitive function decline in elderly patients with T2DM at 1 year was 13.3%. Univariate analysis revealed that there were statistically significant differences between the cognitive function decline group and the cognitive function maintenance group in age, educational level, marital status, smoking history, amount of physical exercise, housework performance, Instrumental Activities of Daily Living (IADL) score, and 2 hours postprandial glucose (2hPG) (P<0.05). Multivariate logistic regression analysis showed that age (OR=2.795, 95% CI 1.785 to 4.375, P<0.001), 2hPG (OR=1.232, 95% CI 1.087 to 1.397, P=0.001), housework performance (OR=2.438, 95% CI 1.017 to 5.844, P=0.046), and physical exercise time ≥1 hour/day (OR=0.107, 95% CI 0.012 to 0.916, P=0.041) were independent influencing factors for cognitive function decline in patients with T2DM.

Conclusions: Advanced age, high 2hPG, less housework, and physical exercise time <1 hour/day are risk factors for cognitive function decline in patients with T2DM. Reasonable control of postprandial blood glucose and increasing physical activity and housework time may help delay cognitive function decline in patients with T2DM.

2型糖尿病(T2DM)的全球患病率持续上升,由T2DM引起的认知功能障碍在老年患者中尤为常见。本研究旨在探讨老年T2DM患者认知功能下降的影响因素,为老年T2DM患者认知功能障碍的预防提供参考。方法:选取2019年6月至2020年12月湘雅第三医院老年与内分泌科首次就诊的60岁以上无认知功能障碍T2DM患者376例。收集一般信息、生活方式行为、实验室相关指标、日常生活活动和抑郁评分。出院一年后,重新评估认知功能。根据再评估得分将患者分为认知功能维持组和认知功能下降组。采用Logistic回归分析探讨老年T2DM患者认知功能下降的危险因素。结果:老年T2DM患者1年认知功能下降发生率为13.3%。单因素分析显示,认知功能下降组与认知功能维持组在年龄、受教育程度、婚姻状况、吸烟史、体育锻炼量、家务劳动表现、日常生活工具活动(IADL)评分、餐后2小时血糖(2hPG) (POR=2.795, 95% CI 1.785 ~ 4.375, POR=1.232, 95% CI 1.087 ~ 1.397, P=0.001)、家务劳动表现(OR=2.438, P=0.001)、家务劳动表现(OR=2.438, P=0.001)等方面差异均有统计学意义。95% CI 1.017 ~ 5.844, P=0.046)、体育锻炼时间≥1小时/天(OR=0.107, 95% CI 0.012 ~ 0.916, P=0.041)是T2DM患者认知功能下降的独立影响因素。结论:高龄、2hPG高、家务劳动少、体育锻炼时间多
{"title":"[Influencing factors of cognitive function decline in elderly patients with type 2 diabetes mellitus].","authors":"Hui Zeng, Guanxiu Tang, Qian Liu, Yue He, Hongmei Zhou, Pingping Yan","doi":"10.11817/j.issn.1672-7347.2025.250081","DOIUrl":"https://doi.org/10.11817/j.issn.1672-7347.2025.250081","url":null,"abstract":"<p><strong>Objectives: </strong>The global prevalence of type 2 diabetes mellitus (T2DM) continues to rise, and cognitive impairment caused by T2DM is particularly common among elderly patients. This study aims to explore the influencing factors of cognitive function decline in elderly patients with T2DM, so as to provide references for the prevention of cognitive impairment in elderly patients with T2DM.</p><p><strong>Methods: </strong>A total of 376 patients aged over 60 years with T2DM without cognitive impairment who visited the Department of Geriatrics and Endocrinology of Third Xiangya Hospital for the first time from June 2019 to December 2020 were selected. General information, lifestyle behaviors, laboratory-related indicators, activities of daily living, and depression scores were collected. One year after discharge, cognitive function was reassessed. According to the reassessment scores, patients were divided into a cognitive function maintenance group and a cognitive function decline group. Logistic regression analysis was used to explore the risk factors for cognitive function decline in elderly patients with T2DM.</p><p><strong>Results: </strong>The incidence of cognitive function decline in elderly patients with T2DM at 1 year was 13.3%. Univariate analysis revealed that there were statistically significant differences between the cognitive function decline group and the cognitive function maintenance group in age, educational level, marital status, smoking history, amount of physical exercise, housework performance, Instrumental Activities of Daily Living (IADL) score, and 2 hours postprandial glucose (2hPG) (<i>P</i><0.05). Multivariate logistic regression analysis showed that age (<i>OR</i>=2.795, 95% <i>CI</i> 1.785 to 4.375, <i>P</i><0.001), 2hPG (<i>OR</i>=1.232, 95% <i>CI</i> 1.087 to 1.397, <i>P</i>=0.001), housework performance (<i>OR</i>=2.438, 95% <i>CI</i> 1.017 to 5.844, <i>P</i>=0.046), and physical exercise time ≥1 hour/day (<i>OR</i>=0.107, 95% <i>CI</i> 0.012 to 0.916, <i>P</i>=0.041) were independent influencing factors for cognitive function decline in patients with T2DM.</p><p><strong>Conclusions: </strong>Advanced age, high 2hPG, less housework, and physical exercise time <1 hour/day are risk factors for cognitive function decline in patients with T2DM. Reasonable control of postprandial blood glucose and increasing physical activity and housework time may help delay cognitive function decline in patients with T2DM.</p>","PeriodicalId":39801,"journal":{"name":"中南大学学报(医学版)","volume":"50 11","pages":"2062-2070"},"PeriodicalIF":0.0,"publicationDate":"2025-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144227","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","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 self-stigma, impulsivity, and insomnia with anxiety and depression in patients with Kallmann syndrome. 自我耻辱感、冲动、失眠与Kallmann综合征患者焦虑和抑郁的关系
Q3 Medicine Pub Date : 2025-11-28 DOI: 10.11817/j.issn.1672-7347.2025.250433
Xiong Tang, Feifei Wu, Yafang He, Han Wu, Jinfan Zhang, Haimiao Huang, Meichao Men, Xiaoping Yi, T Bihong Chen

Objectives: Kallmann syndrome (KS) is a rare inherited disorder characterized by congenital hypogonadotropic hypogonadism and reduced or absent olfactory function. In addition to gonadal dysgenesis and structural abnormalities, KS patients may present with extensive psychosocial dysfunction and behavioral changes. This study aims to evaluate the effects of self-stigma, impulsivity, and insomnia on anxiety and depression in KS patients and to explore the interrelationships among these factors.

