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Impact of transferrin levels on iron accumulation in transfusion-dependent beta-thalassemia: A genotype-specific analysis. 转铁蛋白水平对输血依赖性-地中海贫血中铁积累的影响:一项基因型特异性分析。
IF 1.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-10-28 DOI: 10.5937/jomb0-54839
Yidan Liang, Xinhua Zhang, Binbin Huang, Yushan Huang, Liuhua Liao, Yueyan Huang, Ken Huang, Jinquan Lao, Xiaoqin Feng, Bin Lin, Xingjiang Long, Zhixiang Liu, Weijian Zhu, Lian Yu, Deguo Tang, Tianyu Zhong, Yuhua Ye, Xiangmin Xu

Background: Serum ferritin (SF) monitors secondary iron overload in beta-thalassemia (b-thalassemia). Transferrin (TRF) has been shown to reverse iron accumulation in experimental models, but its role in transfusion-dependent beta-thalassemia (TDT) patients remains unclear. This study aims to explore the relationship between TRF and SF in TDT patients and to reveal the unique connection between specific genotypes and iron metabolism, providing potential therapeutic targets for clinical practice.

Methods: This cross-sectional study includes 817 TDT patients (b0/b0 genotype: n=560; b0/b+ genotype: n=257). We use genotype-phenotype analysis and employ logistic regression and restricted cubic spline (RCS) curves to assess the association between TRF and SF.

Results: Significant differences were observed between the b0/b0 and b0/b+ genotypes in terms of age at first transfusion, transfusion requirements, chelation initiation age, reticulocyte count, red blood cell count, red cell distribution width-coefficient of variation (RDW-CV), fetal haemoglobin (HbF) level, splenomegaly, and SF. b0/b0 patients presented with more severe clinical phenotypes. SF was significantly associated with TRF, HbF, RDW-CV, and chelation therapy. RCS analysis revealed a dose-response relationship with a negative linear correlation between TRF and SF (OR=0.26, P<0.001), indicating that higher TRF levels are linked to lower SF risk.

Conclusions: This study systematically confirms for the first time a significant negative correlation between high TRF levels and high SF risk in TDT patients. This new finding may help clinicians more effectively manage iron overload, especially in patients with different genotypes.

背景:血清铁蛋白(SF)监测β -地中海贫血(b-地中海贫血)的继发性铁超载。在实验模型中,转铁蛋白(TRF)已被证明可以逆转铁的积累,但其在输血依赖性-地中海贫血(TDT)患者中的作用尚不清楚。本研究旨在探讨TDT患者TRF和SF之间的关系,揭示特定基因型与铁代谢之间的独特联系,为临床提供潜在的治疗靶点。方法:横断面研究纳入817例TDT患者(b0/b0基因型560例,b0/b+基因型257例)。我们使用基因型-表型分析,并使用逻辑回归和限制性三次样条(RCS)曲线来评估TRF和SF之间的关系。结果:b0/b0和b0/b+基因型在首次输血年龄、输血需用、螯合起始年龄、网织红细胞计数、红细胞分布宽度变异系数(RDW-CV)、胎儿血红蛋白(HbF)水平、脾肿大和SF方面存在显著差异。B0 / B0患者表现出更严重的临床表型。SF与TRF、HbF、RDW-CV和螯合治疗显著相关。RCS分析显示,TRF和SF之间存在剂量-反应关系(OR=0.26, P<0.001),表明较高的TRF水平与较低的SF风险相关。结论:本研究首次系统地证实了TDT患者高TRF水平与SF高风险之间的显著负相关。这一新发现可能有助于临床医生更有效地管理铁超载,特别是在不同基因型的患者中。
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引用次数: 0
Prognostic value of inflammatory cytokine levels, clinical efficacy, and prognosis of the hybrid artificial liver support system in chronic liver failure treatment. 混合人工肝支持系统治疗慢性肝衰竭的炎性细胞因子水平、临床疗效及预后的预测价值。
IF 1.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-10-28 DOI: 10.5937/jomb0-55735
Lihua Liu, Xiaoling Li, Juan Wang, Jing Ma, Xueping Nan

Background: This study aimed to evaluate the effectiveness and safety of the hybrid artificial liver support system (HALSS) in patients with chronic liver failure (CLF). It also sought to analyze the inflammatory response and patient prognosis.

Methods: A total of 126 CLF patients were divided into three treatment groups: plasma exchange (PEG), double plasma molecular adsorption system (DPMASG), and a combination therapy group (CG). Key parameters, including liver and kidney function, blood coagulation, T lymphocyte subgroups, and inflammatory cytokine levels (TNF-a, procalcitonin [PCT], interferon-gamma [IFN-g], IL-2, IL-6, and IL-10), were assessed before and after treatment. The clinical efficacy, adverse reactions, and short-term prognosis were compared across the groups.

Results: Compared to PEG and DPMASG, the combination group (CG) showed significant improvement in liver and kidney function markers, including reduced ALT, AST, total bilirubin (TBil), creatinine (Cr), INR, and prothrombin time (PT). Additionally, CG demonstrated increased levels of cholinesterase (ChE), albumin, and prothrombin activity (PTA). The CG group had a higher total clinical efficacy (92.0%) compared to PEG (76.3%) and DPMASG (78.9%). It also showed a lower rate of adverse reactions (8.0%) and improved one-year survival (36.0% vs. 18.4% and 21.1%, respectively). Furthermore, CG had the most favourable effects on inflammatory cytokine levels and T lymphocyte subsets, significantly reducing TNF-a, PCT, IFN-g, IL-2, IL-6, and IL-10.

