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MicroRNA-411-3p Attenuates Cell Senescence in SiO 2-Induced Pulmonary Fibrosis. MicroRNA-411-3p减缓二氧化硅诱导肺纤维化的细胞衰老。
IF 4.1 Pub Date : 2025-08-20 DOI: 10.3967/bes2025.097
Ze Lin Xu, Si Qi Liu, Xiao Yu, Si Yi Wang, Bing Bing Li, Xin Yu Wang, Si Yuan Shan, Hong Xu, Bo Nan Zhang, Yi Wei Shi, Xue Min Gao
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引用次数: 0
Influence of Outdoor Light at Night on Early Reproductive Outcomes of In Vitro Fertilization and Its Threshold Effect: Evidence from a Couple-Based Preconception Cohort Study. 夜间室外光照对体外受精早期生殖结局的影响及其阈值效应:来自一对夫妇的孕前队列研究证据
IF 4.1 Pub Date : 2025-08-20 DOI: 10.3967/bes2025.101
Wen Bin Fang, Ying Tang, Ya Ning Sun, Yan Lan Tang, Yin Yin Chen, Ya Wen Cao, Ji Qi Fang, Kun Jing He, Yu Shan Li, Ya Ning Dai, Shuang Shuang Bao, Peng Zhu, Shan Shan Shao, Fang Biao Tao, Gui Xia Pan
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引用次数: 0
Association between PM 2.5 Chemical Constituents and Preterm Birth: The Undeniable Role of Preconception H19 Gene Variation. pm2.5化学成分与早产的关系:孕前H19基因变异的不可否认的作用。
IF 4.1 Pub Date : 2025-08-20 DOI: 10.3967/bes2025.076
Ya Long Wang, Pan Pan Sun, Xin Ying Wang, Jun Xi Zhang, Xiang Yu Yu, Jian Chai, Ruo Du, Wen Yi Liu, Fang Fang Yu, Yue Ba, Guo Yu Zhou
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引用次数: 0
MYCN-Mediated Transcriptional Activation of IDH2 Enhances Proliferation, Migration, and Invasion in Cervical Squamous Cell Carcinoma through the HIF1-α Pathway. mycn介导的IDH2转录激活通过HIF1-α途径增强宫颈鳞状细胞癌的增殖、迁移和侵袭
IF 4.1 Pub Date : 2025-08-20 DOI: 10.3967/bes2025.075
Xiao Juan Liu, Hui Ma, Xiao Yan Li, Chun Xing Ma, Li Sha Shu, Hui Ying Zhang
{"title":"MYCN-Mediated Transcriptional Activation of IDH2 Enhances Proliferation, Migration, and Invasion in Cervical Squamous Cell Carcinoma through the HIF1-α Pathway.","authors":"Xiao Juan Liu, Hui Ma, Xiao Yan Li, Chun Xing Ma, Li Sha Shu, Hui Ying Zhang","doi":"10.3967/bes2025.075","DOIUrl":"https://doi.org/10.3967/bes2025.075","url":null,"abstract":"","PeriodicalId":93903,"journal":{"name":"Biomedical and environmental sciences : BES","volume":"38 8","pages":"1003-1008"},"PeriodicalIF":4.1,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145031416","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
Hypertrophic Cardiomyopathy: Mechanisms of Pathogenicity. 肥厚性心肌病:致病机制。
IF 4.1 Pub Date : 2025-08-20 DOI: 10.3967/bes2025.096
Bao Xi Wang, Yue Ting Zhou, Yi Pin Zhao, Yong Cheng, Jun Ren, Guan Chang Tan, Xiao Hu Wang

Hypertrophic cardiomyopathy (HCM) is a major contributor to cardiovascular diseases (CVD), the leading cause of death globally. HCM can precipitate heart failure (HF) by causing the cardiac tissue to weaken and stretch, thereby impairing its pumping efficiency. Moreover, HCM increases the risk of atrial fibrillation, which in turn elevates the likelihood of thrombus formation and stroke. Given these significant clinical ramifications, research into the etiology and pathogenesis of HCM is intensifying at multiple levels. In this review, we discuss and synthesize the latest findings on HCM pathogenesis, drawing on key experimental studies conducted both in vitro and in vivo. We also offer our insights and perspectives on these mechanisms, while highlighting the limitations of current research. Advancing fundamental research in this area is essential for developing effective therapeutic interventions and enhancing the clinical management of HCM.

