The prevalence of positive C-reactive protein and elevated erythrocyte sedimentation rate among individuals with type 2 diabetes mellitus and non-alcoholic fatty liver disease

Authors

  • Halime Aali Department of Internal Medicine, School of Medicine, Amir Al Momenin Hospital, Zabol University of Medical Sciences, Zabol, Iran
  • Jafar Poodineh Department of Clinical Biotechnology, School of Medicine, Zabol University of Medical Sciences, Zabol, Iran
  • Amirhossein Azariyan Student Research Committee, Zabol University of Medical Sciences, Zabol, Iran https://orcid.org/0009-0000-7118-8926

DOI:

https://doi.org/10.66224/jcbior.7.1.349

Keywords:

Type 2 diabetes mellitus, Non-alcoholic fatty liver disease, C-reactive protein, Erythrocyte sedimentation rate

Abstract

Chronic inflammation plays a central role in both type 2 diabetes mellitus (T2DM) and non-alcoholic fatty liver disease (NAFLD). This study evaluated the association of C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) among patients with T2DM, NAFLD, and concurrent disease. In this cross-sectional study, 150 participants were equally divided into three groups: T2DM or NAFLD, and concurrent T2DM and NAFLD. Demographic and clinical data were recorded, and CRP and ESR levels were measured. Statistical analyses included ANOVA, Kruskal–Wallis, Chi-square tests, and logistic regression models adjusted for age and gender by reporting odds ratios (ORs) and 95% confidence intervals (CIs). A p-value <0.05 was considered statistically significant. ESR levels differed significantly among groups (p <0.001), with the highest values observed in the T2DM+NAFLD group. Adjusted logistic regression showed that patients with T2DM+NAFLD had a 3.8-fold increased odds of elevated ESR compared to NAFLD alone (95% CI: 1.345–10.759, p=0.012). CRP positivity did not significantly differ between groups; however, categorical CRP analysis revealed significant distribution differences (p <0.001). Coexistence of T2DM and NAFLD is associated with greater systemic inflammatory burden, particularly reflected by elevated ESR. ESR may serve as a more sensitive inflammatory marker than CRP in patients with combined metabolic disorders.

References

1. Młynarska E, Czarnik W, Dzieża N, Jędraszak W, Majchrowicz G, Prusinowski F, et al. Type 2 Diabetes Mellitus: New Pathogenetic Mechanisms, Treatment and the Most Important Complications. Int J Mol Sci. 2025;26(3):1094.

DOI: 10.3390/ijms26031094 PMID: 39940862

2. Gieroba B, Kryska A, Sroka-Bartnicka A. Type 2 diabetes mellitus - conventional therapies and future perspectives in innovative treatment. Biochem Biophys Rep. 2025;42:102037. DOI: 10.1016/j.bbrep.2025.102037 PMID: 40395625

3. Faraji N, Abbaspour S, Ajamian F, Keshavarz P. Role of ENPP1 Gene Variants in the Susceptibility to Diabetic Nephropathy in Patients with type 2 Diabetes Mellitus. Biochem Genet. 2023;61(6):2710-2723.

DOI: 10.1007/s10528-023-10402-z PMID: 37231232

4. Yaseri M, Fayazi HS, Mortazavi SS, Faraji N. Uric Acid Level and Glycemic Status in Patients With Type 2 Diabetes. JGUMS. 2022;30(4):268-275.

URL: http://journal.gums.ac.ir/article-1-2393-en.html

5. Joukar F, Khoshgoftar SS, Ghanbari A, et al. Sleep quality and associated factors among individuals with and without diabetes: PERSIAN Guilan Cohort Study (PGCS). J Public Health (Berl). 2024;32:2083-2090. DOI: 10.1007/s10389-023-01958-6

6. Obeagu EI. Unraveling the connection: Inflammatory markers and diabetes mellitus pathogenesis. Medicine (Baltimore). 2026;105(4):e47338.