Conclusions: The combination of PEG and DPMAS (HALSS) demonstrated superior clinical efficacy in improving liver and kidney function, reducing inflammation, and enhancing patient prognosis compared to single therapies. These findings support HALSS as a promising adjunctive therapy for CLF patients, improving short-term outcomes and long-term survival.

背景:本研究旨在评价混合型人工肝支持系统(HALSS)在慢性肝衰竭(CLF)患者中的有效性和安全性。它还试图分析炎症反应和患者预后。方法:将126例CLF患者分为血浆置换(PEG)组、双血浆分子吸附系统(DPMASG)组和联合治疗组(CG)。治疗前后评估肝肾功能、凝血功能、T淋巴细胞亚群、炎症细胞因子(TNF-a、降钙素原[PCT]、干扰素- γ [IFN-g]、IL-2、IL-6、IL-10)水平等关键参数。比较两组患者的临床疗效、不良反应及短期预后。结果:与PEG和DPMASG相比,联合用药组(CG)肝肾功能指标有显著改善,包括ALT、AST、总胆红素(TBil)、肌酐(Cr)、INR、凝血酶原时间(PT)降低。此外,CG显示胆碱酯酶(ChE),白蛋白和凝血酶原活性(PTA)水平升高。CG组总临床疗效(92.0%)高于PEG组(76.3%)和DPMASG组(78.9%)。不良反应发生率较低(8.0%),一年生存率提高(36.0%,分别为18.4%和21.1%)。此外,CG对炎症细胞因子水平和T淋巴细胞亚群有最有利的影响,显著降低TNF-a、PCT、IFN-g、IL-2、IL-6和IL-10。结论:PEG联合DPMAS (HALSS)在改善肝肾功能、减轻炎症、改善患者预后方面优于单一治疗。这些发现支持HALSS作为CLF患者有希望的辅助治疗,改善短期预后和长期生存率。
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引用次数: 0
Serum level of (interleukin (IL)-2, IL-10, tumor necrosis factor (TNF)-a, motilin (MTL), gastrin (GAS), pepsinogen (PG), after adjunctive treatment in patients with chronic atrophic gastritis. 慢性萎缩性胃炎患者辅助治疗后血清白细胞介素(IL)-2、IL-10、肿瘤坏死因子(TNF)-a、胃动素(MTL)、胃泌素(GAS)、胃蛋白酶原(PG)水平的变化。
IF 1.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-10-28 DOI: 10.5937/jomb0-56027
Pan Xue

Background: The study aimed to demonstrate the impact of traditional Chinese medicine (TCM) matrine combined with omeprazole enteric-coated tablets on gastric mucosal histopathology, gastric function, inflammatory cytokines, and Helicobacter pylori (H. pylori) eradication in patients with chronic atrophic gastritis (CAG).

Methods: A retrospective collection of case data from 110 patients with CAG admitted to the TCM Department of the hospital was conducted. Patients were rolled into the test group (TG, matrine + omeprazole enteric-coated tablets) and the control group (CG, omeprazole enteric-coated tablets). The gastric mucosal histopathological scores, serological indicators (interleukin (IL)-2, IL-10, tumour necrosis factor (TNF-a), gastric function (motilin (MTL), gastrin (GAS), pepsinogen (PG)), H. pylori eradication rate, and clinical efficacy were compared.

Results: The degree of glandular atrophy, intestinal meta-plasia, dysplasia, and inflammatory activity index in patients of TG post-treatment were lower than CG (P<0.05). Post-treatment, IL-2, IL-10, and TNF-a levels in patients of TG were inferior to CG (P<0.05), and the H. pylori eradication rate in patients of TG (87.27%) was inferior to CG (63.64%) (P<0.05). The effective treatment rate in patients of TG post-treatment (92.73%) was higher than CG (78.18%) (P<0.05).

Conclusions: Matrine combined with omeprazole enteric-coated tablets significantly improved gastric mucosal histopathology, reduced inflammatory cytokine levels, enhanced gastric function, and increased the H. pylori eradication rate compared to omeprazole monotherapy.

背景:本研究旨在探讨中药苦参碱联合奥美拉唑肠溶片对慢性萎缩性胃炎(CAG)患者胃黏膜组织病理学、胃功能、炎症因子及幽门螺杆菌根除的影响。方法:回顾性收集我院中医科收治的110例CAG患者的病例资料。将患者分为试验组(TG,苦参碱+奥美拉唑肠溶片)和对照组(CG,奥美拉唑肠溶片)。比较两组胃黏膜组织病理学评分、血清学指标(白细胞介素(IL)-2、IL-10、肿瘤坏死因子(TNF-a)、胃功能指标(胃动素(MTL)、胃泌素(GAS)、胃蛋白酶原(PG))、幽门螺杆菌根除率及临床疗效。结果:TG组患者治疗后腺体萎缩程度、肠间质增生、发育不良程度及炎症活动指数均低于CG组(P<0.05)。治疗后,TG患者IL-2、IL-10、TNF-a水平均低于CG (p < 0.05),幽门螺杆菌根除率(87.27%)低于CG (63.64%) (p < 0.05)。治疗后TG患者的有效治愈率(92.73%)高于CG (78.18%) (p < 0.05)。结论:与奥美拉唑单药治疗相比,苦参碱联合奥美拉唑肠溶片可显著改善胃黏膜组织病理学,降低炎症细胞因子水平,增强胃功能,提高幽门螺杆菌根除率。
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引用次数: 0
Myocardial enzyme profile and short-term prognosis of patients with prolonged myocardial damage after transcatheter aortic valve replacement. 经导管主动脉瓣置换术后长期心肌损伤患者的心肌酶谱与短期预后。
IF 1.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-10-28 DOI: 10.5937/jomb0-52087
Yan Guo, Meili Liu, Jing Li, Ke Han

