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[Treatment options for multiple myeloma with renal injury]. [多发性骨髓瘤合并肾损伤的治疗方案]。
Pub Date : 2024-04-01 DOI: 10.3760/cma.j.cn112138-20240108-00016
J Lu
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引用次数: 0
[Clinical features and lymphocyte subtypes in patients with IgG4-related diseases]. [IgG4相关疾病患者的临床特征和淋巴细胞亚型]。
Pub Date : 2024-04-01 DOI: 10.3760/cma.j.cn112138-20231103-00291
L P Guo, W R Wang, J P Liu, B M Wang, L Zhou

Objective: To deepen understanding of IgG4-related diseases (RDs), we analyzed the associated lymphocyte subtypes, and explored the pathogenesis and potential immunotherapeutic targets. Methods: Eighty-six patients with IgG4-RDs were enrolled, and their clinical characteristics, peripheral lymphocyte subtypes, and disease course were analyzed. Results: The mean age of the participants was 36-87(62±11) years; 51 were male (59.3%) and 35 were women (40.7%); and 34.9% had a history of allergy. Follow-up lasted 4.8 (0.4, 14.1) months. The most common symptoms were abdominal pain, and submandibular gland and lacrimal gland swelling (each 20.9%). Sixty-five (75.6%) participants had multiple organ involvement, and the most frequently affected organs were the pancreas (52.3%), submandibular gland (51.2%), and lacrimal gland (34.9%). A high eosinophil count; high IgE, IgG, IgG1, and IgG4 concentrations; and low complement C3 and C4 concentrations were present in 18.8% (16/85), 30.0% (24/80), 72.9% (62/85), 58.3% (28/48), 89.5% (77/86), 61.2% (52/85), and 50.0% (42/84), respectively, of the participants. In addition, 64.7% (55/85) were positive for autoantibodies, and the most frequent was anti-nuclear antibody (63.5%). The proportion of CD4+T lymphocytes increased in 25.7% (9/35) of the participants, which was accompanied by an increase in the ratio of CD4+/CD8+T lymphocytes (22.9%, 8/35). Importantly, most participants (90.0%, 18/20) had a high proportion of regulatory T (Treg) cells. High interleukin (IL)-2, IL-6, and IL-10 concentrations were present in 50.0% (11/22), 33.3% (10/30), and 16.7% (5/30), respectively, of the participants. Substantial lymphoplasmacytic infiltration, fibrosis, IgG4-positive plasma cell infiltration, and lymphoid follicle hyperplasia or ectopic formation were present in 79.2% (42/53), 67.9%(36/53), 35.8%(19/53) and 30.2% (16/53), respectively, of the participants. Fifty-three participants with detailed pathologic data were also further evaluated, of whom 24.5% (13/53), 3.8% (2/53), and 67.9% (36/53) had definite, probable, and possible diagnoses; and 3.8% (2/53) could not be diagnosed. Compared with baseline, the percentage of eosinophils and the IgE, IgG, and IgG4 concentrations decreased significantly; and the complement C3 and C4 concentrations had increased significantly after 6 months of treatment (all P<0.05). The IgG4 concentration after 6 months of treatment negatively correlated with that of C4, and positively correlated with the baseline concentration of IgE and the IgG4/IgG ratio. Conclusion: IgG4-RDs are a group of diseases characterized by male predisposition; multiple organ involvement; a high eosinophil count; high IgE, IgG, IgG1, and IgG4 concentrations; and a low C3 concentration. Peripheral CD4+T cells and

