Diagnostic utility of neutrophil to lymphocyte ratio in adult population of type 2 diabetes mellitus: A tertiary care centre experience

Authors

  • Kavya Varshney Author
  • Mukul Singh Author
  • Sonam Sharma Author
  • Sunil Ranga Author

DOI:

https://doi.org/10.18231/j.pjms.2024.148

Keywords:

Diabetes Mellitus, Glycated hemoglobin A, Ratios

Abstract

Background: Diabetes mellitus is a multifactorial, multisystemic, and chronic low-grade metabolic condition. Neutrophil to lymphocyte ratio (NLR) is a basic and novel parameter to assess underlying inflammation and diabetic control levels. This study aimed to compare the values of NLR between type 2 diabetes mellitus cases and normal healthy individuals. Also, to establish a possible correlation, if any between NLR and Glycated hemoglobin A (HbA1c).
Materials and Methods: This case-control study included 100 cases of type 2 diabetes mellitus patients and similar age & sex-matched healthy controls. The NLR in type 2 diabetic patients and healthy controls were compared to find a possible correlation between NLR and HbA1c levels.
Results : The mean NLR in type 2 diabetes mellitus patients (mean= 4.56±1.3) in comparison with the mean NLR of healthy controls (mean= 1.94±0.95) was found to be significantly elevated (p < 0> Conclusion : An elevated NLR in individuals with no pre-existing health conditions could potentially signify compromised glucose metabolism and ongoing low-level inflammation. Additionally, when paired with HbA1c, it serves as a dependable indicator of diabetes management in type 2 diabetes mellitus patients. NLR testing is a secure, uncomplicated, and budget-friendly method that is widely available and can be employed to track the advancement of diseases, ultimately lessening the risk of complications and fatalities.

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Published

2024-12-21

How to Cite

Diagnostic utility of neutrophil to lymphocyte ratio in adult population of type 2 diabetes mellitus: A tertiary care centre experience. (2024). Panacea Journal of Medical Sciences, 14(3), 830-833. https://doi.org/10.18231/j.pjms.2024.148

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