Methods: A total of 206 patients with confirmed KS were recruited from the Xiangya Hospital and Henan Provincial People's Hospital. Multivariable Logistic regression analysis was used to identify independent factors associated with anxiety and depression, and a serial multiple-mediator model was applied to characterize pathway effects.

Results: The cohort of KS patients demonstrated substantial psychological and social burden, including self-stigma, impulsivity, insomnia, loneliness, anxiety, depression, and overall social isolation tendencies. Logistic regression analysis indicated that self-stigma (OR=1.112, P=0.003), loneliness (OR=1.198, P=0.007), and insomnia (OR=1.098, P=0.017) were independent factors the presence of anxiety and depression in KS patients. Mediation-effect modeling further showed that impulsivity and insomnia significantly mediated the effect of self-stigma on anxiety and depression in KS (indirect effect 3=0.013, P=0.008; 95% CI 0.004 to 0.024; c'=0.147, P<0.001; 95% CI 0.091 to 0.201).

Conclusions: This study preliminarily identified the major modifiable factors associated with anxiety and depression in KS patients, including self-stigma, loneliness, and insomnia. Impulsivity and insomnia demonstrated significant serial mediation effects linking self-stigma to affective outcomes. Multidimensional intervention strategies targeting stigma reduction, impulsivity regulation, and sleep-quality improvement may help alleviate anxiety-depression symptoms and ultimately improve overall quality of life in patients with KS.

目的:卡尔曼综合征(Kallmann syndrome, KS)是一种罕见的遗传性疾病,其特征是先天性促性腺功能低下和嗅觉功能下降或缺失。除了性腺发育不良和结构异常外,KS患者还可能出现广泛的社会心理功能障碍和行为改变。本研究旨在评估自我耻感、冲动和失眠对KS患者焦虑和抑郁的影响,并探讨这些因素之间的相互关系。方法:选取湘雅医院和河南省人民医院确诊的KS患者206例。采用多变量Logistic回归分析确定与焦虑和抑郁相关的独立因素,并采用一系列多中介模型来表征通路效应。结果:该队列KS患者表现出严重的心理和社会负担,包括自我耻辱、冲动、失眠、孤独、焦虑、抑郁和整体社会孤立倾向。Logistic回归分析显示,自我耻感(OR=1.112, P=0.003)、孤独感(OR=1.198, P=0.007)、失眠(OR=1.098, P=0.017)是影响KS患者焦虑、抑郁存在的独立因素。中介效应模型进一步显示,冲动和失眠显著介导了自我耻感对KS焦虑和抑郁的影响(间接效应3=0.013,P=0.008; 95% CI 0.004 ~ 0.024; c′=0.147,PCI 0.091 ~ 0.201)。结论:本研究初步确定了与KS患者焦虑和抑郁相关的主要可改变因素,包括自我耻辱感、孤独感和失眠。冲动性和失眠症表现出显著的系列中介效应,将自我耻辱与情感结果联系起来。针对耻感减少、冲动性调节和睡眠质量改善的多维干预策略可能有助于缓解KS患者的焦虑抑郁症状,并最终改善患者的整体生活质量。
{"title":"Association of self-stigma, impulsivity, and insomnia with anxiety and depression in patients with Kallmann syndrome.","authors":"Xiong Tang, Feifei Wu, Yafang He, Han Wu, Jinfan Zhang, Haimiao Huang, Meichao Men, Xiaoping Yi, T Bihong Chen","doi":"10.11817/j.issn.1672-7347.2025.250433","DOIUrl":"https://doi.org/10.11817/j.issn.1672-7347.2025.250433","url":null,"abstract":"<p><strong>Objectives: </strong>Kallmann syndrome (KS) is a rare inherited disorder characterized by congenital hypogonadotropic hypogonadism and reduced or absent olfactory function. In addition to gonadal dysgenesis and structural abnormalities, KS patients may present with extensive psychosocial dysfunction and behavioral changes. This study aims to evaluate the effects of self-stigma, impulsivity, and insomnia on anxiety and depression in KS patients and to explore the interrelationships among these factors.</p><p><strong>Methods: </strong>A total of 206 patients with confirmed KS were recruited from the Xiangya Hospital and Henan Provincial People's Hospital. Multivariable Logistic regression analysis was used to identify independent factors associated with anxiety and depression, and a serial multiple-mediator model was applied to characterize pathway effects.</p><p><strong>Results: </strong>The cohort of KS patients demonstrated substantial psychological and social burden, including self-stigma, impulsivity, insomnia, loneliness, anxiety, depression, and overall social isolation tendencies. Logistic regression analysis indicated that self-stigma (<i>OR</i>=1.112, <i>P</i>=0.003), loneliness (<i>OR</i>=1.198, <i>P</i>=0.007), and insomnia (<i>OR</i>=1.098, <i>P</i>=0.017) were independent factors the presence of anxiety and depression in KS patients. Mediation-effect modeling further showed that impulsivity and insomnia significantly mediated the effect of self-stigma on anxiety and depression in KS (indirect effect 3=0.013, <i>P</i>=0.008; 95% <i>CI</i> 0.004 to 0.024; c'=0.147, <i>P</i><0.001; 95% <i>CI</i> 0.091 to 0.201).</p><p><strong>Conclusions: </strong>This study preliminarily identified the major modifiable factors associated with anxiety and depression in KS patients, including self-stigma, loneliness, and insomnia. Impulsivity and insomnia demonstrated significant serial mediation effects linking self-stigma to affective outcomes. Multidimensional intervention strategies targeting stigma reduction, impulsivity regulation, and sleep-quality improvement may help alleviate anxiety-depression symptoms and ultimately improve overall quality of life in patients with KS.</p>","PeriodicalId":39801,"journal":{"name":"中南大学学报(医学版)","volume":"50 11","pages":"2095-2103"},"PeriodicalIF":0.0,"publicationDate":"2025-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144271","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Machine learning-based programmed cell death signature model for precise prediction of prognosis and treatment response in melanoma]. [基于机器学习的程序性细胞死亡特征模型用于精确预测黑色素瘤的预后和治疗反应]。
Q3 Medicine Pub Date : 2025-11-28 DOI: 10.11817/j.issn.1672-7347.2025.250286
Benliang Wei, Hong Liu