Background: This work investigated the changes in myocardial enzyme profile (MEP) and short-term prognosis (STP) in patients with myocardial damage (MD) after transcatheter aortic valve replacement (TAVR).

Methods: 100 patients receiving TAVR surgery were selected and rolled into an observation group (Obs group, 50 cases) and a control group (Ctrl group, 50 cases) according to postoperative myocardial status. The changes in MEP before and after the TAVR and the STP within 3 days after surgery were compared and analysed.

Results: Creatine Kinase MB (CK-MB) levels were (21.6±8.8) IU/L, (17.2±7.1) IU/L, and (15.2±6.4) IU/L at 12 h, 24 h, and 72 h after TAVR, respectively, in the Obs group; and the cTnT levels were (0.284±0.13) ng/mL, (0.315±0.15) ng/mL, and (0.363±0.22) ng/mL, respectively, at the same time points. The CK-MB and cTnT levels in the Obs group were increased more obviously based on the conditions in the Ctrl group (P<0.05). After surgery, 23 cases of bleeding occurred in the Obs group, significantly more than 8 cases in the Ctrl group (P<0.05). Differences in ultrasonic test results were not obvious (P>0.05).

Conclusions: The MEP of patients after TAVR generally increased, and the increase in the degree of patients with MD was more significant, which may be an indicator to judge the postoperative MD. Patients with postoperative MD had a higher probability of postoperative bleeding.

背景:本研究探讨心肌损伤(MD)患者经导管主动脉瓣置换术(TAVR)后心肌酶谱(MEP)和短期预后(STP)的变化。方法:选择100例TAVR手术患者,根据术后心肌状态分为观察组(Obs组,50例)和对照组(Ctrl组,50例)。比较分析TAVR术前、术后3 d内MEP及STP的变化。结果:在TAVR后12 h、24 h和72 h, Obs组肌酸激酶MB (CK-MB)水平分别为(21.6±8.8)IU/L、(17.2±7.1)IU/L和(15.2±6.4)IU/L;同一时间点cTnT水平分别为(0.284±0.13)ng/mL、(0.315±0.15)ng/mL和(0.363±0.22)ng/mL。ob组CK-MB和cTnT水平在对照组基础上明显升高(p < 0.05)。术后,Obs组出血23例,显著高于对照组8例(p < 0.05)。超声检查结果差异不明显(P>0.05)。结论:TAVR术后患者MEP普遍升高,且患者MD加重程度更为显著,可能是判断术后MD的一个指标,术后MD患者术后出血的概率较高。
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引用次数: 0
Serum biomarkers in oral lichen planus: A biochemical perspective. 口腔扁平苔藓的血清生物标志物:生化观点。
IF 1.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-05 DOI: 10.5937/jomb0-57322
Jiawei Zhang, Jie Yang, Wei Lu, Shasha Zang, Chengbi Tong

Background: Oral lichen planus (OLP) is a chronic inflammatory disease that affects the mucosal tissues of the oral cavity. Its pathogenesis involves immune dysregulation, angiogenesis, and psychological stress. Identifying reliable biomarkers can enhance diagnosis, monitor disease progression, and guide personalised treatment strategies. This study aimed to investigate five key serum biomarkers in OLP patients, including angiopoietin-2 (Ang-2), vitamin D, IgA, IgG, and cortisol, to explore their associations with disease severity.

Methods: This observational, case-control study enrolled 100 OLP patients and 80 healthy controls. The OLP patients were classified into three subtypes: reticular (n=30), atrophic (n=35), and erosive (n=35). Fasting blood samples were collected, and serum levels of Ang-2, vitamin D, IgA, IgG, and cortisol were measured using ELISA, HPLC, immunoturbidimetry, and chemiluminescent immunoassays. Statistical analyses, including t-tests, ANOVA, and Pearson correlation, were performed to assess biomarker levels and their correlations with disease severity.

Results: Ang-2, IgA, and IgG levels were significantly elevated in OLP patients, particularly in the erosive subtype (P<0.001), with positive correlations between these markers and disease severity. Vitamin D and cortisol levels were significantly reduced in OLP patients compared to controls (P<0.01) and showed negative correlations with disease severity. These findings indicate the role of vascular, immune, metabolic, and stress-related factors in OLP pathogenesis.

Conclusions: Ang-2, vitamin D, IgA, IgG, and cortisol are valuable biomarkers for assessing OLP severity and guiding personalised treatment. Monitoring these biomarkers can aid in diagnosing OLP, tracking disease progression, and optimising therapeutic strategies.