DOI: 10.1097/MD.0000000000047338 PMID: 41578487

7. Zhao L, Yuan J, Yang Q, Ma J, Yang F, Zou Y, et al. Diabetes and its complications: molecular mechanisms, prevention and treatment. Signal Transduct Target Ther. 2026;11(1):22.

DOI: 10.1038/s41392-025-02401-w PMID: 41549124

8. Roy B. Pathophysiological Mechanisms of Diabetes-Induced Macrovascular and Microvascular Complications: The Role of Oxidative Stress. Med Sci (Basel). 2025;13(3):87.

DOI: 10.3390/medsci13030087 PMID: 40700116

9. Khaled Elbaruni, Abdulwahed E, Khalfalla W, Alsudany R, Jerbi R, Alwaseea N, et al. Association Between Some Inflammatory Markers and HbA1c in Patients with Type 2 Diabetes Mellitus. Alq J Med App Sci. 2023;6(1):137-41. URL:https://journal.utripoli.edu.ly/index.php/Alqalam/article/view/230

10. Bassami F, Yavari M, Feizi A, Siavash M, Akbari M, Karimifar M. Association between high-sensitivity C-reactive protein and diabetic nephropathy: a systematic review and meta-analysis. BMC Nephrol. 2025;26(1):418.

DOI: 10.1186/s12882-025-04358-y PMID: 40713563

11. Seo YH, Shin HY. Relationship between hs-CRP and HbA1c in Diabetes Mellitus Patients: 2015-2017 Korean National Health and Nutrition Examination Survey. Chonnam Med J. 2021;57(1):62-67.

DOI: 10.4068/cmj.2021.57.1.62 PMID: 33537221

12. Bellentani S. The epidemiology of non-alcoholic fatty liver disease. Liver Int. 2017;37 Suppl 1:81-84.

DOI: 10.1111/liv.13299 PMID: 28052624

13. Amini-Salehi E, Letafatkar N, Norouzi N, Joukar F, Habibi A, Javid M, et al. Global Prevalence of Nonalcoholic Fatty Liver Disease: An Updated Review Meta-Analysis comprising a Population of 78 million from 38 Countries. Arch Med Res. 2024;55(6):103043.

DOI: 10.1016/j.arcmed.2024.103043 PMID: 39094335

14. Shahdkar M, Goorabzarmakhi MO, Shafizadeh M, Joukar F, Maroufizadeh S, Faraji N, et al. Association between dyslipidemia and elevated liver enzymes: a cross-sectional study from the PERSIAN Guilan cohort study. Endocrine Metab Sci. 2025:100272. DOI: 10.1016/j.endmts.2025.100272

15. Santos-Laso A, Gutiérrez-Larrañaga M, Alonso-Peña M, Medina JM, Iruzubieta P, Arias-Loste MT, et al. Pathophysiological Mechanisms in Non-Alcoholic Fatty Liver Disease: From Drivers to Targets. Biomedicines. 2021;10(1):46.

DOI: 10.3390/biomedicines10010046 PMID: 35052726

16. Ashoobi MT, Joukar F, Mojtahedi K, Maroufizadeh S, Javid M, Parvaneh A, et al. Elevated liver enzymes and diabetes in the PERSIAN Guilan cohort study. Caspian J Intern Med. 2024;16(1):73-82. DOI: 10.22088/cjim.16.1.73 PMID: 39619755

17. Caturano A, Nilo D, Lorenzo GD, Rocco M, Tagliaferri G, Piacevole A, et al. Cardiovascular Health in the Shadow of Diabetes and Metabolic Dysfunction-Associated Steatotic Liver Disease: An Emerging Paradigm. Rev Cardiovasc Med. 2025;26(11):43143.

DOI: 10.31083/RCM43143 PMID: 41356318

18. Kosmalski M, Ziółkowska S, Czarny P, Szemraj J, Pietras T. The Coexistence of Nonalcoholic Fatty Liver Disease and Type 2 Diabetes Mellitus. J Clin Med. 2022;11(5):1375.

