The role of urine β2-MG concentration and the urine MAU/UA ratio in the diagnosis and risk stratification of hypertension-induced renal damage

urine β2-MG concentration and the urine MAU/UA ratio in hypertension-induced renal damage

  • Chezhao Huang 1.Department of Nephrology, Taizhou Affiliated Hospital of Nanjing University of Chinese Medicine; 2. The First Clinical Medical College, Nanjing University of Chinese Medicine.
  • Yanshuang Zhuang Department of Pharmacy, Taizhou Affiliated Hospital of Nanjing University of Chinese Medicine
  • Peng Xue Department of Geriatrics, Taizhou Affiliated Hospital of Nanjing University of Chinese Medicine
  • Hui Zhang The First Clinical Medical College, Nanjing University of Chinese Medicine
  • Yucong Zhao Medical Laboratory Department, The First Affiliated Hospital of University of Science and Technology of China
  • Zeyu Huang Medical Laboratory Department, The First Affiliated Hospital of University of Science and Technology of China
  • Hu Tian Department of Science and Technology, Taizhou Affiliated Hospital of Nanjing University of Chinese Medicine
  • Liping Zhai Department of Endocrine, Taizhou Affiliated Hospital of Nanjing University of Chinese Medicine
  • Teng Ma Department of Nephrology, Taizhou Affiliated Hospital of Nanjing University of Chinese Medicine
Keywords: Primary H-type hypertension, Renal damage, β2-microglobulin, Microalbuminuria, Uric acid, Prognostic risk stratification

Abstract


Objective To explore the roles of urineβ2-microglobulin (β2-MG) and the ratio of microalbuminuria (MAU) to uric acid (UA) in the diagnosis of renal damage and risk stratification assessment of the prognosis of essential hypertension with H-type (EH) hypertension.

Methods From January to December 2025, 204 patients with H-type EH and renal damage who were admitted to our hospital were selected and included in the renal damage group, whereas 102 patients with H-type EH but without renal damage were included in the EH group. The baseline data of all patients were collected. The urine β2-MG, urinary MAU, and UA levels of all patients were detected, and the MAU/UA ratio was calculated. The β2-MG levels and MAU/UA ratios of the two groups were compared, and multivariate logistic regression analysis was used to explore the factors influencing renal damage in patients with H-type EH. Patients with EH-related renal damage were divided into a low- to moderate-risk group and a high-risk group on the basis of the prognostic risk stratification at admission. A receiver operating characteristic (ROC) curve was drawn to analyze the predictive value of the urine β2-MG concentration and the urine MAU/UA ratio for the prognostic risk stratification of H-type EH renal damage.

Results Compared with those in the EH group, the proportion of patients with renal damage combined with diabetes, the urine β2-MG level, and the urine MAU/UA ratio were significantly greater (P<0.05). The results of multivariate logistic regression analysis revealed that elevated urine β2-MG levels and the urine MAU/UA ratio were independent risk factors for renal damage in H-type EH patients (P<0.05). The prognostic risk stratification results revealed that there were 122 patients in the low- to moderate-risk group and 82 patients in the high-risk group; the urine β2-MG level and urine MAU/UA ratio in the high-risk group were significantly greater than those in the low- to moderate-risk group (P<0.05). The ROC curve analysis results revealed that the individual and combined prediction of the urine β2-MG concentration and the urine MAU/UA ratio for high-risk renal damage in H-type EH patients had AUC values of 0.781, 0.786, and 0.860, respectively, and the combined prediction AUC was significantly greater than the individual prediction AUC of the urine β2-MG concentration and the urine MAU/UA ratio (Z = 2.035, 1.953; both P<0.05).

Conclusion The urine β2-MG level and urine MAU/UA ratio in patients with H-type EH renal damage are high. Moreover, increases in the urine β2-MG level and the urine MAU/UA ratio are independent risk factors for the occurrence of renal damage in H-type EH patients. The combined detection of these two indicators has high predictive value for the risk stratification assessment of renal damage in H-type EH patients.