肥厚性心肌病(HCM)是导致心血管疾病(CVD)的主要原因,是全球死亡的主要原因。HCM会导致心脏组织变弱和拉伸,从而降低其泵送效率,从而导致心力衰竭(HF)。此外,HCM增加了房颤的风险,这反过来又增加了血栓形成和中风的可能性。鉴于这些重要的临床后果,对HCM的病因和发病机制的研究正在多个层面上加强。在这篇综述中,我们根据体外和体内的重要实验研究,讨论和综合了HCM发病机制的最新发现。我们还提供了我们对这些机制的见解和观点,同时强调了当前研究的局限性。推进这一领域的基础研究对于开发有效的治疗干预措施和加强HCM的临床管理至关重要。
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引用次数: 0
Re-Exploration for Dietary Iodine Intake in Chinese Adults using the Obligatory Iodine Loss Hypothesis. 用强制性碘流失假说对中国成人膳食碘摄入量的再探讨。
IF 4.1 Pub Date : 2025-08-20 DOI: 10.3967/bes2025.017
Xiao Bing Liu, Jun Wang, Ya Jie Li, Hong Xing Tan, De Qian Mao, Yan Yan Liu, Wei Dong Li, Wei Yu, Jun An Yan, Jian Hua Piao, Chong Zheng Guo, Xiao Li Liu, Xiao Guang Yang

Objective: This study aimed to reexplore minimum iodine excretion and to build a dietary iodine recommendation for Chinese adults using the obligatory iodine loss hypothesis.

Methods: Data from 171 Chinese adults (19-21 years old) were collected and analyzed based on three balance studies in Shenzhen, Yinchuan, and Changzhi. The single exponential equation was accordingly used to simulate the trajectory of 24 h urinary iodine excretion as the low iodine experimental diets offered (iodine intake: 11-26 μg/day) and to further deduce the dietary reference intakes (DRIs) for iodine, including estimated average requirement (EAR) and recommended nutrient intake (RNI).

Results: The minimum iodine excretion was estimated as 57, 58, and 51 μg/day in three balance studies, respectively. Moreover, it was further suggested as 57, 58, and 51 μg/day for iodine EAR, and 80, 81, and 71 μg/day for iodine RNI or expressed as 1.42, 1.41, and 1.20 μg/(day·kg) of body weight.

Conclusion: The iodine DRIs for Chinese adults were established based on the obligatory iodine loss hypothesis, which provides scientific support for the amendment of nutrient requirements.

目的:本研究旨在利用强制性碘流失假说,重新探讨中国成年人的最低碘排泄量,并建立中国成年人的膳食碘推荐量。方法:收集深圳、银川、长治3个城市171名19-21岁的中国成年人的数据并进行分析。利用单指数方程模拟低碘实验日粮(碘摄入量:11 ~ 26 μg/d)下24 h尿碘排泄量的变化轨迹,进一步推导出碘的膳食参考摄入量(DRIs),包括估计平均需水量(EAR)和推荐营养摄入量(RNI)。结果:在三个平衡研究中,碘的最小排泄量分别为57、58和51 μg/d。此外,碘的EAR值分别为57、58、51 μg/d,碘的RNI值分别为80、81、71 μg/d,或分别为1.42、1.41、1.20 μg/(天·kg)体重。结论:我国成人碘需要量指标建立在强制性碘流失假说的基础上,为修正营养需要量提供了科学依据。
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引用次数: 0
Beams of Hope: Shedding New Light on Alzheimer's Treatment with Low-Dose Radiation Therapy. 希望之光:用低剂量放射疗法治疗阿尔茨海默病的新曙光。
IF 4.1 Pub Date : 2025-08-20 DOI: 10.3967/bes2025.100
Jing Xuan Fu, Wei Ping Wang, Yi Dan Wang, Pei Chang Wang
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引用次数: 0
Association of Longitudinal Change in Fasting Blood Glucose with Risk of Cerebral Infarction in a Patients with Diabetes. 糖尿病患者空腹血糖纵向变化与脑梗死风险的关系
IF 4.1 Pub Date : 2025-08-20 DOI: 10.3967/bes2025.052
Tai Yang Luo, Xuan Deng, Xue Yu Chen, Yu He Liu, Shuo Hua Chen, Hao Ran Sun, Zi Wei Yin, Shou Ling Wu, Yong Zhou, Xing Dong Zheng

Objective: To investigate the association between long-term glycemic control and cerebral infarction risk in patients with diabetes through a large-scale cohort study.

Methods: This prospective, community-based cohort study included 12,054 patients with diabetes. From 2006 to 2012, 38,272 fasting blood glucose (FBG) measurements were obtained from these participants. FBG trajectory patterns were generated using latent mixture modelling. Cox proportional hazards models were applied to assess the subsequent risk of cerebral infarction associated with different FBG trajectory patterns.

