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Psychiatric symptoms are not associated with circulating CRP concentrations after controlling for medical, social,
Leandra K Figueroa-Hall1, Bohan Xu2,3, Rayus Kuplicki2
1Laureate Institute for Brain Research, Tulsa, OK, 74136, USA. lfigueroa-hall@laureateinstitute.org.
Insights
C-reactive protein (CRP) levels are linked to inflammation and cardiovascular risk. This study found no direct association between CRP and psychiatric symptoms like depression or substance use after adjusting for other factors, suggesting complex relationships.
Area of Science:
- Psychiatry and Immunology
- Biomarkers and Inflammation
Background:
- Elevated C-reactive protein (CRP) indicates inflammation and is a cardiovascular disease risk factor.
- Psychiatric populations, particularly those with depression, often exhibit higher CRP levels.
- Previous research suggests links between inflammation, anxiety, and substance abuse, with high comorbidity in depressed individuals.
Purpose of the Study:
- To investigate the association between depression and substance use symptoms with C-reactive protein (CRP) concentrations.
- To adjust for medical, social, and demographic covariates in a large psychiatric screening sample.
- To clarify the relationship between psychiatric symptoms and inflammation markers.
Main Methods:
- Multivariate linear regression analysis of 1,724 participants undergoing psychiatric screening.
- Assessment of depression using the Patient Health Questionnaire 9 (PHQ-9) and substance use with the Drug Abuse Screening Test (DAST).
- Analysis of C-reactive protein (CRP) concentrations against psychiatric symptoms, controlling for various covariates.
Main Results:
- Unadjusted models showed associations between PHQ-9 and CRP, and DAST and CRP in males.
- Adjusted models revealed significant associations of CRP with mood-stabilizer treatment, opioid medication, BMI, body fat percentage, nicotine use, and sleep disturbance.
- Specific covariates like oral contraceptive use and waist-to-hip ratio in females, and NSAID use in males, also correlated with CRP. No significant association was found between CRP and individual psychiatric symptoms after covariate adjustment.
Conclusions:
- The association between C-reactive protein (CRP) and psychiatric symptom severity is influenced by the covariates included in the analysis.
- Medical and lifestyle factors, rather than direct symptom severity, appear to be more strongly associated with CRP levels in this psychiatric screening population.
- Further research is needed to understand the complex interplay between inflammation, psychiatric conditions, and confounding variables.
Abstract:
Elevated serum concentrations (>3 mg/L) of the acute-phase protein, C-reactive protein (CRP), is used as a clinical marker of inflammation and is reported to be a strong risk factor for cardiovascular disease. In psychiatric populations, CRP concentration is reported to be higher in depressed versus healthy individuals. Positive associations between CRP and depression have been established in both clinical and community samples, but effect sizes are attenuated after controlling for confounding variables. Similarly, emerging research has begun to draw a link between inflammation, symptoms of anxiety, and substance abuse. Given the high level of comorbid anxiety and substance use disorders in many depressed populations, this study examined whether depression (Patient Health Questionnaire 9 [PHQ-9]) and substance use-related (Drug Abuse Screening Test [DAST]) symptoms were associated with CRP concentrations in the blood after adjusting for relevant medical, social, and demographic covariates in a large sample undergoing screening for several transdiagnostic psychiatric research studies. A total of 1,724 participants were analyzed for association of CRP with variables using multivariate linear regression. An unadjusted model with no covariates showed that PHQ-9 was significantly associated with CRP in All (β = 0.125), Female (β = 0.091), and Male (β = 0.154) participants, but DAST was significantly associated with CRP in males only (β = 0.120). For the adjusted model, in both males and females, mood-stabilizer treatment (β = 0.630), opioid medication (β = 0.360), body mass index (β = 0.244), percent body fat (β = 0.289), nicotine use (β = 0.063), and self-reported sleep disturbance (β = 0.061) were significantly associated with increased CRP concentrations. In females, oral contraceptive use (β = 0.576), and waist-to-hip ratio (β = 0.086), and in males, non-steroidal anti-inflammatory drug use (β = 0.367) were also associated with increased CRP concentrations. There was no significant association between CRP and individual depressive, anxiety, or substance use-related symptoms when covariates were included in the regression models. These results suggest that associations between circulating CRP and the severity of psychiatric symptoms are dependent on the type of covariates controlled for in statistical analyses.
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