<p><strong>Objectives: </strong>The occurrence, metastasis, and drug resistance of melanoma pose major challenges to patient prognosis, and predictive models capable of accurately forecasting patient outcomes and guiding treatment are still lacking. This study aims to develop predictive models for melanoma prognosis and drug sensitivity based on mechanisms of programmed cell death (PCD).</p><p><strong>Methods: </strong>Genes related to 19 PCD patterns were collected and integrated from gene set enrichment analysis (GSEA), the Kyoto Encyclopedia of Genes and Genomes (KEGG), relevant reviews, and published studies to establish a comprehensive PCD signature gene set. Transcriptomic and clinical data from The Cancer Genome Atlas (TCGA) skin cutaneous melanoma (SKCM) cohort were obtained, and 3 untreated Gene Expression Omnibus (GEO) datasets (GSE65904, GSE19234, and GSE100797) were included as external validation cohorts. In addition, immunotherapy cohorts PRJEB23709, GSE136961, and GSE215222 were collected to validate the predictive value for immunotherapy. Single-cell transcriptomic data (GSE115978 and GSE215120) were processed using Seurat for quality control, normalization, dimensionality reduction, clustering, and cell annotation; spatial transcriptomic data were obtained from 10× Genomics and combined with Cottrazm for spatial partitioning and SpaCET deconvolution. Cell-cell communication was evaluated using CellChat to assess secreted signaling, extracellular matrix (ECM)-receptor interactions, and cell contact-mediated communication patterns. Based on the TCGA training set, a machine learning strategy comprising 10 algorithms and 101 combinations was used to construct PCD-related prognostic signatures, and the optimal model was selected using the average concordance index (C-index) across multiple cohorts. Differential analysis, GSEA, CIBERSORT, and Estimation of STromal and Immune cells in MAlignant Tumor tissues using Expression data (ESTIMATE) were further applied to evaluate immune infiltration, calculate T-cell receptor (TCR) clonal diversity, cytolytic activity, and T-cell effector gene expression profiles, and to explore the association between the PCD score (PCDS) and drug sensitivity.</p><p><strong>Results: </strong>The activities of the 19 PCD pathways differed significantly between normal skin and SKCM, suggesting that dysregulation is involved in melanoma progression. Mutation analysis showed that titin (<i>TTN</i>) and mucin 16 (<i>MUC16</i>) had the highest mutation frequencies. After controlling for collinearity and correlation screening, 314 candidate genes were obtained. Among the 101 model combinations, StepCox (backward)+Ridge performed best (average C-index across 4 cohorts=0.677). The PCDS constructed based on this model stably stratified prognosis: The high-PCDS group showed significantly worse survival in TCGA and 3 external validation cohorts and remained an independent prognostic indicator after adjustment for age, se
本研究深入阐明了PCD在肿瘤免疫微环境中的调控机制,为黑色素瘤患者个性化治疗决策提供了重要的理论依据。
{"title":"[Machine learning-based programmed cell death signature model for precise prediction of prognosis and treatment response in melanoma].","authors":"Benliang Wei, Hong Liu","doi":"10.11817/j.issn.1672-7347.2025.250286","DOIUrl":"https://doi.org/10.11817/j.issn.1672-7347.2025.250286","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objectives: &lt;/strong&gt;The occurrence, metastasis, and drug resistance of melanoma pose major challenges to patient prognosis, and predictive models capable of accurately forecasting patient outcomes and guiding treatment are still lacking. This study aims to develop predictive models for melanoma prognosis and drug sensitivity based on mechanisms of programmed cell death (PCD).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;Genes related to 19 PCD patterns were collected and integrated from gene set enrichment analysis (GSEA), the Kyoto Encyclopedia of Genes and Genomes (KEGG), relevant reviews, and published studies to establish a comprehensive PCD signature gene set. Transcriptomic and clinical data from The Cancer Genome Atlas (TCGA) skin cutaneous melanoma (SKCM) cohort were obtained, and 3 untreated Gene Expression Omnibus (GEO) datasets (GSE65904, GSE19234, and GSE100797) were included as external validation cohorts. In addition, immunotherapy cohorts PRJEB23709, GSE136961, and GSE215222 were collected to validate the predictive value for immunotherapy. Single-cell transcriptomic data (GSE115978 and GSE215120) were processed using Seurat for quality control, normalization, dimensionality reduction, clustering, and cell annotation; spatial transcriptomic data were obtained from 10× Genomics and combined with Cottrazm for spatial partitioning and SpaCET deconvolution. Cell-cell communication was evaluated using CellChat to assess secreted signaling, extracellular matrix (ECM)-receptor interactions, and cell contact-mediated communication patterns. Based on the TCGA training set, a machine learning strategy comprising 10 algorithms and 101 combinations was used to construct PCD-related prognostic signatures, and the optimal model was selected using the average concordance index (C-index) across multiple cohorts. Differential analysis, GSEA, CIBERSORT, and Estimation of STromal and Immune cells in MAlignant Tumor tissues using Expression data (ESTIMATE) were further applied to evaluate immune infiltration, calculate T-cell receptor (TCR) clonal diversity, cytolytic activity, and T-cell effector gene expression profiles, and to explore the association between the PCD score (PCDS) and drug sensitivity.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;The activities of the 19 PCD pathways differed significantly between normal skin and SKCM, suggesting that dysregulation is involved in melanoma progression. Mutation analysis showed that titin (&lt;i&gt;TTN&lt;/i&gt;) and mucin 16 (&lt;i&gt;MUC16&lt;/i&gt;) had the highest mutation frequencies. After controlling for collinearity and correlation screening, 314 candidate genes were obtained. Among the 101 model combinations, StepCox (backward)+Ridge performed best (average C-index across 4 cohorts=0.677). The PCDS constructed based on this model stably stratified prognosis: The high-PCDS group showed significantly worse survival in TCGA and 3 external validation cohorts and remained an independent prognostic indicator after adjustment for age, se","PeriodicalId":39801,"journal":{"name":"中南大学学报(医学版)","volume":"50 11","pages":"1961-1978"},"PeriodicalIF":0.0,"publicationDate":"2025-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144194","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Rare massive upper gastrointestinal bleeding: Three cases of Dieulafoy's disease within diverticula of the descending duodenal and a literature review]. [罕见上消化道大出血:十二指肠降憩室内diulafoy病3例并文献复习]。
