Pub Date : 2025-12-30DOI: 10.3760/cma.j.cn112137-20250729-01879
Y Du, Q R Deng, J W Gao, J Chen, Z T Zhong, Y Guo, P M Liu, S L Zhang
Objective: To evaluate the effect of targeted therapy for primary aldosteronism (PA) on the clinical outcome of coexisting obstructive sleep apnea (OSA). Methods: A prospective study was conducted on patients diagnosed with both PA and OSA in the Sun Yat-sen Memorial Hospital between June 2023 and January 2025. All patients received PA targeted treatment. Full-night portable sleep monitoring was performed before and 3-12 months after treatment. Participants were divided into the OSA improvement group or the non-improvement group based on the change in the apnea-hypopnea index (AHI). Differences in clinical characteristics before and after PA treatment, as well as between the two patient groups, were compared. Multivariate logistic regression model was employed to identify risk factors influencing the lack of OSA improvement. Results: A total of 46 patients were enrolled, including 35 males and 11 females, with a mean age of (51.0±12.0) years. Among them, 34 patients were classified into the OSA improvement group, while 12 patients into the non-improvement group the non-improvement group. Of these, 21 patients underwent unilateral adrenalectomy, and 25 received mineralocorticoid receptor antagonist therapy. Patients were followed up for a duration of [M (Q1,Q3)] 6.0 (3.0,8.0) months. After treatment, patients with PA complicated by OSA exhibited a reduction in antihypertensive medication use, the increases in serum potassium, renin activity, and serum creatinine levels, along with the decreases in plasma aldosterone and the aldosterone-to-renin ratio (all P<0.05). Specifically, the AHI declined from 23.8 (9.0,40.2) events/h to 13.1 (8.1,21.8) events/h (P=0.003). In the non-improvement group, baseline body mass index [(30.1±6.4) vs (25.8±5.0) kg/m²] and the clinical non-remission rate of PA [6/12 vs 5.9% (2/34)] were both higher than those in the improvement group (both P<0.05). Multivariate logistic regression model analysis revealed that a higher baseline body mass index (OR=1.18, 95%CI: 1.01-1.39) and clinical non-remission of PA (OR=11.69, 95%CI: 2.13-64.08) were risk factors for lack of improvement in OSA. Conclusions: In patients with PA complicated by OSA, PA-targeted therapy effectively reduces OSA severity. Higher baseline body mass index and clinical non-remission of PA are identified as risk factors for unimproved OSA.
目的:探讨原发性醛固酮增多症(PA)靶向治疗对合并阻塞性睡眠呼吸暂停(OSA)患者临床预后的影响。方法:对2023年6月至2025年1月在中山纪念医院诊断为PA和OSA的患者进行前瞻性研究。所有患者均接受PA靶向治疗。治疗前及治疗后3-12个月进行全夜便携式睡眠监测。根据呼吸暂停低通气指数(AHI)的变化将参与者分为OSA改善组和非改善组。比较PA治疗前后及两组患者临床特征的差异。采用多因素logistic回归模型确定影响OSA改善不足的危险因素。结果:共纳入46例患者,其中男性35例,女性11例,平均年龄(51.0±12.0)岁。其中34例患者分为OSA改善组,12例患者分为非改善组和非改善组。其中,21例患者接受单侧肾上腺切除术,25例接受矿皮质激素受体拮抗剂治疗。随访时间为[M (Q1,Q3)] 6.0(3.0,8.0)个月。经治疗后,PA合并OSA患者降压药使用减少,血清钾、肾素活性、血清肌酐水平升高,血浆醛固酮及醛固酮-肾素比值降低(均PP=0.003)。在非改善组中,基线体重指数[(30.1±6.4)vs(25.8±5.0)kg/m²]和PA临床不缓解率[6/12 vs 5.9%(2/34)]均高于改善组(POR=1.18, 95%CI: 1.01-1.39)和PA临床不缓解率(OR=11.69, 95%CI: 2.13-64.08)是OSA缺乏改善的危险因素。结论:在PA合并OSA患者中,PA靶向治疗可有效降低OSA严重程度。较高的基线体重指数和临床未缓解的PA被确定为未改善的OSA的危险因素。
{"title":"[The impact of primary aldosteronism treatment on the clinical outcome of coexisting obstructive sleep apnea].","authors":"Y Du, Q R Deng, J W Gao, J Chen, Z T Zhong, Y Guo, P M Liu, S L Zhang","doi":"10.3760/cma.j.cn112137-20250729-01879","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250729-01879","url":null,"abstract":"<p><p><b>Objective:</b> To evaluate the effect of targeted therapy for primary aldosteronism (PA) on the clinical outcome of coexisting obstructive sleep apnea (OSA). <b>Methods:</b> A prospective study was conducted on patients diagnosed with both PA and OSA in the Sun Yat-sen Memorial Hospital between June 2023 and January 2025. All patients received PA targeted treatment. Full-night portable sleep monitoring was performed before and 3-12 months after treatment. Participants were divided into the OSA improvement group or the non-improvement group based on the change in the apnea-hypopnea index (AHI). Differences in clinical characteristics before and after PA treatment, as well as between the two patient groups, were compared. Multivariate logistic regression model was employed to identify risk factors influencing the lack of OSA improvement. <b>Results:</b> A total of 46 patients were enrolled, including 35 males and 11 females, with a mean age of (51.0±12.0) years. Among them, 34 patients were classified into the OSA improvement group, while 12 patients into the non-improvement group the non-improvement group. Of these, 21 patients underwent unilateral adrenalectomy, and 25 received mineralocorticoid receptor antagonist therapy. Patients were followed up for a duration of [<i>M</i> (<i>Q</i><sub>1</sub>,<i>Q</i><sub>3</sub>)] 6.0 (3.0,8.0) months. After treatment, patients with PA complicated by OSA exhibited a reduction in antihypertensive medication use, the increases in serum potassium, renin activity, and serum creatinine levels, along with the decreases in plasma aldosterone and the aldosterone-to-renin ratio (all <i>P</i><0.05). Specifically, the AHI declined from 23.8 (9.0,40.2) events/h to 13.1 (8.1,21.8) events/h (<i>P</i>=0.003). In the non-improvement group, baseline body mass index [(30.1±6.4) vs (25.8±5.0) kg/m²] and the clinical non-remission rate of PA [6/12 vs 5.9% (2/34)] were both higher than those in the improvement group (both <i>P</i><0.05). Multivariate logistic regression model analysis revealed that a higher baseline body mass index (<i>OR</i>=1.18, 95%<i>CI</i>: 1.01-1.39) and clinical non-remission of PA (<i>OR</i>=11.69, 95%<i>CI</i>: 2.13-64.08) were risk factors for lack of improvement in OSA. <b>Conclusions:</b> In patients with PA complicated by OSA, PA-targeted therapy effectively reduces OSA severity. Higher baseline body mass index and clinical non-remission of PA are identified as risk factors for unimproved OSA.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 48","pages":"4488-4495"},"PeriodicalIF":0.0,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145850944","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}
Pub Date : 2025-12-30DOI: 10.3760/cma.j.cn112137-20250630-01591
Y N Li, J Li, W Lu, Z Y Shi, F Fang, D Z Yu, Y M Feng, H B Shi, P J Wang
Objective: To investigate the characteristics of theta rhythm functional connectivity and their clinical implications in patients with Meniere's disease. Methods: A cross-sectional study was conducted. Patients diagnosed with Meniere's disease along with matched healthy controlsat the Department of Otolaryngology-Head and Neck Surgery, Shanghai Sixth People's Hospital between August 2020 and January 2024 were enrolled. Phase-locking value (PLV) was used to calculate theta-band functional connectivity between brain regions in source space. Intergroup differences of the functional connectivity were compared, and its correlations with clinical characteristics were analyzed. Results: The study included 32 Meniere's disease patients (9 males and 23 female) with a mean age of (54.8±11.9) years, along with 29 healthy controls (7 males and 22 females) with a mean age of (56.7±14.5) years. Compared with the healthy controls, Meniere's disease patients exhibited enhanced theta functional connectivity within a network centered on the paracentral lobule and cingulate gyrus (all P<0.05). This enhanced connectivity between the medial/paracingulate gyri and the paracentral lobule positively correlated with the severity of subjective symptoms (r=0.355, P=0.046) and scores on the anxiety-autonomic symptom subscale (r=0.402, P=0.023). However, no statistically significant correlation was found with hearing levels or dynamic posturography scores (all P>0.05). Conclusions: Patients with Meniere's disease demonstrate enhanced theta rhythm functional connectivity involving the paracentral lobule and cingulate gyrus. This neural signature is dissociated from hearing loss and overall balance performance but is linked to subjective anxiety and autonomic symptoms.