背景:口腔扁平苔藓(OLP)是一种影响口腔粘膜组织的慢性炎症性疾病。其发病机制涉及免疫失调、血管生成和心理应激。确定可靠的生物标志物可以增强诊断,监测疾病进展,并指导个性化治疗策略。本研究旨在研究OLP患者的5个关键血清生物标志物,包括血管生成素-2 (ang2)、维生素D、IgA、IgG和皮质醇,以探讨它们与疾病严重程度的关系。方法:本观察性病例对照研究纳入100例OLP患者和80例健康对照者。OLP患者分为网状型(n=30)、萎缩性(n=35)和糜烂性(n=35)三种亚型。采集空腹血样,采用ELISA、HPLC、免疫比浊法和化学发光免疫法检测血清中Ang-2、维生素D、IgA、IgG和皮质醇水平。进行统计分析,包括t检验、方差分析和Pearson相关性,以评估生物标志物水平及其与疾病严重程度的相关性。结论:ang2、维生素D、IgA、IgG和皮质醇是评估OLP严重程度和指导个性化治疗的有价值的生物标志物。监测这些生物标志物可以帮助诊断OLP,跟踪疾病进展,优化治疗策略。
{"title":"Serum biomarkers in oral lichen planus: A biochemical perspective.","authors":"Jiawei Zhang, Jie Yang, Wei Lu, Shasha Zang, Chengbi Tong","doi":"10.5937/jomb0-57322","DOIUrl":"10.5937/jomb0-57322","url":null,"abstract":"<p><strong>Background: </strong>Oral lichen planus (OLP) is a chronic inflammatory disease that affects the mucosal tissues of the oral cavity. Its pathogenesis involves immune dysregulation, angiogenesis, and psychological stress. Identifying reliable biomarkers can enhance diagnosis, monitor disease progression, and guide personalised treatment strategies. This study aimed to investigate five key serum biomarkers in OLP patients, including angiopoietin-2 (Ang-2), vitamin D, IgA, IgG, and cortisol, to explore their associations with disease severity.</p><p><strong>Methods: </strong>This observational, case-control study enrolled 100 OLP patients and 80 healthy controls. The OLP patients were classified into three subtypes: reticular (n=30), atrophic (n=35), and erosive (n=35). Fasting blood samples were collected, and serum levels of Ang-2, vitamin D, IgA, IgG, and cortisol were measured using ELISA, HPLC, immunoturbidimetry, and chemiluminescent immunoassays. Statistical analyses, including t-tests, ANOVA, and Pearson correlation, were performed to assess biomarker levels and their correlations with disease severity.</p><p><strong>Results: </strong>Ang-2, IgA, and IgG levels were significantly elevated in OLP patients, particularly in the erosive subtype (P<0.001), with positive correlations between these markers and disease severity. Vitamin D and cortisol levels were significantly reduced in OLP patients compared to controls (P<0.01) and showed negative correlations with disease severity. These findings indicate the role of vascular, immune, metabolic, and stress-related factors in OLP pathogenesis.</p><p><strong>Conclusions: </strong>Ang-2, vitamin D, IgA, IgG, and cortisol are valuable biomarkers for assessing OLP severity and guiding personalised treatment. Monitoring these biomarkers can aid in diagnosing OLP, tracking disease progression, and optimising therapeutic strategies.</p>","PeriodicalId":16175,"journal":{"name":"Journal of Medical Biochemistry","volume":"44 6","pages":"1263-1270"},"PeriodicalIF":1.5,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12497454/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145238878","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Apoptosis in prostate carcinoma tissue: The role of caspase-3, caspase-1, and alkaline DNase activity. 前列腺癌组织凋亡:caspase-3、caspase-1和碱性dna酶活性的作用。
IF 1.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-05 DOI: 10.5937/jomb0-57574
Andrej Veljkovic, Jovan Hadzi-Djokic, Gordana Kocic, Xiaobo Li, Stefanos Roumeliotis, Dušan Sokolović, Aleksandra Klisic

Background: Prostate glandular tissue maintains a delicate balance between cellular proliferation and programmed cell death (apoptosis), ensuring the preservation of normal glandular architecture in healthy individuals. Disruption of this equilibrium - whether due to excessive proliferation or impaired apoptotic mechanisms - can contribute to the initiation and progression of prostate cancer. The objective of this study was to evaluate the expression and activity of caspase-3, caspase-1, and alkaline deoxyribonuclease (DNase) in prostate cancer tissue and tumour-adjacent tissue in comparison to clinically healthy prostate tissue. The aim was to determine whether alterations in these parameters could serve as early biomarkers for the transformation of surrounding tissue into a precancerous phenotype.

Methods: The concentration of caspase-3 and caspase-1, as well as the activity of alkaline DNase, were examined in prostate tissue samples, including cancerous tissue, adjacent tissue near the tumour, and surrounding healthy tissue.

Results: The results revealed a significant reduction in caspase-3 levels in cancerous tissue (p<0.05), with an even more pronounced decrease in the adjacent peritumoural tissue (p<0.05). In contrast, caspase-1 levels were markedly elevated in both cancerous tissue (p<0.00001) and the surrounding non-malignant peritumoural tissue (p<0.0005). Similarly, alkaline DNase activity (both total and specific) was significantly increased in cancerous tissue (p<0.00001), with a moderate but statistically significant elevation in the tumour-adjacent tissue (p<0.000017) compared to control tissue.

