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Prenatal ultrasound diagnosis and quality control of fetal nuchal translucency. 产前超声诊断和胎儿颈部透明层的质量控制。
Q3 Medicine Pub Date : 2024-04-28 DOI: 10.11817/j.issn.1672-7347.2024.240005
Xiaohua Yuan, Yimei Fu

Objectives: In clinical ultrasound examinations, it is challenging to perform quality control on the images of each fetal nuchal translucency (NT) and crown-rump length (CRL). However, small measurement differences can increase the probability of false-positive or false-negative diagnosis. Therefore, it is necessary to establish a quality control system for fetal NT examination. This study aims to control the quality of fetal NT and CRL measurements, evaluate the accuracy of ultrasound physicians in early pregnancy NT measurements, and analyze the impact of increased fetal structure screening on the detection rate of chromosomal abnormalities.

Methods: Data were collected from cases before and after 12 months of NT examination quality control, with 2 214 before quality control and 2 538 cases after quality control. Three quality control data metrics were analyzed: NT multiple of median (NT-MoM), standard deviation (SD) of log10MoM [(SD) log10MoM], and the slope of NT on CRL (SNC). The performance of NT measurements was monitored through the individual CRL NT-MoM within the 0.9-1.1 MoM range of the normal median curve, while grouped based on different years of experience (<3 years, 3-6 years, >6 years), and NT-MoM values among these groups were compared. Data on NT thickening, structural anomalies, and chromosomal abnormalities were retrospectively analyzed during the quality control period.

Results: According to the curve equation of the American NTQR project group, the NT-MoM value before quality control was 0.921 7 MoM, the (SD) log10MoM value was 0.091 92, and the SNC value was 12.20%. After quality control, the NT-MoM value was 0.948 3 MoM, the (SD) log10MoM value was 0.094 81, and the SNC value was 11.43%. The comparison of NT-MoM values before and after quality control showed a statistically significant difference (P<0.000 1). The comparison of NT-MoM values measured by ultrasound physicians with different years of experience before and after quality control also showed statistically significant differences (P<0.000 1). The NT-MoM values for the 3-6 years and >6 years groups were higher after quality control (P<0.05), while the <3 years group showed no significant difference before and after quality control (P>0.05). After quality control, cases of NT thickening without significant structural abnormalities accounted for 19.05%, NT thickening with structural abnormalities accounted for 47.62%, and NT normal with structural abnormalities accounted for 33.33%. There were 36 cases of fetal heart abnormalities, accounting for 20.34% of the total abnormality rate, with a positive rate of 36% in chromosome tests.

Conclusions: After quality control, ultrasound physicians measure NT more accurately, but differences among measurements remain. Measurements by experienced ultrasound physicians

目的:在临床超声检查中,对每个胎儿的颈部透明层(NT)和头臀长(CRL)图像进行质量控制是一项挑战。然而,微小的测量差异会增加假阳性或假阴性诊断的概率。因此,有必要建立胎儿 NT 检查的质量控制体系。本研究旨在控制胎儿NT和CRL测量的质量,评估超声医生在孕早期NT测量中的准确性,并分析增加胎儿结构筛查对染色体异常检出率的影响:方法:收集NT检查质控前后12个月的病例数据,质控前2 214例,质控后2 538例。对三个质控数据指标进行了分析:NT中位数的倍数(NT-MoM)、log10MoM的标准偏差(SD)[(SD) log10MoM]以及NT在CRL上的斜率(SNC)。通过正常中位曲线 0.9-1.1 MoM 范围内的单个 CRL NT-MoM 监测 NT 测量的性能,同时根据不同的工作年限(6 年)进行分组,并比较这些组间的 NT-MoM 值。在质量控制期间,对NT增厚、结构异常和染色体异常的数据进行了回顾性分析:根据美国NTQR项目组的曲线方程,质控前的NT-MoM值为0.921 7 MoM,(SD)log10MoM值为0.091 92,SNC值为12.20%。质控后,NT-MoM 值为 0.948 3 MoM,(标清)log10MoM 值为 0.094 81,SNC 值为 11.43%。质控前后的 NT-MoM 值比较显示,质控后各组 NT-MoM 值较高,差异有统计学意义(PP6 年)(PP>0.05)。质控后,无明显结构异常的 NT 增厚占 19.05%,NT 增厚伴结构异常占 47.62%,NT 正常伴结构异常占 33.33%。胎儿心脏畸形36例,占总畸形率的20.34%,染色体检测阳性率为36%:结论:经过质量控制后,超声医生对 NT 的测量更为准确,但测量结果之间仍存在差异。有经验的超声医生的测量值更接近预期值,通常低于预期值。监测胎儿NT和CRL的测量有助于提高测量的准确性。在 NT 检查中增加结构筛查,尤其是胎儿心脏筛查,可提高染色体异常的检出率。
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引用次数: 0
Application progress of exergames in health interventions for the elderly. 电子游戏在老年人健康干预中的应用进展。
Q3 Medicine Pub Date : 2024-04-28 DOI: 10.11817/j.issn.1672-7347.2024.230420
Xi Chen, Hongting Ning, Shuang Wu, Lina Wu, Dian Jiang, Yifei Chen, Zeng Cao, Hui Feng

