目的 探讨入院时血清淀粉样蛋白A(SAA)、载脂蛋白A1(ApoA1)、C反应蛋白(CRP)水平联合检测对老年急性脑梗死(ACI)患者规范治疗后3个月内发生预后不良的早期预测效能。方法 前瞻性选取2023年1月~2025年1月于焦作市第五人民医院就诊的108例老年ACI患者作为ACI组,另选取同期健康志愿者108例作为对照组。比较两组血清SAA、ApoA1、CRP水平。老年ACI患者予以规范治疗,根据治疗后3个月内预后情况将其分为预后不良(46例)和预后良好(62例)亚组,比较不同预后ACI患者患者临床资料及入院时血清SAA、ApoA1、CRP水平;Logistic回归分析入院时血清SAA、ApoA1、CRP水平是否为老年ACI患者规范治疗后3个月内发生预后不良的独立影响因素;ROC曲线分析入院时血清SAA、ApoA1、CRP水平联合检测对ACI患者预后不良的预测效能。结果 ACI组入院时血清SAA、CRP水平高于对照组,血清ApoA1水平低于对照组(P<0.05);预后不良亚组高血压占比、入院NIHSS评分、梗死体积、入院时血清SAA、CRP水平高于预后良好亚组,血清ApoA1水平低于预后良好亚组(P<0.05);剔除存在多重共线性指标高血压、入院NIHSS评分、梗死体积后,入院时血清SAA、ApoA1、CRP水平仍是老年ACI患者规范治疗后3个月内发生预后不良的独立影响因素(P<0.05);入院时血清SAA、ApoA1、CRP水平联合预测ACI患者预后不良的AUC值为0.873,显高于各指标单独预测值0.738、0.768、0.749(P<0.05)。结论 入院时血清SAA、ApoA1、CRP水平是老年ACI患者预后不良的独立影响因素,联合检测对预后不良具有较高的预测效能,可将其作为ACI患者血清敏感指标,协助临床医师早期制定针对性干预措施,减少ACI患者预后不良的发生。
【摘要】目的:探究血液透析患者C反应蛋白、白蛋白、铁蛋白联合检测对营养不良-炎症综合征的评估价值。方法:回顾性选取2025年2月至2026年2月我院收治的血液透析患者104例作为研究对象,根据是否发生营养不良-炎症综合征(MICS)分为MICS组51例和单纯透析组53例,获取患者临床资料,并于透析前检测血清C反应蛋白、白蛋白、铁蛋白水平,采用多因素logistic回归分析影响血液透析患者发生MICS的危险因素,并采用ROC曲线评估各指标联合检测对MICS的诊断价值。结果:MICS组血清C反应蛋白、铁蛋白水平高于单纯透析组,血清白蛋白水平低于单纯透析组(P<0.05)。logistic回归分析结果显示,C反应蛋白、白蛋白、铁蛋白水平是影响血液透析患者发生MICS的危险因素(P<0.05)。ROC曲线分析结果显示,当白蛋白的最佳诊断截断值为(33.89)g/L,C反应蛋白的最佳诊断截断值为(13.17)mg/L,铁蛋白的最佳诊断截断值为(247.53)ng/mL,此时联合检测诊断MICS的AUC为0.973、敏感度为(98.00)和特异度为(83.02),高于任一单项指标检测(P<0.05)。结论:血液透析患者血清C反应蛋白、铁蛋白升高,血清白蛋白水平下降,三者联合诊断MIAS的临床价值较高。
目的 分析2024年2月至2026年2月郑州人民医院收治的急性下呼吸道感染(ALRTI)患儿的病原体分布情况及其流行病学特征。方法 选取2024年2月—2026年2月于郑州人民医院就诊的193例ALRTI患儿为研究对象,采集患儿咽拭子样本,统计患儿病原体检测结果,比较不同性别、不同年龄段、不同发病季节患儿病原体分布情况。结果 193例患儿中,经病原体检测出阳性患儿165例,总阳性检出率85.49%,检出率最高的前三位为RSV(20.73%)、MP(19.69%)、HRV(15.54%);婴儿期患儿RSV感染占比(44.83%)最高,其次为HRV感染(20.69%),幼儿期患儿RSV、HRV、MP感染占比(17.31%、17.31%、19.23%)均较高,学龄前、学龄期患儿MP感染占比(33.33%、26.32%)最高,婴儿期患儿混合感染占比(6.90%)较低,学龄前患儿混合感染占比(20.00%)较高;春季时,各病原体分布较均衡,HRV、MP、SP感染占比(14.58%、12.50%、14.58%)均较高,夏季、秋季时,MP感染率(31.82%、28.85%)较高,冬季时,RSV感染率(55.10%)较高,四个季节中混合感染患儿占比较接近,其中秋季感染率(17.31%)相对较高。结论 2024年至2026年郑州人民医院收治的急性下呼吸道感染患儿病原体中,RSV、MP为主要病原体,各呼吸道病原体随患儿年龄段、季节变化存在不同发病高峰,临床应结合实际情况早期鉴别病原体,以指导临床制定针对性治疗方案,改善患儿预后。
Objective To analyze the distribution of pathogens and the epidemiological characteristics of children with acute lower respiratory tract infections (ALRTI) admitted to Zhengzhou People’s Hospital from February 2024 to February 2026. Methods: A total of 193 pediatric patients with ALRTI who visited Zhengzhou People’s Hospital between February 2024 and February 2026 were selected as study subjects. Throat swab samples were collected from the patients, and pathogen testing