目的为了加深对 IgG4 相关疾病(RDs)的了解,我们分析了相关的淋巴细胞亚型,并探讨了发病机制和潜在的免疫治疗靶点。研究方法入组 86 例 IgG4-RD 患者,分析他们的临床特征、外周淋巴细胞亚型和病程。结果参与者的平均年龄为36-87(62±11)岁;51人为男性(59.3%),35人为女性(40.7%);34.9%有过敏史。随访时间为 4.8 (0.4, 14.1) 个月。最常见的症状是腹痛、颌下腺和泪腺肿胀(各占 20.9%)。65名(75.6%)患者有多个器官受累,最常受累的器官是胰腺(52.3%)、颌下腺(51.2%)和泪腺(34.9%)。18.8%(16/85)、30.0%(24/80)、72.9%(62/85)、58.3%(28/48)、89.5%(77/86)、61.2%(52/85)和 50.0%(42/84)的参与者嗜酸性粒细胞计数高;IgE、IgG、IgG1 和 IgG4 浓度高;补体 C3 和 C4 浓度低。此外,64.7%(55/85)的人自身抗体呈阳性,其中最常见的是抗核抗体(63.5%)。25.7%的参与者(9/35)的 CD4+T 淋巴细胞比例升高,CD4+/CD8+T 淋巴细胞比例也随之升高(22.9%,8/35)。重要的是,大多数参与者(90.0%,18/20)的调节性 T(Treg)细胞比例较高。50.0%(11/22)、33.3%(10/30)和 16.7%(5/30)的参与者体内白细胞介素 (IL)-2、IL-6 和 IL-10 浓度较高。79.2%(42/53)、67.9%(36/53)、35.8%(19/53)和 30.2%(16/53)的参与者分别出现大量淋巴浆细胞浸润、纤维化、IgG4 阳性浆细胞浸润、淋巴滤泡增生或异位形成。此外,还对 53 名有详细病理数据的参与者进行了进一步评估,其中 24.5%(13/53)、3.8%(2/53)和 67.9%(36/53)的参与者有明确、可能和可能的诊断;3.8%(2/53)的参与者无法确诊。与基线相比,嗜酸性粒细胞的百分比以及 IgE、IgG 和 IgG4 的浓度显著下降;补体 C3 和 C4 的浓度在治疗 6 个月后显著上升(治疗 6 个月后所有 P4 的浓度与 C4 的浓度呈负相关,与 IgE 的基线浓度和 IgG4/IgG 比值呈正相关)。结论IgG4-RD是一组以男性易感性、多器官受累、嗜酸性粒细胞计数高、IgE、IgG、IgG1和IgG4浓度高以及C3浓度低为特征的疾病。外周 CD4+T 细胞和 Treg 细胞也较多。在大多数情况下,糖皮质激素和免疫抑制剂可以控制疾病。治疗 6 个月后的 IgG4 浓度与基线补体 C4 浓度呈负相关,与 IgE 浓度和 IgG4/IgG 比值呈正相关,这表明应密切监测 IgG4/IgG、IgE 和补体,以评估此类患者的疾病活动性和治疗效果。
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引用次数: 0
[Inflammatory myopathy associated with anti-mitochondrial antibodies: a case report]. [与抗线粒体抗体相关的炎性肌病:病例报告]。
Pub Date : 2024-04-01 DOI: 10.3760/cma.j.cn112138-20231028-00258
J Y Huo, A P Sun, X Y Zhang, Y Fu, D S Fan
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引用次数: 0
[Advances on extracellular vesicles derived from dead cells]. [从死亡细胞中提取细胞外囊泡的研究进展]。
Pub Date : 2024-04-01 DOI: 10.3760/cma.j.cn112138-20231024-00247
W T Li, W Huang, Y Yang, F Peng
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引用次数: 0
[Magnetic resonance imaging T2 mapping could reflect disease status in patients with dermatomyositis or polymyositis]. [磁共振成像 T2 映射可反映皮肌炎或多发性肌炎患者的疾病状态]。
Pub Date : 2024-04-01 DOI: 10.3760/cma.j.cn112138-20231014-00211
F Zhang, J Xu, X X Wang, Y Q Cheng, W Chen

This study aimed to explore the value of magnetic resonance imaging (MRI) T2 mapping in the assessment of dermatomyositis (DM) and polymyositis (PM). Thirty-three confirmed cases (myosin group) and eight healthy volunteers (healthy control group) at the Department of Rheumatology and Immunology, the First Affiliated Hospital of Kunming Medical University, from October 2016 to December 2017, were collected and analyzed. Multiple parameters of the myosin group were quantified, including creatine kinase (CK), erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), complement C3, and complement C4. Disease status was evaluated using a panel of tools: myositis disease activity assessment tool-muscle (MDAAT-muscle), myositis disease activity assessment tool-whole (MDAAT-all), health assessment questionnaire (HAQ), medical outcomes study health survey short form-36 item (SF-36), hand muscle strength test (MMT-8) score, and MRI T2 mapping of muscle (22 muscles in the pelvis and thighs) T2 values. The results showed that in the myositis group, the measurements for CK, ESR, CRP, complement C3, and complement C4 were 457.2 (165.6, 1 229.2) IU/L, 20 (10, 42) mm/1h, 3.25 (2.38, 10.07) mg/L, 0.90 (0.83, 1.06) g/L, and 0.18 (0.14, 0.23) g/L, respectively. The scores for MMT-8, MDAAT-muscle, MDAAT-all, HAQ, and SF-36 were 57.12±16.23, 5.34 (4.00, 6.00), 34.63±12.62, 1.55 (0.66, 2.59), and 44.66±7.98, respectively. T2 values were significantly higher in all 22 muscles of the pelvis and thighs of patients with DM or PM compared with the healthy controls [(54.99±11.60)ms vs. (36.62±1.66)ms, P<0.001], with the most severe lesions in the satrorius, iliopsoas, piriformis, gluteus minimus, and gluteus medius muscles. The total muscle T2 value in the myositis group was positively correlated with CK, MDAAT-muscle, MDAAT-all, and HAQ (r=0.461, 0.506, 0.347, and 0.510, respectively, all P<0.05). There was a negative correlation between complement C4, SF-36, and MMT-8 scores (r=-0.424, -0.549, and -0.686, respectively, all P<0.05). Collectively, the findings from this study suggest that MRI T2 mapping can objectively reflect the disease status of DM and PM.

