Development of transplantation vasculopathy and progression of donor-transmitted atherosclerosis - Comparison by serial intravascular ultrasound imaging
Sr. Kapadia et al., Development of transplantation vasculopathy and progression of donor-transmitted atherosclerosis - Comparison by serial intravascular ultrasound imaging, CIRCULATION, 98(24), 1998, pp. 2672-2678
Citations number
37
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Background-Transplant coronary artery disease isa combination of atheroscle
rosis transmitted from the donor and new lesions of allograft vasculopathy.
We sought to determine the morphological characteristics of allograft vasc
ulopathy and differentiate it from donor-transmitted atherosclerosis with s
erial intravascular ultrasound.
Methods and Results-Intravascular ultrasound examination was performed in 9
3 patients at 27.2+/-15.0 and 369.7+/-23.9 days after transplantation. The
maximally and minimally diseased sites were selected in each segment as def
ined by Coronary Artery Surgery Study classification. For each matched site
, maximal plaque thickness was measured. Lesions (maximum plaque thickness
greater than or equal to 0.5 mm) present at baseline examination were defin
ed as donor lesions. On follow-up, lesions that developed at previously nor
mal sites were defined as de novo lesions. The distribution and severity of
donor and de novo lesions were similar in proximal, mid, and distal segmen
ts. The de novo lesions were less focal (43% vs 74%) and more circumferenti
al (69% vs 45%) compared with the donor lesions, but there was significant
morphological heterogeneity, Similar numbers of patients with and those wit
hout donor lesions developed de novo lesions. Moreover, progression of dono
r lesions was not associated with the presence or absence of de novo lesion
s.
Conclusions-Differentiation between early allograft vasculopathy from conve
ntional atherosclerosis by distribution and morphology of lesions alone is
difficult. Serial intravascular ultrasound imaging with early baseline exam
ination is necessary to make this distinction. This distinction is importan
t because the progression of donor lesions and the development of de novo l
esions are independent of each other.