{"title":"[Functional connectivity characteristics of electroencephalography theta rhythm and their clinical significance in patients with Meniere's disease].","authors":"Y N Li, J Li, W Lu, Z Y Shi, F Fang, D Z Yu, Y M Feng, H B Shi, P J Wang","doi":"10.3760/cma.j.cn112137-20250630-01591","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250630-01591","url":null,"abstract":"<p><p><b>Objective:</b> To investigate the characteristics of theta rhythm functional connectivity and their clinical implications in patients with Meniere's disease. <b>Methods:</b> A cross-sectional study was conducted. Patients diagnosed with Meniere's disease along with matched healthy controlsat the Department of Otolaryngology-Head and Neck Surgery, Shanghai Sixth People's Hospital between August 2020 and January 2024 were enrolled. Phase-locking value (PLV) was used to calculate theta-band functional connectivity between brain regions in source space. Intergroup differences of the functional connectivity were compared, and its correlations with clinical characteristics were analyzed. <b>Results:</b> The study included 32 Meniere's disease patients (9 males and 23 female) with a mean age of (54.8±11.9) years, along with 29 healthy controls (7 males and 22 females) with a mean age of (56.7±14.5) years. Compared with the healthy controls, Meniere's disease patients exhibited enhanced theta functional connectivity within a network centered on the paracentral lobule and cingulate gyrus (all <i>P</i><0.05). This enhanced connectivity between the medial/paracingulate gyri and the paracentral lobule positively correlated with the severity of subjective symptoms (<i>r</i>=0.355, <i>P</i>=0.046) and scores on the anxiety-autonomic symptom subscale (<i>r</i>=0.402, <i>P</i>=0.023). However, no statistically significant correlation was found with hearing levels or dynamic posturography scores (all <i>P</i>>0.05). <b>Conclusions:</b> Patients with Meniere's disease demonstrate enhanced theta rhythm functional connectivity involving the paracentral lobule and cingulate gyrus. This neural signature is dissociated from hearing loss and overall balance performance but is linked to subjective anxiety and autonomic symptoms.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 48","pages":"4459-4464"},"PeriodicalIF":0.0,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145850970","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}
Pub Date : 2025-12-30DOI: 10.3760/cma.j.cn112137-20250624-01538
von Hippel-Lindau (VHL) syndrome is an autosomal dominant hereditary disorder caused by germline heterozygous pathogenic variants of the VHL gene or promoter hypermethylation. It is characterized by multiple tumors and cystic lesions, primarily affecting the central nervous system, retina, kidneys, pancreas, adrenal glands, and other organs. In recent years, significant progress has been made in both basic and clinical research on VHL syndrome, particularly in genotype-phenotype correlations and targeted therapies, such as the clinical application of hypoxia-inducible factor-2α inhibitors. To further standardize the diagnosis and management of VHL syndrome in China, the Chinese Society of Rare Diseases of the Chinese Medical Association, the Beijing Society of Rare Diseases, and the Chinese Alliance for Genetic and Rare Diseases of the Urinary System of the Chinese Urological Association have updated the epidemiological, genetic, and clinical characteristics, diagnostic criteria, treatment strategies, and long-term management protocols based on the latest evidence-based medical findings and the "Chinese expert consensus for the diagnosis and treatment of von Hippel-Lindau syndrome" in the 2018 edition, and forms 12 recommended suggestions, aiming to provide scientific guidance for clinical practice.
