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Association of Biomarkers with the Severity of Depression
Shruti Agnihotri1, Suresh Daripelly1, Shirley Keerthana Cherla1
1Dept. of Psychiatry, Gandhi Medical College and Hospital, Secunderabad, Telangana, India.
Insights
Depression may be linked to systemic inflammation, high cortisol, and low magnesium. These markers, including C-reactive protein and neutrophil-lymphocyte ratio, correlate with depression severity, suggesting a biological basis.
Area of Science:
- Neuroscience
- Psychiatry
- Immunology
Background:
- The exact causes of depression are not fully understood.
- Emerging research suggests a potential role for low-grade systemic inflammation in depression's development.
- Serum magnesium and cortisol levels are also investigated as potential contributing factors.
Purpose of the Study:
- To investigate the association between inflammatory markers, serum magnesium, serum cortisol, and the severity of depression.
- To explore the potential biological underpinnings of depressive disorders.
Main Methods:
- A cross-sectional study was conducted with 40 participants.
- Data collected included socio-demographics and depression severity assessed by the Hamilton Depression Rating Scale (HAM-D).
- Blood samples were analyzed for C-reactive protein (CRP), neutrophil-lymphocyte ratio (NLR), serum magnesium, and serum cortisol.
Main Results:
- Participants exhibited elevated levels of CRP and NLR, indicating systemic inflammation.
- Serum cortisol levels were higher, while serum magnesium levels were lower in the study group.
- All measured markers (CRP, NLR, cortisol, and magnesium) showed significant correlations with depression severity (HAM-D scores).
Conclusions:
- Depressive disorders are characterized by a state of systemic inflammation.
- Hypercortisolemia (elevated cortisol) and hypomagnesemia (low magnesium) are observed in individuals with depression.
- These findings highlight potential biomarkers and pathophysiological pathways involved in depression.
Background:
The pathogenesis of depression remains elusive and uncertain. The literature suggests that low-grade systemic inflammation might contribute to the etiology of depression. Other markers that are studied are serum magnesium and serum cortisol. The association between these factors might help understand the etiology.
Methods:
This was a cross-sectional study conducted on a sample of 40 participants. Socio-demographic data was noted, and the Hamilton depression rating scale was applied to rate the severity of depression. Blood samples were drawn at 8 a.m. to record a complete blood picture (to derive the neutrophil-lymphocyte ratio (NLR)), C-reactive protein, serum magnesium, and serum cortisol.
Results:
In this study, conducted on a sample size of 40, inflammatory markers such as C-reactive protein (CRP: mg/dl) and NLR were significantly increased to 15.52 ± 13.10 and 6.46 ± 2.92, respectively, showing an underlying inflammatory pathology. Serum cortisol (µg/dl) was also raised to 22.30 ± 5.46, and there was a fall in serum magnesium. Also, it is noteworthy that all these markers were significantly associated with the severity of depression, as the Pearson correlation between the Hamilton depression rating scale-21 item (HAM-D-21) score and CRP, NLR, and serum cortisol was positive and statistically significant (r = 0.55, p < .01; r = 0.51, p = .01; r = 0.46, p = .002). The Pearson correlation between the HAM-D score and serum magnesium was negative and statistically significant (r = -0.82, p < .01).
Conclusion:
There is a state of systemic inflammation, hypercortisolemia, and hypomagnesemia in depressive disorders.
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