本研究旨在探讨磁共振成像(MRI)T2图在皮肌炎(DM)和多发性肌炎(PM)评估中的价值。研究收集并分析了昆明医科大学第一附属医院风湿免疫科2016年10月至2017年12月的33例确诊病例(肌酶组)和8名健康志愿者(健康对照组)。对肌苷组的多个参数进行了量化,包括肌酸激酶(CK)、红细胞沉降率(ESR)、C反应蛋白(CRP)、补体C3和补体C4。采用一系列工具对疾病状态进行评估:肌炎疾病活动评估工具-肌肉(MDAAT-muscle)、肌炎疾病活动评估工具-全身(MDAAT-all)、健康评估问卷(HAQ)、医疗结果研究健康调查短表-36项(SF-36)、手部肌力测试(MMT-8)评分以及肌肉(骨盆和大腿的22块肌肉)磁共振成像T2图T2值。结果显示,肌炎组的肌酸激酶、血沉、CRP、补体C3和补体C4的测量值分别为457.2(165.6,1 229.2)IU/L、20(10,42)mm/1h、3.25(2.38,10.07)mg/L、0.90(0.83,1.06)g/L和0.18(0.14,0.23)g/L。MMT-8、MDAAT-muscle、MDAAT-all、HAQ 和 SF-36 评分分别为 57.12±16.23、5.34(4.00,6.00)、34.63±12.62、1.55(0.66,2.59)和 44.66±7.98。与健康对照组相比,DM 或 PM 患者骨盆和大腿所有 22 块肌肉的 T2 值均明显升高[(54.99±11.60)ms vs. (36.62±1.66)ms,P0.001],其中以坐骨肌、髂腰肌、梨状肌、臀小肌和臀中肌的病变最为严重。肌炎组的肌肉 T2 总值与肌酸激酶、肌肉 MDAAT、全部 MDAAT 和 HAQ 呈正相关(r 分别为 0.461、0.506、0.347 和 0.510,均为 P0.05)。补体 C4、SF-36 和 MMT-8 评分之间呈负相关(r=-0.424、-0.549 和 -0.686,均为 P0.05)。总之,本研究的结果表明,磁共振成像 T2 映像可以客观地反映 DM 和 PM 的疾病状态。
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引用次数: 0
[Investigation of the immune profile of multiple myeloma patients achieving long-term survival after autologous stem cell transplantation]. [调查自体干细胞移植后长期存活的多发性骨髓瘤患者的免疫概况]。
Pub Date : 2024-04-01 DOI: 10.3760/cma.j.cn112138-20230906-00112
J L Gu, C H Zhong, M L Chen, L F Kuang, X Z Li, B H Huang, J R Liu, J Li

Objective: To identify the characteristics of the bone marrow immune microenvironment associated with long-term survival in multiple myeloma (MM) patients. Methods: In the follow-up cohort of patients with newly diagnosed MM and who received "novel agent induction therapy and subsequent autologous stem cell transplantation and immunomodulator maintenance therapy" in the First Affiliated Hospital of Sun Yat-sen University, a cross-sectional study was carried out between August 2019 and May 2020. Using NanoString technology, the RNA expression of 770 bone marrow immune-related markers was compared between 16 patients who had progression-free survival ≥5 years and 5 patients with progressive disease. Among the 16 patients who achieved long-term survival, 9 achieved persistent minimal residual disease (MRD) negative while the other 7 had persistent positive MRD. The functional scores of each kind of immune cells were calculated based on the expression level of characteristic genes, so as to indirectly obtained the proportion of each immune cell subset. The Mann-Whitney U test and the Kruskal Wallis test were used for statistical analysis. Results: The proportion of neutrophils was significantly higher in long-surviving MM patients than in patients with progressive disease [functional scores, 13.61 (13.33, 14.25) vs. 12.93 (12.58, 13.38); Z=2.31, P=0.021]. Among long-surviving patients, those who were MRD-positive had a significantly greater number of mast cells compared with those who were MRD-negative [functional scores, 7.09 (6.49, 8.57) vs. 6.03 (5.18, 6.69); H=2.18, P=0.029]. Compared with patients with progressive disease, four genes (CTSG, IFIT2, S100B, and CHIT1) were significantly downregulated and six (C4B, TNFRSF17, CD70, IRF4, C2, and GAGE1) were upregulated in long-surviving patients. Among long-surviving patients, only gene CMA1 was significantly upgraded, 10 genes (ISG15, OAS3, MX1, IFIT2, DDX58, SIGLEC1, CXCL10, IL1RN, SERPING and TNFSF10) were significantly downregulated in the MRD-positive group compared with that in the MRD-negative group, the first 5 of which are related to the interferon response pathway. Conclusions: The increased neutrophil and mast cell numbers may be related to long-term survival in MM. Interferon signaling activation may be a key bone marrow immune profiling feature for MRD-negative, long-surviving patients with MM.