results were compiled to compare the distribution of pathogens across different genders, age groups, and seasons of onset. Results: Among the 193 children, 165 tested positive for pathogens, resulting in an overall positive detection rate of 85.49%. The top three most frequently detected pathogens were RSV (20.73%), MP (19.69%), and HRV (15.54%); RSV infection had the highest prevalence (44.83%) among infants, followed by HRV infection (20.69%). Among preschoolers, the prevalence of RSV, HRV, and MP infections (17.31%, 17.31%, and 19.23%, respectively) was relatively high. MP infections were most common among preschool and school-age children (33.33% and 26.32%, respectively); the proportion of mixed infections was lower among infants (6.90%) but higher among preschoolers (20.00%); In spring, the distribution of pathogens was relatively balanced, with high proportions of HRV, MP, and SP infections (14.58%, 12.50%, and 14.58%, respectively). In summer and fall, the MP infection rate was high (31.82% and 28.85%, respectively). In winter, the RSV infection rate (55.10%) was high. The proportion of children with mixed infections was relatively similar across the four seasons, with a relatively higher infection rate (17.31%) in autumn. Conclusion: Among the pathogens identified in children with acute lower respiratory tract infections admitted to Zhengzhou People’s Hospital from 2024 to 2026, RSV and MP were the primary pathogens. The incidence peaks of various respiratory pathogens varied according to the children’s age groups and seasons. Clinicians should conduct early pathogen identification based on actual conditions to guide the development of targeted treatment plans and improve patient outcomes.
目的 探讨急性心肌梗死(AMI)患者经皮冠状动脉介入(PCI)术后6个月内预后不良的影响因素及术前血清髓过氧化物酶(MPO)、淀粉样蛋白A(SAA)、肌酸激酶同工酶(CK-MB)水平联合检测对预后不良的预测效能。方法 前瞻性选取2023年1月~2025年1月许昌市人民医院诊治的204例AMI患者作为AMI组,另选取同期102例健康志愿者作为对照组。比较两组血清MPO、SAA、CK-MB水平。AMI组患者予以PCI术治疗,依据PCI术后6个月内(失访8例)预后情况将分为预后不良亚组(42例)和预后良好亚组(154例),比较不同预后AMI患者临床资料及术前血清MPO、SAA、CK-MB水平。分析AMI患者PCI术后6个月内预后不良的影响因素;分析术前血清MPO、SAA、CK-MB水平联合检测对预后不良的预测效能。结果 AMI组血清MPO、SAA、CK-MB水平高于对照组(P<0.05);预后不良亚组多支病变占比、Killip分级Ⅲ级占比、支架置入数、术前血清MPO、SAA、CK-MB水平高于预后良好亚组(P<0.05);校正病变支数、Killip分级、支架置入数后,术前血清MPO、SAA、CK-MB水平是AMI患者PCI术后6个月内预后不良的独立影响因素(P<0.05);术前血清MPO、SAA、CK-MB联合预测预后不良的AUC值明显高于各血清指标单度指标预测(P<0.05)。结论 AMI患者血清MPO、SAA、CK-MB水平明显升高,且是AMI患者PCI术后预后不良的独立影响因素,联合检测其水平对预后不良具有较高的预测效能。