References

1.Lee SA, McMahon GM. A spurious elevation of serum creatinine level in a patient with Crohn's disease without histologic kidney damage: a case report and review of the literature. J Bras Nefrol. 2023 Oct-Dec;45(4):497-501. doi: 10.1590/2175-8239-JBN-2023-0071en. PMID: 37930142; PMCID: PMC10726663.
2.Basolo A, Salvetti G, Giannese D, Genzano SB, Ceccarini G, Giannini R, Sotgia G, Fierabracci P, Piaggi P, Santini F. Obesity, Hyperfiltration, and Early Kidney Damage: A New Formula for the Estimation of Creatinine Clearance. J Clin Endocrinol Metab. 2023 Nov 17;108(12):3280-3286. doi: 10.1210/clinem/dgad330. PMID: 37296533; PMCID: PMC10655541.
3.Taylor KM, Au AYM, Herath S, Succar L, Wong J, Erlich JH, Endre ZH. Kidney functional reserve and damage biomarkers in subclinical chronic kidney disease and acute kidney injury. Am J Physiol Renal Physiol. 2023 Dec 1;325(6):F888-F898. doi: 10.1152/ajprenal.00133.2023. Epub 2023 Sep 21. PMID: 37733876.
4.Mikami Y, Ogawa M, Hayasaka Y, Yamakami A, Hattori K, Fukazawa C, Ito T, Kanomata N, Terawaki H. Kidney damage relates to agonal bacteremia: a single-center retrospective study. Clin Exp Nephrol. 2024 Aug;28(8):773-783. doi: 10.1007/s10157-024-02485-8. Epub 2024 Mar 20. PMID: 38506981.
5.Habeichi NJ, Amin G, Lakkis B, Kataya R, Mericskay M, Booz GW, Zouein FA. Potential Alternative Receptors for SARS-CoV-2-Induced Kidney Damage: TLR-4, KIM-1/TIM-1, and CD147. Front Biosci (Landmark Ed). 2024 Jan 12;29(1):8. doi: 10.31083/j.fbl2901008. PMID: 38287815; PMCID: PMC10924798.
6.Park J, Sim J, Yi HJ, Rhee SG, Woo HA. Cisplatin induces kidney damage through the downregulation of Prx I by autophagic degradation. Free Radic Biol Med. 2024 Nov 20;225:236-246. doi: 10.1016/j.freeradbiomed.2024.09.049. Epub 2024 Oct 2. PMID: 39366472.
7.Yao X, Liu Y, Yang Y, Li Y, Hu N, Song F, Yang F. Microcystin-LR-Exposure-Induced Kidney Damage by Inhibiting MKK6-Mediated Mitophagy in Mice. Toxins (Basel). 2023 Jun 19;15(6):404. doi: 10.3390/toxins15060404. PMID: 37368704; PMCID: PMC10301610.
8.Taylor KM, Au AYM, Herath S, Succar L, Wong J, Erlich JH, Endre ZH. Kidney functional reserve and damage biomarkers in subclinical chronic kidney disease and acute kidney injury. Am J Physiol Renal Physiol. 2023 Dec 1;325(6):F888-F898. doi: 10.1152/ajprenal.00133.2023. Epub 2023 Sep 21. PMID: 37733876.
9.Azırak S, Özgöçmen M. Linalool prevents kidney damage by inhibiting rifampicin-induced oxidative stress and apoptosis. Tissue Cell. 2023 Jun;82:102097. doi: 10.1016/j.tice.2023.102097. Epub 2023 Apr 17. PMID: 37104973.
10.Calderón-Garcidueñas AL, Barradas-Dermitz DM, Nolasco-Hypolito C, López-Amador N, Ajibola OO, Carvajal-Zarrabal O. Functional and histological effects of Anthurium schlechtendalii Kunth extracts on adenine-induced kidney damage of adult Wistar rats. Toxicon. 2023 Sep;233:107272. doi: 10.1016/j.toxicon.2023.107272. Epub 2023 Aug 29. PMID: 37652102.
11.Pereira RO, Correia LA, Farah D, Komoni G, Farah V, Fiorino P. Wistar rat as an animal model to study high-fat induced kidney damage: a systematic review. Arch Physiol Biochem. 2024 Apr;130(2):205-214. doi: 10.1080/13813455.2021.2017462. Epub 2021 Dec 16. PMID: 34915796.
12.Veloso-Giménez V, Cárdenas-Calderón C, Castillo V, Carvajal F, Gallardo-Agüero D, González-Itier S, Corrales-Orovio R, Becerra D, Miranda M, Rebolledo R, San Martín S, Boric MP, Egaña JT. Oxygenation by Intravascular Photosynthesis Reduces Kidney Damage During ex Vivo Preservation. ACS Appl Bio Mater. 2024 Dec 16;7(12):8528-8542. doi: 10.1021/acsabm.4c01327. Epub 2024 Nov 8. PMID: 39514332.
13.Raya AI, Vidal A, López I, Rodríguez M, Aguilera-Tejero E, Pineda C. Phosphorus Restriction Prevents Rapamycin-Induced Kidney Damage in Rats. Am J Nephrol. 2025;56(1):48-57. doi: 10.1159/000541411. Epub 2024 Oct 9. PMID: 39383849.