Q3 Medicine Pub Date : 2025-11-28 DOI: 10.11817/j.issn.1672-7347.2025.240653
Qiuling Zhao, Jian Zhang, Qiao Zhou, Zhaohui He, Hongping Li

Dieulafoy's disease is a rare condition that can cause acute, life-threatening massive gastrointestinal bleeding and is prone to misdiagnosis and missed diagnosis. From May 2023 to April 2024, 3 patients with Dieulafoy's disease within diverticula of the descending duodenum complicated by upper gastrointestinal bleeding were admitted to the Affiliated Hospital of Zunyi Medical University and Dafang County People's Hospital. Their clinical data and diagnostic and therapeutic processes are reported to enhance awareness of this disease. All patients presented with massive gastrointestinal bleeding, manifested as recurrent hematemesis and hematochezia with large-volume bleeding, and were diagnosed by emergency gastroscopy as having Dieulafoy's disease within diverticula of the descending duodenum. After medical therapy, the outcomes were unsatisfactory in all 3 cases. Endoscopic examination revealed active bleeding located in the descending duodenum; using a side-viewing duodenoscope, the lesions were observed to be within the diverticula of the descending duodenum. Hemostasis was successfully achieved in all cases by endoscopic hemoclip placement. Dieulafoy's disease within diverticula of the descending duodenum complicated by gastrointestinal bleeding is relatively rare in clinical practice. For gastrointestinal bleeding of unclear etiology, endoscopic examination should maintain a high index of suspicion for the descending duodenum, and duodenoscopy should be used when necessary. Particular attention should be paid to rare bleeding causes occurring within diverticula to avoid missed or incorrect diagnoses that could delay treatment.

diulafoy病是一种罕见的疾病,可引起急性,危及生命的大量胃肠道出血,容易误诊和漏诊。2023年5月至2024年4月,在遵义医学院附属医院及大方县人民医院共收治了3例十二指肠降憩室内diulafoy病合并上消化道出血患者。报告他们的临床数据和诊断和治疗过程,以提高对这种疾病的认识。所有患者均表现为胃肠道大量出血,表现为反复呕血、便血并大量出血,经急诊胃镜检查诊断为十二指肠降憩室内diulafoy病。经药物治疗后,3例均不理想。内镜检查发现活动性出血位于十二指肠降部;在侧视十二指肠镜下,病变位于十二指肠降憩室内。所有病例均通过内窥镜止血钳成功止血。十二指肠降憩室内的十二指肠溃疡合并消化道出血在临床上是比较少见的。对于病因不明的消化道出血,内镜检查应保持对十二指肠降部的高度怀疑,必要时应进行十二指肠镜检查。应特别注意憩室内发生的罕见出血原因,以避免遗漏或错误的诊断,可能延误治疗。
{"title":"[Rare massive upper gastrointestinal bleeding: Three cases of Dieulafoy<b>'</b>s disease within diverticula of the descending duodenal and a literature review].","authors":"Qiuling Zhao, Jian Zhang, Qiao Zhou, Zhaohui He, Hongping Li","doi":"10.11817/j.issn.1672-7347.2025.240653","DOIUrl":"https://doi.org/10.11817/j.issn.1672-7347.2025.240653","url":null,"abstract":"<p><p>Dieulafoy's disease is a rare condition that can cause acute, life-threatening massive gastrointestinal bleeding and is prone to misdiagnosis and missed diagnosis. From May 2023 to April 2024, 3 patients with Dieulafoy's disease within diverticula of the descending duodenum complicated by upper gastrointestinal bleeding were admitted to the Affiliated Hospital of Zunyi Medical University and Dafang County People's Hospital. Their clinical data and diagnostic and therapeutic processes are reported to enhance awareness of this disease. All patients presented with massive gastrointestinal bleeding, manifested as recurrent hematemesis and hematochezia with large-volume bleeding, and were diagnosed by emergency gastroscopy as having Dieulafoy's disease within diverticula of the descending duodenum. After medical therapy, the outcomes were unsatisfactory in all 3 cases. Endoscopic examination revealed active bleeding located in the descending duodenum; using a side-viewing duodenoscope, the lesions were observed to be within the diverticula of the descending duodenum. Hemostasis was successfully achieved in all cases by endoscopic hemoclip placement. Dieulafoy's disease within diverticula of the descending duodenum complicated by gastrointestinal bleeding is relatively rare in clinical practice. For gastrointestinal bleeding of unclear etiology, endoscopic examination should maintain a high index of suspicion for the descending duodenum, and duodenoscopy should be used when necessary. Particular attention should be paid to rare bleeding causes occurring within diverticula to avoid missed or incorrect diagnoses that could delay treatment.</p>","PeriodicalId":39801,"journal":{"name":"中南大学学报(医学版)","volume":"50 11","pages":"2133-2140"},"PeriodicalIF":0.0,"publicationDate":"2025-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144237","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Finite element analysis of skeletal injury mechanisms in adult standing positions with both feet landed on the ground]. [成人双脚着地站立时骨骼损伤机制的有限元分析]。
Q3 Medicine Pub Date : 2025-11-28 DOI: 10.11817/j.issn.1672-7347.2025.250450
Hongmin Yuan, Shuhui Gao, Zhibin Wei

Objectives: The prevalence and complexity of high-fall injuries pose major challenges to injury-mechanism interpretation, which currently relies largely on forensic autopsy. The finite element method (FEM) can elucidate biomechanical mechanisms of skeletal injury and quantify the relationship between fracture risk and fall height, providing evidence for forensic injury analysis and scene reconstruction.

