TY - JOUR
T1 - Renal artery plaque composition is associated with changes in renal frame count following renal artery stenting
AU - Prasad, Anand
AU - Ilapakurti, Manjusha
AU - Hu, Patrick
AU - Zafar, Nayab
AU - Palakodeti, Vachaspathi
AU - Tsimikas, Sotirios
AU - Mahmud, Ehtisham
PY - 2011/6
Y1 - 2011/6
N2 - Background: Benefit of percutaneous revascularization for atherosclerotic renal artery stenosis (RAS) may be attenuated by distal embolization of atheroemboli. The purpose of this study was to characterize RAS plaque composition with intravascular ultrasound virtual histology (IVUS-VH) and to explore the relationship between plaque components and renal frame count (RFC) after renal revascularization. METHODS: Seventeen patients (75 ± 7.5 years; 18 lesions) undergoing RAS revascularization were included. Before stenting, automated IVUS-VH pullback (0.5 mm/sec) with analysis of the minimal luminal diameter (MLD) frame and entire atherosclerotic segment was performed. RFC was also determined before and after stenting. Results: The VH component analysis of the segment demonstrated predominantly fibrous tissue (56.3 ± 11.4), followed by necrotic core (21.8 ± 8.6), dense calcification (13.2 ± 6.6) and fibrofatty tissue (8.7 ± 4.0). Analysis of the MLD frame also demonstrated mostly fibrous tissue (62.1 ± 11.1), with smaller amounts of necrotic core (15.6 ± 7.3), fibrofatty (13.9 ± 9.6), and dense calcification (8.4 ± 6.0). A trend toward more fibrous tissue (p ≤ 0.074), less necrotic core (p ≤ 0.095) and less dense calcification (p ≤ 0.075) at the MLD compared to the segment was observed. Analysis of the entire atherosclerotic segment revealed a positive correlation between necrotic core and change in RFC (r ≤ 0.582; p ≤ 0.029), with increasing necrotic core associated with an increase in RFC after revascularization. Conclusion: Both the MLD frame and segmental analysis of atherosclerotic RAS lesions demonstrate predominantly fibrous tissue with smaller amounts of necrotic core, fibrofatty tissue, and dense calcification. Increased necrotic core correlates with a lack of improvement in RFC after stenting.
AB - Background: Benefit of percutaneous revascularization for atherosclerotic renal artery stenosis (RAS) may be attenuated by distal embolization of atheroemboli. The purpose of this study was to characterize RAS plaque composition with intravascular ultrasound virtual histology (IVUS-VH) and to explore the relationship between plaque components and renal frame count (RFC) after renal revascularization. METHODS: Seventeen patients (75 ± 7.5 years; 18 lesions) undergoing RAS revascularization were included. Before stenting, automated IVUS-VH pullback (0.5 mm/sec) with analysis of the minimal luminal diameter (MLD) frame and entire atherosclerotic segment was performed. RFC was also determined before and after stenting. Results: The VH component analysis of the segment demonstrated predominantly fibrous tissue (56.3 ± 11.4), followed by necrotic core (21.8 ± 8.6), dense calcification (13.2 ± 6.6) and fibrofatty tissue (8.7 ± 4.0). Analysis of the MLD frame also demonstrated mostly fibrous tissue (62.1 ± 11.1), with smaller amounts of necrotic core (15.6 ± 7.3), fibrofatty (13.9 ± 9.6), and dense calcification (8.4 ± 6.0). A trend toward more fibrous tissue (p ≤ 0.074), less necrotic core (p ≤ 0.095) and less dense calcification (p ≤ 0.075) at the MLD compared to the segment was observed. Analysis of the entire atherosclerotic segment revealed a positive correlation between necrotic core and change in RFC (r ≤ 0.582; p ≤ 0.029), with increasing necrotic core associated with an increase in RFC after revascularization. Conclusion: Both the MLD frame and segmental analysis of atherosclerotic RAS lesions demonstrate predominantly fibrous tissue with smaller amounts of necrotic core, fibrofatty tissue, and dense calcification. Increased necrotic core correlates with a lack of improvement in RFC after stenting.
KW - hypertension
KW - intravascular ultrasound
KW - renal stent
KW - virtual histology
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M3 - Article
C2 - 21646647
AN - SCOPUS:79958100224
SN - 1042-3931
VL - 23
SP - 227
EP - 231
JO - Journal of Invasive Cardiology
JF - Journal of Invasive Cardiology
IS - 6
ER -