Reham Hammad, Mona A Eldosoky, Lamiaa Ismaiel, Fatma M Kotb, Omaima I Abo-Elkheir, Hend G Kotb, Wafaa A Emam, Amena R Mohammed, Amany M Tawfik, Mona A Raafat, Doaa L Ali, Sarah F Fahmy, Rasha Elgamal, Fatma El-Zahraa Abd El Hakam, Sonia Distante
{"title":"无细胞DNA、hepcidin和白细胞介素-6之间的相互作用在慢性肾脏疾病诱导炎症和进展到血液透析依赖状态。","authors":"Reham Hammad, Mona A Eldosoky, Lamiaa Ismaiel, Fatma M Kotb, Omaima I Abo-Elkheir, Hend G Kotb, Wafaa A Emam, Amena R Mohammed, Amany M Tawfik, Mona A Raafat, Doaa L Ali, Sarah F Fahmy, Rasha Elgamal, Fatma El-Zahraa Abd El Hakam, Sonia Distante","doi":"10.55133/eji.320201","DOIUrl":null,"url":null,"abstract":"<p><p>Inflammation drives chronic kidney disease (CKD) progression to end-stage renal disease (ESRD). Cell-free DNA (cfDNA) release is linked to systemic inflammation. Pro-inflammatory interleukin-6 (IL-6) is believed to induce hepcidin, the master regulator of iron metabolism. This study attempts to assess the link between cfDNA, IL-6, and hepcidin in CKD induced inflammation and evaluate their usefulness as indicators for progression. This study included 90 participants, divided into three equal groups. Group 1 comprised non-dialysis dependent CKD (ND-CKD) patients (stages IV and V); Group 2 comprised hemodialysis dependent ESRD (HD-ESRD) patients; and Group 3 comprised study normal controls. cfDNA concentration was determined using the real-time quantitative polymerase chain reaction (RT-qPCR). Serum hepcidin and IL-6 were assessed using enzyme-linked immunosorbent assay (ELISA) kits. The HD-ESRD group showed significant up-regulation of cfDNA, IL-6, and hepcidin compared to the ND-CKD group (p =0.008, p < 0.001, and p < 0.001, respectively) and to the control group (p =0.007, p < 0.001, and p < 0.001, respectively). The ND-CKD group showed no significant up-regulation in cfDNA compared to the control group. cfDNA was positively correlated with IL-6, hepcidin, and carotid intima-media thickness (CIMT). IL-6 had the highest discriminative power to detect CKD progression [area under the curve (AUC) of 0.84, 83% sensitivity (SN) and 73% specificity (SP)], followed by hepcidin [AUC 0.77, SN = 80%, and SP = 63%] and cfDNA [AUC 0.67, SN = 70%, and SP = 50%]. Logistic regression analysis revealed that up-regulated IL-6 and hepcidin were independent predictors of HD-ESRD progression, (odds ratio = 1.005 and 1.006, respectively). In conclusion, cfDNA was associated with IL-6 and hepcidin in CKD. Up-regulated IL-6 and hepcidin can serve as predictors of HD-ESRD progression. cfDNA was associated with CIMT in renal patients. IL-6 and hepcidin up-regulations may act as predictors of HD-ESRD progression.</p>","PeriodicalId":39724,"journal":{"name":"The Egyptian journal of immunology / Egyptian Association of Immunologists","volume":"32 2","pages":"1-16"},"PeriodicalIF":0.0000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The interplay between cell-free DNA, hepcidin, and interleukin-6 in chronic kidney disease induced inflammation and progression to a hemodialysis dependent state.\",\"authors\":\"Reham Hammad, Mona A Eldosoky, Lamiaa Ismaiel, Fatma M Kotb, Omaima I Abo-Elkheir, Hend G Kotb, Wafaa A Emam, Amena R Mohammed, Amany M Tawfik, Mona A Raafat, Doaa L Ali, Sarah F Fahmy, Rasha Elgamal, Fatma El-Zahraa Abd El Hakam, Sonia Distante\",\"doi\":\"10.55133/eji.320201\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Inflammation drives chronic kidney disease (CKD) progression to end-stage renal disease (ESRD). Cell-free DNA (cfDNA) release is linked to systemic inflammation. Pro-inflammatory interleukin-6 (IL-6) is believed to induce hepcidin, the master regulator of iron metabolism. This study attempts to assess the link between cfDNA, IL-6, and hepcidin in CKD induced inflammation and evaluate their usefulness as indicators for progression. This study included 90 participants, divided into three equal groups. Group 1 comprised non-dialysis dependent CKD (ND-CKD) patients (stages IV and V); Group 2 comprised hemodialysis dependent ESRD (HD-ESRD) patients; and Group 3 comprised study normal controls. cfDNA concentration was determined using the real-time quantitative polymerase chain reaction (RT-qPCR). Serum hepcidin and IL-6 were assessed using enzyme-linked immunosorbent assay (ELISA) kits. The HD-ESRD group showed significant up-regulation of cfDNA, IL-6, and hepcidin compared to the ND-CKD group (p =0.008, p < 0.001, and p < 0.001, respectively) and to the control group (p =0.007, p < 0.001, and p < 