Methods: Using adult upright feet-first landing as a representative scenario, a finite element approach based on the total human model for safety (THUMS) was applied to simulate bilateral feet-first impacts onto a rigid surface from heights of 1 to 50 m. Skeletal biomechanical responses were systematically evaluated using von Mises stress analysis, Logistic regression modeling, and hierarchical clustering.

Results: Stress concentration followed a longitudinal axial distribution along the body's vertical axis, with a dual-path load-transmission mechanism identified. Step-change biomechanical responses were observed at the foot, tibial ends, femoral neck, and spine, indicating abrupt increases in fracture risk at critical heights. Logistic regression successfully generated fracture-risk prediction models for fibular ends, pelvis, and skull. The fastest height-dependent fracture-risk escalation occurred at the fibular ends, followed by the skull, whereas the pelvis showed the slowest but still significant risk increase. Hierarchical clustering combined with biomechanical-mechanism interpretation stratified fall heights into 5 clusters and 3 injury phases: Local energy-dissipation phase (<7 meters), axial conduction stage (7 to 16 meters), and systemic composite injury phase (>16 meters).

Conclusions: FEM reveals the dual-path load-transmission mechanism of skeletal injury in upright feet-first landing. The established fracture-risk-height prediction models and injury-pattern-to-height mapping models provide biomechanical evidence for forensic inference of fall height.

目的:高跌落伤的普遍性和复杂性对损伤机制的解释提出了重大挑战,目前主要依赖于法医尸检。有限元方法可以阐明骨骼损伤的生物力学机制,量化骨折风险与坠落高度的关系,为法医损伤分析和现场重建提供依据。方法:以成人直立脚先着地为代表,采用基于全人体安全模型(THUMS)的有限元方法模拟双侧脚先着地在1 ~ 50 m高度的刚性表面上的碰撞。采用von Mises应力分析、Logistic回归模型和分层聚类对骨骼生物力学响应进行了系统评估。结果:应力集中遵循沿机体纵轴的纵向轴向分布,确定了双路径荷载传递机制。在足部、胫骨末端、股骨颈和脊柱处观察到阶梯变化的生物力学反应,表明在临界高度骨折风险突然增加。逻辑回归成功地生成了腓骨末端、骨盆和颅骨骨折风险预测模型。与身高相关的骨折风险增加最快的是腓骨末端,其次是颅骨,而骨盆的风险增加速度最慢,但仍显着。结合生物力学机制解释的分层聚类将坠落高度分为5个聚类和3个损伤阶段:局部能量耗散阶段(16米)。结论:有限元分析揭示了直立足先着地时骨骼损伤的双路径载荷传递机制。建立的骨折风险-高度预测模型和损伤模式-高度映射模型为坠落高度的法医推断提供了生物力学依据。
{"title":"[Finite element analysis of skeletal injury mechanisms in adult standing positions with both feet landed on the ground].","authors":"Hongmin Yuan, Shuhui Gao, Zhibin Wei","doi":"10.11817/j.issn.1672-7347.2025.250450","DOIUrl":"https://doi.org/10.11817/j.issn.1672-7347.2025.250450","url":null,"abstract":"<p><strong>Objectives: </strong>The prevalence and complexity of high-fall injuries pose major challenges to injury-mechanism interpretation, which currently relies largely on forensic autopsy. The finite element method (FEM) can elucidate biomechanical mechanisms of skeletal injury and quantify the relationship between fracture risk and fall height, providing evidence for forensic injury analysis and scene reconstruction.</p><p><strong>Methods: </strong>Using adult upright feet-first landing as a representative scenario, a finite element approach based on the total human model for safety (THUMS) was applied to simulate bilateral feet-first impacts onto a rigid surface from heights of 1 to 50 m. Skeletal biomechanical responses were systematically evaluated using von Mises stress analysis, Logistic regression modeling, and hierarchical clustering.</p><p><strong>Results: </strong>Stress concentration followed a longitudinal axial distribution along the body's vertical axis, with a dual-path load-transmission mechanism identified. Step-change biomechanical responses were observed at the foot, tibial ends, femoral neck, and spine, indicating abrupt increases in fracture risk at critical heights. Logistic regression successfully generated fracture-risk prediction models for fibular ends, pelvis, and skull. The fastest height-dependent fracture-risk escalation occurred at the fibular ends, followed by the skull, whereas the pelvis showed the slowest but still significant risk increase. Hierarchical clustering combined with biomechanical-mechanism interpretation stratified fall heights into 5 clusters and 3 injury phases: Local energy-dissipation phase (<7 meters), axial conduction stage (7 to 16 meters), and systemic composite injury phase (>16 meters).</p><p><strong>Conclusions: </strong>FEM reveals the dual-path load-transmission mechanism of skeletal injury in upright feet-first landing. The established fracture-risk-height prediction models and injury-pattern-to-height mapping models provide biomechanical evidence for forensic inference of fall height.</p>","PeriodicalId":39801,"journal":{"name":"中南大学学报(医学版)","volume":"50 11","pages":"2051-2061"},"PeriodicalIF":0.0,"publicationDate":"2025-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144230","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Changes and forecast of the disease burden of senile dementias among Chinese residents from 1992 to 2021]. [1992 - 2021年中国居民老年痴呆疾病负担变化及预测]。
Q3 Medicine Pub Date : 2025-11-28 DOI: 10.11817/j.issn.1672-7347.2025.250464
Xie Zhang, Mengmeng Pan
