医学检查与临床诊断

血浆PPARγ作为女性间质性膀胱炎/膀胱疼痛综合征潜在诊断标志物的评估及其预测价值

  • 王照 ,
  • 左解鹏 ,
  • 车航 ,
  • 任凌云 ,
  • 徐哲 ,
  • 王磊
展开
  • 河北医科大学第一医院泌尿外科 (河北 石家庄 050000 )

收稿日期: 2024-08-01

  网络出版日期: 2025-01-26

基金资助

河北省卫健委医学科学研究课题计划(20241597)

Evaluation of plasma PPARγ as a potential diagnostic marker for female interstitial cystitis/painful bladder syndrome and its predictive model

  • Zhao WANG ,
  • Jiepeng ZUO ,
  • Hang CHE ,
  • Lingyun REN ,
  • Zhe XU ,
  • Lei. WANG
Expand
  • Department of Urology,First Hospital of Hebei Medical University,Shijiazhuang 050000,Hebei,China

Received date: 2024-08-01

  Online published: 2025-01-26

摘要

目的 探讨PPARγ与女性间质性膀胱炎/膀胱疼痛综合征(IC/BPS)的相关性,并构建预测模型。 方法 收集2022年6月至2023年12月医院收治的89例女性IC/BPS患者(观察组)和同期90例健康女性体检志愿者(对照组)的临床资料。检测血浆炎症因子水平、总抗氧化能力(TAC)、总谷胱甘肽(GSH)和丙二醛(MDA)含量以及血浆PPARγ水平;通过LASSO回归筛选显著临床特征,使用多因素二元logistic回归模型进行拟合;通过受试者工作特征(ROC)曲线评估其诊断效能。 结果 与对照组比较,观察组患者的年龄、BMI、NLR、绝对中性粒细胞计数、IFN-α、IL-1β、IL-6、IL-8、TNF-α和CD3+CD4+T表达水平显著升高,而绝对淋巴细胞计数、IL-10、TAC、GSH和血浆PPARγ表达水平显著降低,差异具有统计学意义(均P < 0.05)。LASSO回归筛选出,NLR、IFN-α、绝对中性粒细胞计数、IL-1β、IL-6、TNF-α、CD3+CD4+T及PPARγ共8个自变量进入预测模型。多因素二元logistic回归分析显示,IL-1β、TNF-α和CD3+CD4+T水平升高及PPARγ水平降低是IC/BPS的独立危险因素。ROC曲线结果显示,PPARγ联合临床参数(IL-1β、TNF-α和CD3+CD4+T)的诊断IC/PBS的曲线下面积0.901(95%CI:0.885 ~ 0.963)高于PPARγ单一指标诊断[0.839(95%CI:0.730 ~ 0.902)]效能(AUC = 0.901)优于单独PPARγ(AUC = 0.839)。 结论 IC/BPS女性患者血浆PPARγ水平明显降低,可作为IC/BPS的潜在诊断标志物,联合临床指标提高诊断效能。

本文引用格式

王照 , 左解鹏 , 车航 , 任凌云 , 徐哲 , 王磊 . 血浆PPARγ作为女性间质性膀胱炎/膀胱疼痛综合征潜在诊断标志物的评估及其预测价值[J]. 实用医学杂志, 2025 , 41(2) : 258 -263 . DOI: 10.3969/j.issn.1006-5725.2025.02.016

Abstract

Objective To investigate the correlation between PPARγ and female interstitial cystitis/bladder pain syndrome (IC/BPS) and to establish a predictive model. Methods Clinical data were collected from 89 female IC/BPS patients (observational group) admitted to the hospital from June 2022 to December 2023, and 90 healthy female volunteers undergoing physical examinations during the same period (control group). Plasma levels of inflammatory factors, total antioxidant capacity (TAC), total glutathione (GSH), malondialdehyde (MDA), and PPARγ levels were measured. Significant clinical features were identified using LASSO regression and fitted into a multivariate logistic regression model. The diagnostic efficacy was assessed through receiver operating characteristic (ROC) curves. Results Compared to the control group, the observation group exhibited significantly elevated age, BMI, NLR, absolute neutrophil count, IFN-α, IL-1β, IL-6, IL-8, TNF-α and CD3+CD4+T expression levels, while absolute lymphocyte count, IL-10, TAC, GSH and plasma PPARγ expression levels were significantly decreased (all P < 0.05). LASSO regression identified 8 variables, including NLR, IFN-α, absolute neutrophil count, IL-1β, IL-6, TNF-α, CD3+CD4+T and PPARγ, which were incorporated into the predictive model. Multivariate binary logistic regression analysis revealed that elevated levels of IL-1β, TNF-α and CD3+CD4+T cells, along with reduced PPARγ levels, were independent risk factors for IC/BPS. ROC curve analysis indicated that the diagnostic efficacy of the combined PPARγ and clinical parameters (age, IL-1β, TNF-α and CD3+CD4+T) (AUC = 0.901) was superior to PPARγ alone (AUC = 0.839). Conclusion Plasma PPARγ levels are significantly reduced in female IC/BPS patients and serve as a potential diagnostic marker, with combined clinical parameters enhancing diagnostic accuracy.

