CCL22 and Leptin associated with steroid resistance in childhood idiopathic nephrotic syndrome

被引:0
|
作者
Peng, Peng [1 ]
Li, Wei [1 ]
Jin, Yanyan [2 ]
Xiang, Wenqing [1 ]
Fu, Haidong [2 ]
Mao, Jianhua [2 ]
机构
[1] Zhejiang Univ, Dept Clin Lab, Natl Clin Res Ctr Child Hlth, Childrens Hosp,Sch Med, Hangzhou, Peoples R China
[2] Zhejiang Univ, Childrens Hosp, Natl Clin Res Ctr Child Hlth, Dept Nephrol,Sch Med, Hangzhou, Peoples R China
来源
FRONTIERS IN PEDIATRICS | 2023年 / 11卷
关键词
CCL22; leptin; steroid-resistant nephrotic syndrome; T regulatory cells; idiopathic nephrotic syndrome; CHILDREN;
D O I
10.3389/fped.2023.1261034
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
ObjectivePrevious studies have indicated a decrease in T regulatory cells (Tregs) among patients with steroid-resistant nephrotic syndrome. CCL22 and Leptin influenced the immune function of Tregs through their respective pathways. This study aimed to compare patients with steroid-sensitive nephrotic syndrome (SSNS) and steroid-resistant nephrotic syndrome (SRNS) in terms of CCL22 and Leptin levels.MethodsThis prospective study included 117 children diagnosed with idiopathic nephrotic syndrome (INS). Peripheral blood samples were collected before initiating steroid therapy, and serum levels of CCL22 and Leptin were measured. Patients were categorized into three groups based on their response to steroid treatment. Renal biopsies were recommended for all children diagnosed with INS, with higher acceptance rates in glucocorticoid resistance patients.ResultsBased on the response to steroid treatment, 117 children were divided as groups of SSNS (82 cases), frequent relapse nephrotic syndrome (FRNS) (10 cases), and SRNS (25 cases). A total of 41 patients underwent kidney biopsy, 11 cases (13.4%) in SSNS, 7 cases (70.0%) in FRNS and 24 cases (96.0%) in SRNS. 30 cases were minimal change disease (MCD), 9 cases were mesangial proliferative glomerulonephritis (MsPGN) and 3 cases were focal segmental glomerulosclerosis (FSGS). The levels of Leptin were significantly higher in SR patients (1208.1 & PLUSMN; 1044.1 pg/ml) compared to SS patients (515.4 & PLUSMN; 676.9 pg/ml) and controls (507.9 & PLUSMN; 479.8 pg/ml), regardless of the pathological type. CCL22 levels were significantly elevated in SRNS (92.2 & PLUSMN; 157.0 pg/ml), but the difference seemed to be attributed to the specific type of pathology, such as Minimal change disease (MCD) (127.4 & PLUSMN; 206.7 pg/ml) and focal segmental glomerulosclerosis (FSGS) (114.8 & PLUSMN; 22.0 pg/ml). For SRNS prediction, the AUC of Leptin, CCL22, and the joint prediction index were 0.764, 0.640, and 0.806, respectively.ConclusionSerum levels of CCL22 and Leptin, detected prior to steroid therapy, were associated with steroid resistance in childhood INS.
引用
收藏
页数:7
相关论文
共 50 条
  • [21] Atopy in childhood idiopathic nephrotic syndrome
    Salsano, Maria Esposito
    Graziano, Luisa
    Luongo, Ilaria
    Pilla, Paola
    Giordano, Mario
    Lama, Giuliana
    ACTA PAEDIATRICA, 2007, 96 (04) : 561 - 566
  • [22] Childhood idiopathic nephrotic syndrome in Turkey
    Bircan, Z
    Yilmaz, AY
    Katar, S
    Vitrinel, A
    Yildirim, M
    PEDIATRICS INTERNATIONAL, 2002, 44 (06) : 608 - 611
  • [23] MicroRNAs in idiopathic childhood nephrotic syndrome
    Aditi Sinha
    Manraj Sra
    Aijaz Ahmed
    Saumyaranjan Mallick
    Himanshi Saini
    Kshetrimayum Ghanapriya Devi
    Pankaj Hari
    Arvind Bagga
    Clinical and Experimental Nephrology, 2025, 29 (4) : 477 - 484
  • [24] NEPHROTIC SYNDROME Rituximab in childhood steroid-dependent nephrotic syndrome
    Boyer, Olivia
    Niaudet, Patrick
    NATURE REVIEWS NEPHROLOGY, 2013, 9 (10) : 562 - 563
  • [25] Prognostic value of early vs late steroid resistance in idiopathic nephrotic syndrome
    Gulati, S
    Kumar, A
    INDIAN PEDIATRICS, 2006, 43 (04) : 373 - 374
  • [26] Long Term Evolution Of Childhood Steroid-sensitive Idiopathic Nephrotic Syndrome.
    Zarauza Santovena, Alejandro
    Pena Carrion, Antonia
    Fernandez Camblor, Carlota
    Melgosa Hijosa, Marta
    Garcia Meseguer, Carmen
    Alonso Melgar, Angel
    Espinosa Roman, Laura
    PEDIATRIC NEPHROLOGY, 2014, 29 (09) : 1730 - 1730
  • [27] Recurrence of severe steroid dependency in cyclosporin A-treated childhood idiopathic nephrotic syndrome
    Kemper, MJ
    Kuwertz-Broeking, E
    Bulla, M
    Mueller-Wiefel, DE
    Neuhaus, TJ
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2004, 19 (05) : 1136 - 1141
  • [28] Seasonal variation in first episode of childhood idiopathic steroid-sensitive nephrotic syndrome and adult minimal change nephrotic syndrome
    Jun Odaka
    Takahiro Kanai
    Ritei Uehara
    Eiji Kusano
    Takanori Yamagata
    Clinical and Experimental Nephrology, 2015, 19 : 146 - 147
  • [29] Seasonal variation in first episode of childhood idiopathic steroid-sensitive nephrotic syndrome and adult minimal change nephrotic syndrome
    Odaka, Jun
    Kanai, Takahiro
    Uehara, Ritei
    Kusano, Eiji
    Yamagata, Takanori
    CLINICAL AND EXPERIMENTAL NEPHROLOGY, 2015, 19 (01) : 146 - 147
  • [30] CCL22 signaling contributes to sorafenib resistance in hepatitis B virus-associated hepatocellular carcinoma
    Gao, Yanan
    Fan, Xing
    Li, Nan
    Du, Chengzhi
    Yang, Bin
    Qin, Wenhao
    Fu, Jing
    Markowitz, Geoffrey J.
    Wang, Hongyang
    Ma, Jianli
    Cheng, Shuqun
    Yang, Pengyuan
    PHARMACOLOGICAL RESEARCH, 2020, 157