DOI: 10.3390/jcm11051375 PMID: 35268466

19. Ding Z, Wei Y, Peng J, Wang S, Chen G, Sun J. The Potential Role of C-Reactive Protein in Metabolic-Dysfunction-Associated Fatty Liver Disease and Aging. Biomedicines. 2023;11(10):2711. DOI: 10.3390/biomedicines11102711 PMID: 37893085

20. Alharthi AH, Al-Shehri SH, Albarqi MA, Alshehri MS, Alshehri AM, Amer AM, Alshehri MH, Alshehri AH, Alshehri SH, Alassiry AM. Laboratory Markers of Inflammation: CRP and ESR in Clinical Practice. J Int Crisis Risk Commun Res. 2024; 7(S8):2376-92. DOI: https://doi.org/10.63278/jicrcr.vi.1233

21. Rajbhandari PM, Gyawali P, Mahato RV, Chaudhary D. A Cross-Sectional Prospective Study of Glycated Hemoglobin (HbA1c) and Fasting Blood Glucose (FBG) Level In Both Diabetic and Non-Diabetic Patients in Context to Nepalese General Population. MJ Diab. 2017;2(2):007. URL: https://www.mathewsopenaccess.com/scholarly-articles/a-cross-sectional-prospective-study-of-glycated-hemoglobin-hba1c-and-fasting-blood-glucose-fbg-level-in-both-diabetic-and-non-diabetic-patients-in-context-to-nepalese-general-population.pdf

22. Kotsiliti E. NAFLD prevalence in older patients with T2DM. Nat Rev Gastroenterol Hepatol. 2023;20(2):65.

DOI: 10.1038/s41575-022-00733-4 PMID: 36526903

23. Goh GB, Pagadala MR, Dasarathy J, Unalp-Arida A, Sargent R, Hawkins C, et al. Clinical spectrum of non-alcoholic fatty liver disease in diabetic and non-diabetic patients. BBA Clin. 2014;3:141-5.

DOI: 10.1016/j.bbacli.2014.09.001 PMID: 26675585

24. Obeagu EI, Muhimbura E, Kagenderezo BP, Nakyeyune S, Obeagu GU. An Insight of Interleukin -6 and Fibrinogen: In Regulating the Immune System. J Biomed Sci. 2022;11(10):83. DOI: 10.36648/2254-609X.11.10.83

25. Wu D, Lan Y, Chen S, Ding X, Chen G, Wu C, et al. Combined effect of adiposity and elevated inflammation on incident type 2 diabetes: a prospective cohort study. Cardiovasc Diabetol. 2023;22(1):351.

DOI: 10.1186/s12933-023-02067-0 PMID: 38124083

26. Cai Z, Huang Y, He B. New Insights into Adipose Tissue Macrophages in Obesity and Insulin Resistance. Cells. 2022;11(9):1424. DOI: 10.3390/cells11091424 PMID: 35563728

27. Xu GX, Wei S, Yu C, Zhao SQ, Yang WJ, Feng YH, et al. Activation of Kupffer cells in NAFLD and NASH: mechanisms and therapeutic interventions. Front Cell Dev Biol. 2023;11:1199519.

DOI: 10.3389/fcell.2023.1199519 PMID: 37261074

28. Sukumar M, Vikram NK, Ranjan P, Pandey M, Bhalla AS, Ramakrishnan L, et al. Linking Non-alcoholic Fatty Liver Disease Severity With Metabolic Syndrome Features: An Integrative Study on Clinical and Radiological Fronts. Cureus. 2024;16(5):e59788.

DOI: 10.7759/cureus.59788 PMID: 38846245

29. Christopher Aloy Simeon, Godae Fidelis Beega, Sheudeen Abubakar Abiola, Chinwendu Doris Wofuru, Chinemerem Cynthia Eze. Significance of inflammatory biomarkers in clinical diagnostics: Erythrocyte sedimentation rate versus other inflammatory biomarkers: A review. Int J Sci Res Arch. 2024;12(02):1980-1995. DOI: 10.30574/ijsra.2024.12.2.1469

30. Moursi EY, Moez PE, Hassouna EM, Elkemary EZ, Marei GM, Shater MSS, et al. MALAT1 and MEG3 genes expression in non-alcoholic fatty liver disease in type 2 diabetes mellitus patients: a case-control study. Alex J Med. 2023;59(1):86-94.