With the aging population in China, health issues among the elderly are becoming increasingly prominent, leading to a rapidly growing demand for health interventions for the elderly. Exergames are one of the important emerging methods in the field of health interventions for the elderly, widely used and yielding positive results. While research on exergames is well-established abroad, it is still in its infancy in China, lacking reports on the types, interaction forms, intervention content, application status, and effectiveness of exergames. Exergames are suitable for widespread use among the elderly in China, and there is a need to accelerate the development and application of exergames in the field of health interventions for the elderly in China.

随着中国人口老龄化的加剧,老年人健康问题日益突出,导致对老年人健康干预的需求迅速增长。体外游戏是老年人健康干预领域重要的新兴方法之一,应用广泛,效果良好。虽然国外对电子游戏的研究已经比较成熟,但在国内还处于起步阶段,缺乏对电子游戏的类型、互动形式、干预内容、应用现状和效果等方面的报道。外显子游戏适合在中国老年人中广泛使用,有必要加快外显子游戏在中国老年人健康干预领域的开发和应用。
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引用次数: 0
Identification of ceRNA networks in type H and L vascular endothelial cells through integrated bioinformatics methods. 通过综合生物信息学方法识别 H 型和 L 型血管内皮细胞中的 ceRNA 网络。
Q3 Medicine Pub Date : 2024-04-28 DOI: 10.11817/j.issn.1672-7347.2024.230343
Zhi Liu, Zhe Ruan, Haitao Long, Ruibo Zhao, Yong Zhu, Zhangyuan Lin, Peng Chen, Shushan Zhao

Objectives: Type H blood vessels are a subtype of bone-specific microvessels (CD31hiEmcnhi) that play an important regulatory role in the coupling of angiogenesis and osteogenesis. Despite reports on the distinct roles of type H and L vessels under physiological and pathological bone conditions, their genetic differences remain to be elucidated. This study aims to construct a competitive endogenous RNA (ceRNA) network of key gene for differencial expression (DE) in type H and L vascular endothelial cells (ECs) through integrated bioinformatic methods.

Methods: We downloaded relevant raw data from the ArrayExpress and the Gene Expression Omnibus (GEO) database and used the Limma R-Bioconductor package to screen for DE lncRNAs, DE miRNAs, and DE mRNAs between type H and L vascular ECs. A total ceRNA network was constructed based on their interactions, followed by refinement using protein-protein interaction (PPI) networks to select upregulated and downregulated key genes. Enrichment analysis was performed on these key genes. Random validation was conducted using flow cytometry and real-time RT-PCR.

Results: A total of 1 761 DE mRNAs, 187 DE lncRNAs, and 159 DE miRNAs were identified, and a comprehensive ceRNA network was constructed based on their interactions. Six upregulated (Itga5, Kdr, Tjp1, Pecam1, Cdh5, and Ptk2) and 2 downregulated (Csf1r and Il10) key genes were selected via PPI network to construct a subnetwork of ceRNAs related to these key genes. Upregulated key genes were mainly enriched in negative regulation of angiogenesis and vascular apoptosis. Results from flow cytometry and real-time RT-PCR were consistent with bioinformatics analysis.