Conclusions: These findings suggest a disruption in the interplay between caspase-3 and alkaline DNase, potentially as a consequence of necrotic processes or enzyme release from inhibitory complexes. Furthermore, the increased expression of caspase-1 implies that inflammatory responses may play a role in tumourigenesis.

背景:前列腺组织在细胞增殖和程序性细胞死亡(凋亡)之间保持着微妙的平衡,确保了健康个体正常腺体结构的保存。这种平衡的破坏——无论是由于过度增殖还是凋亡机制受损——都可能导致前列腺癌的发生和发展。本研究的目的是评估caspase-3、caspase-1和碱性脱氧核糖核酸酶(DNase)在前列腺癌组织和肿瘤邻近组织中的表达和活性,并与临床健康前列腺组织进行比较。目的是确定这些参数的改变是否可以作为周围组织转化为癌前表型的早期生物标志物。方法:检测前列腺癌组织、癌旁组织及周围健康组织中caspase-3、caspase-1的浓度及碱性dna酶活性。结果:结果显示癌组织中caspase-3水平显著降低(结论:这些发现表明caspase-3和碱性dna酶之间的相互作用被破坏,可能是坏死过程或抑制复合物释放酶的结果。此外,caspase-1表达的增加表明炎症反应可能在肿瘤发生中起作用。
{"title":"Apoptosis in prostate carcinoma tissue: The role of caspase-3, caspase-1, and alkaline DNase activity.","authors":"Andrej Veljkovic, Jovan Hadzi-Djokic, Gordana Kocic, Xiaobo Li, Stefanos Roumeliotis, Dušan Sokolović, Aleksandra Klisic","doi":"10.5937/jomb0-57574","DOIUrl":"10.5937/jomb0-57574","url":null,"abstract":"<p><strong>Background: </strong>Prostate glandular tissue maintains a delicate balance between cellular proliferation and programmed cell death (apoptosis), ensuring the preservation of normal glandular architecture in healthy individuals. Disruption of this equilibrium - whether due to excessive proliferation or impaired apoptotic mechanisms - can contribute to the initiation and progression of prostate cancer. The objective of this study was to evaluate the expression and activity of caspase-3, caspase-1, and alkaline deoxyribonuclease (DNase) in prostate cancer tissue and tumour-adjacent tissue in comparison to clinically healthy prostate tissue. The aim was to determine whether alterations in these parameters could serve as early biomarkers for the transformation of surrounding tissue into a precancerous phenotype.</p><p><strong>Methods: </strong>The concentration of caspase-3 and caspase-1, as well as the activity of alkaline DNase, were examined in prostate tissue samples, including cancerous tissue, adjacent tissue near the tumour, and surrounding healthy tissue.</p><p><strong>Results: </strong>The results revealed a significant reduction in caspase-3 levels in cancerous tissue (p<0.05), with an even more pronounced decrease in the adjacent peritumoural tissue (p<0.05). In contrast, caspase-1 levels were markedly elevated in both cancerous tissue (p<0.00001) and the surrounding non-malignant peritumoural tissue (p<0.0005). Similarly, alkaline DNase activity (both total and specific) was significantly increased in cancerous tissue (p<0.00001), with a moderate but statistically significant elevation in the tumour-adjacent tissue (p<0.000017) compared to control tissue.</p><p><strong>Conclusions: </strong>These findings suggest a disruption in the interplay between caspase-3 and alkaline DNase, potentially as a consequence of necrotic processes or enzyme release from inhibitory complexes. Furthermore, the increased expression of caspase-1 implies that inflammatory responses may play a role in tumourigenesis.</p>","PeriodicalId":16175,"journal":{"name":"Journal of Medical Biochemistry","volume":"44 6","pages":"1297-1304"},"PeriodicalIF":1.5,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12497462/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145238895","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Vitamin D status among pregnant women of North Macedonia: Assessing deficiency rates and associated risks factors. 北马其顿孕妇的维生素D状况:评估缺乏率和相关风险因素
IF 1.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-05 DOI: 10.5937/jomb0-55601
Boshku Aleksandra Atanasova, Vasko Aleksovski, Krstevska Slagana Simeonova, Nikolovska Elena Gjorgievska, Igor Samardjiski, Markova Ana Daneva

Background: Vitamin D is an essential vitamin that plays a key role in maintaining overall health. During pregnancy, the demand for vitamin D increases to support the growing needs of the fetus. Vitamin D deficiency is highly prevalent in pregnant women worldwide. Our study aimed to evaluate the vitamin D deficiency rate among pregnant women in the Republic of North Macedonia, along with influencing factors.

Methods: We conducted a prospective study of randomly selected pregnant women with different body mass indexes among vitamin supplementation users and non-users in two different seasons.

Results: A total of 309 pregnant women aged > 18 years were recruited from June 2022 to April 2023, with an average vitamin D concentration of 38.9 (36.6-40.2) nmol/L. During winter, 80.8 % of pregnant women had vitamin D deficiency.

Conclusions: Even though more than 77.3 % of pregnant women consume multivitamins containing vitamin D, vitamin D deficiency is highly prevalent among pregnant women, especially among obese pregnant women and during the winter months.

