The value of the platelet/high-density lipoprotein cholesterol ratio in predicting depression and its cardiovascular
Huifeng Zhang1, Ying Xu2, Yaying Xu3
1Department of Cardiovascular, The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang, China.
Insights
The platelet-to-HDL-C ratio (PHR) is linked to increased depression risk and cardiovascular disease (CVD) mortality in US adults. PHR also shows better depression prediction than HDL-C and mediates the link between Life's Essential 8 and depression.
Area of Science:
- Cardiovascular Health
- Mental Health
- Biomarker Research
Background:
- Cardiovascular disease (CVD) and depression share bidirectional links, often influenced by inflammation and metabolic factors.
- The platelet-to-HDL-C ratio (PHR), a novel inflammatory and metabolic marker, has not been extensively studied in relation to both CVD and depression.
Purpose of the Study:
- To investigate the association between the platelet-to-HDL-C ratio (PHR) and depression in U.S. adults.
- To examine the relationship between PHR and cardiovascular disease (CVD) mortality in individuals with depression.
- To evaluate PHR's predictive performance for depression compared to HDL-C and its mediating role in the association between Life's Essential 8 (LE8) and depression.
Main Methods:
- Utilized data from the 2005-2018 National Health and Nutrition Examination Survey (NHANES) database for participants aged 20 and older.
- Calculated PHR and diagnosed depression using the Patient Health Questionnaire (PHQ-9). Employed weighted logistic regression, restricted cubic spline (RCS), and weighted COX regression analyses.
- Assessed predictive accuracy using Receiver Operating Characteristic (ROC) curves and explored mediation using mediation analysis.
Main Results:
- A higher PHR was significantly associated with an increased odds ratio for depression (OR=1.06 per SD increase) and a higher risk of CVD mortality in depressed patients (HR=1.38 per SD increase).
- PHR demonstrated a better predictive advantage for depression than HDL-C (AUC for PHR=0.556 vs. HDL-C=0.536).
- PHR was found to mediate 5.02% of the association between Life's Essential 8 (LE8) scores and depression.
Conclusions:
- Increased PHR is linearly associated with higher depression risk and CVD mortality among U.S. adults with depression.
- PHR exhibits superior predictive capability for depression compared to HDL-C.
- PHR acts as a significant mediator in the relationship between LE8 scores and depression, highlighting its potential clinical relevance.
Background:
Cardiovascular disease (CVD) and depression have a bidirectional association, with inflammation and metabolic factors being common important triggers for both conditions. However, as a novel inflammatory and metabolic marker, platelet-to-HDL-C ratio (PHR) has not been established in relation to depression and cardiovascular disease.
Materials And Methods:
Participants aged 20 years and older were included in the 2005-2018 NHANES database. PHR was calculated as the ratio of platelet count (1000 cells/μL) to HDL-C (mmol/L). The Patient Health Questionnaire (PHQ-9) was used to diagnose depression, with a cutoff value of 10. Weighted logistic regression analysis and restricted cubic spline (RCS) analysis were employed to examine the association between PHR and depression-related features. Additionally, weighted COX regression and RCS were used to analyze the association of PHR with CVD mortality in patients with depression. Receiver operating characteristic curves were used to assess whether PHR had an advantage over HDL-C in predicting depression. Finally, the mediating role of PHR in the latest cardiovascular health indicator Life's Essential 8 and depression was explored.
Results:
A total of 26,970 eligible participants were included, including 2,308 individuals with depression, representing approximately 160 million U.S. adults when weighted. After full adjustment, we estimated that the odds ratio (OR) of depression associated with a per standard deviation (SD) increase in PHR was 1.06 (95% CI: 1.01-1.12, P=0.03). The restricted cubic spline (RCS) analysis indicated a linear association (Nonlinear P=0.113). When PHR was divided into four groups based on quartiles and included in the model after full adjustment for depression risk factors, participants in quartile 2, quartile 3, and quartile 4 of PHR showed a trend of increasing risk of depression compared to the lowest quartile group (P trend=0.01). In addition, weighted COX regression and RCS revealed that a per SD increase in PHR was associated with a higher risk of CVD mortality among patients with depression (HR: 1.38, 95% CI: 1.05-1.81, P=0.02, Nonlinear P=0.400). Subgroup analyses showed that current alcohol consumption enhanced the association between PHR and depression (P for interaction=0.017). Furthermore, the areas under the ROC curves (AUC) were 0.556 (95% CI, 0.544-0.568; P < 0.001) for PHR and 0.536 (95% CI, 0.524-0.549; P < 0.001) for HDL-C (PDeLong = 0.025). Finally, mediation analysis indicated that PHR was an intermediate mechanism between LE8 and depression (mediation proportion=5.02%, P=0.02).
Conclusion:
In U.S. adults, an increase in PHR linearly increases the risk of depression and CVD mortality among individuals with depression. Additionally, PHR has a better predictive advantage for depression compared to HDL-C. Furthermore, PHR significantly mediates the association between LE8 scores and depression.
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