全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

miR-146a、UAER等指标联合检测对早期2型糖尿病肾脏病临床诊断的应用价值
The Clinical Diagnostic Value of Combined Detection of miR-146a, UAER, and Other Indicators for Early-Stage Type 2 Diabetic Nephropathy

DOI: 10.12677/acm.2024.1472124, PP. 1138-1146

Keywords: 糖尿病肾病,早期诊断,miR-146a,SLPI,IGFBP7,TIMP-2,UAER
Diabetic Nephropathy
, Early Diagnosis, miR-146a, SLPI, IGFBP7, TIMP-2, UAER

Full-Text   Cite this paper   Add to My Lib

Abstract:

目的:探讨血清miR-146a、SLPI、IGFBP7、TIMP-2对早期糖尿病肾病(DN)的诊断价值。方法:选取2022年1月至2023年12月在杭州市富阳区第一人民医院就诊的临床诊断为T2DM患者192例,按24 h尿微量清蛋白排泄率(24 h UAER)分为糖尿病肾脏病患者(DN) 48例(A组),早期糖尿病肾病患者48例(B组),糖尿病无肾脏病患者48例(C组),另外选取同期健康体检者作为对照组48例(D组)。检测四组患者血清miR-146a、SLPI、IGFBP7、TIMP-2及24h UAER表达水平,并分析其对早期DN的诊断价值。结果:A组患者血清中miR-146a水平显著高于B、C、D组 (p < 0.05),A组血清中SLPI、TIMP-2、IGFBP7指标显著低于B、C、D组(p < 0.05),血清五个分子指标仅miR-146a、UAER单项诊断DN患者AUC面积分别为0.623、0.801 (p < 0.05),同时小样本金标准诊断对比,miR-146a、UAER单项诊断DN患者AUC面积分别为0.643、0.850 (p < 0.05),SLPI、TIMP-2、IGFBP7诊断DN患者AUC面积分别为0.464、0.586、0.425 (p < 0.05),最终我们分析所有样本中五个分子联合诊断DN患者AUC面积为0.903 (p < 0.05)。结论:miR-146a检测对早期DN具有诊断价值,可作为糖尿病肾损伤早期的评估指标,miR-146a、SLPI、IGFBP7、TIMP-2联合UAER检测对早期DN具有更高的诊断价值。
Objective: To explore the diagnostic value of serum miR-146a, SLPI, IGFBP7, and TIMP-2 for early diabetic nephropathy (DN). Methods: A total of 192 patients clinically diagnosed with type 2 diabetes mellitus (T2DM) from January 2022 to December 2024 at the Fuyang District First People’s Hospital in Hangzhou were selected. Based on the 24-hour urinary albumin excretion rate (24 h UAER), the patients were divided into three groups: DN patients (48 cases, Group A), early DN patients (48 cases, Group B), and diabetes patients without kidney disease (48 cases, Group C). Additionally, 48 healthy individuals undergoing routine health check-ups during the same period were selected as the control group (Group D). The expression levels of serum miR-146a, SLPI, IGFBP7, TIMP-2, and 24 h UAER were measured in all four groups, and their diagnostic value for early DN was analyzed. Results: The serum miR-146a levels in Group A were significantly higher than those in Groups B, C, and D (p < 0.05). The indicators SLPI, TIMP-2, and IGFBP7 in Group A were significantly lower than those in Groups B, C, and D (p < 0.05). The diagnostic AUC areas of miR-146a and UAER for DN in Group A were 0.623 and 0.801, respectively (p < 0.05). With small sample gold standard diagnostics, the AUC areas for miR-146a and UAER were 0.643 and 0.850, respectively (p < 0.05). The AUC areas for SLPI, TIMP-2, and IGFBP7 were 0.464, 0.586, and 0.425, respectively (p < 0.05). Ultimately, the combined diagnostic AUC area for the five molecular markers in DN was 0.903 (p < 0.05). Conclusion: miR-146a testing has diagnostic value for early DN and can serve as an early assessment marker for diabetic kidney damage. The combination of miR-146a, SLPI, IGFBP7, and TIMP-2 with UAER provides higher diagnostic value for early DN.

