TY - JOUR
T1 - Serum amyloid A in atherosclerosis
AU - King, Victoria L.
AU - Thompson, Joel
AU - Tannock, Lisa R.
PY - 2011/8
Y1 - 2011/8
N2 - Purpose of Review: Serum amyloid A (SAA) is a family of acute-phase proteins which are shown to correlate with cardiovascular disease, but whether this SAA contributes causally to atherosclerosis development or reflects underlying disease or risk factors remains unclear. Recent Findings: SAA has been detected within atherosclerotic lesions and within adipose tissue where it is hypothesized that it may play a contributory role in disease development. In the acute-phase response SAA is synthesized by the liver and transported primarily in association with HDL. However, there is a growing literature suggesting that localized synthesis of SAA within the vasculature, or adipose tissue, may play a distinct role in disease development. Furthermore, SAA can be found in association with apoB-containing lipoproteins, in which its biological activity may be different. Summary: This review will discuss recent experimental evidence supporting a causal role of SAA with atherosclerosis.
AB - Purpose of Review: Serum amyloid A (SAA) is a family of acute-phase proteins which are shown to correlate with cardiovascular disease, but whether this SAA contributes causally to atherosclerosis development or reflects underlying disease or risk factors remains unclear. Recent Findings: SAA has been detected within atherosclerotic lesions and within adipose tissue where it is hypothesized that it may play a contributory role in disease development. In the acute-phase response SAA is synthesized by the liver and transported primarily in association with HDL. However, there is a growing literature suggesting that localized synthesis of SAA within the vasculature, or adipose tissue, may play a distinct role in disease development. Furthermore, SAA can be found in association with apoB-containing lipoproteins, in which its biological activity may be different. Summary: This review will discuss recent experimental evidence supporting a causal role of SAA with atherosclerosis.
KW - HDL
KW - cardiovascular disease
KW - inflammation
KW - obesity
KW - proteoglycans
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U2 - 10.1097/MOL.0b013e3283488c39
DO - 10.1097/MOL.0b013e3283488c39
M3 - Review article
C2 - 21734573
AN - SCOPUS:79960648848
SN - 0957-9672
VL - 22
SP - 302
EP - 307
JO - Current Opinion in Lipidology
JF - Current Opinion in Lipidology
IS - 4
ER -