von Hippel-Lindau (VHL)综合征是一种常染色体显性遗传病,由VHL基因的种系杂合致病性变异或启动子超甲基化引起。它的特点是多发肿瘤和囊性病变,主要影响中枢神经系统、视网膜、肾脏、胰腺、肾上腺和其他器官。近年来,VHL综合征的基础研究和临床研究都取得了重大进展,特别是在基因型-表型相关性和靶向治疗方面,如缺氧诱导因子-2α抑制剂的临床应用。为进一步规范VHL综合征在中国的诊断和管理,中华医学会罕见病学会、北京市罕见病学会、中国泌尿系统遗传与罕见病联盟更新了VHL综合征的流行病学、遗传学、临床特征、诊断标准、治疗策略、根据最新循证医学成果和2018年版《中国希佩尔-林道综合征诊疗专家共识》制定长期管理方案,形成12条推荐意见,旨在为临床实践提供科学指导。
{"title":"[Chinese expert consensus for the diagnosis and treatment of von Hippel-Lindau syndrome (2025 edition)].","authors":"","doi":"10.3760/cma.j.cn112137-20250624-01538","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250624-01538","url":null,"abstract":"<p><p>von Hippel-Lindau (VHL) syndrome is an autosomal dominant hereditary disorder caused by germline heterozygous pathogenic variants of the VHL gene or promoter hypermethylation. It is characterized by multiple tumors and cystic lesions, primarily affecting the central nervous system, retina, kidneys, pancreas, adrenal glands, and other organs. In recent years, significant progress has been made in both basic and clinical research on VHL syndrome, particularly in genotype-phenotype correlations and targeted therapies, such as the clinical application of hypoxia-inducible factor-2α inhibitors. To further standardize the diagnosis and management of VHL syndrome in China, the Chinese Society of Rare Diseases of the Chinese Medical Association, the Beijing Society of Rare Diseases, and the Chinese Alliance for Genetic and Rare Diseases of the Urinary System of the Chinese Urological Association have updated the epidemiological, genetic, and clinical characteristics, diagnostic criteria, treatment strategies, and long-term management protocols based on the latest evidence-based medical findings and the \"Chinese expert consensus for the diagnosis and treatment of von Hippel-Lindau syndrome\" in the 2018 edition, and forms 12 recommended suggestions, aiming to provide scientific guidance for clinical practice.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 48","pages":"4441-4452"},"PeriodicalIF":0.0,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145850990","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}
Pub Date : 2025-12-30DOI: 10.3760/cma.j.cn112137-20250620-01508
C Wu, X Fang, C Y Shi, R Wang, X Z Gao, M Hua, Y Cao, P X Zhang, C J Xu
Objective: To investigate the clinical efficacy of short-term spinal cord stimulation (stSCS) in the treatment of segmental zoster paresis (SZP). Methods: A retrospective analysis was performed to collect the clinical data of patients with SZP at the Department of Pain Medicine, Nanjing Hospital Affiliated to Nanjing Medical University from January 2023 to December 2024. The patients were divided into two groups based on whether they received stSCS therapy: the stSCS group (stSCS combined with medication) and the control group (medication only). Evaluations were performed before treatment (T0) and at the following time points after treatment: day 14 (T1), 1 month (T2), 3 months (T3), and 6 months (T4). The following parameters were compared between the two groups at different time points: peak torque (PT) of elbow extensors and flexors at an angular velocity of 60°/s, motor nerve conduction velocity (MNCV) of the ulnar and median nerves, as well as scores on the Numerical Rating Scale (NRS) of pain, Self-Rating Anxiety Scale (SAS), and Self-Rating Depression Scale (SDS). Results: The stSCS group consisted of 20 patients (8 males, 12 females) with a median [Q1, Q3] age of 73.5 (70.3, 77.3) years and disease duration of 0.9 (0.3, 1.6) months. The control group included 20 patients (6 males, 14 females) with a median age of 69.5 (64.5, 79.0) years and disease duration of 0.7 (0.4, 1.2) months. There were no statistically significant differences in age or gender between the two groups (all P>0.05). At the T3 and T4 follow-ups after treatment, the stSCS group demonstrated significantly higher elbow extensor PT [(24.7±1.8) Nm vs (21.9±2.3) Nm], flexor peak PT [(18.6±2.0) Nm vs (20.6±1.9) Nm], ulnar nerve MNCV [(49.0±1.8) m/s vs (52.4±2.3) m/s], and median nerve MNCV [47.3 (46.7, 48.1) m/s vs 51.1 (49.4, 52.1) m/s] compared to the control group, while NRS of pain, SAS, and SDS scores were significantly lower than those in the control group, with significant differences (all P<0.05). No serious stSCS-related adverse reactions occurred, and there were no patient deaths. Conclusion: The stSCS facilitates the recovery of motor function, significantly alleviates pain, and effectively mitigates anxiety and depression symptoms in patients with SZP.
目的:探讨短期脊髓刺激(stSCS)治疗节段性带状疱疹性麻痹(SZP)的临床疗效。方法:回顾性分析南京医科大学附属南京医院疼痛内科2023年1月至2024年12月收治的SZP患者的临床资料。根据患者是否接受stSCS治疗分为两组:stSCS组(stSCS联合药物治疗)和对照组(仅药物治疗)。治疗前(T0)和治疗后第14天(T1)、1个月(T2)、3个月(T3)、6个月(T4)分别进行评估。比较两组患者在不同时间点肘关节伸屈肌角速度为60°/s时的峰值扭矩(PT)、尺神经和正中神经的运动神经传导速度(MNCV)、疼痛数值评定量表(NRS)、焦虑自评量表(SAS)和抑郁自评量表(SDS)得分。结果:stSCS组共有20例患者(男性8例,女性12例),中位[Q1, Q3]年龄为73.5(70.3,77.3)岁,病程为0.9(0.3,1.6)个月。对照组患者20例,男6例,女14例,中位年龄69.5(64.5,79.0)岁,病程0.7(0.4,1.2)个月。两组患者年龄、性别差异无统计学意义(P < 0.05)。治疗后T3、T4随访时,stSCS组肘关节伸肌PT[(24.7±1.8)Nm vs(21.9±2.3)Nm]、屈肌峰PT[(18.6±2.0)Nm vs(20.6±1.9)Nm]、尺神经MNCV[(49.0±1.8)m/s vs(52.4±2.3)m/s]、正中神经MNCV [47.3 (46.7, 48.1) m/s vs 51.1 (49.4, 52.1) m/s]均显著高于对照组,疼痛、SAS、SDS评分NRS均显著低于对照组,差异均有统计学意义(p < 0.05)。stSCS促进SZP患者运动功能恢复,显著缓解疼痛,有效缓解焦虑、抑郁症状。
{"title":"[Effect analysis of short-term spinal cord stimulation on segmental zoster paralysis of limbs].","authors":"C Wu, X Fang, C Y Shi, R Wang, X Z Gao, M Hua, Y Cao, P X Zhang, C J Xu","doi":"10.3760/cma.j.cn112137-20250620-01508","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250620-01508","url":null,"abstract":"<p><p><b>Objective:</b> To investigate the clinical efficacy of short-term spinal cord stimulation (stSCS) in the treatment of segmental zoster paresis (SZP). <b>Methods:</b> A retrospective analysis was performed to collect the clinical data of patients with SZP at the Department of Pain Medicine, Nanjing Hospital Affiliated to Nanjing Medical University from January 2023 to December 2024. The patients were divided into two groups based on whether they received stSCS therapy: the stSCS group (stSCS combined with medication) and the control group (medication only). Evaluations were performed before treatment (T<sub>0</sub>) and at the following time points after treatment: day 14 (T<sub>1</sub>), 1 month (T<sub>2</sub>), 3 months (T<sub>3</sub>), and 6 months (T<sub>4</sub>). The following parameters were compared between the two groups at different time points: peak torque (PT) of elbow extensors and flexors at an angular velocity of 60°/s, motor nerve conduction velocity (MNCV) of the ulnar and median nerves, as well as scores on the Numerical Rating Scale (NRS) of pain, Self-Rating Anxiety Scale (SAS), and Self-Rating Depression Scale (SDS). <b>Results:</b> The stSCS group consisted of 20 patients (8 males, 12 females) with a median [<i>Q</i><sub>1</sub><i>, Q</i><sub>3</sub>] age of 73.5 (70.3, 77.3) years and disease duration of 0.9 (0.3, 1.6) months. The control group included 20 patients (6 males, 14 females) with a median age of 69.5 (64.5, 79.0) years and disease duration of 0.7 (0.4, 1.2) months. There were no statistically significant differences in age or gender between the two groups (all <i>P</i>>0.05). At the T<sub>3</sub> and T<sub>4</sub> follow-ups after treatment, the stSCS group demonstrated significantly higher elbow extensor PT [(24.7±1.8) Nm vs (21.9±2.3) Nm], flexor peak PT [(18.6±2.0) Nm vs (20.6±1.9) Nm], ulnar nerve MNCV [(49.0±1.8) m/s vs (52.4±2.3) m/s], and median nerve MNCV [47.3 (46.7, 48.1) m/s vs 51.1 (49.4, 52.1) m/s] compared to the control group, while NRS of pain, SAS, and SDS scores were significantly lower than those in the control group, with significant differences (all <i>P</i><0.05). No serious stSCS-related adverse reactions occurred, and there were no patient deaths. <b>Conclusion:</b> The stSCS facilitates the recovery of motor function, significantly alleviates pain, and effectively mitigates anxiety and depression symptoms in patients with SZP.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 48","pages":"4504-4509"},"PeriodicalIF":0.0,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145850951","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}
Pub Date : 2025-12-30DOI: 10.3760/cma.j.cn112137-20250710-01692
R Cao, Y R Liu, X N Zhang, Q Mu, K X Wei, L Zhang