References

[1]  Naaman, S.C. and Bakris, G.L. (2023) Diabetic Nephropathy: Update on Pillars of Therapy Slowing Progression. Diabetes Care, 46, 1574-1586.
https://doi.org/10.2337/dci23-0030
[2]  Hu, Q., Chen, Y., Deng, X., Li, Y., Ma, X., Zeng, J., et al. (2023) Diabetic Nephropathy: Focusing on Pathological Signals, Clinical Treatment, and Dietary Regulation. Biomedicine & Pharmacotherapy, 159, Article ID: 114252.
https://doi.org/10.1016/j.biopha.2023.114252
[3]  Zhao, P., Sun, T., Lyu, C., Liang, K. and Du, Y. (2023) Cell Mediated ECM-Degradation as an Emerging Tool for Anti-Fibrotic Strategy. Cell Regeneration, 12, Article No. 29.
https://doi.org/10.1186/s13619-023-00172-9
[4]  Satta, E., Strollo, F., Borgia, L., et al. (2023) Urinary L-FABP: A Potential Novel Early Biomarker for Diabetic Nephropathy? A Systematic Review of the Literature. Research Square, 1-11.
[5]  Rossing, P. and Flyvbjerg, A. (2024) Diabetic Nephropathy. In: Holt, Richard, I.G., Cockram, C., Flyvbjerg, A. and Goldstein, B.J., Eds., Textbook of Diabetes, Blackwell, 640-654.
[6]  Thipsawat, S. (2021) Early Detection of Diabetic Nephropathy in Patient with Type 2 Diabetes Mellitus: A Review of the Literature. Diabetes and Vascular Disease Research, 18, 1-9.
https://doi.org/10.1177/14791641211058856
[7]  中华医学会糖尿病学分会. 中国2型糖尿病防治指南(2020年版) [J]. 国际内分泌代谢杂志, 2021, 41(5): 482-548.
[8]  中华医学会肾脏病学分会专家组. 糖尿病肾脏疾病临床诊疗中国指南[J]. 中华肾脏病杂志, 2021, 37(3): 255-304.
[9]  李静雅, 李亮亮, 肖洪玲. 血清miR-155和miR-146a检测对早期糖尿病肾病的诊断价值[J]. 医学临床研究, 2019, 36(8): 1620-1622.
[10]  孟雪, 王慧文. 糖尿病肾病的早期诊断相关指标研究进展[J]. 沈阳医学院学报, 2024, 26(2): 188-192, 199.
[11]  Begum, F., Ramesh, J. and Lakshmanan, K. (2023) Association of Urinary Biomarkers of Chronic Kidney Disease with Type 2 Diabetes. Romanian Journal of Diabetes Nutrition and Metabolic Diseases, 30, 494-499.
[12]  Mahapatra, H., Kulshreshtha, B., Goyal, P., Chitkara, A., Kumari, A., Arora, A., et al. (2022) Comparative Diagnostic Utility of Different Urinary Biomarkers during Pre-Albuminuric Stages of Non-Hypertensive Type 2 Diabetic Nephropathy. Indian Journal of Medical Research, 156, 46-55.
https://doi.org/10.4103/ijmr.ijmr_455_21
[13]  贺炜, 刘泓键, 易艳霞, 等. 血清骨生成诱导因子及miR-22-3p表达水平对2型糖尿病肾病早期诊断价值研究[J]. 现代检验医学杂志, 2023, 38(2): 37-42.
[14]  Fan, B., Chopp, M., Zhang, Z.G. and Liu, X.S. (2020) Emerging Roles of Micrornas as Biomarkers and Therapeutic Targets for Diabetic Neuropathy. Frontiers in Neurology, 11, Article 558758.
https://doi.org/10.3389/fneur.2020.558758
[15]  Guerrieri, D., Ambrosi, N.G., Romeo, H., Salaberry, J., Toniolo, M.F., Remolins, C., et al. (2021) Secretory Leukocyte Proteinase Inhibitor Protects Acute Kidney Injury through Immune and Non-Immune Pathways. Shock, 56, 1019-1027.
https://doi.org/10.1097/shk.0000000000001785
[16]  赵登旺. 尿胰岛素样生长因子结合蛋白7在急性肾损伤中的诊断价值及意义[D]: [硕士学位论文]. 石河子: 石河子大学, 2017.
[17]  Brew, K. and Nagase, H. (2010) The Tissue Inhibitors of Metalloproteinases (timps): An Ancient Family with Structural and Functional Diversity. Biochimica et Biophysica Acta (BBA)—Molecular Cell Research, 1803, 55-71.
https://doi.org/10.1016/j.bbamcr.2010.01.003
[18]  Yuan, S., Guo, D., Liang, X., Zhang, L., Zhang, Q. and Xie, D. (2023) Relaxin in Fibrotic Ligament Diseases: Its Regulatory Role and Mechanism. Frontiers in Cell and Developmental Biology, 11, Article 1131481.
https://doi.org/10.3389/fcell.2023.1131481
[19]  Genovese, F., Manresa, A.A., Leeming, D.J., Karsdal, M.A. and Boor, P. (2014) The Extracellular Matrix in the Kidney: A Source of Novel Non-Invasive Biomarkers of Kidney Fibrosis? Fibrogenesis & Tissue Repair, 7, Article No. 4.
https://doi.org/10.1186/1755-1536-7-4
[20]  Ni, W., Ding, H., Zhou, H., Qiu, Y. and Tang, L. (2015) Renoprotective Effects of Berberine through Regulation of the MMPs/TIMPs System in Streptozocin-Induced Diabetic Nephropathy in Rats. European Journal of Pharmacology, 764, 448-456.
https://doi.org/10.1016/j.ejphar.2015.07.040

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133