Conclusions: This study proposes a ceRNA network associated with upregulated and downregulated type H and L vascular ECs based on selected key genes, providing new insights into the regulatory mechanisms of type H and L vascular ECs in bone metabolism.

目的:H 型血管是骨特异性微血管(CD31hiEmcnhi)的一种亚型,在血管生成和骨生成的耦合过程中发挥着重要的调节作用。尽管有报道称 H 型血管和 L 型血管在生理和病理骨条件下发挥着不同的作用,但它们的遗传差异仍有待阐明。本研究旨在通过综合生物信息学方法,构建H型和L型血管内皮细胞(ECs)差异表达(DE)关键基因的竞争性内源性RNA(ceRNA)网络:我们从ArrayExpress和Gene Expression Omnibus(GEO)数据库中下载了相关原始数据,并使用Limma R-Bioconductor软件包筛选了H型和L型血管内皮细胞中的DE lncRNAs、DE miRNAs和DE mRNAs。根据它们之间的相互作用构建了一个总的 ceRNA 网络,然后利用蛋白质-蛋白质相互作用(PPI)网络进行细化,以选择上调和下调的关键基因。对这些关键基因进行了富集分析。使用流式细胞仪和实时 RT-PCR 进行随机验证:结果:共鉴定出 1 761 个 DE mRNA、187 个 DE lncRNA 和 159 个 DE miRNA,并根据它们之间的相互作用构建了一个全面的 ceRNA 网络。通过PPI网络筛选出6个上调(Itga5、Kdr、Tjp1、Pecam1、Cdh5和Ptk2)和2个下调(Csf1r和Il10)的关键基因,构建了与这些关键基因相关的ceRNA子网络。上调的关键基因主要富集在血管生成和血管凋亡的负调控中。流式细胞术和实时 RT-PCR 的结果与生物信息学分析一致:本研究根据选定的关键基因,提出了与H型和L型血管内皮细胞上调和下调相关的ceRNA网络,为H型和L型血管内皮细胞在骨代谢中的调控机制提供了新的见解。
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引用次数: 0
Clinicopathological characteristics of secondary trigeminal neuralgia due to cerebellopontine angle tumors. 小脑角肿瘤引起的继发性三叉神经痛的临床病理特征。
Q3 Medicine Pub Date : 2024-04-28 DOI: 10.11817/j.issn.1672-7347.2024.230369
Ying Wang, Ruijie Liu, Zhiquan Yang, Zhuanyi Yang

Objectives: Cerebellopontine angle (CPA) tumors are a common cause of secondary trigeminal neuralgia (TN), characterized by their concealed location, slow progression, and difficulty in early detection. This study aims to explore the clinicopathological characteristics of patients with secondary TN due to CPA tumors to enhance understanding and management of secondary TN.

Methods: A retrospective analysis was conducted on clinical data and pathological results of 116 patients with CPA tumor-related TN treated at Xiangya Hospital of Central South University from January 1, 2017 to December 31, 2022. The study analyzed the relationship of tumor pathological types with clinical manifestations, tumor location, surgical methods, and treatment outcomes.

Results: Among the cases, 95.7% (111/116) were benign tumors, 3.4% (4/116) were malignant tumors, and 0.9% (1/116) were borderline tumors. Benign tumors were predominantly acoustic neuromas, meningiomas, and schwannomas. Among the patients, 46.6% (54/116) presented with isolated TN, while 53.4% (62/116) exhibited other associated symptoms depending on factors such as tumor growth location and rate. The complete resection rate in this group was over 90%, with 41.4% (48/116) of patients undergoing concurrent microvascular decompression after tumor resection, predominantly for schwannomas. The overall effective rate of surgical treatment reached 93.9%, with schwannomas showing higher efficacy rates compared with acoustic neuromas and meningiomas (P<0.05). The recurrence rate of acoustic neuromas was significantly higher than that of meningiomas and schwannomas (P<0.05).

Conclusions: CPA tumors are a major cause of secondary TN, predominantly benign, with occasional underdiagnosed malignant tumors. Early diagnosis and treatment significantly impact prognosis. Different tumor types vary in clinical symptoms, surgical approaches, and treatment efficacy. Surgical strategies should balance tumor resection extent and neural function preservation, with microvascular decompression as necessary.