<p><p><b>Objective:</b> To investigate the molecular mechanism by which fibroblast growth factor 1 (FGF1) participates in neural tube defects (NTD) through regulating cell proliferation in a retinoic acid (RA)-induced mouse model, and to elucidate the role of FGF1 during neural tube closure in mice. <b>Methods:</b> An NTD mouse model was established using RA induction, with mice divided into a treatment group and a control group (<i>n</i>=9 each). Pregnant mice in the treatment group received 28 mg/kg RA via gavage at embryonic day 7.5 (E7.5), while the control group received sesame oil. Embryonic brain vesicle tissues were collected at E8.5, E9.5, and E10.5 for RNA and protein extraction to assess gene expression. Embryonic brain sections from E9.5 and E10.5 were prepared for pathological examination and gene expression analysis. At the mouse embryonic brain tissue level, quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to validate FGF1 mRNA expression, and immunohistochemistry (IHC) was performed to detect FGF1 protein expression. An FGF1 knockdown plasmid was constructed, and cell proliferation was assessed in vitro. Western blot was used to measure the expression of the proliferation marker proliferating cell nuclear antigen (PCNA), 5-Ethynyl-2'-deoxyuridine (EdU) staining was employed to evaluate cell proliferation, and flow cytometry was conducted to analyze apoptosis. <b>Results:</b> The RA treatment group of mice showed delayed embryonic development, abnormal brain structure, and unclosed neural tubes, inducing the formation of NTD mouse models. At the animal level, both the mRNA and protein expressions of FGF1 were abnormally highly expressed in the brain tissues of NTD mouse embryos at embryonic day 9.5 (E9.5) and E10.5 (<i>P</i><0.001). At the cellular level, FGF1 was significantly highly expressed in HT-22 cells treated with RA (<i>P</i><0.001), while its expression was significantly downregulated after FGF1 knockdown (<i>P</i><0.001); the protein expression of PCNA (a cellular proliferation marker) in RA-treated cells was significantly increased (<i>P</i><0.01), and this expression was significantly decreased after FGF1 gene knockdown in the RA-treated group (<i>P</i><0.01). EdU staining experiments also showed that excessive cell proliferation occurred after RA treatment (<i>P</i><0.001), whereas cell proliferation was reduced in RA-treated cells with FGF1 knockdown (<i>P</i><0.001); flow cytometry analysis indicated that the proportion of apoptotic cells increased significantly after RA intervention (<i>P</i><0.001), and this proportion continued to increase after FGF1 knockdown (<i>P</i><0.05). <b>Conclusions:</b> FGF1 was significantly upregulated in the RA-induced NTD model. Overexpression of FGF1 inhibited cell proliferation and induced apoptosis. Knockdown of FGF1 restored the reduced cell proliferation caused by RA intervention and further increased RA-induced apoptosis. It provides a new perspe
{"title":"[Mechanistic investigation of fibroblast growth factor 1-mediated regulation of cell proliferation and apoptosis in retinoic acid-induced neural tube defects in mice].","authors":"R Cao, Y R Liu, X N Zhang, Q Mu, K X Wei, L Zhang","doi":"10.3760/cma.j.cn112137-20250710-01692","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250710-01692","url":null,"abstract":"<p><p><b>Objective:</b> To investigate the molecular mechanism by which fibroblast growth factor 1 (FGF1) participates in neural tube defects (NTD) through regulating cell proliferation in a retinoic acid (RA)-induced mouse model, and to elucidate the role of FGF1 during neural tube closure in mice. <b>Methods:</b> An NTD mouse model was established using RA induction, with mice divided into a treatment group and a control group (<i>n</i>=9 each). Pregnant mice in the treatment group received 28 mg/kg RA via gavage at embryonic day 7.5 (E7.5), while the control group received sesame oil. Embryonic brain vesicle tissues were collected at E8.5, E9.5, and E10.5 for RNA and protein extraction to assess gene expression. Embryonic brain sections from E9.5 and E10.5 were prepared for pathological examination and gene expression analysis. At the mouse embryonic brain tissue level, quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to validate FGF1 mRNA expression, and immunohistochemistry (IHC) was performed to detect FGF1 protein expression. An FGF1 knockdown plasmid was constructed, and cell proliferation was assessed in vitro. Western blot was used to measure the expression of the proliferation marker proliferating cell nuclear antigen (PCNA), 5-Ethynyl-2'-deoxyuridine (EdU) staining was employed to evaluate cell proliferation, and flow cytometry was conducted to analyze apoptosis. <b>Results:</b> The RA treatment group of mice showed delayed embryonic development, abnormal brain structure, and unclosed neural tubes, inducing the formation of NTD mouse models. At the animal level, both the mRNA and protein expressions of FGF1 were abnormally highly expressed in the brain tissues of NTD mouse embryos at embryonic day 9.5 (E9.5) and E10.5 (<i>P</i><0.001). At the cellular level, FGF1 was significantly highly expressed in HT-22 cells treated with RA (<i>P</i><0.001), while its expression was significantly downregulated after FGF1 knockdown (<i>P</i><0.001); the protein expression of PCNA (a cellular proliferation marker) in RA-treated cells was significantly increased (<i>P</i><0.01), and this expression was significantly decreased after FGF1 gene knockdown in the RA-treated group (<i>P</i><0.01). EdU staining experiments also showed that excessive cell proliferation occurred after RA treatment (<i>P</i><0.001), whereas cell proliferation was reduced in RA-treated cells with FGF1 knockdown (<i>P</i><0.001); flow cytometry analysis indicated that the proportion of apoptotic cells increased significantly after RA intervention (<i>P</i><0.001), and this proportion continued to increase after FGF1 knockdown (<i>P</i><0.05). <b>Conclusions:</b> FGF1 was significantly upregulated in the RA-induced NTD model. Overexpression of FGF1 inhibited cell proliferation and induced apoptosis. Knockdown of FGF1 restored the reduced cell proliferation caused by RA intervention and further increased RA-induced apoptosis. It provides a new perspe","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 48","pages":"4510-4516"},"PeriodicalIF":0.0,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145850998","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}
Pub Date : 2025-12-30DOI: 10.3760/cma.j.cn112137-20250626-01561
D Chen, W Y Deng, X D Shi, G Z Shi, Y F Ye, Q B Tang, X H Yu, C Liu
Objective: To compare the efficacy and safety of left hepatectomy with sequential embolization of the tumor-invaded right hepatic artery (RHA) followed by resection without reconstruction versus left hepatectomy with RHA resection and reconstruction for the treatment of hilar cholangiocarcinoma (HCCA). Methods: A retrospective cohort of 10 HCCA patients undergoing the SERRHA protocol between January 2023 and January 2025 at the Sun Yat-sen Memorial Hospital, Department of Biliary and Pancreatic Surgery, was included (SERRHA group). A control group of 24 HCCA patients undergoing left hepatectomy with RHA resection and reconstruction between January 2014 and January 2025 was established (RRRHA group). Follow-up was conducted until April 30, 2025. The incidence of 90-day Clavien-Dindo≥Grade Ⅲ complications, R0 resection rates, and postoperative survival were compared. Results: The SERRHA group included 10 cases, aged (57.6 ± 16.3) years, with 3 males. The RRRHA group included 24 cases, aged (57.3 ± 11.1) years, with 15 males. In the SERRHA group, 2 patients (2/10) developed left liver abscesses post-embolization. There were no 90-day or in-hospital deaths. Median follow-up was 9.3 months (95%CI: 3.6-15.0). In the RRRHA group, there was 1 peri-operative death due to anastomotic haemorrhage. Median follow-up was 44.5 months (95%CI: 25.8-63.2). Median overall survival (OS) was 29.0 months (95%CI: 9.3-48.7), with 1-, 3-, and 5-year OS rates of 90.8%, 45.6%, and 20.3%, respectively. There were no statistically significant differences (P>0.05) between the SERRHA and RRRHA groups in 90-day Clavien-Dindo≥Grade Ⅲ complications [5/10 vs 20.8% (5/24)], R0 resection rate [4/10 vs 70.8% (17/24)], or 1-year OS (83.3% vs 90.8%). Conclusion: For HCCA with RHA invasion where resection and reconstruction are difficult, left hepatectomy following RHA embolization demonstrates a certain degree of safety, and its short-term efficacy is similar to that of cases with RHA resection and reconstruction.