<p><strong>Objectives: </strong>The China Alzheimer's Disease Report 2024 reveals that the number of deaths in China due to Alzheimer's disease (AD) and other types of dementia reached 320 715, accounting for 19.8% of global dementia-related deaths. The socioeconomic burden is increasingly prominent and poses a serious threat to the health of Chinese residents. This study aims to analyze the changes in the disease burden of dementias among Chinese residents from 1992 to 2021 and to predict future trends, so as to provide a reference for dementia prevention and control.</p><p><strong>Methods: </strong>Based on data from the Global Burden of Disease (GBD) Study 2021, Joinpoint regression models were used to analyze the incidence and age-standardized incidence rate, deaths and age-standardized mortality rate, disability-adjusted life year (DALY) and age-standardized DALY rate of senile dementia among Chinese residents aged 60 years and above from 1992 to 2021. Age-period-cohort models were used to analyze incidence and mortality under different effects. Bayesian age-period-cohort models were applied to predict the age-standardized incidence rate of dementias among Chinese residents from 2022 to 2031.</p><p><strong>Results: </strong>From 1992 to 2021, the disease burden of senile dementia among Chinese residents increased year by year. The age-standardized incidence rate and age-standardized DALY rate showed fluctuating upward trends, while the age-standardized mortality rate declined. The average annual percent change (AAPC) of the age-standardized incidence rate, age-standardized mortality rate, and age-standardized DALY rate were 0.57%, -0.07%, and 0.09%, respectively (all <i>P</i><0.05). From 2019 to 2021, the numbers of incident cases, deaths, and DALY of dementia among Chinese residents aged 60 years and above increased significantly, with higher values in females than in males. The age-period-cohort model indicated that incidence and mortality risks increased with age, with a marked increase after 70 years of age; incidence risk showed a "wave-like" pattern of increase-decrease-increase over periods, while mortality risk showed a trend of decrease followed by increase; incidence risk fluctuated upward across birth cohorts, whereas mortality risk fluctuated downward. Predictions from the Bayesian age-period-cohort model indicate that from 2022 to 2031, the age-standardized incidence rate of dementia in China may continue to increase, reaching 1 616.87 per 100 000 in the total population, 1 304.71 per 100 000 in males, and 1 809.09 per 100 000 in females by 2031.</p><p><strong>Conclusions: </strong>From 1992 to 2021, the disease burden of senile dementia in China has increased year by year, with a particularly heavy burden among older women. Senile dementia remains a major public health problem, and its disease burden may continue to increase in the future. It is recommended to promote early screening to promote early screening among high-risk p
目的:《中国阿尔茨海默病报告2024》显示,中国因阿尔茨海默病(AD)和其他类型的痴呆症死亡人数达到320 715人,占全球痴呆症相关死亡人数的19.8%。社会经济负担日益突出,对我国居民的健康构成严重威胁。本研究旨在分析1992 - 2021年中国居民痴呆症疾病负担的变化,并预测未来趋势,为痴呆防控提供参考。方法:基于全球疾病负担(GBD)研究2021的数据,采用Joinpoint回归模型分析1992 - 2021年中国60岁及以上居民老年痴呆的发病率和年龄标准化发病率、死亡率和年龄标准化死亡率、残疾调整生命年(DALY)和年龄标准化DALY率。采用年龄-时期-队列模型分析不同影响下的发病率和死亡率。应用贝叶斯年龄-时期-队列模型预测2022 - 2031年中国居民痴呆年龄标准化发病率。结果:1992 - 2021年,我国居民老年痴呆疾病负担逐年增加。年龄标准化发病率和年龄标准化DALY率呈波动上升趋势,而年龄标准化死亡率呈下降趋势。年龄标准化发病率、年龄标准化死亡率和年龄标准化DALY的年均变化率(AAPC)分别为0.57%、-0.07%和0.09%(均为p)。结论:1992 - 2021年,中国老年痴呆疾病负担逐年增加,其中老年女性负担尤重。老年痴呆症仍然是一个主要的公共卫生问题,其疾病负担可能在未来继续增加。建议推广早期筛查,促进高危人群早期筛查,通过广泛的健康教育提高公众意识,降低发病率风险,全面提高老年痴呆防治效果。
{"title":"[Changes and forecast of the disease burden of senile dementias among Chinese residents from 1992 to 2021].","authors":"Xie Zhang, Mengmeng Pan","doi":"10.11817/j.issn.1672-7347.2025.250464","DOIUrl":"https://doi.org/10.11817/j.issn.1672-7347.2025.250464","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objectives: &lt;/strong&gt;The China Alzheimer's Disease Report 2024 reveals that the number of deaths in China due to Alzheimer's disease (AD) and other types of dementia reached 320 715, accounting for 19.8% of global dementia-related deaths. The socioeconomic burden is increasingly prominent and poses a serious threat to the health of Chinese residents. This study aims to analyze the changes in the disease burden of dementias among Chinese residents from 1992 to 2021 and to predict future trends, so as to provide a reference for dementia prevention and control.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;Based on data from the Global Burden of Disease (GBD) Study 2021, Joinpoint regression models were used to analyze the incidence and age-standardized incidence rate, deaths and age-standardized mortality rate, disability-adjusted life year (DALY) and age-standardized DALY rate of senile dementia among Chinese residents aged 60 years and above from 1992 to 2021. Age-period-cohort models were used to analyze incidence and mortality under different effects. Bayesian age-period-cohort models were applied to predict the age-standardized incidence rate of dementias among Chinese residents from 2022 to 2031.