背景:维生素D是一种必需的维生素,在维持整体健康方面起着关键作用。在怀孕期间,对维生素D的需求增加,以支持胎儿不断增长的需求。维生素D缺乏症在全世界的孕妇中非常普遍。本研究旨在评估北马其顿共和国孕妇维生素D缺乏率及其影响因素。方法:在两个不同季节随机选择不同体质指数的孕妇进行维生素补充者和未补充者的前瞻性研究。结果:从2022年6月至2023年4月共招募了309名年龄在bb0 - 18岁之间的孕妇,平均维生素D浓度为38.9 (36.6-40.2)nmol/L。在冬季,80.8%的孕妇缺乏维生素D。结论:尽管超过77.3%的孕妇服用含有维生素D的复合维生素,但维生素D缺乏症在孕妇中非常普遍,尤其是在肥胖孕妇和冬季。
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引用次数: 0
The prognosis of primary aldosteronism achieved incomplete surgical remission and changes in plasma aldosterone, plasma renin activity, and biochemical indicators. 原发性醛固酮增多症的预后达到手术不完全缓解,血浆醛固酮、血浆肾素活性和生化指标发生变化。
IF 1.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-05 DOI: 10.5937/jomb0-54960
Zihao Guo, Jing Wang, Xiang Ren, Xing Li, Yisheng Yin, Yiqun Tian, Zhenliang Qin, Kun Yuan, Xiaoyong Zeng

Background: Some primary aldosteronism (PA) patients with spontaneous hypokalemia achieved incomplete remission after surgical treatment. In this study, we aimed to construct a nomogram to predict surgical benefits for primary aldosteronism (PA) patients with typical symptoms, incorporating changes in plasma aldosterone, plasma renin activity (PRA), and aldosterone/renin ratio (ARR) to help clinicians assess prognosis and develop optimised treatment plans.

Methods: This retrospective cohort study enrolled 162 patients between January 2017 and January 2024. Baseline characteristics, clinical indicators, and biochemical results, including plasma aldosterone, PRA, ARR, and serum potassium, were compared among patients with different clinical and biochemical outcomes. A nomogram was developed and internally validated with risk factors selected from univariate and multivariate logistic regression analyses.

Results: Complete clinical and biochemical success was achieved in 69 (42.6%) and 129 (79.6%). Five risk factors were used to develop a nomogram. The area under the receiver operating characteristic curve (AUC) was 0.856 (0.788-0.924) in the training dataset and 0.726 (0.580-0.872) in the validation dataset. The calibration curve showed good agreement, and the decision curve analysis demonstrated the clinical utility of this model.

Conclusions: PA patients with older age, higher systolic blood pressure, lower plasma aldosterone, more than 5 years of hypertension, and an adrenal gland mass on the left side or both sides had more probability of achieving incomplete remission after the surgery.

背景:一些原发性醛固酮增多症(PA)患者自发性低钾血症在手术治疗后达到不完全缓解。在这项研究中,我们旨在构建一个nomogram来预测具有典型症状的原发性醛固酮增多症(PA)患者的手术效果,包括血浆醛固酮、血浆肾素活性(PRA)和醛固酮/肾素比值(ARR)的变化,以帮助临床医生评估预后并制定优化的治疗方案。方法:该回顾性队列研究于2017年1月至2024年1月期间纳入162例患者。比较不同临床及生化结局患者的基线特征、临床指标及血浆醛固酮、PRA、ARR、血钾等生化结果。从单变量和多变量逻辑回归分析中选择风险因素,开发并内部验证了nomogram。结果:69例(42.6%)和129例(79.6%)临床及生化完全成功。五个危险因素被用来形成一个nomogram。训练数据集的受试者工作特征曲线下面积(AUC)为0.856(0.788-0.924),验证数据集的AUC为0.726(0.580-0.872)。校正曲线吻合良好,决策曲线分析证明了该模型的临床实用性。结论:年龄较大、收缩压较高、血浆醛固酮较低、高血压≥5年、左侧或两侧有肾上腺肿块的PA患者术后不完全缓解的可能性较大。
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引用次数: 0
Effectiveness of treating NELL1-positive idiopathic membranous nephropathy on clinical outcomes, serum cytokine levels (IL-6, IL-10, IL-2, IL-17), nutritional status, and immune responses. 治疗nell1阳性特发性膜性肾病对临床结果、血清细胞因子水平(IL-6、IL-10、IL-2、IL-17)、营养状况和免疫反应的影响
IF 1.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-05 DOI: 10.5937/jomb0-56892
Xiaojing Liu, Yanqiu Yu, Kang Li

Background: This study aimed to evaluate the therapeutic effects of glucocorticoids (GCs) combined with tacrolimus (TAC) in the treatment of Neural Epidermal Growth Factor-Like 1 (NELL1)-positive idiopathic membranous nephropathy (IMN), with a focus on clinical outcomes, nutritional status, and inflammatory response.

Methods: A total of 84 NELL1-positive IMN patients from Cangzhou Central Hospital (January 2020-February 2024) were randomly assigned to a research group (GCs+TAC) and a control group (GCs alone). The research group received methylprednisolone (0.5 g), prednisone (0.5 mg/kg), and tacrolimus (0.05 mg/kg/day), while the control group was treated with methylprednisolone and prednisone alone. Clinical parameters, including renal function, blood glucose, lipids, nutritional proteins, and cytokine levels (IL-6, IL-10, IL-2, IL-17), were measured at baseline and after six months of treatment. Nutritional status was assessed using the Nutritional Risk Screening 2002 (NRS 2002).