目的:比较左肝切除术合并肿瘤侵犯右肝动脉(RHA)序贯栓塞后切除不重建与左肝切除术合并RHA切除重建治疗肝门部胆管癌(HCCA)的疗效和安全性。方法:选取2023年1月至2025年1月在中山纪念医院胆胰外科接受SERRHA治疗的10例HCCA患者(SERRHA组)作为回顾性队列。选取2014年1月至2025年1月间行左肝切除术并RHA切除重建的24例HCCA患者作为对照组(RRRHA组)。随访至2025年4月30日。比较90天Clavien-Dindo≥Ⅲ级并发症发生率、R0切除率和术后生存率。结果:SERRHA组10例,年龄(57.6±16.3)岁,男3例。RRRHA组24例,年龄(57.3±11.1)岁,男性15例。在SERRHA组中,2例(2/10)患者在栓塞后出现左肝脓肿。没有90天内死亡或院内死亡。中位随访时间为9.3个月(95%CI: 3.6-15.0)。RRRHA组术中因吻合口出血死亡1例。中位随访时间为44.5个月(95%CI: 25.8-63.2)。中位总生存期(OS)为29.0个月(95%CI: 9.3-48.7), 1年、3年和5年OS率分别为90.8%、45.6%和20.3%。SERRHA组与RRRHA组在90天Clavien-Dindo≥级Ⅲ并发症[5/10 vs 20.8%(5/24)]、R0切除率[4/10 vs 70.8%(17/24)]、1年OS (83.3% vs 90.8%)方面差异无统计学意义(P>0.05)。结论:对于难以切除重建的RHA侵袭HCCA, RHA栓塞左肝切除术具有一定的安全性,其近期疗效与RHA切除重建病例相似。
{"title":"[Efficacy and safety of resection of hilar cholangiocarcinoma with left hepatectomy after pre-operative embolization of the invaded right hepatic artery].","authors":"D Chen, W Y Deng, X D Shi, G Z Shi, Y F Ye, Q B Tang, X H Yu, C Liu","doi":"10.3760/cma.j.cn112137-20250626-01561","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250626-01561","url":null,"abstract":"<p><p><b>Objective:</b> To compare the efficacy and safety of left hepatectomy with sequential embolization of the tumor-invaded right hepatic artery (RHA) followed by resection without reconstruction versus left hepatectomy with RHA resection and reconstruction for the treatment of hilar cholangiocarcinoma (HCCA). <b>Methods:</b> A retrospective cohort of 10 HCCA patients undergoing the SERRHA protocol between January 2023 and January 2025 at the Sun Yat-sen Memorial Hospital, Department of Biliary and Pancreatic Surgery, was included (SERRHA group). A control group of 24 HCCA patients undergoing left hepatectomy with RHA resection and reconstruction between January 2014 and January 2025 was established (RRRHA group). Follow-up was conducted until April 30, 2025. The incidence of 90-day Clavien-Dindo≥Grade Ⅲ complications, R0 resection rates, and postoperative survival were compared. <b>Results:</b> The SERRHA group included 10 cases, aged (57.6 ± 16.3) years, with 3 males. The RRRHA group included 24 cases, aged (57.3 ± 11.1) years, with 15 males. In the SERRHA group, 2 patients (2/10) developed left liver abscesses post-embolization. There were no 90-day or in-hospital deaths. Median follow-up was 9.3 months (95%<i>CI</i>: 3.6-15.0). In the RRRHA group, there was 1 peri-operative death due to anastomotic haemorrhage. Median follow-up was 44.5 months (95%<i>CI</i>: 25.8-63.2). Median overall survival (OS) was 29.0 months (95%<i>CI</i>: 9.3-48.7), with 1-, 3-, and 5-year OS rates of 90.8%, 45.6%, and 20.3%, respectively. There were no statistically significant differences (<i>P</i>>0.05) between the SERRHA and RRRHA groups in 90-day Clavien-Dindo≥Grade Ⅲ complications [5/10 vs 20.8% (5/24)], R0 resection rate [4/10 vs 70.8% (17/24)], or 1-year OS (83.3% vs 90.8%). <b>Conclusion:</b> For HCCA with RHA invasion where resection and reconstruction are difficult, left hepatectomy following RHA embolization demonstrates a certain degree of safety, and its short-term efficacy is similar to that of cases with RHA resection and reconstruction.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 48","pages":"4496-4503"},"PeriodicalIF":0.0,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145850940","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}
Pub Date : 2025-12-30DOI: 10.3760/cma.j.cn112137-20250524-01281
X N Wu, C S Shan, C Y Liu, Y Cao, J Li, J Guan, Q J Wang
Objective: To explore the association between blood lipid levels and prognosis in patients with sudden sensorineural hearing loss (SSNHL) and develop a predictive model. Methods: The clinical data of unilateral SSNHL patients from the Chinese PLA General Hospital between January 2008 and December 2022 were retrospectively analyzed. Patients were divided into treatment-effective and ineffective groups based on their hearing recovery (prognosis) after treatment. Restricted cubic spline (RCS) analysis was used to examine the nonlinear relationship between blood lipid levels and prognosis. The data were randomly split into training and testing sets at a 7∶3 ratio using a computer-based algorithm, and sex-stratified predictive models for prognosis were developed using stepwise logistic regression. The performance of the models was evaluated through receiver operating characteristic (ROC) curves, Hosmer-Lemeshow goodness-of-fit tests, and decision curve analysis (DCA), respectively. Results: A total of 1 329 patients aged (41.4±10.9) years were included, with 682 males and 647 females. RCS analysis showed no nonlinear relationship between lipid metabolism indicators and prognosis in sudden sensorineural hearing loss (all P>0.05). The male predictive model included eight variables: age, low-density lipoprotein cholesterol (LDL-C), smoking, drinking, time of onset, tinnitus, vertigo, and audiogram type. The areas under the ROC curve (AUC) for the training set and validation set were 0.873 (95%CI: 0.839-0.908) and 0.823 (95%CI: 0.760-0.886), respectively. The female predictive model included sevenvariables: age, body mass index (BMI), triglycerides (TG), time of onset, vertigo, hearing level, and audiogram type. The AUC was 0.864 (95%CI: 0.828-0.901) for the training set and 0.833 (95%CI: 0.766-0.900) for the validation set. The model evaluation showed no significant bias in the Hosmer-Lemeshow test for both groups (both P>0.05). The DCA showed a positive net benefit for risk-threshold probabilities of 0-0.93 in both the training and validation sets for male patients. For female patients, the net benefit was positive for thresholds of 0-0.94 in the training set and across nearly the entire range in the validation set. Conclusions: The prognosis of male patients is significantly influenced by smoking, drinking, and LDL-C metabolism disorders, while female patients are affected by BMI and TG levels. The predictive models based on blood lipid levels demonstrated good discrimination, calibration, and clinical applicability.