0.001, respectively). The ND-CKD group showed no significant up-regulation in cfDNA compared to the control group. cfDNA was positively correlated with IL-6, hepcidin, and carotid intima-media thickness (CIMT). IL-6 had the highest discriminative power to detect CKD progression [area under the curve (AUC) of 0.84, 83% sensitivity (SN) and 73% specificity (SP)], followed by hepcidin [AUC 0.77, SN = 80%, and SP = 63%] and cfDNA [AUC 0.67, SN = 70%, and SP = 50%]. Logistic regression analysis revealed that up-regulated IL-6 and hepcidin were independent predictors of HD-ESRD progression, (odds ratio = 1.005 and 1.006, respectively). In conclusion, cfDNA was associated with IL-6 and hepcidin in CKD. Up-regulated IL-6 and hepcidin can serve as predictors of HD-ESRD progression. cfDNA was associated with CIMT in renal patients. IL-6 and hepcidin up-regulations may act as predictors of HD-ESRD progression.</p>\",\"PeriodicalId\":39724,\"journal\":{\"name\":\"The Egyptian journal of immunology / Egyptian Association of Immunologists\",\"volume\":\"32 2\",\"pages\":\"1-16\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Egyptian journal of immunology / Egyptian Association of Immunologists\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.55133/eji.320201\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Egyptian journal of immunology / Egyptian Association of Immunologists","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55133/eji.320201","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
摘要
炎症驱动慢性肾脏疾病(CKD)进展到终末期肾脏疾病(ESRD)。游离DNA (cfDNA)的释放与全身炎症有关。促炎白细胞介素-6 (IL-6)被认为可以诱导铁代谢的主要调节因子hepcidin。本研究试图评估cfDNA、IL-6和hepcidin在CKD诱导炎症中的联系,并评估它们作为进展指标的有效性。这项研究包括90名参与者,分为三组。组1包括非透析依赖性CKD (ND-CKD)患者(IV期和V期);第二组为血液透析依赖性ESRD (HD-ESRD)患者;第三组为研究正常对照组。采用实时定量聚合酶链反应(RT-qPCR)测定cfDNA浓度。采用酶联免疫吸附测定(ELISA)试剂盒检测血清hepcidin和IL-6。与ND-CKD组(p =0.008, p < 0.001, p < 0.001)和对照组(p =0.007, p < 0.001, p < 0.001)相比,HD-ESRD组cfDNA、IL-6和hepcidin均显著上调。与对照组相比,ND-CKD组cfDNA无明显上调。cfDNA与IL-6、hepcidin、颈动脉内膜-中膜厚度(CIMT)呈正相关。IL-6对CKD进展的鉴别能力最高[曲线下面积(AUC)为0.84,灵敏度(SN)为83%,特异性(SP)为73%],其次是hepcidin [AUC 0.77, SN = 80%, SP = 63%]和cfDNA [AUC 0.67, SN = 70%, SP = 50%]。Logistic回归分析显示,IL-6和hepcidin上调是HD-ESRD进展的独立预测因子(优势比分别为1.005和1.006)。总之,CKD中cfDNA与IL-6和hepcidin相关。上调IL-6和hepcidin可作为HD-ESRD进展的预测因子。cfDNA与肾脏患者的CIMT相关。IL-6和hepcidin上调可作为HD-ESRD进展的预测因子。
The interplay between cell-free DNA, hepcidin, and interleukin-6 in chronic kidney disease induced inflammation and progression to a hemodialysis dependent state.
Inflammation drives chronic kidney disease (CKD) progression to end-stage renal disease (ESRD). Cell-free DNA (cfDNA) release is linked to systemic inflammation. Pro-inflammatory interleukin-6 (IL-6) is believed to induce hepcidin, the master regulator of iron metabolism. This study attempts to assess the link between cfDNA, IL-6, and hepcidin in CKD induced inflammation and evaluate their usefulness as indicators for progression. This study included 90 participants, divided into three equal groups. Group 1 comprised non-dialysis dependent CKD (ND-CKD) patients (stages IV and V); Group 2 comprised hemodialysis dependent ESRD (HD-ESRD) patients; and Group 3 comprised study normal controls. cfDNA concentration was determined using the real-time quantitative polymerase chain reaction (RT-qPCR). Serum hepcidin and IL-6 were assessed using enzyme-linked immunosorbent assay (ELISA) kits. The HD-ESRD group showed significant up-regulation of cfDNA, IL-6, and hepcidin compared to the ND-CKD group (p =0.008, p < 0.001, and p < 0.001, respectively) and to the control group (p =0.007, p < 0.001, and p < 0.001, respectively). The ND-CKD group showed no significant up-regulation in cfDNA compared to the control group. cfDNA was positively correlated with IL-6, hepcidin, and carotid intima-media thickness (CIMT). IL-6 had the highest discriminative power to detect CKD progression [area under the curve (AUC) of 0.84, 83% sensitivity (SN) and 73% specificity (SP)], followed by hepcidin [AUC 0.77, SN = 80%, and SP = 63%] and cfDNA [AUC 0.67, SN = 70%, and SP = 50%]. Logistic regression analysis revealed that up-regulated IL-6 and hepcidin were independent predictors of HD-ESRD progression, (odds ratio = 1.005 and 1.006, respectively). In conclusion, cfDNA was associated with IL-6 and hepcidin in CKD. Up-regulated IL-6 and hepcidin can serve as predictors of HD-ESRD progression. cfDNA was associated with CIMT in renal patients. IL-6 and hepcidin up-regulations may act as predictors of HD-ESRD progression.