目的:小脑角(CPA)肿瘤是继发性三叉神经痛(TN)的常见病因,其特点是位置隐蔽、进展缓慢、难以早期发现。本研究旨在探讨CPA肿瘤导致的继发性三叉神经痛患者的临床病理特征,以加深对继发性三叉神经痛的理解和管理:对中南大学湘雅医院2017年1月1日至2022年12月31日收治的116例CPA肿瘤相关TN患者的临床资料和病理结果进行回顾性分析。研究分析了肿瘤病理类型与临床表现、肿瘤位置、手术方式及治疗效果的关系:病例中,95.7%(111/116)为良性肿瘤,3.4%(4/116)为恶性肿瘤,0.9%(1/116)为边缘性肿瘤。良性肿瘤主要是听神经瘤、脑膜瘤和裂隙瘤。在患者中,46.6%(54/116)表现为孤立的 TN,而 53.4%(62/116)表现为其他相关症状,这取决于肿瘤生长的位置和速度等因素。该组患者的完全切除率超过90%,其中41.4%(48/116)的患者在肿瘤切除后同时进行了微血管减压术,主要用于治疗裂隙瘤。手术治疗的总有效率达到 93.9%,与听神经瘤和脑膜瘤相比,分裂瘤的有效率更高(PPConclusions:CPA肿瘤是继发性TN的主要病因,以良性为主,偶尔也有诊断不足的恶性肿瘤。早期诊断和治疗对预后有重大影响。不同肿瘤类型的临床症状、手术方法和治疗效果各不相同。手术策略应兼顾肿瘤切除范围和神经功能保护,必要时进行微血管减压。
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引用次数: 0
ALK fusion small cell transformation of lung adenocarcinoma: A case report and literature review. ALK融合小细胞肺腺癌转化:病例报告和文献综述。
Q3 Medicine Pub Date : 2024-04-28 DOI: 10.11817/j.issn.1672-7347.2024.230506
Guangyan Xu, Liang Zhou

Patients with anaplastic lymphoma kinase (ALK) fusion lung adenocarcinoma may develop drug resistance after treatment with ALK-tyrosine kinase inhibitor (ALK-TKI), and the mechanisms of this resistance are not yet fully defined. The Affiliated Hospital of Zunyi Medical University admitted a patient who was resistant to ALK fusion after ALK-TKI treatment, leading to disease progression and subsequent biopsy indicating a transformation to small cell lung cancer in September 2021. The patient, a 54-year-old female, initially presented with symptoms of cough, sputum production, and chest pain for 4 months. Chest CT showed a neoplastic lesion in the posterior segment of the right upper lobe to right lower lobe with obstructive pneumonia, metastasis in the right lower lobe, increased and enlarged mediastinal and right hilar lymph nodes, and thickening of the right hilar soft tissue. Bronchoscopy and pathological biopsy confirmed the diagnosis of lung adenocarcinoma. The results of next-generation sequencing indicated that echinoderm microtubule associated protein like 4-anaplastic lymphoma kinase (EML4-ALK) fusion is associated with tumor protein 53 (TP53) and retinoblastoma 1 (RB1) gene mutations. The patient received second-generation ALK-TKI aletinib, achieving a progression-free survival of 11 months before disease progression suggested aletinib resistance. Subsequently, the third-generation ALK-TKI lorlatinib administered for one month without efficacy, resulting in rapid systemic disease progression. The neuron specific enolase (NSE) was significantly increased, and the patient developed new pleural, pericardial, intracranial, liver, and multiple bone metastases occurred in a short period. A second biopsy indicated small cell lung cancer. Modification of treatment regimen to chemotherapy combined with immunotherapy proved effective. The mechanisms of drug resistance of ALK-TKI treatment for advanced non-small cell lung cancer with ALK fusion are complex, and small cell transformation of pathological type is one such mechanism, although rare. Concurrent TP53 and RB1 gene mutations may be characteristic of this transformation. Elevated NSE can serve as a predictive serum marker for adenocarcinoma transforming to small cell carcinoma. Timely re-biopsy and selection of subsequent treatments based on different resistance mechanisms are crucial for comprehensive disease management.