参考文献

1 CLEMENS J Q, ERICKSON D R, VARELA N P, et al. Diagnosis and treatment of interstitial cystitis/bladder pain syndrome[J]. J Urol, 2022, 208(1): 34-42. doi:10.1097/ju.0000000000002756
2 PESKAR D, KURET T, LAKOTA K, et al. Molecular profiling of inflammatory processes in a mouse model of ic/bps: From the complete transcriptome to major sex-related histological features of the urinary bladder[J]. Int J Mol Sci, 2023, 24(6): 5758. doi:10.3390/ijms24065758
3 OGAWA T, ISHIZUKA O, UEDA T, et al. Pharmacological management of interstitial cystitis/bladder pain syndrome and the role cyclosporine and other immunomodulating drugs play[J]. Expert Rev Clin Pharmacol, 2018, 11(5): 495-505. doi:10.1080/17512433.2018.1457435
4 MOLDWIN R M, NURSEY V, YASKIV O, et al. Immune cell profiles of patients with interstitial cystitis/bladder pain syndrome[J]. J Transl Med, 2022, 20(1): 97. doi:10.1186/s12967-022-03236-7
5 JHANG J F, JIANG Y H, KUO H C. Current understanding of the pathophysiology and novel treatments of interstitial cystitis/bladder pain syndrome[J]. Biomedicines, 2022, 10(10): 2380. doi:10.3390/biomedicines10102380
6 DUH K, FUNARO M G, DEGOUVEIA W, et al. Crosstalk between the immune system and neural pathways in interstitial cystitis/bladder pain syndrome[J]. Discov Med, 2018, 25(139): 243-250.
7 JIANG Y H, JHAN G J F, HO H C, et al. Urine oxidative stress biomarkers as novel biomarkers in interstitial cystitis/bladder pain syndrome[J]. Biomedicines, 2022, 10(7): 1701. doi:10.3390/biomedicines10071701
8 YU W R, JIANG Y H, JHANG J F, et al. Use of urinary cytokine and chemokine levels for identifying bladder conditions and predicting treatment outcomes in patients with interstitial cystitis/bladder pain syndrome[J]. Biomedicines, 2022, 10(5): 1149. doi:10.3390/biomedicines10051149
9 易莎, 胡楠, 李粤, 等. 过氧化物酶体增殖物激活受体-γ对P.acnes诱导的人角质形成细胞焦亡、增殖及凋亡的影响[J].实用医学杂志, 2023, 39(16): 2043-2049. doi:10.3969/j.issn.1006-5725.2023.16.006
10 DE AZAMBUJA G, JORGE C O, GOMES B B, et al. Regular swimming exercise prevented the acute and persistent mechanical muscle hyperalgesia by modulation of macrophages phenotypes and inflammatory cytokines via PPARγ receptors[J]. Brain Behav Immun, 2021, 95: 462-476. doi:10.1016/j.bbi.2021.05.002
11 KURET T, KREFT M E, ROMIH R, et al. Cannabidiol as a Promising therapeutic option in ic/bps: In vitro evaluation of its protective effects against inflammation and oxidative stress[J]. Int J Mol Sci, 2023, 24(5): 5055. doi:10.3390/ijms24055055
12 ZENG Y, HE H, AN Z. Advance of serum biomarkers and combined diagnostic panels in nonalcoholic fatty liver disease[J]. Dis Markers, 2022, 2022: 1254014. doi:10.1155/2022/1254014
13 DE JONG J J, PIJPERS O M, VAN KESSEL K E M, et al. A urine-based genomic assay improves risk stratification for patients with high-risk hematuria stratified according to the american urological association guidelines[J]. Eur Urol Oncol, 2023, 6(2): 183-189. doi:10.1016/j.euo.2022.08.002
14 LERNER L B, MCVARY K T, BARRY M J, et al. Management of lower urinary tract symptoms attributed to benign prostatic hyperplasia: Aua guideline part II-surgical evaluation and treatment[J]. J Urol, 2021, 206(4): 818-826. doi:10.1097/ju.0000000000002184
