Circulating endothelial progenitor cell dysfunction in patients with bipolar disorder
Ying-Jay Liou1,2, Mu-Hong Chen1,2,3, Ju-Wei Hsu1,2
1Department of Psychiatry, Taipei Veterans General Hospital, No. 201, Shih-Pai Road, Sec. 2, 11217, Taipei, Taiwan.
Insights
Circulating endothelial progenitor cells (cEPCs) show impaired adhesive function in bipolar disorder (BPD), linked to manic symptoms. Lower apoptosis in cEPCs correlates with cognitive deficits in BPD patients.
Area of Science:
- Cardiovascular Research
- Neuroscience
- Cell Biology
Background:
- Circulating endothelial progenitor cells (cEPCs) are vital for cardiovascular health.
- Bipolar disorder (BPD) patients face elevated cardiovascular disorder (CVD) risks.
- Understanding cEPC dysfunction in BPD is crucial for risk assessment.
Purpose of the Study:
- To investigate the functional characteristics of cEPCs in BPD.
- To correlate cEPC function with BPD clinical and cognitive features.
Main Methods:
- Compared cEPC adhesion and apoptosis in 69 BPD patients and 41 healthy controls (HCs).
- Assessed BPD symptoms using YMRS, CGI-BP, HDRS, MADRS, HARS, DSS.
- Evaluated cognitive function via 2-back and Go/No-Go tasks.
Main Results:
- BPD patients exhibited significantly reduced cEPC adhesive function compared to HCs (Pcorr=0.027).
- Lower cEPC adhesion correlated with higher YMRS (Pcorr=0.0002) and CGI-BP (Pcorr=0.0009) scores.
- Reduced cEPC apoptosis linked to increased errors in 2-back (Pcorr=0.028) and Go/No-Go (Pcorr=0.029) tasks.
Conclusions:
- BPD is associated with attenuated cEPC adhesive function.
- Altered cEPC adhesion and apoptosis correlate with BPD symptom severity and cognitive deficits, particularly response inhibition.
Abstract:
Dysfunction in circulating endothelial progenitor cells (cEPCs) plays a crucial role in cardiovascular disorders (CVDs). Patients with bipolar disorder (BPD) are at increased risk of developing CVDs. This study examined the associations of the functional properties of cEPCs with BPD and its clinical and cognitive characteristics. We recruited 69 patients with BPD and 41 healthy controls (HCs). The levels of manic, depressive, anxiety, psychosomatic symptoms, subjective cognitive dysfunction, quality of life, and functional disability of the BPD group were evaluated using the Young Mania Rating Scale (YMRS), Clinical Global Impression for BPD (CGI-BP), Hamilton Depression Rating Scale, Montgomery-Åsberg Depression Rating Scale, Hamilton Anxiety Rating Scale, Depression and Somatic Symptoms Scale, Perceived Deficits Questionnaire-Depression, 12-Item Short-Form Health Survey, and Sheehan Disability Scale, respectively. Cognitive function was assessed using 2-back and Go/No-Go tasks. Through in vitro assays, the adhesion to fibronectin and the percentage of apoptosis of cEPCs were examined. Under correction for multiple comparisons, the adhesive function of cEPCs in BPD was significantly lower than that in the HCs (corrected P [Pcorr] = 0.027). The reduced adhesive function of cEPCs correlated significantly with increased scores in the YMRS (Pcorr = 0.0002) and the CGI-BP (Pcorr = 0.0009). A lower percentage of apoptotic cEPC cells was associated with greater commission errors in the 2-back (Pcorr = 0.028) and Go/No-Go tasks (Pcorr = 0.029). The cEPCs of the BPD group exhibited attenuated adhesive function. The altered adhesive and apoptotic functions of cEPCs are associated with manic symptom severity and response inhibition deficits in patients with BPD.
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