Results: The two groups had no significant differences in clinical efficacy or adverse reactions. However, the research group exhibited significant improvements in renal function, glycemic control, lipid profile, and nutritional status (P<0.05). Furthermore, the research group showed a more favourable cytokine profile, with more significant reductions in pro-inflammatory cytokines (IL-6, IL-17) and increases in anti-inflammatory cytokines (IL-10, IL-2) compared to the control group (P<0.05). Both groups had comparable safety profiles, with no significant increase in adverse events.

Conclusions: Combining GCs and TAC is an effective and safe therapeutic option for NELL1-positive IMN. It improves clinical outcomes, maintains nutritional stability, and modulates immune responses without increasing adverse reactions.

背景:本研究旨在评估糖皮质激素(GCs)联合他克莫司(TAC)治疗神经表皮生长因子样1 (NELL1)阳性特发性膜性肾病(IMN)的疗效,重点关注临床结局、营养状况和炎症反应。方法:将2020年1月~ 2024年2月沧州市中心医院收治的84例nell1阳性IMN患者随机分为研究组(GCs+TAC)和对照组(GCs单独)。研究组给予甲基强的松龙(0.5 g)、强的松(0.5 mg/kg)、他克莫司(0.05 mg/kg/d)治疗,对照组给予甲基强的松龙和强的松单独治疗。临床参数,包括肾功能、血糖、血脂、营养蛋白和细胞因子水平(IL-6、IL-10、IL-2、IL-17),在基线和治疗6个月后测量。利用2002年营养风险筛查(NRS 2002)评估营养状况。结果:两组临床疗效及不良反应均无显著差异。然而,研究组在肾功能、血糖控制、血脂和营养状况方面均有显著改善(p结论:GCs和TAC联合治疗nell1阳性IMN是一种有效且安全的治疗选择。它改善临床结果,保持营养稳定,调节免疫反应而不增加不良反应。
{"title":"Effectiveness of treating NELL1-positive idiopathic membranous nephropathy on clinical outcomes, serum cytokine levels (IL-6, IL-10, IL-2, IL-17), nutritional status, and immune responses.","authors":"Xiaojing Liu, Yanqiu Yu, Kang Li","doi":"10.5937/jomb0-56892","DOIUrl":"10.5937/jomb0-56892","url":null,"abstract":"<p><strong>Background: </strong>This study aimed to evaluate the therapeutic effects of glucocorticoids (GCs) combined with tacrolimus (TAC) in the treatment of Neural Epidermal Growth Factor-Like 1 (NELL1)-positive idiopathic membranous nephropathy (IMN), with a focus on clinical outcomes, nutritional status, and inflammatory response.</p><p><strong>Methods: </strong>A total of 84 NELL1-positive IMN patients from Cangzhou Central Hospital (January 2020-February 2024) were randomly assigned to a research group (GCs+TAC) and a control group (GCs alone). The research group received methylprednisolone (0.5 g), prednisone (0.5 mg/kg), and tacrolimus (0.05 mg/kg/day), while the control group was treated with methylprednisolone and prednisone alone. Clinical parameters, including renal function, blood glucose, lipids, nutritional proteins, and cytokine levels (IL-6, IL-10, IL-2, IL-17), were measured at baseline and after six months of treatment. Nutritional status was assessed using the Nutritional Risk Screening 2002 (NRS 2002).</p><p><strong>Results: </strong>The two groups had no significant differences in clinical efficacy or adverse reactions. However, the research group exhibited significant improvements in renal function, glycemic control, lipid profile, and nutritional status (P<0.05). Furthermore, the research group showed a more favourable cytokine profile, with more significant reductions in pro-inflammatory cytokines (IL-6, IL-17) and increases in anti-inflammatory cytokines (IL-10, IL-2) compared to the control group (P<0.05). Both groups had comparable safety profiles, with no significant increase in adverse events.</p><p><strong>Conclusions: </strong>Combining GCs and TAC is an effective and safe therapeutic option for NELL1-positive IMN. It improves clinical outcomes, maintains nutritional stability, and modulates immune responses without increasing adverse reactions.</p>","PeriodicalId":16175,"journal":{"name":"Journal of Medical Biochemistry","volume":"44 6","pages":"1201-1209"},"PeriodicalIF":1.5,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12497463/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145238824","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Combination of prostate cancer antigen 3 (PCA3), sarcosine, glypican-1 (GPC1), urokinase plasminogen activator receptor (uPAR), and thymidine kinase 1 (TK1), and T2WI and DWI radiomics model for distinguishing benign prostatic hyperplasia, prostate cancer, and prostatitis. 联合前列腺癌抗原3 (PCA3)、肌氨酸甘聚糖-1 (GPC1)、尿激酶纤溶酶原激活物受体(uPAR)、胸苷激酶1 (TK1),结合T2WI、DWI放射组学模型鉴别良性前列腺增生、前列腺癌、前列腺炎。
IF 1.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-05 DOI: 10.5937/jomb0-57639
Fan Yang, Wei Guo, Siqin Sun, Yanan Huang

Background: To measure the diagnostic value of T2WI and DWI radiomics model, combined with advanced biomarkers, in distinguishing benign prostatic hyperplasia (BPH), prostate cancer (PCa) and prostatitis.