15 SATARI M, BAHMANI F, REINER Z, et al. Metabolic and anti-inflammatory response to melatonin administration in patients with diabetic nephropathy[J]. Iran J Kidney Dis, 2021, 1(1): 22-30.
16 LIN H Y, LU J H, CHUANG S M, et al. Urinary biomarkers in interstitial cystitis/bladder pain syndrome and its impact on therapeutic outcome[J]. Diagnostics (Basel), 2021, 12(1): 75. doi:10.3390/diagnostics12010075
17 ABID M S R, QIU H, TRIPP B A, et al. Peptidomics analysis reveals changes in small urinary peptides in patients with interstitial cystitis/bladder pain syndrome[J]. Sci Rep, 2022, 12(1): 8289. doi:10.1038/s41598-022-12197-2
18 JIANG Y H, JHANG J F, BIRDER L A, et al. Sensory receptor, inflammatory, and apoptotic protein expression in the bladder urothelium of patients with different subtypes of interstitial cystitis/bladder pain syndrome[J]. Int J Mol Sci, 2023, 24(1): 820. doi:10.3390/ijms24010820
19 许庆元, 袁伟锋, 陈沐, 等. 人类免疫缺陷病毒相关肺动脉高压患者的肺动脉管径特征及联合肿瘤坏死因子-α的诊断价值[J].实用医学杂志, 2024, 40(13): 1869-1873.
20 JIANG Y H, JHANG J F, KUO H C. Can we use urinary cytokine/chemokine analysis in discriminating ulcer-type interstitial cystitis/bladder pain syndrome?[J]. Diagnostics (Basel), 2022, 12(5): 1093. doi:10.3390/diagnostics12051093
21 BIRDER L A. Is there a role for oxidative stress and mitochondrial dysfunction in age-associated bladder disorders?[J]. Tzu Chi Med J, 2020, 32(3): 223-226. doi:10.4103/tcmj.tcmj_250_19
22 JIANG Y H, JHANG J F, HSU Y H, et al. Usefulness of urinary biomarkers for assessing bladder condition and histopathology in patients with interstitial cystitis/bladder pain syndrome[J]. Int J Mol Sci, 2022, 23(19): 12044. doi:10.3390/ijms231912044
23 ENER K, KESKE M, ALDEMIR M, et al. Evaluation of oxidative stress status and antioxidant capacity in patients with painful bladder syndrome/interstitial cystitis: Preliminary results of a randomised study[J]. Int Urol Nephrol, 2015, 47(8): 1297-1302. doi:10.1007/s11255-015-1021-1
24 KE H, ZHU L, WANG Q, et al. Neutrophil-to-lymphocyte ratio as a promising non-invasive biomarker for symptom assessment and diagnosis of interstitial cystitis/bladder pain syndrome[J]. BMC Urol, 2023, 23(1): 180. doi:10.1186/s12894-023-01353-z
25 LI X, GUO Q, YE Z, et al. PPARγ prevents neuropathic pain by down-regulating cx3cr1 and attenuating m1 activation of microglia in the spinal cord of rats using a sciatic chronic constriction injury model[J]. Front Neurosci, 2021, 15: 620525. doi:10.3389/fnins.2021.620525
26 XU T, LIU R, LU X, et al. Lycium barbarum polysaccharides alleviate LPS- induced inflammatory responses through PPARγ/MAPK/NF-κB pathway in bovine mammary epithelial cells[J]. J Anim Sci, 2022, 100(1): skab345. doi:10.1093/jas/skab345
27 MAHAL A, YOUNG-LIN N, DOBBERFUHL A, et al. Peroxisome proliferator- activated receptor gamma agonist as a novel treatment for interstitial cystitis: A rat model[J]. Investig Clin Urol, 2018, 59(4): 257-262. doi:10.4111/icu.2018.59.4.257
文章导航

/