目的 探讨血清白蛋白(ALB)、纤维蛋白原(FIB)、乳酸脱氢酶(LDH)水平联合检测对急性心肌梗死患者短期预后的预测价值,以期为临床早期制定相应干预方案、改善患者预后提供参考。 方法 回顾性选取我院2023年1月~2025年1月收治的132例急性心肌梗死患者,入院后均接受经皮冠脉介入术(PCI)术治疗,根据术后6个月是否发生心血管主要不良事件(MACE)分为预后不良组(n=34)、预后良好组(n=98),比较两组临床资料及入院时血清ALB、FIB、LDH水平,Logistic回归方程分析血清ALB、FIB、LDH水平与急性心肌梗死患者PCI术后预后的关系,受试者工作特征(ROC)曲线分析其预测价值。 结果 两组病变血管支数、Killip分级及入院时血清ALB、FIB、LDH水平比较,差异具有统计学意义(P<0.05);入院时血清ALB、FIB、LDH水平与PCI术后预后显著相关,均为其独立影响因素(P<0.05);绘制ROC曲线结果显示,入院时血清ALB、FIB、LDH对于PCI术后预后不良的预测AUC分别为0.795、0.856、0.832,联合预测预后不良的AUC为0.927(95%CI:0.892~0.963),大于各方案单独预测,敏感度为91.18%,特异度为89.80%;危险度分析显示,血清ALB低水平患者预后不良风险是高水平患者的6.127倍,血清FIB、LDH高水平患者预后不良风险是低水平患者的10.493、8.170倍(P<0.05)。 结论 血清ALB、FIB、LDH水平联合检测对急性心肌梗死患者PCI术后预后具有较高预测价值,临床可根据其早期评估患者预后不良风险,以制定个体化干预方案,改善患者预后。
目的 探讨靶向治疗前晚期非小细胞肺癌(NSCLC)患者血清肿瘤特异性生长因子(TSGF)、乳酸脱氢酶(LDH)、同型半胱氨酸(Hcy)水平与靶向治疗无效的相关性,并分析其对靶向治疗无效的预测价值。方法 选取2023年1月~2025年1月于本院就诊的晚期NSCLC患者108例作为研究组,另选取同期健康志愿者108例作为对照组。比较两组血清TSGF、LDH、Hcy水平。研究组予以靶向治疗(治疗3个疗程),依据靶向治疗无效将其分为无效亚组36例、有效亚组72例,比较其血清TSGF、LDH、Hcy水平。分析血清TSGF、LDH、Hcy与靶向治疗无效的相关性,并分析其对靶向治疗无效的预测价值。结果 研究组血清TSGF、LDH、Hcy水平高于对照组(P<0.05);无效亚组血清TSGF、LDH、Hcy水平高于有效亚组(P<0.05);校正吸烟史、分化程度、TNM分期后,治疗1个疗程后血清TSGF、LDH、Hcy水平仍与靶向治疗无效独立相关(P<0.05);靶向治疗前血清TSGF、LDH、Hcy水平预测靶向治疗无效的AUC值明显大于各指标单独预测(P<0.05)。结论 晚期NSCLC患者血清TSGF、LDH、Hcy水平升高与靶向治疗无效独立相关,检测其水平对靶向治疗无效具有一定预测价值,且联合预测的效能更高,可指导临床制定及调整诊治方案。
1型糖尿病(T1DM)是一种免疫介导的胰岛β细胞特异性破坏的自身免疫性疾病,全球发病率逐年上升。胰岛自身抗体(IAbs)是T1DM最可靠的生物标志物,用于早期预测和诊断。然而,传统的放射配体法(RBA)虽然具有高实验特异度,但在疾病特异度方面存在局限性,尤其是单抗体阳性的预测价值较低。近年来,电化学发光法(ECL)作为一种无放射性污染的新方法,能够区分高亲和力和低亲和力的IAbs,显著提高了疾病特异度。多项研究表明,ECL法在预测T1DM风险方面优于RBA法,特别是在单抗体阳性的情况下。本文综述了IAbs检测方法的进展及其在T1DM预测和诊断中的应用,强调了ECL法在提高疾病特异度方面的优势。
Type 1 diabetes mellitus(T1DM)is an autoimmune disease characterized by the immune-mediated destruction of pancreatic β-cells,with a rising global incidence.Islet autoantibodies(IAbs)are the most reliable biomarkers for early prediction and diagnosis of T1DM.However,the traditional radio-binding assay(RBA),despite its high experimental specificity,has limitations in disease specificity,particularly in the predictive value of single autoantibody positivity.Recently,the electrochemiluminescence(ECL)method,a non-radioactive approach,has been developed to distinguish high-affinity from low-affinity IAbs,significantly improving disease specificity.Multiple studies have shown that the ECL method outperforms RBA in predicting T1DM risk,especially in cases of single autoantibody positivity.This review discusses the advancements in IAbs detection methods and their applications in T1DM prediction and diagnosis,highlighting the advantages of the ECL method in enhancing disease specificity.