无性淋巴瘤激酶(ALK)融合型肺腺癌患者在接受ALK-酪氨酸激酶抑制剂(ALK-TKI)治疗后可能出现耐药,而这种耐药的机制尚未完全明确。遵义医学院附属医院于2021年9月收治了一名经ALK-TKI治疗后出现ALK融合耐药,导致疾病进展,随后活检显示转变为小细胞肺癌的患者。患者为 54 岁女性,最初出现咳嗽、咳痰和胸痛症状,已持续 4 个月。胸部 CT 显示右上叶后段至右下叶有肿瘤病变,伴有阻塞性肺炎,右下叶有转移,纵隔和右侧肺门淋巴结增大,右侧肺门软组织增厚。支气管镜检查和病理活检确诊为肺腺癌。新一代测序结果表明,棘皮微管相关蛋白样4-无性淋巴瘤激酶(EML4-ALK)融合与肿瘤蛋白53(TP53)和视网膜母细胞瘤1(RB1)基因突变有关。患者接受了第二代 ALK-TKI 阿来替尼治疗,在疾病进展提示阿来替尼耐药前获得了 11 个月的无进展生存期。随后,第三代ALK-TKI洛拉替尼(lorlatinib)用药一个月后未见疗效,导致全身疾病迅速进展。神经元特异性烯醇化酶(NSE)明显升高,患者在短期内出现新的胸膜、心包、颅内、肝脏和多处骨转移。第二次活检显示为小细胞肺癌。将治疗方案调整为化疗联合免疫治疗证明有效。ALK-TKI治疗ALK融合的晚期非小细胞肺癌的耐药机制非常复杂,病理类型的小细胞转化是其中一种机制,但并不多见。同时发生的 TP53 和 RB1 基因突变可能是这种转化的特征。NSE 升高可作为腺癌向小细胞癌转化的预测性血清标志物。及时进行再活检并根据不同的耐药机制选择后续治疗方法,对于疾病的综合管理至关重要。
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引用次数: 0
Curcumin inhibits the proliferation and migration of osteosarcoma by regulating the expression of super-enhancer-associated genes. 姜黄素通过调节超级增强子相关基因的表达抑制骨肉瘤的增殖和迁移。
Q3 Medicine Pub Date : 2024-04-28 DOI: 10.11817/j.issn.1672-7347.2024.230224
Zhanbo Ouyang, Haihong Zhu, Zhongyue Liu, Chao Tu, Jian Qu, Qiong Lu, Min Xu

Objectives: Super-enhancer-associated genes may be closely related to the progression of osteosarcoma, curcumin exhibits a certain inhibitory effect on tumors such as osteosarcoma. This study aims to investigate the effects of curcumin on osteosarcoma in vitro and in vivo, and to determine whether curcumin can inhibit the progression of osteosarcoma by suppressing the expression of super-enhancer-associated genes LIM and senescent cell antigen-like-containing domain 1 (LIMS1), secreted protein acidic and rich in cysteine (SPARC), and sterile alpha motif domain containing 4A (SAMD4A).

Methods: Human osteosarcoma cell lines (MG63 cells or U2OS cells) were treated with 5 to 50 μmol/L curcumin for 24, 48, and 72 hours, followed by the methyl thiazolyl tetrazolium (MTT) assay to detect cell viability. Cells were incubated with dimethyl sulfoxide (DMSO) or curcumin (2.5, 5.0 μmol/L) for 7 days, and a colony formation assay was used to measure in vitro cell proliferation. After treatment with DMSO or curcumin (10, 15 μmol/L), a scratch healing assay and a transwell migration assay were performed to evaluate cell migration ability. Real-time reverse transcription polymerase chain reaction (real-time RT-PCR) and Western blotting were used to detect mRNA and protein expression levels of LIMS1, SPARC, and SAMD4A in the cells. An osteosarcoma-bearing nude mouse model was established, and curcumin was administered via gavage for 14 days to assess the impact of curcumin on tumor volume and weight in vivo. Real-time RT-PCR was used to measure mRNA expression levels of LIMS1, SPARC, and SAMD4A in the cancer and adjacent tissues from 12 osteosarcoma patients.