Results: At baseline, the mean age of the participants was 55.2 years. Four distinct FBG trajectories were identified based on FBG concentrations and their changes over the 6-year follow-up period. After a median follow-up of 6.9 years, 786 cerebral infarction events were recorded. Different trajectory patterns were associated with significantly varied outcome risks (Log-Rank P < 0.001). Compared with the low-stability group, Hazard Ratio ( HR) adjusted for potential confounders were 1.37 for the moderate-increasing group, 1.23 for the elevated-decreasing group, and 2.08 for the elevated-stable group.

Conclusion: Sustained high FBG levels were found to play a critical role in the development of ischemic stroke among patients with diabetes. Controlling FBG levels may reduce the risk of cerebral infarction.

目的:通过大规模队列研究,探讨糖尿病患者长期血糖控制与脑梗死风险的关系。方法:这项前瞻性、基于社区的队列研究纳入了12054例糖尿病患者。从2006年到2012年,从这些参与者那里获得了38,272个空腹血糖(FBG)测量值。利用潜在混合模型生成FBG轨迹模式。应用Cox比例风险模型评估与不同FBG轨迹模式相关的脑梗死后续风险。结果:基线时,参与者的平均年龄为55.2岁。根据FBG浓度及其在6年随访期间的变化,确定了四种不同的FBG轨迹。中位随访6.9年后,记录了786例脑梗死事件。不同的轨迹模式与显著不同的结局风险相关(Log-Rank P < 0.001)。与低稳定组相比,经潜在混杂因素调整后的风险比(HR),中等升高组为1.37,升高-降低组为1.23,升高-稳定组为2.08。结论:持续的高FBG水平在糖尿病患者缺血性卒中的发展中起关键作用。控制空腹血糖水平可以降低脑梗死的风险。
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引用次数: 0
Analysis of Tongue and Face Image Features of Anemic Women and Construction of Risk-Screening Model. 贫血妇女舌脸图像特征分析及风险筛查模型构建。
IF 4.1 Pub Date : 2025-08-20 DOI: 10.3967/bes2025.047
Hong Yuan Fu, Yi Chun, Ya Han Zhang, Yu Wang, Yu Lin Shi, Tao Jiang, Xiao Juan Hu, Li Ping Tu, Yong Zhi Li, Jia Tuo Xu

Objective: To identify the key features of facial and tongue images associated with anemia in female populations, establish anemia risk-screening models, and evaluate their performance.

Methods: A total of 533 female participants (anemic and healthy) were recruited from Shuguang Hospital. Facial and tongue images were collected using the TFDA-1 tongue and face diagnosis instrument. Color and texture features from various parts of facial and tongue images were extracted using Face Diagnosis Analysis System (FDAS) and Tongue Diagnosis Analysis System version 2.0 (TDAS v2.0). Least Absolute Shrinkage and Selection Operator (LASSO) regression was used for feature selection. Ten machine learning models and one deep learning model (ResNet50V2 + Conv1D) were developed and evaluated.

Results: Anemic women showed lower a-values, higher L- and b-values across all age groups. Texture features analysis showed that women aged 30-39 with anemia had higher angular second moment (ASM)and lower entropy (ENT) values in facial images, while those aged 40-49 had lower contrast (CON), ENT, and MEAN values in tongue images but higher ASM. Anemic women exhibited age-related trends similar to healthy women, with decreasing L-values and increasing a-, b-, and ASM-values. LASSO identified 19 key features from 62. Among classifiers, the Artificial Neural Network (ANN) model achieved the best performance [area under the curve (AUC): 0.849, accuracy: 0.781]. The ResNet50V2 model achieved comparable results [AUC: 0.846, accuracy: 0.818].

Conclusion: Differences in facial and tongue images suggest that color and texture features can serve as potential TCM phenotype and auxiliary diagnostic indicators for female anemia.