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;From 1992 to 2021, the disease burden of senile dementia among Chinese residents increased year by year. The age-standardized incidence rate and age-standardized DALY rate showed fluctuating upward trends, while the age-standardized mortality rate declined. The average annual percent change (AAPC) of the age-standardized incidence rate, age-standardized mortality rate, and age-standardized DALY rate were 0.57%, -0.07%, and 0.09%, respectively (all &lt;i&gt;P&lt;/i&gt;&lt;0.05). From 2019 to 2021, the numbers of incident cases, deaths, and DALY of dementia among Chinese residents aged 60 years and above increased significantly, with higher values in females than in males. The age-period-cohort model indicated that incidence and mortality risks increased with age, with a marked increase after 70 years of age; incidence risk showed a \"wave-like\" pattern of increase-decrease-increase over periods, while mortality risk showed a trend of decrease followed by increase; incidence risk fluctuated upward across birth cohorts, whereas mortality risk fluctuated downward. Predictions from the Bayesian age-period-cohort model indicate that from 2022 to 2031, the age-standardized incidence rate of dementia in China may continue to increase, reaching 1 616.87 per 100 000 in the total population, 1 304.71 per 100 000 in males, and 1 809.09 per 100 000 in females by 2031.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;From 1992 to 2021, the disease burden of senile dementia in China has increased year by year, with a particularly heavy burden among older women. Senile dementia remains a major public health problem, and its disease burden may continue to increase in the future. It is recommended to promote early screening to promote early screening among high-risk p","PeriodicalId":39801,"journal":{"name":"中南大学学报(医学版)","volume":"50 11","pages":"2071-2081"},"PeriodicalIF":0.0,"publicationDate":"2025-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144121","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Patterns and mechanisms of the "treating skin with skin" therapy under traditional Chinese medicine analogical thinking based on data mining and network pharmacology]. [基于数据挖掘和网络药理学的中医类比思维下“以皮治皮”疗法的模式与机制]。
Q3 Medicine Pub Date : 2025-11-28 DOI: 10.11817/j.issn.1672-7347.2025.250250
Xiaoli Hu, Hui Guo, Guoyan Sun, Xuefeng Wang
<p><strong>Objectives: </strong>Under the guidance of analogical thinking in traditional Chinese medicine (TCM), the "treating of skin with skin" therapy, using processed animal and plant skin-derived medicinal materials to treat skin diseases, has a long history but lacks scientific evidence-based support. This study aims to apply data mining and network pharmacology techniques to explore the prescription patterns and mechanisms of action of the "treating skin with skin" therapy, and to interpret its rationality, effectiveness, and scientific basis using modern scientific methods.</p><p><strong>Methods: </strong>Relevant literature from Chinese and English databases over the past 20 years was retrieved and integrated according to inclusion and exclusion criteria. Data were integrated and mined using software such as Excel, OriginPro 2021, and SPSS Modeler 18.0. Frequency analysis, cluster analysis, and association rule analysis were performed sequentially to summarize high-frequency plant skin-derived Chinese medicinal materials and extract the core prescription. Core prescription drugs and skin disease-related gene targets were obtained from drug and disease target databases, including the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform and GeneCards. Intersection targets were identified using Venny 2.1.0, and core targets were further extracted. Protein-protein interaction (PPI) network analysis, Gene Ontology (GO) functional enrichment analysis, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis were conducted for the intersection targets, and finally a "core drug-component-target-pathway" network was constructed and visualized.</p><p><strong>Results: </strong>Based on the inclusion and exclusion criteria, 563 eligible articles were ultimately included, from which 32 prescriptions were extracted, involving 21 plant skin-derived Chinese medicinal materials. Among them, 15 medicinal materials had a usage frequency exceeding 50%, with bitter, sweet, and cold properties predominating. Cluster analysis yielded 4 effective clusters. Cluster 1: <i>Phellodendron</i> cortex-<i>Dictamni</i> cortex; Cluster 2: <i>Eucommia</i> cortex-<i>Mori</i> cortex-<i>Meliae</i> cortex-<i>Pseudolaricis</i> cortex; Cluster 3: <i>Moutan</i> cortex-<i>Poriae Cutis</i>-Lycii cortex-<i>Fraxini</i> cortex-<i>Acanthopanacis</i> cortex-<i>Benincasae Pericarpium</i>; Cluster 4: <i>Ailanthi</i> cortex-<i>Periplocae</i> cortex-<i>Erycibes</i> cortex. Association rule analysis generated 92 association rules, with 4 strong links, 90 moderate links, and 10 weak links between herb pairs. Based on the association rules and linkage strength, the core prescription of the "treating skin with skin" therapy was summarized as "Phellodendri Cortex-Moutan Cortex-Dictamni Cortex-Benincasae Pericarpium-Poriae Cutis-Lycii Cortex." A total of 46 active ingredients were screened from this core prescription, involving 781 gene targets.
