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Cyclophilins in Ischemic Heart Disease: Differences Between Acute and Chronic Coronary Artery Disease Patients
Jeremias Bayon1, Amparo Alfonso2, Sandra Gegunde2
1Cardiology Department, Hospital Universitario Lucus Augusti, c/Ulises Romero n°1, 27003 Lugo, Spain.
Insights
Cyclophilins A and C (CypA, CypC) are elevated in coronary artery disease (CAD) patients. High CypC serum levels may indicate a more severe CAD condition, serving as a potential novel biomarker.
Area of Science:
- Cardiovascular Research
- Biochemistry
- Immunology
Background:
- Cyclophilins (Cyps) are implicated in cardiovascular diseases via inflammation.
- This study investigates serum levels of four Cyps (CypA, CypB, CypC, CypD) in coronary artery disease (CAD).
Purpose of the Study:
- To determine serum levels of CypA, CypB, CypC, and CypD in CAD patients.
- To correlate these levels with clinical characteristics and inflammation markers.
Main Methods:
- An observational prospective study included 125 subjects (40 acute CAD, 40 chronic CAD, 45 controls).
- Serum levels of Cyps, interleukins, and metalloproteinases were measured.
Main Results:
- CypA levels were significantly higher in CAD patients versus controls.
- CypC levels were significantly higher in CAD patients (32.42 ± 3.71 pg/mL) compared to controls (9.38 ± 1.51 pg/mL).
- A CypC cut-off (> 17.5 pg/mL) correlated with older age, hypertension, dyslipidemia, and more extensive CAD.
Conclusions:
- Serum CypA and CypC levels are elevated in patients with coronary artery disease.
- Elevated CypC may serve as a novel biomarker for more severe CAD.
Background:
Cyclophilins (Cyps) are a family of peptidyl-prolyl cis/trans isomerases consistently involved in cardiovascular diseases through the inflammation pathway. This study aims to investigate the serum levels of Cyps (CypA, CypB, CypC and CypD) in patients with coronary artery disease (CAD) and the correlation with clinical characteristics and inflammation parameters.
Methods:
We developed an observational prospective study with a total of 125 subjects: 40 patients with acute CAD, 40 patients with chronic CAD and 45 control volunteers, in whom serum levels of Cyps (CypA, CypB, CypC and CypD), interleukins and metalloproteinases were measured.
Results:
CypA levels increased significantly in CAD patients compared with control subjects, but no differences were noted between acute CAD (7.80 ± 1.30 ng/mL) and chronic CAD (5.52 ± 0.76 ng/mL) patients (P = 0.13). No differences in CypB and CypD levels were showed between CAD patients and controls and between acute CAD and chronic CAD patients. In relation with CypC, the levels in CAD patients were significantly higher compared to controls (32.42 ± 3.71 pg/mL vs. 9.38 ± 1.51 pg/mL, P < 0.001), but no differences between acute and chronic CAD groups were obtained (P = 0.62). We analyzed the CypC > 17.5 pg/mL cut-off point, and it was significantly associated with older age, hypertension, dyslipidemia and more extensive CAD in acute and chronic CAD groups.
Conclusions:
CypA and CypC levels are increased in CAD patients. High CypC serum levels could be a novel biomarker in CAD patients correlating with a more severe disease.
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