Interplay between PAPP-A, inflammation and adiposity in patients with angiographically proven acute coronary syndrome
Abstract:
Introduction Studies conducted in the recent past have demonstrated the role of inflammation, obesity and dysfunctional insulin signaling as contributing factors in the pathogenesis of acute coronary syndrome (ACS). However, pharmacological interventions targeting a single pathway have not proven useful in the long run. This indicates that a synergism occurs between the various risk factors and hence calls for a combinatorial approach. This study was planned to study the interplay, if any, between pregnancy associated plasma protein-A (PAPP-A), inflammation and adiposity in patients with ACS. Materials and methods The study was conducted in a tertiary care hospital in Delhi. The study population consisted of 128 subjects, divided into two groups. The control group consisted of 64 healthy subjects without ACS. Cases consisted of 64 subjects with angiographically proven ACS cases. PAPP-A and high sensitivity C-reactive protein (hs-CRP) were estimated by enzyme-linked immunosorbent assay (ELIZA) kits. Results The mean level of PAPP-A and hs-CRP were significantly higher in cases as compared to the controls. A positive correlation of PAPP-A was observed with hs-CRP, insulin, ApoB and Lp(a). The relative risk for ACS was 14.2 with a p value of <0.001 when all the three parameters - hs-CRP, PAPP-A and body mass index (BMI) were considered together. This was significantly higher when each risk factor was assessed standalone. Conclusions Our study results suggest a possible interplay between chronic inflammation, obesity and plaque instability among patients with ACS. This interaction can accelerate the process of plaque rupture in patients with increased BMI as compare to those patients with low/normal BMI.
Insights
This study reveals a significant interplay between inflammation, obesity, and pregnancy-associated plasma protein-A (PAPP-A) in acute coronary syndrome (ACS) patients. Combined risk factors, including PAPP-A, hs-CRP, and BMI, dramatically increase ACS risk.
Area of Science:
- Cardiology
- Biochemistry
- Metabolic Syndrome
Background:
- Inflammation, obesity, and insulin resistance are implicated in acute coronary syndrome (ACS) pathogenesis.
- Single-pathway interventions for ACS have limited long-term efficacy, suggesting synergistic interactions between risk factors.
- Understanding these complex interactions is crucial for developing effective combinatorial therapeutic approaches.
Purpose of the Study:
- To investigate the interplay between pregnancy-associated plasma protein-A (PAPP-A), inflammation, and adiposity in patients with ACS.
- To determine if PAPP-A, hs-CRP, and BMI collectively influence ACS risk.
- To explore the relationship between these factors and plaque instability in ACS.
Main Methods:
- A case-control study involving 128 subjects (64 ACS patients, 64 controls) in a tertiary care hospital.
- Estimation of PAPP-A and high-sensitivity C-reactive protein (hs-CRP) using enzyme-linked immunosorbent assay (ELISA) kits.
- Analysis of correlations between PAPP-A, hs-CRP, insulin, ApoB, Lp(a), and body mass index (BMI).
Main Results:
- Mean levels of PAPP-A and hs-CRP were significantly elevated in ACS patients compared to controls.
- PAPP-A showed a positive correlation with hs-CRP, insulin, ApoB, and Lp(a).
- The combined assessment of hs-CRP, PAPP-A, and BMI yielded a significantly higher relative risk (14.2, p<0.001) for ACS compared to individual factors.
Conclusions:
- A significant interplay exists between chronic inflammation, obesity, and plaque instability in ACS patients.
- Increased BMI exacerbates plaque rupture risk in the presence of elevated PAPP-A and inflammation.
- These findings support a combinatorial approach to managing ACS risk by addressing multiple interacting factors.
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