目的:确定与多发性骨髓瘤(MM)患者长期生存相关的骨髓免疫微环境特征:确定与多发性骨髓瘤(MM)患者长期生存相关的骨髓免疫微环境特征。方法在2019年8月至2020年5月期间,对中山大学附属第一医院接受 "新药诱导治疗及随后的自体干细胞移植和免疫调节剂维持治疗 "的新诊断MM患者进行了一项横断面研究。利用NanoString技术,比较了16名无进展生存期≥5年的患者和5名疾病进展期患者的770个骨髓免疫相关标志物的RNA表达。在 16 名获得长期生存的患者中,9 人的最小残留病灶(MRD)持续阴性,另外 7 人的 MRD 持续阳性。根据特征基因的表达水平计算各类免疫细胞的功能评分,从而间接得出各类免疫细胞亚群所占的比例。统计分析采用 Mann-Whitney U 检验和 Kruskal Wallis 检验。结果长期存活的 MM 患者的中性粒细胞比例明显高于疾病进展期患者[功能评分,13.61 (13.33, 14.25) vs. 12.93 (12.58, 13.38);Z=2.31,P=0.021]。在长期存活的患者中,MRD阳性患者的肥大细胞数量明显多于MRD阴性患者[功能评分,7.09(6.49,8.57) vs. 6.03(5.18,6.69);H=2.18,P=0.029]。与进展期患者相比,长存活期患者的四个基因(CTSG、IFIT2、S100B 和 CHIT1)明显下调,六个基因(C4B、TNFRSF17、CD70、IRF4、C2 和 GAGE1)上调。与 MRD 阴性组相比,MRD 阳性组中只有 CMA1 基因明显上调,10 个基因(ISG15、OAS3、MX1、IFIT2、DDX58、SIGLEC1、CXCL10、IL1RN、SERPING 和 TNFSF10)明显下调,其中前 5 个基因与干扰素反应途径有关。结论中性粒细胞和肥大细胞数量的增加可能与 MM 的长期生存有关。干扰素信号激活可能是MRD阴性、长期存活的MM患者骨髓免疫图谱的一个关键特征。
{"title":"[Investigation of the immune profile of multiple myeloma patients achieving long-term survival after autologous stem cell transplantation].","authors":"J L Gu, C H Zhong, M L Chen, L F Kuang, X Z Li, B H Huang, J R Liu, J Li","doi":"10.3760/cma.j.cn112138-20230906-00112","DOIUrl":"10.3760/cma.j.cn112138-20230906-00112","url":null,"abstract":"<p><p><b>Objective:</b> To identify the characteristics of the bone marrow immune microenvironment associated with long-term survival in multiple myeloma (MM) patients. <b>Methods:</b> In the follow-up cohort of patients with newly diagnosed MM and who received \"novel agent induction therapy and subsequent autologous stem cell transplantation and immunomodulator maintenance therapy\" in the First Affiliated Hospital of Sun Yat-sen University, a cross-sectional study was carried out between August 2019 and May 2020. Using NanoString technology, the RNA expression of 770 bone marrow immune-related markers was compared between 16 patients who had progression-free survival ≥5 years and 5 patients with progressive disease. Among the 16 patients who achieved long-term survival, 9 achieved persistent minimal residual disease (MRD) negative while the other 7 had persistent positive MRD. The functional scores of each kind of immune cells were calculated based on the expression level of characteristic genes, so as to indirectly obtained the proportion of each immune cell subset. The Mann-Whitney <i>U</i> test and the Kruskal Wallis test were used for statistical analysis. <b>Results:</b> The proportion of neutrophils was significantly higher in long-surviving MM patients than in patients with progressive disease [functional scores, 13.61 (13.33, 14.25) vs. 12.93 (12.58, 13.38); <i>Z</i>=2.31, <i>P</i>=0.021]. Among long-surviving patients, those who were MRD-positive had a significantly greater number of mast cells compared with those who were MRD-negative [functional scores, 7.09 (6.49, 8.57) vs. 6.03 (5.18, 6.69); <i>H</i>=2.18, <i>P</i>=0.029]. Compared with patients with progressive disease, four genes (CTSG, IFIT2, S100B, and CHIT1) were significantly downregulated and six (C4B, TNFRSF17, CD70, IRF4, C2, and GAGE1) were upregulated in long-surviving patients. Among long-surviving patients, only gene CMA1 was significantly upgraded, 10 genes (ISG15, OAS3, MX1, IFIT2, DDX58, SIGLEC1, CXCL10, IL1RN, SERPING and TNFSF10) were significantly downregulated in the MRD-positive group compared with that in the MRD-negative group, the first 5 of which are related to the interferon response pathway. <b>Conclusions:</b> The increased neutrophil and mast cell numbers may be related to long-term survival in MM. Interferon signaling activation may be a key bone marrow immune profiling feature for MRD-negative, long-surviving patients with MM.