Results: After treating cells with different concentrations of curcumin for 24, 48, and 72 hours, cell viability were all significantly decreased. Compared with the DMSO group, the colony formation rates in the 2.5 μmol/L and 5.0 μmol/L curcumin groups significantly declined (both P<0.01). The scratch healing assay showed that, compared with the DMSO group, the migration rates of cells in the 10 μmol/L and 15 μmol/L curcumin groups were significantly reduced. The exception was the 10 μmol/L curcumin group at 24 h, where the migration rate of U2OS cells did not show a statistically significant difference (P>0.05), while all other differences were statistically significant (P<0.01 or P<0.001). The transwell migration assay results showed that the number of migrating cells in the 10 μmol/L and 15 μmol/L curcumin groups was significantly lower than that in the DMSO group (both P<0.001). In the in vivo tumor-bearing mouse experiment, the curcumin group showed a reduction in tumor mass (P<0.01) and a significant reduction in tumor volume (P<0.001) compared with the control group. Compared with the DMSO group, the mRNA expression lev

研究目的超级增强子相关基因可能与骨肉瘤的进展密切相关,姜黄素对骨肉瘤等肿瘤具有一定的抑制作用。本研究旨在探讨姜黄素在体外和体内对骨肉瘤的影响,并确定姜黄素是否能通过抑制超级增强子相关基因LIM和衰老细胞抗原样结构域1(LIMS1)、富含半胱氨酸的酸性分泌蛋白(SPARC)和含无菌α基序结构域4A(SAMD4A)的表达来抑制骨肉瘤的进展。方法:用 5 至 50 μmol/L 姜黄素处理人骨肉瘤细胞系(MG63 细胞或 U2OS 细胞)24、48 和 72 小时,然后用甲基噻唑基四氮唑(MTT)试验检测细胞活力。用二甲基亚砜(DMSO)或姜黄素(2.5、5.0 μmol/L)培养细胞 7 天,然后用菌落形成试验来检测体外细胞增殖。用二甲基亚砜或姜黄素(10、15 μmol/L)处理后,进行划痕愈合试验和透孔迁移试验,以评估细胞迁移能力。采用实时逆转录聚合酶链反应(real-time RT-PCR)和 Western 印迹法检测细胞中 LIMS1、SPARC 和 SAMD4A 的 mRNA 和蛋白表达水平。建立骨肉瘤裸鼠模型,通过灌胃给药姜黄素 14 天,以评估姜黄素对体内肿瘤体积和重量的影响。采用实时 RT-PCR 技术检测了 12 例骨肉瘤患者的癌组织和邻近组织中 LIMS1、SPARC 和 SAMD4A 的 mRNA 表达水平:结果:用不同浓度的姜黄素处理细胞 24、48 和 72 小时后,细胞活力均显著下降。与二甲基亚砜组相比,2.5 μmol/L 和 5.0 μmol/L 姜黄素组的集落形成率明显下降(PP 均>0.05),而其他差异均有统计学意义(10 μmol/L和15 μmol/L姜黄素组的PPPLIMS1、SPARC和SAMD4A均明显下调(骨肉瘤组织中的PPSPARC均明显升高(PLIMS1和SAMD4A差异无统计学意义(均P>0.05).结论:姜黄素在体外和体内均能抑制骨肉瘤的增殖和迁移,这可能与超级增强子相关基因LIMS1的失活有关。
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引用次数: 0
Exercise perspective: Benefits and mechanisms of gut microbiota on the body. 从运动的角度看问题:肠道微生物群对人体的益处和机制。
Q3 Medicine Pub Date : 2024-04-28 DOI: 10.11817/j.issn.1672-7347.2024.230550
Xin Gao, Peizhen Zhang

Gut microbiota refers to the vast and diverse community of microorganisms residing in the intestines. Factors such as genetics, environmental influences (e.g., exercise, diet), and early life experiences (e.g., infant feeding methods) can all affect the ecological balance of gut microbiota within the body. Dysbiosis of the gut microbiota is associated with extra-intestinal diseases such as Parkinson's syndrome, osteoporosis, and autoimmune diseases, suggesting that disturbances in gut microbiota may be one of the causes of these diseases. Exercise benefits various diseases, with gut microbiota playing a role in regulating the nervous, musculoskeletal, and immune systems. Gut microbiota can impact the body's health status through the gut-brain axis, gut-muscle axis, and immune pathways. Moderate-intensity aerobic exercise can increase the quantity of gut microbiota and change microbial abundance, although short-term exercise does not significantly affect the alpha diversity of the microbiota. Resistance exercise also does not have a significant regulatory effect on gut microbiota.