Methods: A total of 90 patients with prostate diseases were selected from our hospital from January 2022 to January 2024. All patients underwent T2WI and DWI MRI examinations. Regions of interest (ROI) were delineated, and imaging features were extracted using radiomics analysis. In addition, novel biomarkers, including Prostate Cancer Antigen 3 (PCA3), Sarcosine, Glypican-1 (GPC1), Urokinase Plasminogen Activator Receptor (uPAR), and Thymidine Kinase 1 (TK1), were analysed for their diagnostic significance. Feature selection was performed using LASSO regression, and a random forest model was established for classification. The receiver operating characteristic (ROC) curve was used to evaluate the diagnostic performance of the T2WI and DWI radiomics model with and without biomarker integration.

Results: Among the 90 patients with prostate diseases, 50 cases were PCa, 20 cases of prostatitis and 20 cases of BPH were detected by biopsy. The PI-RADS v2 score in the PCa group presented elevation relative to those in the BPH and prostatitis groups (P<0.01). The ADC values in the PCa group were reduced relative to those in the BPH and prostatitis groups (P<0.01). The integration of biomarkers with radiomics analysis led to improved diagnostic performance. The AUC value, sensitivity, and specificity of the T2WI and DWI radiomics model were higher relative to those of PI-RADS V2.

Conclusions: The T2WI and DWI radiomics model, when combined with novel biomarkers, enhances the accuracy of distinguishing PCa, BPH, and prostatitis. This approach may provide an advanced diagnostic tool for personalised prostate disease management.

背景:探讨T2WI和DWI放射组学模型结合先进生物标志物对良性前列腺增生(BPH)、前列腺癌(PCa)和前列腺炎的诊断价值。方法:选择2022年1月~ 2024年1月我院收治的前列腺疾病患者90例。所有患者均行T2WI和DWI MRI检查。绘制感兴趣区域(ROI),并使用放射组学分析提取成像特征。此外,还分析了新的生物标志物,包括前列腺癌抗原3 (PCA3)、肌氨酸甘聚糖-1 (GPC1)、尿激酶纤溶酶原激活物受体(uPAR)和胸苷激酶1 (TK1)的诊断意义。采用LASSO回归进行特征选择,建立随机森林模型进行分类。采用受试者工作特征(ROC)曲线评价T2WI和DWI放射组学模型有无生物标志物整合的诊断性能。结果:90例前列腺疾病患者中,前列腺癌50例,前列腺炎20例,前列腺增生20例。与BPH和前列腺炎组相比,PCa组PI-RADS v2评分升高(结论:T2WI和DWI放射组学模型与新型生物标志物结合可提高区分PCa、BPH和前列腺炎的准确性。该方法可为个性化前列腺疾病管理提供先进的诊断工具。
{"title":"Combination of prostate cancer antigen 3 (PCA3), sarcosine, glypican-1 (GPC1), urokinase plasminogen activator receptor (uPAR), and thymidine kinase 1 (TK1), and T2WI and DWI radiomics model for distinguishing benign prostatic hyperplasia, prostate cancer, and prostatitis.","authors":"Fan Yang, Wei Guo, Siqin Sun, Yanan Huang","doi":"10.5937/jomb0-57639","DOIUrl":"10.5937/jomb0-57639","url":null,"abstract":"<p><strong>Background: </strong>To measure the diagnostic value of T2WI and DWI radiomics model, combined with advanced biomarkers, in distinguishing benign prostatic hyperplasia (BPH), prostate cancer (PCa) and prostatitis.</p><p><strong>Methods: </strong>A total of 90 patients with prostate diseases were selected from our hospital from January 2022 to January 2024. All patients underwent T2WI and DWI MRI examinations. Regions of interest (ROI) were delineated, and imaging features were extracted using radiomics analysis. In addition, novel biomarkers, including Prostate Cancer Antigen 3 (PCA3), Sarcosine, Glypican-1 (GPC1), Urokinase Plasminogen Activator Receptor (uPAR), and Thymidine Kinase 1 (TK1), were analysed for their diagnostic significance. Feature selection was performed using LASSO regression, and a random forest model was established for classification. The receiver operating characteristic (ROC) curve was used to evaluate the diagnostic performance of the T2WI and DWI radiomics model with and without biomarker integration.</p><p><strong>Results: </strong>Among the 90 patients with prostate diseases, 50 cases were PCa, 20 cases of prostatitis and 20 cases of BPH were detected by biopsy. The PI-RADS v2 score in the PCa group presented elevation relative to those in the BPH and prostatitis groups (P<0.01). The ADC values in the PCa group were reduced relative to those in the BPH and prostatitis groups (P<0.01). The integration of biomarkers with radiomics analysis led to improved diagnostic performance. The AUC value, sensitivity, and specificity of the T2WI and DWI radiomics model were higher relative to those of PI-RADS V2.</p><p><strong>Conclusions: </strong>The T2WI and DWI radiomics model, when combined with novel biomarkers, enhances the accuracy of distinguishing PCa, BPH, and prostatitis. This approach may provide an advanced diagnostic tool for personalised prostate disease management.</p>","PeriodicalId":16175,"journal":{"name":"Journal of Medical Biochemistry","volume":"44 6","pages":"1376-1385"},"PeriodicalIF":1.5,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12497469/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145238868","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Journal of Medical Biochemistry
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