</p>","PeriodicalId":68309,"journal":{"name":"中华内科杂志","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140337781","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
[Progress of kidney disease in the past decade]. [过去十年肾脏病的进展]。
Pub Date : 2024-04-01 DOI: 10.3760/cma.j.cn112138-20240220-00113
M Chen, M H Zhao
{"title":"[Progress of kidney disease in the past decade].","authors":"M Chen, M H Zhao","doi":"10.3760/cma.j.cn112138-20240220-00113","DOIUrl":"10.3760/cma.j.cn112138-20240220-00113","url":null,"abstract":"","PeriodicalId":68309,"journal":{"name":"中华内科杂志","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140337783","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
[Analysis of the factors influencing the severity of coronavirus disease 2019 in patients with myeloproliferative neoplasms based on an online questionnaire]. [基于在线问卷对骨髓增生性肿瘤患者 2019 年冠状病毒疾病严重程度的影响因素分析]。
Pub Date : 2024-04-01 DOI: 10.3760/cma.j.cn112138-20230822-00073
F Y Qi, M Bao, H L Gao, Q Jiang

Objective: To explore the variables associated with the severity of coronavirus disease 2019 (COVID-19) caused by the SARS-CoV-2 omicron variant during the epidemic in patients with myeloproliferative neoplasms (MPN). Methods: A cross-sectional study. During the SARS-CoV-2 omicron variant pandemic from December 15, 2022, to March 15, 2023, COVID-19 related data for patients with MPN who were treated at Peking University People's Hospital were collected through an online questionnaire-based survey. All questionnaires and clinical data were checked by medical assistants. Logistic multivariate analysis was used to explore the prevalence and variables associated with the severity of COVID-19 in patients with MPN. Results: A total of 239 patients with MPN, including 90 (37.7%) presenting with essential thrombocythemia (ET), 50 (20.9%) with polycythemia vera (PV), and 99 (41.4%) with myelofibrosis (MF), were enrolled in the study. The 99 patients with MF included 87 (87.9%) with primary MF, 5 (5.1%) with post-PV MF, and 7 (7.1%) with post-ET MF. Overall, 239 (100%) patients reported that they experienced COVID-19 during the pandemic. Of these, 226 (94.6%) had mild disease, 4 (1.7%) had moderate disease, 7 (2.9%) had severe disease, and 2 (0.8%) had critical disease. Two (0.8%) patients with severe COVID-19 died, one of which suffered from MT and the other from PV. Multivariate analysis showed that older age (OR=2.36, 95%CI 1.24-4.49), MF (OR=10.22, 95%CI 1.13-92.80), or comorbidity (OR=5.25, 95%CI 1.25-22.03) were associated with a significantly higher risk of developing moderate, severe, or critical COVID-19. Among patients with MF, higher risk stratification reflected an increased risk of developing moderate, severe, or critical COVID-19 (P=0.034). Conclusion: During the omicron pandemic, older age, MF (especially higher-risk categories), and comorbidity were associated with a higher risk of developing moderate, severe, or critical COVID-19.