目的 探讨单克隆免疫球蛋白血症患者M蛋白质量浓度检测的临床意义。方法 选取2018年6月—2023年6月龙岩人民医院收治的88例单克隆免疫球蛋白血症患者为研究对象,其中意义未明单克隆免疫球蛋白血症(MGUS)21例,具有肾脏意义单克隆免疫球蛋白血症(MGRS)50例,血液系统恶性肿瘤17例。对比其M蛋白质量浓度及临床实验室相关指标表达水平,采用Spearman相关分析法分析临床实验室相关指标的与M蛋白的相关性,对所有患者进行半年随访,以预后情况作为因变量,纳入Logistics回归模型分析M蛋白质量浓度对单克隆免疫球蛋白血症预后的预测价值。结果 不同病种M蛋白水平分别为(2.42±0.55)(2.57±0.64)(4.36±0.64)g/L、24 h尿蛋白分别为(1.45±0.16)(2.98±0.68)(2.43±0.44)g/24 h、血清白蛋白质量浓度分别为(31.01±3.06)(35.03±5.04)(39.05±7.08)g/L、总胆固醇水平分别为(3.42±1.25)(3.87±0.64)、(4.16±0.64)mmol/L、血肌酐水平分别为(114.35±23.23)(81.18±12.12)(146.36±21.12)μmol/L、血红蛋白质量浓度分别为(148.12±15.26)(141.69±12.15)(133.34±15.31)g/L,组间对比差异均有统计学意义(F分别为23.890,19.700,12.044,25.767,36.572,10.267,P<0.05)。MGUS患者24h尿蛋白与M蛋白有相关性(r=-0.384,P=0.033),24 h尿蛋白、血清白蛋白、总胆固醇、血肌酐与MGRS患者M蛋白有相关性(r=-0.586,P=0.006;r=0.431,P=0.018;r=-0.457,P=0.020;r=0.523,P=0.009),血清白蛋白、总胆固醇、血红蛋白与血液系统恶性肿瘤患者M蛋白有相关性(r=0.374,P=0.029;r=-0.617,P=0.001;r=-0.414,P=0.024);年龄、M蛋白为单克隆免疫球蛋白血症患者预后的影响因素(P<0.05)。结论 不同单克隆免疫球蛋白血症患者M蛋白水平存在差异,其中血液系统恶性肿瘤患者的M蛋白水平最高,且M蛋白为单克隆免疫球蛋白血症预后的独立影响因素。
Objective To explore the clinical significance of detecting M protein concentration in patients with monoclonal gammopathy.Methods From June 2018 to June 2023,88 patients with monoclonal gammopathy admitted to the hospital were selected as the study subjects.Among them,21 cases of monoclonal gammopathy with undetermined significance(MGUS),50 cases of monoclonal gammopathy with renal significance(MGRS),and 17 cases of hematological malignancies were selected. Concentration of M protein and the expression levels of clinical laboratory related indicators were compared,Spearman correlation analysis was used to analyze the correlation between clinical laboratory related indicators and M protein.All patients were followed up for six months,with prognosis as the dependent variable,included in the logistic regression model to analyze the predictive value of M protein concentration on the prognosis of monoclonal gammopathy.Results There were significant differences in the expression levels of M protein([2.42±0.55],[2.57±0.64],[4.36±0.64])g/L,24-hour urine protein([1.45±0.16],[2.98±0.68],[2.43±0.44])g/24 h,serum albumin([31.01±3.06],[35.03±5.04],[39.05±7.08])g/L,total cholesterol([3.42±1.25],[3.87±0.64],[4.16±0.64])mmol/L,blood creatinine([114.35±23.23],[81.18±12.12],[146.36±21.12])μmol/L,and hemoglobin([148.12±15.26],[141.69±12.15],[133.34±15.31])g/L among different diseases(F=23.890,19.700,12.044,25.767,36.572,10.267;P<0.05).There was a significant correlation between 24 h urinary protein and M protein in MGUS patients(r=-0.384,P=0.033).Urinary protein,serum albumin,serum cholesterol and blood creatinine were significantly associated with M protein in MGRS patients(r=-0.586,P=0.006;r=0.431,P=0.018;r=-0.457,P=0.020;r=0.523,P=0.009),Serum albumin,total cholesterol,and hemoglobin were significantly associated with M protein in patients with hematological