Serum complement (C3, C4) levels in patients with acute myocardial infarction and angina pectoris
A S M Giasuddin1, Jamila M ElMahdawi, Fakhri M ElHassadi
1Department of Laboratory Medicine, Al-Arab Medical University, Benghazi, Libya. asmgias@proshikanet.com
Insights
Serum complement C3 and C4 levels are elevated in patients with acute myocardial infarction (AMI) and angina pectoris (AP). Levels increase further in AMI by day 7, indicating an inflammatory response.
Area of Science:
- Cardiology
- Immunology
- Biochemistry
Background:
- Serum complement proteins C3 and C4 play roles in inflammatory processes.
- Elevated complement levels are observed in various cardiovascular conditions.
Purpose of the Study:
- To investigate serum complement C3 and C4 levels in Libyan patients with acute myocardial infarction (AMI) and angina pectoris (AP).
- To compare complement levels between AMI and AP patients and healthy controls.
Main Methods:
- Serum C3 and C4 levels were measured in 31 AMI patients, 11 AP patients, and 26 healthy controls.
- Measurements were taken on the 1st and 7th day following the onset of symptoms.
- Statistical analysis included ANOVA and correlation tests.
Main Results:
- Both AMI and AP patients showed elevated C3 and C4 levels on day 1 compared to controls.
- C3 and C4 levels further increased in AMI patients by day 7, while remaining elevated in AP patients.
- Significant positive correlations between C3/C4 levels and disease severity were observed in AMI patients.
Conclusions:
- Serum C3 and C4 levels are elevated in both AMI and AP, suggesting an acute phase and inflammatory response.
- The more profound elevation in AMI patients indicates a stronger inflammatory component compared to AP.
Abstract:
Serum complement (C3, C4) levels in Libyan patients with acute myocardial infarction (AMI; 31 patients) and angina pectoris (AP; 11 patients) at the 1st day and 7th day of attack were estimated. A group of 26 healthy Libyans were taken as control subjects (CS). Serum C3 and C4 levels (mean +/- SD, mg/dl) were elevated at the 1st day in AMI as well as AP patients (C3 --> AMI1: 154.0 +/- 28.5, AP1: 152.0 +/- 45.0, CS: 132.0 +/- 8.0, ANOVA: p = 0.0072; C4 --> AMII1: 38 +/- 13, AP1: 37 +/- 17, CS: 29 +/- 6, ANOVA: p = 0.0160). No significant differences for the elevated C3 and C4 levels at the 1st day were observed between the two diseases groups (AMI1 vs AP1 --> C3: p = 0.879, C4: p = 0.818). At the 7th day, C3 and C4 levels were further elevated in AMI, while they remained at the similar elevated levels in AP (C3 --> AMI 7: 173.1 +/- 28.0, AP 7: 149.0 +/- 41.0, CS: 132.0 +/- 8.0, ANOVA: p = 0.0000; C4 --> AMI 7: 46.0 +/- 7.0, AP 7: 36.0 +/- 15.0, CS: 29.0 +/- 6.0, ANOVA: p = 0.0000). Again, no significance differences for the raised C3 and C4 levels at the 7th day was observed between AMI and AP patients (AMI 7 vs AP 7 --> C3: P = 0.059, C4: p = 0.06). The C3 elevation showed significant positive correlation in AMI group (r = 0.522, p = 0.003) while it was insignificant in AP patients (r = 0.037, p = 0.915). Regarding C4 levels, it was significantly correlated in AMI (r = 0.483, p = 0.006), and in AP, although it was positively correlated (r = 0.656, P = 0.028) the observed difference was not significant (t = 0.29, p = 0.778). In conclusion, serum C3 and C4 levels were more profoundly elevated in AMI compared to AP patients suggestive of an acute phase and inflammatory response.
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