目的探讨骨髓增生性肿瘤(MPN)患者在流行期间由 SARS-CoV-2 omicron 变体引起的冠状病毒病 2019(COVID-19)严重程度的相关变量。方法:横断面研究:横断面研究。在 2022 年 12 月 15 日至 2023 年 3 月 15 日 SARS-CoV-2 omicron 变体大流行期间,通过在线问卷调查收集了在北京大学人民医院接受治疗的骨髓增殖性肿瘤患者的 COVID-19 相关数据。所有问卷和临床数据均由医疗助理进行核对。采用逻辑多变量分析法探讨 MPN 患者 COVID-19 的患病率以及与 COVID-19 严重程度相关的变量。结果共有239名骨髓增生性疾病患者参与了研究,其中包括90名(37.7%)原发性血小板增多症(ET)患者、50名(20.9%)真性多血细胞增多症(PV)患者和99名(41.4%)骨髓纤维化(MF)患者。在 99 名骨髓纤维化患者中,87 人(87.9%)为原发性骨髓纤维化,5 人(5.1%)为 PV 后骨髓纤维化,7 人(7.1%)为ET 后骨髓纤维化。总体而言,239 名(100%)患者报告在大流行期间经历过 COVID-19。其中,226 人(94.6%)病情轻微,4 人(1.7%)病情中度,7 人(2.9%)病情严重,2 人(0.8%)病情危重。两名(0.8%)重度 COVID-19 患者死亡,其中一名患有 MT,另一名患有 PV。多变量分析显示,年龄较大(OR=2.36,95%CI 1.24-4.49)、MF(OR=10.22,95%CI 1.13-92.80)或合并症(OR=5.25,95%CI 1.25-22.03)与罹患中度、重度或危重COVID-19的风险显著升高有关。在中耳炎患者中,风险分层越高,患中度、重度或危重 COVID-19 的风险越高(P=0.034)。结论在奥米克大流行期间,高龄、MF(尤其是高风险类别)和合并症与罹患中度、重度或危重 COVID-19 的较高风险有关。
{"title":"[Analysis of the factors influencing the severity of coronavirus disease 2019 in patients with myeloproliferative neoplasms based on an online questionnaire].","authors":"F Y Qi, M Bao, H L Gao, Q Jiang","doi":"10.3760/cma.j.cn112138-20230822-00073","DOIUrl":"10.3760/cma.j.cn112138-20230822-00073","url":null,"abstract":"<p><p><b>Objective:</b> To explore the variables associated with the severity of coronavirus disease 2019 (COVID-19) caused by the SARS-CoV-2 omicron variant during the epidemic in patients with myeloproliferative neoplasms (MPN). <b>Methods:</b> A cross-sectional study. During the SARS-CoV-2 omicron variant pandemic from December 15, 2022, to March 15, 2023, COVID-19 related data for patients with MPN who were treated at Peking University People's Hospital were collected through an online questionnaire-based survey. All questionnaires and clinical data were checked by medical assistants. Logistic multivariate analysis was used to explore the prevalence and variables associated with the severity of COVID-19 in patients with MPN. <b>Results:</b> A total of 239 patients with MPN, including 90 (37.7%) presenting with essential thrombocythemia (ET), 50 (20.9%) with polycythemia vera (PV), and 99 (41.4%) with myelofibrosis (MF), were enrolled in the study. The 99 patients with MF included 87 (87.9%) with primary MF, 5 (5.1%) with post-PV MF, and 7 (7.1%) with post-ET MF. Overall, 239 (100%) patients reported that they experienced COVID-19 during the pandemic. Of these, 226 (94.6%) had mild disease, 4 (1.7%) had moderate disease, 7 (2.9%) had severe disease, and 2 (0.8%) had critical disease. Two (0.8%) patients with severe COVID-19 died, one of which suffered from MT and the other from PV. Multivariate analysis showed that older age (<i>OR</i>=2.36, 95%<i>CI</i> 1.24-4.49), MF (<i>OR</i>=10.22, 95%<i>CI</i> 1.13-92.80), or comorbidity (<i>OR</i>=5.25, 95%<i>CI</i> 1.25-22.03) were associated with a significantly higher risk of developing moderate, severe, or critical COVID-19. Among patients with MF, higher risk stratification reflected an increased risk of developing moderate, severe, or critical COVID-19 (<i>P</i>=0.034). <b>Conclusion:</b> During the omicron pandemic, older age, MF (especially higher-risk categories), and comorbidity were associated with a higher risk of developing moderate, severe, or critical COVID-19.</p>","PeriodicalId":68309,"journal":{"name":"中华内科杂志","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140337837","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
[Clinical and electrophysiological characteristics and treatment outcomes of anti-neutrophil cytoplasmic antibody ANCA-associated vasculitic neuropathy]. [抗中性粒细胞胞浆抗体 ANCA 相关血管炎性神经病的临床和电生理特点及治疗效果]。
Pub Date : 2024-04-01 DOI: 10.3760/cma.j.cn112138-20231031-00267
Y F Li, M Li, F Yang, H F Wang, F Xu, S Y Chen, B Sun, Z H Chen, X S Huang