malignancies(r=0.374,P=0.029;r=- 0.617,P=0.001;r=-0.414,P=0.024;P<0.05).Age and M protein were independent risk factors for the prognosis of patients with monoclonal gammopathy(P<0.05).Conclusions There are significant differences in the concentration of M protein among patients with different levels of monoclonal gammopathy,with the highest level observed in patients with hematological malignancies.M protein is an independent prognostic factor for monoclonal gammopathy.
目的 探讨痰涂片找抗酸杆菌、痰利福平耐药实时荧光定量核酸扩增检测技术(Xpert MTB/RIF)、分枝杆菌菌种鉴定、痰抗酸杆菌培养和血γ-干扰素释放检测技术(TB-IGRA)5种检测技术在尘肺合并肺结核临床诊断中的应用价值。方法 纳入2016年7月—2021年5月在厦门大学附属第一医院住院治疗的尘肺合并肺结核患者,按照尘肺患者是否合并肺结核,将患者分为尘肺组(156例)和尘肺合并肺结核组(111例);比较两组患者的性别、年龄、接尘时间等一般资料,以及患者痰涂片、Xpert MTB/RIF、分枝杆菌菌种鉴定、痰培养和TB-IGRA的检测结果,分析尘肺合并肺结核患者5种检测技术阳性检出率的差异及其诊断价值。结果 在尘肺合并肺结核组中,TB-IGRA检测方法的阳性检出率最高(81.1%),高于其他4种检测方法(P<0.01);两两联合检测,以Xpert MTB/RIF+TB-IGRA组合的检测方式检出率最高(96.4%),高于其他9种组合(P<0.01)。结论 TB-IGRA检测方法对尘肺合并肺结核患者的阳性检出率较高,联合Xpert MTB/RIF检测后可进一步提高诊断效率,对早期诊断尘肺是否合并结核具有重要的临床诊断价值。
Objective To investigate the value of five testing techniques in the clinical diagnosis of pneumoconiosis combined pulmonary tuberculosis,including sputum smear,Xpert Mycobacterium tuberculosis/rifampicin(Xpert MTB/RIF),identification of Mycobacterium species,sputum acid-fast bacilli culture and tuberculosis-interferon-gamma release assays(TB-IGRA).Methods Patients with pneumoconiosis combined with tuberculosis who were hospitalized in the First Hospital of Xiamen University from July 2016 to May 2021 were included in the study.The patients were divided into the pneumoconiosis group(156 cases)and pneumoconiosis combined with tuberculosis group(111 cases)according to whether the pneumoconiosis patients were combined with tuberculosis or not.The general data of the patients in the two groups were compared with respect to gender,age,and dust exposure time,and the results of sputum smears,Xpert MTB/RIF,identification of Mycobacterium species,sputum acid-fast bacilli culture and TB-IGRA were collected to analyze the differences and the diagnostic value in the five testing techniques of the positivity rates for patients who have pneumoconiosis combined with pulmonary tuberculosis.Results In the group with pneumoconiosis combined with tuberculosis,the positive detection rate of TB-IGRA was the highest(81.1%),which was higher than other 4 testing methods(P<0.01).Combined testing in pairs suggested that the testing method of Xpert MTB/RIF and TB-IGRA combination was the highest(96.4%),significantly higher than the other 9 combinations(P<0.01).Conclusions TB-IGRA has higher positive detection rate for patients with pneumoconiosis combined with tuberculosis,and diagnostic efficiency can be further improved by combining Xpert MTB/RIF assay testing,which is of great clinical diagnostic value for the early diagnosis of pneumoconiosis combined with tuberculosis.