14.Jiang Y, Peng Y, Yang X, Yu J, Yu F, Yuan J, Zha Y. PM2.5 exposure aggravates kidney damage by facilitating the lipid metabolism disorder in diabetic mice. PeerJ. 2023 Sep 1;11:e15856. doi: 10.7717/peerj.15856. PMID: 37671359; PMCID: PMC10476618.
15.Güner G, Erbaş O. Candesartan protects from cisplatin-induced kidney damage via the GDF-15 pathway. Eur Rev Med Pharmacol Sci. 2024 Feb;28(3):1103-1110. doi: 10.26355/eurrev_202402_35347. PMID: 38375716.
16.Kara O. Protective effect of coenzyme Q10 in cyclophosphamide-induced kidney damage in rats. Rev Assoc Med Bras (1992). 2024 May 3;70(4):e20230990. doi: 10.1590/1806-9282.20230990. PMID: 38716935; PMCID: PMC11068380.
17.Flores-Estrada J, Cano-Martínez A, Ibarra-Lara L, Jiménez A, Palacios-Reyes C, García LJP, Ortiz-López MG, Rodríguez-Peña ON, Hernández-Portilla LB. Spinach Extract Reduces Kidney Damage in Diabetic Rats by Impairing the AGEs/RAGE Axis. Int J Mol Sci. 2025 May 15;26(10):4730. doi: 10.3390/ijms26104730. PMID: 40429870; PMCID: PMC12111706.
18.Ma F, Shao X, Zhang Y, Li J, Li Q, Sun H, Wang T, Liu H, Zhao F, Chen L, Chen J, Zhou S, Ji Q, Yu P. An arterial spin labeling-based radiomics signature and machine learning for the prediction and detection of various stages of kidney damage due to diabetes. Front Endocrinol (Lausanne). 2024 Nov 18;15:1333881. doi: 10.3389/fendo.2024.1333881. PMID: 39624821; PMCID: PMC11608948.
19.Liu S, Qiu B, Li Y, Wang HP, Zhong ZJ, Wang L. Trehalose prevents glyphosate-induced kidney damage in roosters by inhibiting apoptosis. Vet Res Commun. 2025 Jul 25;49(5):263. doi: 10.1007/s11259-025-10832-7. PMID: 40711623.
20.Futorian A, Armon L, Waldman Ben-Asher H, Shoval I, Hazut I, Munitz A, Urbach A. Nephron-Specific Lin28A Overexpression Triggers Severe Inflammatory Response and Kidney Damage. Int J Biol Sci. 2024 Jul 22;20(10):4044-4054. doi: 10.7150/ijbs.97434. PMID: 39113694; PMCID: PMC11302891.
21.Gubina-Vakulik GІ, Nakonechna OA, Sorokina IV, Gorbach ТV, Denisenko SA, Stepanova SI, Yarmysh NV. Experimental evidence of kidney damage following oral administration of gadolinium nanoparticles GdYVO4:Eu3. Wiad Lek. 2025;78(7):1302-1308. doi: 10.36740/WLek/208990. PMID: 40847863.
22.Zhang H, Li X, Bai J, Zhang C. Mice with NOP2/sun RNA methyltransferase 5 deficiency die before reaching puberty due to fatal kidney damage. Ren Fail. 2024 Dec;46(1):2349139. doi: 10.1080/0886022X.2024.2349139. Epub 2024 May 7. PMID: 38712768; PMCID: PMC11078075.
23.Chen Z, Tessmer G, Nguyen BA, Meyer J, Saleem M, Ahmad T, Bogle R, Tsoi LC, Yang TS, Gudjonsson JE, Kirabo A, Ward NL, Alexander MR. G-CSF Mediates Increased Renal Neutrophils and Kidney Damage in a Psoriasis Mouse Model. Hypertension. 2025 Nov;82(11):2027-2039. doi: 10.1161/HYPERTENSIONAHA.125.25111. Epub 2025 Sep 4. PMID: 40905133; PMCID: PMC12529989.
24.Erdemli Z, Gul M, Kayhan E, Gokturk N, Bag HG, Erdemli ME. High-fat and carbohydrate diet caused chronic kidney damage by disrupting kidney function, caspase-3, oxidative stress and inflammation. Prostaglandins Other Lipid Mediat. 2024 Jun;172:106822. doi: 10.1016/j.prostaglandins.2024.106822. Epub 2024 Feb 22. PMID: 38395139.
25.Ren H, Shen X. Molybdenum exposure causes kidney damage related to the excretion of heavy metals. Ecotoxicol Environ Saf. 2025 Sep 1;302:118635. doi: 10.1016/j.ecoenv.2025.118635. Epub 2025 Jul 9. PMID: 40639232.
26.Jiang S, Du L, Zhao Q, Su S, Huang S, Zhang J. Tropical postbiotics alleviate the disorders in the gut microbiota and kidney damage induced by ochratoxin A exposure. Food Funct. 2024 Apr 22;15(8):3980-3992. doi: 10.1039/d3fo05213c. Erratum in: Food Funct. 2025 Sep 29;16(19):7959-7960. doi: 10.1039/d5fo90079d. PMID: 38482731.
27.Zhou Q, Cui J, Liu Y, Gu L, Teng X, Tang Y. EGCG alleviated Mn exposure-caused carp kidney damage via trpm2-NLRP3-TNF-α-JNK pathway: Oxidative stress, inflammation, and tight junction dysfunction. Fish Shellfish Immunol. 2023 Mar;134:108582. doi: 10.1016/j.fsi.2023.108582. Epub 2023 Feb 7. PMID: 36754155.
Published
2026/05/04
Section
Original paper