{"title":"[Association between blood lipid levels and prognosis in patients with sudden sensorineural hearing loss and development of a predictive model].","authors":"X N Wu, C S Shan, C Y Liu, Y Cao, J Li, J Guan, Q J Wang","doi":"10.3760/cma.j.cn112137-20250524-01281","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250524-01281","url":null,"abstract":"<p><p><b>Objective:</b> To explore the association between blood lipid levels and prognosis in patients with sudden sensorineural hearing loss (SSNHL) and develop a predictive model. <b>Methods:</b> The clinical data of unilateral SSNHL patients from the Chinese PLA General Hospital between January 2008 and December 2022 were retrospectively analyzed. Patients were divided into treatment-effective and ineffective groups based on their hearing recovery (prognosis) after treatment. Restricted cubic spline (RCS) analysis was used to examine the nonlinear relationship between blood lipid levels and prognosis. The data were randomly split into training and testing sets at a 7∶3 ratio using a computer-based algorithm, and sex-stratified predictive models for prognosis were developed using stepwise logistic regression. The performance of the models was evaluated through receiver operating characteristic (ROC) curves, Hosmer-Lemeshow goodness-of-fit tests, and decision curve analysis (DCA), respectively. <b>Results:</b> A total of 1 329 patients aged (41.4±10.9) years were included, with 682 males and 647 females. RCS analysis showed no nonlinear relationship between lipid metabolism indicators and prognosis in sudden sensorineural hearing loss (all <i>P</i>>0.05). The male predictive model included eight variables: age, low-density lipoprotein cholesterol (LDL-C), smoking, drinking, time of onset, tinnitus, vertigo, and audiogram type. The areas under the ROC curve (AUC) for the training set and validation set were 0.873 (95%<i>CI</i>: 0.839-0.908) and 0.823 (95%<i>CI</i>: 0.760-0.886), respectively. The female predictive model included sevenvariables: age, body mass index (BMI), triglycerides (TG), time of onset, vertigo, hearing level, and audiogram type. The AUC was 0.864 (95%<i>CI</i>: 0.828-0.901) for the training set and 0.833 (95%<i>CI</i>: 0.766-0.900) for the validation set. The model evaluation showed no significant bias in the Hosmer-Lemeshow test for both groups (both <i>P</i>>0.05). The DCA showed a positive net benefit for risk-threshold probabilities of 0-0.93 in both the training and validation sets for male patients. For female patients, the net benefit was positive for thresholds of 0-0.94 in the training set and across nearly the entire range in the validation set. <b>Conclusions:</b> The prognosis of male patients is significantly influenced by smoking, drinking, and LDL-C metabolism disorders, while female patients are affected by BMI and TG levels. The predictive models based on blood lipid levels demonstrated good discrimination, calibration, and clinical applicability.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 48","pages":"4465-4472"},"PeriodicalIF":0.0,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145850979","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}
Pub Date : 2025-12-30DOI: 10.3760/cma.j.cn112137-20250901-02257
S J Cai, Z Q Li, X Wang, J Wang, Q L Zhu, Q J Wang, R Chen
<p><p><b>Objective:</b> To investigate the characteristics of event-related potential (ERP) in adult males with obstructive sleep apnea (OSA) comorbid with depressive state and their correlation with polysomnography (PSG) parameters. <b>Methods:</b> Cross-sectional study. A total of 77 adult male OSA patients aged 18 to 60 from the Sleep Center of the Second Affiliated Hospital of Soochow University were prospectively enrolled between August 2023 and June 2024. General clinical data, Epworth sleepiness scale (ESS), Pittsburgh sleep quality index (PSQI), self-rating depression scale (SDS), self-rating anxiety scale (SAS), and PSG parameters were collected. Task-state EEG signals were acquired using a 64-channel system under an emotional facial stimulation paradigm. ERP components were analyzed, including the negative wave occurring at approximately 170 ms (N170) and the positive wave occurring at approximately 300 ms (P300) post-stimulus. Based on the apnea-hypopnea index (AHI) and SDS scores, patients were divided into two groups: the OSA without depressive state group (AHI≥5 events/h and SDS<50) and the OSA with depressive state group (AHI≥5 events/h and SDS≥50). Differences in relevant indicators between the two groups were compared. Spearman correlation analysis was employed to assess the relationships between ERP amplitude/latency and PSG parameters. <b>Results:</b> The 77 OSA patients had a mean age of (40.3±8.1) years. Among them, 51 were classified as the OSA without depressive state group, while 26 comprised the OSA with depressive state group, indicating a depression comorbidity rate of 33.8% in the OSA cohort. The OSA with depressive state group demonstrated significantly higher values compared to the OSA without depressive state group in the following parameters: hypertension comorbidity rate [46.2% (12/26) vs 21.6% (11/51)], ESS score [<i>M</i> (<i>Q</i><sub>1</sub>, <i>Q</i><sub>3</sub>): 10.0 (5.0, 15.0) vs 7.0 (4.0, 11.0) points], SDS [(55.2±4.4) vs (40.4±6.0) points], and SAS [(43.3±6.0) vs (37.9±7.4) points] (all <i>P</i><0.05). The OSA with depressive state group exhibited a lower proportion of slow-wave sleep (SWS) compared to the OSA without depressive state group [7.1% (2.9%, 11.4%) vs 13.1% (6.8%, 19.3%), <i>P</i>=0.002], and a higher microarousal index [36.2 (24.9, 45.9) vs 27.9 (16.4, 39.4) events/h, <i>P</i>=0.034]. Furthermore, the N170 latencies at both the PO7 electrode [(261.5±22.4) vs (250.2±23.1) ms] and the PO8 electrode [(261.4±20.2) vs (246.8±23.2) ms] were longer in the OSA with depressive state group (all <i>P</i><0.05). Correlation analyses revealed a negative correlation between N170 latency at the PO8 electrode and SWS percentage (<i>r</i>=-0.227, <i>P</i>=0.047). Additionally, N170 amplitudes at both the PO7 electrode (<i>r</i>=-0.351, <i>P</i>=0.002) and the PO8 electrode (<i>r</i>=-0.262, <i>P</i>=0.021) showed negative correlations with the microarousal index. <b>Conclusion:</b> Adult male OSA patients w