Objective: To investigate the clinical and electrophysiological characteristics of ANCA-associated vasculitic neuropathy (VN) and analyze the predictors of treatment outcomes. Methods: Retrospective case series. In all, 652 consecutive patients with ANCA-associated vasculitis were admitted to the First Medical Center of the Chinese PLA General Hospital between January 2006 and December 2022. Peripheral neuropathy occurred in 91 patients. Patients were excluded if other known causes of neuropathy were present. Sixty-one patients were eventually enrolled, including 17 with eosinophilic granulomatosis with polyangiitis (EGPA), 11 with granulomatosis polyangiitis (GPA), and 33 with microscopic polyangiitis (MPA). Their clinical data were collected and clinical characteristics, VN manifestations, electrophysiological findings (including interside amplitude ratio [IAR]), and treatment outcomes were compared among the three subsets of AAV. Then, factors influencing the treatment outcomes were analyzed using multivariable logistic regression analysis. Results: Peripheral neuropathy occurred in 62.1%(18/29) of EGPA, 8.3%(15/180) of GPA, and 13.1%(58/443) of MPA patients. The age at onset and examination was higher in patients with MPA than those with EGPA or GPA (P<0.01). The occurrence of VN was later in patients with GPA than those with EGPA (P<0.01), and the GPA group had fewer affected nerves than the other two groups (P<0.016). The abnormal IARs of motor nerves in lower limbs were more detected in the EGPA than the MPA group (P<0.01). Logistic regression analysis suggested that higher Birmingham vasculitis activity score-version 3 (BVAS-V3) (OR=6.85, 95%CI 1.33-35.30) was associated with better treatment outcomes of VN. However, central nervous system involvement was a risk factor for poor treatment outcomes (OR=0.13, 95%CI 0.02-0.89). Conclusions: The clinical and electrophysiological characteristics of VN were slightly different among subsets of AAV. Patients with GPA often presented with polyneuropathy and had fewer nerves affected; mononeuritis multiplex was more common in EGPA than GPA and MPA. Higher BVAS-V3 and central nervous system involvement might predict the treatment outcome of VN.

目的研究 ANCA 相关血管炎性神经病(VN)的临床和电生理特征,并分析治疗效果的预测因素。方法:回顾性病例系列:回顾性病例系列。2006年1月至2022年12月期间,中国人民解放军总医院第一医学中心连续收治了652例ANCA相关性血管炎患者。91名患者发生了周围神经病变。如果存在其他已知的神经病变原因,则排除患者。最终有61名患者入选,其中包括17名嗜酸性粒细胞肉芽肿伴多血管炎(EGPA)患者、11名肉芽肿性多血管炎(GPA)患者和33名显微镜下多血管炎(MPA)患者。研究人员收集了他们的临床数据,并比较了三个亚组 AAV 的临床特征、血管神经网表现、电生理结果(包括两侧振幅比 [IAR])和治疗效果。然后,采用多变量逻辑回归分析法对影响治疗结果的因素进行了分析。结果62.1%(18/29)的EGPA、8.3%(15/180)的GPA和13.1%(58/443)的MPA患者发生了周围神经病变。与 EGPA 或 GPA 相比,MPA 患者的发病年龄和检查年龄更高(PPPPOR=6.85,95%CI 1.33-35.30),这与更好的 VN 治疗效果有关。然而,中枢神经系统受累是治疗效果不佳的风险因素(OR=0.13,95%CI 0.02-0.89)。结论不同亚型AAV的VN临床和电生理特点略有不同。GPA患者通常表现为多发性神经病,受影响的神经较少;与GPA和MPA相比,多发性单神经炎在EGPA中更为常见。较高的BVAS-V3和中枢神经系统受累可能预示着VN的治疗结果。
{"title":"[Clinical and electrophysiological characteristics and treatment outcomes of anti-neutrophil cytoplasmic antibody ANCA-associated vasculitic neuropathy].","authors":"Y F Li, M Li, F Yang, H F Wang, F Xu, S Y Chen, B Sun, Z H Chen, X S Huang","doi":"10.3760/cma.j.cn112138-20231031-00267","DOIUrl":"10.3760/cma.j.cn112138-20231031-00267","url":null,"abstract":"<p><p><b>Objective:</b> To investigate the clinical and electrophysiological characteristics of ANCA-associated vasculitic neuropathy (VN) and analyze the predictors of treatment outcomes. <b>Methods:</b> Retrospective case series. In all, 652 consecutive patients with ANCA-associated vasculitis were admitted to the First Medical Center of the Chinese PLA General Hospital between January 2006 and December 2022. Peripheral neuropathy occurred in 91 patients. Patients were excluded if other known causes of neuropathy were present. Sixty-one patients were eventually