目的:在中医类比思维的指导下,“以皮治皮”疗法,即利用加工过的动植物皮源药材治疗皮肤病,历史悠久,但缺乏科学的循证支持。本研究旨在运用数据挖掘和网络药理学技术,探索“以皮治皮”疗法的方剂规律和作用机理,并运用现代科学方法解释其合理性、有效性和科学依据。方法:检索近20年来中英文数据库的相关文献,按照纳入标准和排除标准进行整合。使用Excel、OriginPro 2021、SPSS Modeler 18.0等软件对数据进行整合和挖掘。依次进行频率分析、聚类分析和关联规则分析,总结高频植物皮源中药材,提取核心方剂。核心处方药和皮肤病相关基因靶点来源于药物和疾病靶点数据库,包括中药系统药理学数据库与分析平台和GeneCards。利用Venny 2.1.0识别交叉目标,进一步提取核心目标。对交叉靶点进行蛋白-蛋白相互作用(PPI)网络分析、基因本体(GO)功能富集分析、京都基因与基因组百科全书(KEGG)通路富集分析,最终构建“核心药物组分-靶点-通路”网络并进行可视化。结果:根据纳入与排除标准,最终纳入符合条件的文献563篇,从中提取处方32张,涉及植物皮源性中药21种。其中15种药材的使用频率超过50%,以苦、甜、寒性为主。聚类分析得到4个有效聚类。簇1:黄柏皮质-黄柏皮质;集群2:杜仲皮质-桑皮质-蜜兰科皮质-拟金枝皮质;聚类3:牡丹皮-茯苓皮-枸杞子皮-白蜡皮-棘五加皮- benincasae皮;簇4:Ailanthi皮质- periplocae皮质- erycibes皮质。关联规则分析生成了92条关联规则,其中草本对之间有4条强链接、90条中等链接和10条弱链接。根据关联规律和连锁强度,将“以皮治皮”疗法的核心方剂归纳为“黄柏皮-牡丹皮-地黄皮-白皮-枸杞皮”。从该核心方中共筛选出46种有效成分,涉及781个基因靶点。共检索到2 537个皮肤病相关基因靶点,其中核心处方与皮肤病交叉靶点212个。交叉目标的PPI网络分析结果显示,212个节点中有2 723条边,平均节点度为25.9,平均局部聚类系数为0.554。核心目标的PPI网络包含50个节点和784条边;排名前三位的核心淋巴结依次为:白细胞介素-6 (IL-6; 116)、肿瘤坏死因子(TNF; 115)、白细胞介素-1β (IL-1β; 110)。氧化石墨烯分析共获得732个生物过程项,前3位为脂多糖应答、dna模板化转录正调控和microRNA转录正调控;90个细胞成分术语,前3名分别是细胞外空间、细胞外区域和染色质;153个分子功能项,前3个分别是酶结合、核受体活性和相同蛋白结合。KEGG分析鉴定出166条富集信号通路,其中前3位为癌症、脂质和动脉粥样硬化通路,以及糖尿病并发症晚期糖基化终产物-受体晚期糖基化终产物通路。可视化的“核心药物-成分-靶点-通路”网络由854个节点和1 911条边组成,网络集中化系数为0.182,特征路径长度为3.985;按程度排列前3位的淋巴结均为药物成分,分别为维生素E、维生素B和葫芦巴碱。结论:在中医类比思维的指导下,“以皮治皮”疗法的核心方剂通过多成分、多靶点、多途径的协同作用,对皮肤病发挥治疗作用。它的影响是显著的,它的理论基础是有充分根据的,它的起源是很确定的。
{"title":"[Patterns and mechanisms of the <b>\"</b>treating skin with skin<b>\"</b> therapy under traditional Chinese medicine analogical thinking based on data mining and network pharmacology].","authors":"Xiaoli Hu, Hui Guo, Guoyan Sun, Xuefeng Wang","doi":"10.11817/j.issn.1672-7347.2025.250250","DOIUrl":"https://doi.org/10.11817/j.issn.1672-7347.2025.250250","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objectives: &lt;/strong&gt;Under the guidance of analogical thinking in traditional Chinese medicine (TCM), the \"treating of skin with skin\" therapy, using processed animal and plant skin-derived medicinal materials to treat skin diseases, has a long history but lacks scientific evidence-based support. This study aims to apply data mining and network pharmacology techniques to explore the prescription patterns and mechanisms of action of the \"treating skin with skin\" therapy, and to interpret its rationality, effectiveness, and scientific basis using modern scientific methods.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;Relevant literature from Chinese and English databases over the past 20 years was retrieved and integrated according to inclusion and exclusion criteria. Data were integrated and mined using software such as Excel, OriginPro 2021, and SPSS Modeler 18.0. Frequency analysis, cluster analysis, and association rule analysis were performed sequentially to summarize high-frequency plant skin-derived Chinese medicinal materials and extract the core prescription. Core prescription drugs and skin disease-related gene targets were obtained from drug and disease target databases, including the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform and GeneCards. Intersection targets were identified using Venny 2.1.0, and core targets were further extracted. Protein-protein interaction (PPI) network analysis, Gene Ontology (GO) functional enrichment analysis, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis were conducted for the intersection targets, and finally a \"core drug-component-target-pathway\" network was constructed and visualized.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Based on the inclusion and exclusion criteria, 563 eligible articles were ultimately included, from which 32 prescriptions were extracted, involving 21 plant skin-derived Chinese medicinal materials. Among them, 15 medicinal materials had a usage frequency exceeding 50%, with bitter, sweet, and cold properties predominating. Cluster analysis yielded 4 effective clusters. Cluster 1: &lt;i&gt;Phellodendron&lt;/i&gt; cortex-&lt;i&gt;Dictamni&lt;/i&gt; cortex; Cluster 2: &lt;i&gt;Eucommia&lt;/i&gt; cortex-&lt;i&gt;Mori&lt;/i&gt; cortex-&lt;i&gt;Meliae&lt;/i&gt; cortex-&lt;i&gt;Pseudolaricis&lt;/i&gt; cortex; Cluster 3: &lt;i&gt;Moutan&lt;/i&gt; cortex-&lt;i&gt;Poriae Cutis&lt;/i&gt;-Lycii cortex-&lt;i&gt;Fraxini&lt;/i&gt; cortex-&lt;i&gt;Acanthopanacis&lt;/i&gt; cortex-&lt;i&gt;Benincasae Pericarpium&lt;/i&gt;; Cluster 4: &lt;i&gt;Ailanthi&lt;/i&gt; cortex-&lt;i&gt;Periplocae&lt;/i&gt; cortex-&lt;i&gt;Erycibes&lt;/i&gt; cortex. Association rule analysis generated 92 association rules, with 4 strong links, 90 moderate links, and 10 weak links between herb pairs. Based on the association rules and linkage strength, the core prescription of the \"treating skin with skin\" therapy was summarized as \"Phellodendri Cortex-Moutan Cortex-Dictamni Cortex-Benincasae Pericarpium-Poriae Cutis-Lycii Cortex.\" A total of 46 active ingredients were screened from this core prescription, involving 781 gene targets. ","PeriodicalId":39801,"journal":{"name":"中南大学学报(医学版)","volume":"50 11","pages":"2003-2016"},"PeriodicalIF":0.0,"publicationDate":"2025-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146144205","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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中南大学学报(医学版)
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