肠道微生物群是指居住在肠道中的庞大而多样的微生物群落。遗传、环境影响(如运动、饮食)和早期生活经历(如婴儿喂养方法)等因素都会影响体内肠道微生物群的生态平衡。肠道微生物菌群失调与帕金森综合症、骨质疏松症和自身免疫性疾病等肠道外疾病有关,这表明肠道微生物菌群紊乱可能是导致这些疾病的原因之一。运动有益于各种疾病,而肠道微生物群在调节神经、肌肉骨骼和免疫系统方面发挥着作用。肠道微生物群可通过肠道-大脑轴、肠道-肌肉轴和免疫途径影响人体的健康状况。中等强度的有氧运动可以增加肠道微生物群的数量并改变微生物的丰度,但短期运动并不会对微生物群的α多样性产生显著影响。阻力运动对肠道微生物群也没有明显的调节作用。
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引用次数: 0
Regulation of exercise on heart rate variability in perimenopausal and postmenopausal women. 运动对围绝经期和绝经后妇女心率变异性的调节。
Q3 Medicine Pub Date : 2024-04-28 DOI: 10.11817/j.issn.1672-7347.2024.230399
Mengchen Fang, Peizhen Zhang

Heart rate variability (HRV) is a non-invasive quantitative measure of cardiac autonomic nervous activity. Due to the increase of age and the decrease of estrogen level in perimenopausal and postmenopausal women, the cardiac autonomic nervous function is abnormal, increasing the risk of cardiovascular disease. Proper exercise can increase estrogen levels, improve cardiovascular health, regulate cardiac autonomic nervous activity, and reduce the risk of cardiovascular disease. Low-moderate intensity aerobic exercise, resistance exercise, aerobic combined resistance exercise and mind-body exercise have positive effects on HRV in perimenopausal and postmenopausal women. Therefore, summarizing the effects of different exercise modes on HRV in perimenopausal and postmenopausal women, as well as the mechanism of exercise training improvement on HRV, so as to adopt better exercise strategies to improve HRV of perimenopausal and postmenopausal women, and thus reduce the risk of cardiovascular diseases and improve the health level and quality of life of perimenopausal and postmenopausal women.

心率变异性(HRV)是对心脏自律神经活动的一种无创定量测量。围绝经期和绝经后妇女由于年龄的增长和雌激素水平的下降,心脏自主神经功能出现异常,增加了心血管疾病的风险。适当的运动可以提高雌激素水平,改善心血管健康,调节心脏自主神经活动,降低心血管疾病的风险。低中等强度的有氧运动、阻力运动、有氧联合阻力运动和心身运动对围绝经期和绝经后妇女的心率变异有积极影响。因此,总结不同运动方式对围绝经期和绝经后妇女心率变异的影响,以及运动训练改善心率变异的机制,从而采取更好的运动策略改善围绝经期和绝经后妇女的心率变异,进而降低围绝经期和绝经后妇女罹患心血管疾病的风险,提高围绝经期和绝经后妇女的健康水平和生活质量。
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引用次数: 0
Role of exercise in reducing the risk of cardiovascular diseases associated with sleep disorders. 运动在降低与睡眠障碍有关的心血管疾病风险方面的作用。
Q3 Medicine Pub Date : 2024-04-28 DOI: 10.11817/j.issn.1672-7347.2024.230426
Yunheng Qiao, Peizhen Zhang

Cardiovascular diseases are the leading cause of death among urban and rural residents and have become a major global public health problem. The prevention and control of cardiovascular disease risk factors is crucial for preventing, stabilizing, and even reversing cardiovascular disease. Studies have found that certain sleep disorders are directly related to cardiovascular disease and may be induced through pathways such as endothelial dysfunction, dysregulation of autonomic homeostasis, inflammatory response, and metabolic dysfunction. Exercise helps improve sleep disorders and thus reduce the risk of cardiovascular disease, and has irreplaceable advantages over pharmacological treatments for improving sleep. Different types of sleep disorders should be adjusted by factors such as exercise mode, intensity, and duration of exercise. A good sleep state further reduces the risk of cardiovascular disease. Discussing the effect of exercise on the improvement of the risk of cardiovascular disease associated with sleep disorders, and elaborating the mechanism of action of exercise in reducing the risk of cardiovascular disease from the perspective of sleep, can lay a foundation for the treatment of sleep disorders by exercise and propose new directions for reducing cardiovascular disease risk.

