Key result
Stenotic bicuspid aortic valves showed the same degree of T lymphocyte infiltration as degenerative tricuspid aortic valves, with no significant differences in extent or localisation.
Why the study?
Is there a difference in T lymphocyte infiltration between stenotic bicuspid and tricuspid aortic valves?
Observational (n=29)
No
Is there a difference in T lymphocyte infiltration between stenotic bicuspid and tricuspid aortic valves?
Stenotic bicuspid aortic valves show the same degree of T lymphocyte infiltration as degenerative tricuspid aortic valves, suggesting inflammation plays a role in the pathogenesis of acquired aortic stenosis regardless of primary valve anomaly.
Supports shared inflammatory mechanisms across aortic stenosis etiologies; leaves open whether immunomodulation could modify progression in bicuspid or tricuspid valves.
BACKGROUND: The two most common causes of aortic stenosis are primary "degenerative" calcification of tricuspid aortic valves and secondary calcification of congenital bicuspid valves. T lymphocyte infiltration occurs in stenotic tricuspid aortic valves, indicating an inflammatory component, but it has not been shown whether it also occurs in stenotic bicuspid valves. OBJECTIVE: To compare non-rheumatic tricuspid and bicuspid stenotic aortic valves for the presence and distribution of T lymphocytes. SETTING: University hospital. PATIENTS AND DESIGN: Valve specimens were obtained from 29 patients (15 women, 14 men, mean age 69 years (range 52-81 years)), referred to the hospital for aortic valve replacement because of symptomatic aortic valve stenosis. There were 17 tricuspid valves (from 10 women and seven men, mean age 71 years) and 12 bicuspid valves (from five women and seven men, mean age 67 years). To identify mononuclear inflammatory cells, sections were stained with antibodies for CD3 (pan-T cell antigen, Dako 1:400) and then graded histologically according to the degree of T cell infiltrate. RESULTS: T lymphocyte infiltration was present in both tricuspid and bicuspid stenotic aortic valves, without any significant differences in extent or localisation. CONCLUSIONS: Stenotic bicuspid aortic valves show the same degree of T lymphocyte infiltration as degenerative tricuspid aortic valves. Inflammation needs to be considered in the pathogenesis of acquired aortic stenosis, irrespective of the primary valve anomaly.
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Lars Wallby (2002) conducted an observational in Symptomatic aortic valve stenosis (n=29). Bicuspid aortic valve vs. Tricuspid aortic valve was evaluated on Presence and distribution of T lymphocytes. Stenotic bicuspid aortic valves showed the same degree of T lymphocyte infiltration as degenerative tricuspid aortic valves, with no significant differences in extent or localisation.
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