DOI: 10.1080/20905068.2023.2251221

31. González P, Lozano P, Ros G, Solano F. Hyperglycemia and Oxidative Stress: An Integral, Updated and Critical Overview of Their Metabolic Interconnections. Int J Mol Sci. 2023;24(11):9352.

DOI: 10.3390/ijms24119352 PMID: 37298303

32. Li F, Guan Z, Gao Y, Bai Y, Zhan X, Ji X, et al. ER stress promotes mitochondrial calcium overload and activates the ROS/NLRP3 axis to mediate fatty liver ischemic injury. Hepatol Commun. 2024;8(4):e0399.

DOI: 10.1097/HC9.0000000000000399 PMID: 38497930

33. Mehta M, Shah J, Joshi U. Understanding Insulin Resistance in NAFLD: A Systematic Review and Meta-Analysis Focused on HOMA-IR in South Asians. Cureus. 2024;16(10):e70768.

DOI: 10.7759/cureus.70768 PMID: 39364176

34. Elimam H, Abdulla AM, Taha IM. Inflammatory markers and control of type 2 diabetes mellitus. Diabetes Metab Syndr. 2019;13(1):800-804.

DOI: 10.1016/j.dsx.2018.11.061 PMID: 30641811

35. Liu-Galvin R, Orlando FA, Saguil AA, Jo A, Smith KB, Miller AM, et al. More evidence of the health risks of normal weight obesity: the association with systemic inflammation. Front Med (Lausanne). 2025;12:1695935.

DOI: 10.3389/fmed.2025.1695935 PMID: 41341825

36. Tsuriya D, Morita H, Morioka T, Takahashi N, Ito T, Oki Y, et al. Significant correlation between visceral adiposity and high-sensitivity C-reactive protein (hs-CRP) in Japanese subjects. Intern Med. 2011;50(22):2767-73.

DOI: 10.2169/internalmedicine.50.5908 PMID: 22082888

37. Wiwanitkit V. Haematological parameters in patients with non-alcoholic fatty liver disease and alcoholic liver disease: concern on findings. Singapore Med J. 2011;52(5):382. PMID: 21633779

38. Neuman G, Sagi R, Shalitin S, Reif S. Serum inflammatory markers in overweight children and adolescents with non-alcoholic fatty liver disease. Isr Med Assoc J. 2010;12(7):410-5. PMID: 20862821

39. Caussy C, Aubin A, Loomba R. The Relationship Between Type 2 Diabetes, NAFLD, and Cardiovascular Risk. Curr Diab Rep. 2021;21(5):15.

DOI: 10.1007/s11892-021-01383-7 PMID: 33742318

40. Matyas C, Haskó G, Liaudet L, Trojnar E, Pacher P. Interplay of cardiovascular mediators, oxidative stress and inflammation in liver disease and its complications. Nat Rev Cardiol. 2021;18(2):117-135.

DOI: 10.1038/s41569-020-0433-5 PMID: 32999450

41. Airola C, Pallozzi M, Cerrito L, Santopaolo F, Stella L, Gasbarrini A, et al. Microvascular Thrombosis and Liver Fibrosis Progression: Mechanisms and Clinical Applications. Cells. 2023;12(13):1712.

DOI: 10.3390/cells12131712 PMID: 37443746

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Published

2026-03-30

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How to Cite

The prevalence of positive C-reactive protein and elevated erythrocyte sedimentation rate among individuals with type 2 diabetes mellitus and non-alcoholic fatty liver disease. (2026). Journal of Current Biomedical Reports, 7(1). https://doi.org/10.66224/jcbior.7.1.349

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