目的:识别与女性贫血相关的面部和舌头图像的关键特征,建立贫血风险筛查模型,并对其性能进行评价。方法:从曙光医院招募533名女性受试者(贫血和健康)。采用TFDA-1型舌面诊断仪采集面部及舌面图像。使用人脸诊断分析系统(FDAS)和舌头诊断分析系统2.0版本(TDAS v2.0)提取面部和舌头各部位的颜色和纹理特征。最小绝对收缩和选择算子(LASSO)回归用于特征选择。开发并评估了10个机器学习模型和1个深度学习模型(ResNet50V2 + Conv1D)。结果:在所有年龄组中,贫血妇女的a值较低,L值和b值较高。纹理特征分析表明,30 ~ 39岁贫血女性面部图像的角秒矩(ASM)值较高,熵值(ENT)值较低;40 ~ 49岁贫血女性舌部图像的对比度(CON)、熵值(ENT)和MEAN值较低,但熵值较高。贫血妇女表现出与健康妇女相似的年龄相关趋势,l值降低,a-、b-和asm值升高。LASSO从62个关键特征中识别出19个。在分类器中,人工神经网络(ANN)模型取得了最好的性能[曲线下面积(AUC): 0.849,准确率:0.781]。ResNet50V2模型取得了相当的结果[AUC: 0.846,准确率:0.818]。结论:面部和舌部图像的差异提示颜色和纹理特征可作为女性贫血的潜在中医表型和辅助诊断指标。
{"title":"Analysis of Tongue and Face Image Features of Anemic Women and Construction of Risk-Screening Model.","authors":"Hong Yuan Fu, Yi Chun, Ya Han Zhang, Yu Wang, Yu Lin Shi, Tao Jiang, Xiao Juan Hu, Li Ping Tu, Yong Zhi Li, Jia Tuo Xu","doi":"10.3967/bes2025.047","DOIUrl":"https://doi.org/10.3967/bes2025.047","url":null,"abstract":"<p><strong>Objective: </strong>To identify the key features of facial and tongue images associated with anemia in female populations, establish anemia risk-screening models, and evaluate their performance.</p><p><strong>Methods: </strong>A total of 533 female participants (anemic and healthy) were recruited from Shuguang Hospital. Facial and tongue images were collected using the TFDA-1 tongue and face diagnosis instrument. Color and texture features from various parts of facial and tongue images were extracted using Face Diagnosis Analysis System (FDAS) and Tongue Diagnosis Analysis System version 2.0 (TDAS v2.0). Least Absolute Shrinkage and Selection Operator (LASSO) regression was used for feature selection. Ten machine learning models and one deep learning model (ResNet50V2 + Conv1D) were developed and evaluated.</p><p><strong>Results: </strong>Anemic women showed lower a-values, higher L- and b-values across all age groups. Texture features analysis showed that women aged 30-39 with anemia had higher angular second moment (ASM)and lower entropy (ENT) values in facial images, while those aged 40-49 had lower contrast (CON), ENT, and MEAN values in tongue images but higher ASM. Anemic women exhibited age-related trends similar to healthy women, with decreasing L-values and increasing a-, b-, and ASM-values. LASSO identified 19 key features from 62. Among classifiers, the Artificial Neural Network (ANN) model achieved the best performance [area under the curve (AUC): 0.849, accuracy: 0.781]. The ResNet50V2 model achieved comparable results [AUC: 0.846, accuracy: 0.818].</p><p><strong>Conclusion: </strong>Differences in facial and tongue images suggest that color and texture features can serve as potential TCM phenotype and auxiliary diagnostic indicators for female anemia.</p>","PeriodicalId":93903,"journal":{"name":"Biomedical and environmental sciences : BES","volume":"38 8","pages":"935-951"},"PeriodicalIF":4.1,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145031439","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
HIV Pretreatment Drug Resistance and Transmission Clusters among Newly Diagnosed Patients in the China-Myanmar Border Region, 2020-2023. 2020-2023年中缅边境地区新发感染者HIV预处理耐药及传播聚集性分析
IF 4.1 Pub Date : 2025-07-20 DOI: 10.3967/bes2025.080
Huan Liu, Yue Cheng Yang, Xing Duan, Yi Chen Jin, Yan Fen Cao, Yi Feng, Chang Cai, He He Zhao, Hou Lin Tang

Objective: This study aimed to investigate the prevalence of HIV pretreatment drug resistance (PDR) and the transmission clusters associated with PDR-related mutations in newly diagnosed, treatment-naive patients between 2020 and 2023 in Dehong prefecture, Yunnan province, China.

Methods: Demographic information and plasma samples were collected from study participants. PDR was assessed using the Stanford HIV Drug Resistance Database. The Tamura-Nei 93 model within HIV-TRACE was employed to compute pairwise matches with a genetic distance of 0.015 substitutions per site.