enrolled, including 17 with eosinophilic granulomatosis with polyangiitis (EGPA), 11 with granulomatosis polyangiitis (GPA), and 33 with microscopic polyangiitis (MPA). Their clinical data were collected and clinical characteristics, VN manifestations, electrophysiological findings (including interside amplitude ratio [IAR]), and treatment outcomes were compared among the three subsets of AAV. Then, factors influencing the treatment outcomes were analyzed using multivariable logistic regression analysis. <b>Results:</b> Peripheral neuropathy occurred in 62.1%(18/29) of EGPA, 8.3%(15/180) of GPA, and 13.1%(58/443) of MPA patients. The age at onset and examination was higher in patients with MPA than those with EGPA or GPA (<i>P</i><0.01). The occurrence of VN was later in patients with GPA than those with EGPA (<i>P</i><0.01), and the GPA group had fewer affected nerves than the other two groups (<i>P</i><0.016). The abnormal IARs of motor nerves in lower limbs were more detected in the EGPA than the MPA group (<i>P</i><0.01). Logistic regression analysis suggested that higher Birmingham vasculitis activity score-version 3 (BVAS-V3) (<i>OR</i>=6.85, 95%<i>CI</i> 1.33-35.30) was associated with better treatment outcomes of VN. However, central nervous system involvement was a risk factor for poor treatment outcomes (<i>OR</i>=0.13, 95%<i>CI</i> 0.02-0.89). <b>Conclusions:</b> The clinical and electrophysiological characteristics of VN were slightly different among subsets of AAV. Patients with GPA often presented with polyneuropathy and had fewer nerves affected; mononeuritis multiplex was more common in EGPA than GPA and MPA. Higher BVAS-V3 and central nervous system involvement might predict the treatment outcome of VN.</p>","PeriodicalId":68309,"journal":{"name":"中华内科杂志","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140337838","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
[Expert consensus on thermal ablation of papillary thyroid cancer (2024 edition)]. [甲状腺乳头状癌热消融专家共识(2024 年版)]。
Pub Date : 2024-04-01 DOI: 10.3760/cma.j.cn112138-20231104-00296

Ultrasound-guided thermal ablation of papillary thyroid cancer (PTC) has been promoted in clinical practice over the past few years. Thermal ablation has the advantages of being minimally invasive, effective, and safe. However, current guidelines and consensus only focus on low-risk papillary thyroid microcarcinoma. With growing clinical application and accumulating scientific research in thermal ablation for PTC, there is considerable evidence to demonstrate that thermal ablation can treat larger PTC tumors and benefit more patients with PTC. To expand the indications and standardize the technical details and perioperative patient management for PTC ablation, experts from the Society of Tumor Ablation Therapy of the Chinese Anti-Cancer Association, the Ablation Expert Committee of the Chinese Society of Clinical Oncology (CSCO), Chinese Medical Doctor Association College of Interventionalists Tumor Ablation Committee, and Chinese Bethune Spirit Research Association Endocrinology and Diabetes Branch Interventional Endocrine Committee discussed and developed a consensus on thermal ablation of PTC based on the latest research results. This consensus aims to promote the rapid development of thermal ablation for PTC in the clinic.

过去几年来,临床上一直在推广超声引导下的甲状腺乳头状癌(PTC)热消融术。热消融具有微创、有效、安全等优点。然而,目前的指南和共识只关注低风险的甲状腺乳头状微癌。随着热消融治疗PTC临床应用的不断增加和科学研究的不断积累,有大量证据表明热消融可以治疗较大的PTC肿瘤,使更多的PTC患者受益。为了扩大PTC消融术的适应症,规范PTC消融术的技术细节和围手术期患者管理,中国抗癌协会肿瘤消融治疗学分会、中国临床肿瘤学会(CSCO)消融专家委员会、中国医师协会介入医师分会肿瘤消融专业委员会、中国白求恩精神研究会内分泌与糖尿病分会介入内分泌专业委员会的专家们根据最新的研究成果,讨论并制定了PTC热消融共识。该共识旨在促进PTC热消融在临床上的快速发展。
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中华内科杂志
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