心血管疾病是城乡居民死亡的主要原因,已成为全球主要的公共卫生问题。预防和控制心血管疾病的危险因素对于预防、稳定甚至逆转心血管疾病至关重要。研究发现,某些睡眠障碍与心血管疾病直接相关,可能通过内皮功能障碍、自主神经平衡失调、炎症反应和代谢功能障碍等途径诱发。运动有助于改善睡眠障碍,从而降低罹患心血管疾病的风险,在改善睡眠方面具有药物治疗不可替代的优势。不同类型的睡眠障碍应根据运动方式、运动强度和持续时间等因素进行调整。良好的睡眠状态可进一步降低心血管疾病的风险。探讨运动对改善睡眠障碍相关心血管疾病风险的影响,从睡眠角度阐述运动降低心血管疾病风险的作用机制,可以为运动治疗睡眠障碍奠定基础,为降低心血管疾病风险提出新的方向。
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引用次数: 0
Early-onset Parkinson's disease with mutations in both the PRKN gene and the APOB gene: A case report. 同时存在 PRKN 基因和 APOB 基因突变的早发性帕金森病:病例报告。
Q3 Medicine Pub Date : 2024-04-28 DOI: 10.11817/j.issn.1672-7347.2024.230438
Shijia Bing, Xia Yi, Xiangqi Tang

The incidence rate of Parkinson's disease ranks the second among degenerative diseases of the nervous system, only lower than Alzheimer's disease. Early-onset Parkinson's disease (EPOD) refers to Parkinson's disease with initial symptoms appearing before the age of 50. EOPD is associated with certain genetic mutations and has distinct clinical features. This study reports a case of EOPD with mutations in both the PRKN and the APOB genes. The patient presented with the initial symptom of unstable walking at the age of 28, followed by bradykinesia, limb tremors, masked face, shuffling gait, and cogwheel rigidity in both upper limbs. The blood lipid test showed total cholesterol of 6.48 mmol/L and low-density lipoprotein cholesterol of 4.13 mmol/L. Genetic testing showed a deletion in exon 5 and a point mutation [c.850G>C(p.Gly284Arg)] in exon 7 of the PRKN gene, as well as a point mutation [c.10579C>T(p.Arg3527Trp)] in exon 26 of the APOB gene. Based on these clinical manifestations and examination results, the patient was diagnosed with EOPD. The compound heterozygous mutations in the PRKN gene, as well as the combined mutations in the PRKN and APOB genes, are both reported for the first time, expanding the spectrum of genetic mutations associated with EOPD.

帕金森病的发病率在神经系统变性疾病中排名第二,仅低于阿尔茨海默病。早发性帕金森病(EPOD)是指在 50 岁之前出现初期症状的帕金森病。早发帕金森病与某些基因突变有关,具有明显的临床特征。本研究报告了一例 PRKN 和 APOB 基因均发生突变的 EOPD 患者。患者 28 岁时出现行走不稳的最初症状,随后出现运动迟缓、肢体震颤、蒙面、洗牌步态和双上肢齿轮僵直。血脂检测显示总胆固醇为 6.48 毫摩尔/升,低密度脂蛋白胆固醇为 4.13 毫摩尔/升。基因检测显示,PRKN基因第5外显子缺失,第7外显子发生点突变[c.850G>C(p.Gly284Arg)],APOB基因第26外显子发生点突变[c.10579C>T(p.Arg3527Trp)]。根据这些临床表现和检查结果,患者被诊断为 EOPD。PRKN基因的复合杂合突变以及PRKN和APOB基因的联合突变均为首次报道,从而扩大了与EOPD相关的基因突变的范围。
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引用次数: 0
期刊
中南大学学报(医学版)
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