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May 1, 1999Arteriosclerosis Thrombosis and Vascular Biology411 citations

Presence of Oxidized Low Density Lipoprotein in Nonrheumatic Stenotic Aortic Valves

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MOMargareta OlssonJTJohan ThybergJNJan Nilsson

Key Result

Oxidized LDLs colocalized with T-lymphocytes, macrophages, and calcium deposits in stenotic aortic valves, whereas control valves showed no signs of inflammation.

Key Points

  • To determine whether low-density lipoprotein (LDL) particles accumulated in stenotic aortic valve tissue undergo oxidative modification.
  • Analyzed 6 tricuspid stenotic valves excised during valve replacement alongside 3 non-stenotic control valves collected during heart transplantation.
  • Performed Oil Red O staining for neutral lipids and immunohistochemistry for apolipoprotein B (apoB), 4-hydroxynonenal-modified LDL, leukocyte markers, and HLA-DR.
  • Extracellular neutral lipids and apoB were present in all stenotic valves and colocalized with 4-hydroxynonenal-modified (oxidized) LDL along the fibrosa layer.
  • Oxidized LDLs localized around calcium deposits, subendothelially, and in deep fibrosa layers, colocalizing directly with macrophages, T lymphocytes, and HLA-DR expression, whereas control valves showed minimal lipids and no inflammatory infiltrate.

Study Design

Type

Observational (n=9)

PICO

P
Population
Nonrheumatic stenotic aortic valves (n=9)
I
Intervention / Comparator
Stenotic aortic valves vs Control valves
O
Primary Outcome
Presence and localization of oxidized LDL, neutral lipids, and inflammatory cells

Abstract

The aim of the present study was to analyze if LDL particles trapped in stenotic aortic valve tissue undergo oxidative modification. Degenerative aortic stenosis affects >3% of the population >75 years of age in the Western world. Recent studies have revealed the presence of a chronic inflammatory process similar to what has been described in other degenerative diseases such as atherosclerosis. However, the underlying disease mechanisms of degenerative aortic stenosis still remain largely unknown. Six tricuspid stenotic valves, obtained at valve replacement, were compared with 3 control valves collected from hearts taken out during transplantation. The stenotic valves and the control valves were examined by immunohistochemistry, using antibodies against apoB, 4-hydroxynonenal-modified LDL, leukocytes, and HLA-DR. All valves were also stained with oil red O for neutral lipids. Extracellular neutral lipids were found in all stenotic valves, extending from the bases along the fibrosa layer. This lipid colocalized with apoB- and 4-hydroxynonenal-modified LDL immunoreactivity. 4-Hydroxynonenal-modified LDLs were present around calcium deposits, subendothelially, and in the deeper layer of the fibrosa. There was also a colocalization with macrophages, T lymphocytes, and HLA-DR expression. Control valves had a thin area of neutral lipid accumulation, a small amount of apoB, but no signs of inflammation. A distinct colocalization between oxidized LDLs, T-lymphocyte accumulation, and calcium deposits suggests that oxidized lipids may play a role in the disease process.

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Cite This Study

Olsson et al. (1999) conducted an observational in Nonrheumatic stenotic aortic valves (n=9). Stenotic aortic valves vs. Control valves was evaluated on Presence and localization of oxidized LDL, neutral lipids, and inflammatory cells. Oxidized LDLs colocalized with T-lymphocytes, macrophages, and calcium deposits in stenotic aortic valves, whereas control valves showed no signs of inflammation.

synapsesocial.com/papers/6a0d6b666e03bc61cb09c05fhttps://doi.org/10.1161/01.atv.19.5.1218
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