目的:探讨成年男性阻塞性睡眠呼吸暂停(OSA)合并抑郁状态的事件相关电位(ERP)特征及其与多导睡眠图(PSG)参数的相关性。方法:横断面研究。前瞻性研究于2023年8月至2024年6月期间纳入苏州大学第二附属医院睡眠中心18 - 60岁成年男性OSA患者77例。收集一般临床资料、Epworth嗜睡量表(ESS)、匹兹堡睡眠质量指数(PSQI)、抑郁自评量表(SDS)、焦虑自评量表(SAS)及PSG参数。在情绪面部刺激模式下,使用64通道系统获取任务状态脑电图信号。分析了刺激后约170 ms (N170)出现的负波和约300 ms (P300)出现的正波。根据呼吸暂停低通气指数(AHI)和SDS评分将患者分为两组:无抑郁状态OSA组(AHI≥5事件/h和SDS)。结果:77例OSA患者平均年龄(40.3±8.1)岁。其中,51例为OSA无抑郁组,26例为OSA伴抑郁组,OSA队列中抑郁症合并率为33.8%。与无抑郁状态组相比,OSA伴抑郁组在以下参数中表现出更高的数值:高血压合并率[46.2% (12/26)vs 21.6% (11/51)], ESS评分[M (Q1, Q3): 10.0 (5.0, 15.0) vs 7.0(4.0, 11.0)分],SDS[(55.2±4.4)vs(40.4±6.0)分],SAS[(43.3±6.0)vs(37.9±7.4)分](所有PP=0.002),微觉醒指数[36.2 (24.9,45.9)vs 27.9(16.4, 39.4)事件/h, P=0.034]。此外,OSA合并抑郁状态组PO7电极[(261.5±22.4)vs(250.2±23.1)ms]和PO8电极[(261.4±20.2)vs(246.8±23.2)ms]的N170潜伏期均较长(Pr=-0.227, P=0.047)。此外,PO7电极的N170振幅(r=-0.351, P=0.002)和PO8电极的N170振幅(r=-0.262, P=0.021)与微觉醒指数呈负相关。结论:伴有抑郁症的成年男性OSA患者对情绪性面部刺激的N170潜伏期延长,且其振幅和潜伏期的改变与睡眠片段化有关。
{"title":"[Event-related potential characteristics in adult male patients with obstructive sleep apnea comorbid with depressive state and their correlation with polysomnographic parameters].","authors":"S J Cai, Z Q Li, X Wang, J Wang, Q L Zhu, Q J Wang, R Chen","doi":"10.3760/cma.j.cn112137-20250901-02257","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250901-02257","url":null,"abstract":"<p><p><b>Objective:</b> To investigate the characteristics of event-related potential (ERP) in adult males with obstructive sleep apnea (OSA) comorbid with depressive state and their correlation with polysomnography (PSG) parameters. <b>Methods:</b> Cross-sectional study. A total of 77 adult male OSA patients aged 18 to 60 from the Sleep Center of the Second Affiliated Hospital of Soochow University were prospectively enrolled between August 2023 and June 2024. General clinical data, Epworth sleepiness scale (ESS), Pittsburgh sleep quality index (PSQI), self-rating depression scale (SDS), self-rating anxiety scale (SAS), and PSG parameters were collected. Task-state EEG signals were acquired using a 64-channel system under an emotional facial stimulation paradigm. ERP components were analyzed, including the negative wave occurring at approximately 170 ms (N170) and the positive wave occurring at approximately 300 ms (P300) post-stimulus. Based on the apnea-hypopnea index (AHI) and SDS scores, patients were divided into two groups: the OSA without depressive state group (AHI≥5 events/h and SDS<50) and the OSA with depressive state group (AHI≥5 events/h and SDS≥50). Differences in relevant indicators between the two groups were compared. Spearman correlation analysis was employed to assess the relationships between ERP amplitude/latency and PSG parameters. <b>Results:</b> The 77 OSA patients had a mean age of (40.3±8.1) years. Among them, 51 were classified as the OSA without depressive state group, while 26 comprised the OSA with depressive state group, indicating a depression comorbidity rate of 33.8% in the OSA cohort. The OSA with depressive state group demonstrated significantly higher values compared to the OSA without depressive state group in the following parameters: hypertension comorbidity rate [46.2% (12/26) vs 21.6% (11/51)], ESS score [<i>M</i> (<i>Q</i><sub>1</sub>, <i>Q</i><sub>3</sub>): 10.0 (5.0, 15.0) vs 7.0 (4.0, 11.0) points], SDS [(55.2±4.4) vs (40.4±6.0) points], and SAS [(43.3±6.0) vs (37.9±7.4) points] (all <i>P</i><0.05). The OSA with depressive state group exhibited a lower proportion of slow-wave sleep (SWS) compared to the OSA without depressive state group [7.1% (2.9%, 11.4%) vs 13.1% (6.8%, 19.3%), <i>P</i>=0.002], and a higher microarousal index [36.2 (24.9, 45.9) vs 27.9 (16.4, 39.4) events/h, <i>P</i>=0.034]. Furthermore, the N170 latencies at both the PO7 electrode [(261.5±22.4) vs (250.2±23.1) ms] and the PO8 electrode [(261.4±20.2) vs (246.8±23.2) ms] were longer in the OSA with depressive state group (all <i>P</i><0.05). Correlation analyses revealed a negative correlation between N170 latency at the PO8 electrode and SWS percentage (<i>r</i>=-0.227, <i>P</i>=0.047). Additionally, N170 amplitudes at both the PO7 electrode (<i>r</i>=-0.351, <i>P</i>=0.002) and the PO8 electrode (<i>r</i>=-0.262, <i>P</i>=0.021) showed negative correlations with the microarousal index. <b>Conclusion:</b> Adult male OSA patients w","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 48","pages":"4480-4487"},"PeriodicalIF":0.0,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145850965","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}
Pub Date : 2025-12-23DOI: 10.3760/cma.j.cn112137-20250712-01708
Z Y Gao, W Sun, J P Huang, L He, W W Dong, Z H Wang, T Zhang, L Shao, D L Zhang, C Z Lyu, J Z Xiang, P Zhang, H Zhang
To explore the clinical and pathological characteristics of reoperation cases after thermal ablation treatment for thyroid carcinoma, the restrospective analysis included 40 patients with thyroid cancer who underwent reoperation after thermal ablation treatment in the Department of Thyroid Surgery of the First Hospital of China Medical University from December 2014 to April 2025, with an average age of (48.3±12.9) years including 9 male patients. A total of 49 cancer foci underwent thermal ablation treatment. Before thermal ablation, fine-needle aspiration was performed in all 40 patients (49 cancer foci), but 31 patients (37 cancer foci) underwent thermal ablation without obtaining cytological pathology. The maximum diameter of the cancer foci before thermal ablation was (1.50±0.99) cm, with 29 cancer foci≥1 cm and 20 cancer foci <1 cm. Nineteen cancer foci were adjacent to the thyroid capsule. Postoperative pathology confirmed that 29 patients (33 cancer foci) still had residual cancer foci. The residual rate of lesions with a maximum diameter≥1 cm was higher than that of lesions with a maximum diameter<1 cm [79.3% (23/29) vs 50.0% (10/20), P=0.032]. The residual rate of cancer foci adjacent to the thyroid capsule was higher than that of those far from the thyroid capsule [89.5% (17/19) vs 53.3% (16/30), P=0.009)]. Three cases had occult multifocal cancer, and 14 patients had metastatic lymph nodes. One patient with follicular carcinoma had multiple bone metastases. The results of this study suggest that non-standard initial thermal ablation treatment may lead to residual cancer foci or metastatic lymph nodes. For patients that are eligible for surgery,thermal ablation should not be blindly promoted or overused as an initial treatment.
