Key result
Highest CRP quartile linked to higher arterial stiffness after 17 years versus lowest quartile.
Why the study?
Do elevated baseline acute phase proteins increase arterial stiffness (c-f PWV) in a general population cohort?
Cohort (n=2,338)
No
Do elevated baseline acute phase proteins increase arterial stiffness (c-f PWV) in a general population cohort?
Elevated baseline levels of alpha-1-antitrypsin, complement C3, and CRP are independently associated with increased arterial stiffness after 17 years of follow-up, suggesting low-grade inflammation contributes to vascular aging.
Answers are grounded in this paper and cite their sources.
Elevated baseline CRP signals higher long-term arterial stiffness risk; hypothesis-generating for inflammation in vascular aging, needs interventional confirmation.
BACKGROUND AND OBJECTIVES: Arterial stiffness plays a significant role in the development and progression of adverse cardiovascular events and all-cause mortality. This observational study aims to explore the relationship between six acute phase proteins namely, ceruloplasmin, alpha-1-antitrypsin, orosomucoid, haptoglobin, complement C3 and C-reactive protein (CRP), and carotid-femoral pulse wave velocity (c-f PWV) in a population-based cohort, and to also explore the effect of low-grade inflammation on the relationship between diabetes and c-f PWV. METHOD: The study consisted of participants from the Malmö Diet and Cancer study with data from baseline examinations (1991-1994) and follow-up examinations (2007-2012). Arterial stiffness was measured at follow-up by determining c-f PWV. After excluding participants with missing data, the total study population included 2338 subjects. General linear models were used to assess the relationship between baseline acute phase proteins and c-f PWV. RESULTS: After adjusting for traditional risk factors the participants in the 4th quartile vs 1st quartile of alpha-1-antitrypsin (geometric mean: 10.32 m/s vs 10.04 m/s) (p<0.05), C3 (10.35 m/s vs 10.06 m/s) (p<0.05) and CRP (10.37 m/s vs 9.96 m/s) (p<0.001) showed significant association with c-f PWV. Diabetes at follow-up was also associated with high c-f PWV, however, this relationship was independent of low grade inflammation. CONCLUSION: Alpha-1-antitrypsin, C3 and CRP are associated with arterial stiffness. The results indicate that low grade inflammation is associated with arterial stiffness in addition to established cardiovascular risk factors.
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Muhammad et al. (2017) conducted a cohort in Arterial stiffness (n=2,338). High acute phase proteins (4th quartile CRP) vs. Low acute phase proteins (1st quartile CRP) was evaluated on Carotid-femoral pulse wave velocity (c-f PWV) (p=<0.001). Participants in the highest quartile of C-reactive protein had significantly higher arterial stiffness compared to the lowest quartile (c-f PWV 10.37 m/s vs 9.96 m/s) after 17 years.
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