目的 探讨唐氏综合征血清学筛查风险值异常孕妇选择接受无创产前基因检测(NIPT)的影响因素,为临床制定对应策略提供参考依据。方法 选取2022年1月—2022年12月唐氏综合征血清学筛查风险值异常孕妇229例,根据是否接受NIPT分为接受组(195例)与不接受组(34例)。收集两组临床资料,采用Lasso-Logistic回归分析唐氏综合征血清学筛查风险值异常孕妇接受NIPT的影响因素。结果 单因素分析显示,年龄、文化水平、居住地、家庭平均月收入、孕前优生优育检查、孕前合并生殖相关疾病、受孕方式、不良孕产史、家族史、补充叶酸、配偶意愿、NIPT认知水平、血清学风险等级是血清学筛查异常孕妇接受NIPT的影响因素(P<0.05);Lasso回归分析筛选出7个变量,分别为年龄、文化水平、家庭平均月收入、不良孕产史、家族史、NIPT认知水平、血清学风险等级;Logistic回归分析,年龄(OR=6.269,95%CI:2.413~16.285)、文化水平(OR=4.119,95%CI:1.627~10.430)、家庭平均月收入(OR=5.102,95%CI:2.067~12.594)、不良孕产史(OR=5.247,95%CI:1.833~15.021)、家族史(OR=7.416,95%CI:2.952~18.629)、NIPT认知水平(OR=5.751,95%CI:2.338~14.146)、血清学风险等级(OR=7.866,95%CI:3.057~20.238)是血清学筛查异常孕妇接受NIPT的影响因素(P<0.05)。结论 唐氏综合征血清学筛查风险值异常孕妇选择接受NIPT的影响因素较多,包括年龄、文化水平、家庭平均月收入、不良孕产史、家族史、NIPT认知水平、血清学风险等级,能为临床提高NIPT接受度提供指导信息。
Objective To explore the influencing factors of noninvasive prenatal testing(NIPT)for pregnant women with abnormal risk value of serological screening for Down syndrome,and to provide reference for clinical development of corresponding strategies.Methods A total of 229 pregnant women with abnormal serological screening risk values for Down syndrome from January 2022 to December 2022 were selected and divided into acceptance group(195 cases)and non-acceptance group(34 cases)according to whether they received NIPT.The clinical data of the two groups were collected and Lasso-Logistic regression was used to analyze the factors influencing the acceptance of NIPT in pregnant women with abnormal serological screening risk value for Down syndrome.Results In single factor analysis,age,education level,place of residence,average monthly family income,pre-pregnancy and childbearing examination,pre-pregnancy combined with reproductive diseases,conception method,adverse pregnancy history,family history,folic acid supplementation,spouse intention,NIPT cognition level and serological risk grade were the influencing factors for the acceptance of NIPT in pregnant women with abnormal serological screening(P<0.05).Seven variables were selected by Lasso regression analysis,which were age,education level,average monthly family income,adverse pregnancy history,family history,NIPT cognition level and serological risk level.Logistic regression analysis showed that age(OR=6.269,95%CI:2.413-16.285),education level(OR=4.119,95%CI:1.627-10.430),average monthly family income(OR=5.102,95%CI:2.067-12.594),adverse pregnancy history(OR=5.247,95%CI:1.833-15.021),family history(OR=7.416,95%CI:2.952-18.629),NIPT cognitive level(OR=5.751,95%CI:2.338-14.146)and serological risk level(OR=7.866,95%CI:3.057-20.238)were independent influencing factors for NIPT acceptance in pregnant women with abnormal serological screening(P<0.05).Conclusions There are many influencing factors for pregnant women with abnormal serological screening risk value to accept NIPT,including age,education level,average monthly family income,adverse pregnancy history,family history,NIPT cognition level,serological risk grade,etc.,which can provide guidance information for clinical improvement of NIPT acceptance.