Results: Among 948 treatment-naive individuals with eligible sequences, 36 HIV subtypes were identified, with unique recombinant forms (URFs) being the most prevalent (18.8%, 178/948). The overall prevalence of PDR was 12.4% (118/948), and resistance to non-nucleotide reverse transcriptase inhibitors (NNRTIs), nucleotide reverse transcriptase inhibitors (NRTIs), and protease inhibitors (PIs) was 10.7%, 1.3%, and 1.6%, respectively. A total of 91 clusters were identified, among which eight showed evidence of PDR strain transmission. The largest PDR-associated cluster consisted of six CRF01_AE drug-resistant strains carrying K103N and V179T mutations; five of these individuals had initial CD4+ cell counts < 200 cells/μL.

Conclusion: The distribution of HIV subtypes in Dehong is diverse and complex. PDR was moderately prevalent (12.4%) between 2020 and 2023. Evidence of transmission of CRF01_AE strains carrying K103N and V179T mutations was found. Routine surveillance of PDR and the strengthening of control measures are essential to limit the spread of drug-resistance HIV strains.

目的:本研究旨在调查2020 - 2023年云南省德宏州新诊断、初治患者HIV预处理耐药(PDR)的流行情况及与PDR相关突变相关的传播聚集性。方法:收集研究参与者的人口统计信息和血浆样本。PDR使用斯坦福HIV耐药数据库进行评估。利用HIV-TRACE中的Tamura-Nei 93模型计算每位点的遗传距离为0.015个替换的两两匹配。结果:在符合条件的948例初次治疗个体中,共鉴定出36种HIV亚型,其中以独特重组形式(URFs)最为普遍(18.8%,178/948)。PDR的总患病率为12.4%(118/948),对非核苷酸逆转录酶抑制剂(NNRTIs)、核苷酸逆转录酶抑制剂(NRTIs)和蛋白酶抑制剂(pi)的耐药率分别为10.7%、1.3%和1.6%。共鉴定出91个聚类,其中8个聚类有PDR菌株传播的证据。最大的pdr相关簇由6株携带K103N和V179T突变的CRF01_AE耐药菌株组成;其中5例初始CD4+细胞计数< 200细胞/μL。结论:德洪市HIV亚型分布多样、复杂。在2020年至2023年期间,PDR中度流行(12.4%)。发现携带K103N和V179T突变的CRF01_AE菌株传播的证据。对PDR的常规监测和加强控制措施对于限制耐药艾滋病毒毒株的传播至关重要。
{"title":"HIV Pretreatment Drug Resistance and Transmission Clusters among Newly Diagnosed Patients in the China-Myanmar Border Region, 2020-2023.","authors":"Huan Liu, Yue Cheng Yang, Xing Duan, Yi Chen Jin, Yan Fen Cao, Yi Feng, Chang Cai, He He Zhao, Hou Lin Tang","doi":"10.3967/bes2025.080","DOIUrl":"10.3967/bes2025.080","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to investigate the prevalence of HIV pretreatment drug resistance (PDR) and the transmission clusters associated with PDR-related mutations in newly diagnosed, treatment-naive patients between 2020 and 2023 in Dehong prefecture, Yunnan province, China.</p><p><strong>Methods: </strong>Demographic information and plasma samples were collected from study participants. PDR was assessed using the Stanford HIV Drug Resistance Database. The Tamura-Nei 93 model within HIV-TRACE was employed to compute pairwise matches with a genetic distance of 0.015 substitutions per site.</p><p><strong>Results: </strong>Among 948 treatment-naive individuals with eligible sequences, 36 HIV subtypes were identified, with unique recombinant forms (URFs) being the most prevalent (18.8%, 178/948). The overall prevalence of PDR was 12.4% (118/948), and resistance to non-nucleotide reverse transcriptase inhibitors (NNRTIs), nucleotide reverse transcriptase inhibitors (NRTIs), and protease inhibitors (PIs) was 10.7%, 1.3%, and 1.6%, respectively. A total of 91 clusters were identified, among which eight showed evidence of PDR strain transmission. The largest PDR-associated cluster consisted of six CRF01_AE drug-resistant strains carrying K103N and V179T mutations; five of these individuals had initial CD4+ cell counts < 200 cells/μL.</p><p><strong>Conclusion: </strong>The distribution of HIV subtypes in Dehong is diverse and complex. PDR was moderately prevalent (12.4%) between 2020 and 2023. Evidence of transmission of CRF01_AE strains carrying K103N and V179T mutations was found. Routine surveillance of PDR and the strengthening of control measures are essential to limit the spread of drug-resistance HIV strains.</p>","PeriodicalId":93903,"journal":{"name":"Biomedical and environmental sciences : BES","volume":"38 7","pages":"840-847"},"PeriodicalIF":4.1,"publicationDate":"2025-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144877259","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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Biomedical and environmental sciences : BES
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