{"title":"[Clinical and pathological characteristics analysis of 40 reoperation cases after thermal ablation treatment for thyroid carcinoma].","authors":"Z Y Gao, W Sun, J P Huang, L He, W W Dong, Z H Wang, T Zhang, L Shao, D L Zhang, C Z Lyu, J Z Xiang, P Zhang, H Zhang","doi":"10.3760/cma.j.cn112137-20250712-01708","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250712-01708","url":null,"abstract":"<p><p>To explore the clinical and pathological characteristics of reoperation cases after thermal ablation treatment for thyroid carcinoma, the restrospective analysis included 40 patients with thyroid cancer who underwent reoperation after thermal ablation treatment in the Department of Thyroid Surgery of the First Hospital of China Medical University from December 2014 to April 2025, with an average age of (48.3±12.9) years including 9 male patients. A total of 49 cancer foci underwent thermal ablation treatment. Before thermal ablation, fine-needle aspiration was performed in all 40 patients (49 cancer foci), but 31 patients (37 cancer foci) underwent thermal ablation without obtaining cytological pathology. The maximum diameter of the cancer foci before thermal ablation was (1.50±0.99) cm, with 29 cancer foci≥1 cm and 20 cancer foci <1 cm. Nineteen cancer foci were adjacent to the thyroid capsule. Postoperative pathology confirmed that 29 patients (33 cancer foci) still had residual cancer foci. The residual rate of lesions with a maximum diameter≥1 cm was higher than that of lesions with a maximum diameter<1 cm [79.3% (23/29) vs 50.0% (10/20), <i>P</i>=0.032]. The residual rate of cancer foci adjacent to the thyroid capsule was higher than that of those far from the thyroid capsule [89.5% (17/19) vs 53.3% (16/30), <i>P</i>=0.009)]. Three cases had occult multifocal cancer, and 14 patients had metastatic lymph nodes. One patient with follicular carcinoma had multiple bone metastases. The results of this study suggest that non-standard initial thermal ablation treatment may lead to residual cancer foci or metastatic lymph nodes. For patients that are eligible for surgery,thermal ablation should not be blindly promoted or overused as an initial treatment.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 47","pages":"4395-4397"},"PeriodicalIF":0.0,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145811594","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}
Pub Date : 2025-12-23DOI: 10.3760/cma.j.cn112137-20250811-02036
B Han, F Sun, Y He, H D Song
Congenital hypothyroidism (CH) is one of the most common inherited metabolic disorders in children, and delayed diagnosis and treatment can adversely affect intellectual development and growth. In April 2025, the Chinese Society of Endocrinology and the Chinese Society of Pediatrics jointly released the "Guidelines for the diagnosis and treatment of congenital hypothyroidism". Based on the latest evidence-based medical data and clinical experience, these guidelines systematically established a comprehensive management framework covering screening, diagnosis, treatment, and follow-up, aiming to standardize CH screening, diagnosis, treatment, and long-term management. This article provides an interpretation of the main content of the guidelines. The guidelines emphasize that early diagnosis and treatment can improve the prognosis of CH and set a newborn screening cut-off value of≥8-10 mU/L as the standard for recall and examination. In terms of treatment, the guidelines stress the principle of "early and adequate" intervention, recommending levothyroxine (LT4) as the first-line treatment with a starting dose of at least 10 μg/kg. Timely follow-up and avoidance of overtreatment are also highlighted. For transient CH, it is recommended to discontinue LT4 treatment after the age of 3 and conduct further evaluations of thyroid function and imaging examinations. The guidelines also note that genetic testing to identify the molecular etiology of CH has significant guiding value for the treatment of specific types of CH. The guidelines achieve standardization of the diagnostic and therapeutic process, address the gap in lifelong management of CH in China from the neonatal period to adulthood, and provide healthcare professionals with an accurate, effective, and comprehensive normative document.
{"title":"[Interpretation of the 2025 \"Guidelines for the diagnosis and treatment of congenital hypothyroidism\"].","authors":"B Han, F Sun, Y He, H D Song","doi":"10.3760/cma.j.cn112137-20250811-02036","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250811-02036","url":null,"abstract":"<p><p>Congenital hypothyroidism (CH) is one of the most common inherited metabolic disorders in children, and delayed diagnosis and treatment can adversely affect intellectual development and growth. In April 2025, the Chinese Society of Endocrinology and the Chinese Society of Pediatrics jointly released the \"Guidelines for the diagnosis and treatment of congenital hypothyroidism\". Based on the latest evidence-based medical data and clinical experience, these guidelines systematically established a comprehensive management framework covering screening, diagnosis, treatment, and follow-up, aiming to standardize CH screening, diagnosis, treatment, and long-term management. This article provides an interpretation of the main content of the guidelines. The guidelines emphasize that early diagnosis and treatment can improve the prognosis of CH and set a newborn screening cut-off value of≥8-10 mU/L as the standard for recall and examination. In terms of treatment, the guidelines stress the principle of \"early and adequate\" intervention, recommending levothyroxine (LT<sub>4</sub>) as the first-line treatment with a starting dose of at least 10 μg/kg. Timely follow-up and avoidance of overtreatment are also highlighted. For transient CH, it is recommended to discontinue LT<sub>4</sub> treatment after the age of 3 and conduct further evaluations of thyroid function and imaging examinations. The guidelines also note that genetic testing to identify the molecular etiology of CH has significant guiding value for the treatment of specific types of CH. The guidelines achieve standardization of the diagnostic and therapeutic process, address the gap in lifelong management of CH in China from the neonatal period to adulthood, and provide healthcare professionals with an accurate, effective, and comprehensive normative document.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 47","pages":"4345-4350"},"PeriodicalIF":0.0,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145810718","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}