In the present study we compared in

vivo IMT with in vitro US measured IMT and average wall thickness. Finally, histological processing of selected frozen arterial specimens was also performed. We aimed to validate in vitro US as alternative method, if in vivo US data were not available, for postmortem vascular wall investigation, and to examine the applicability of snap freezing histotechnique on utilized vascular specimens. Comparisons between ultrasound and postmortem findings were performed in 25 patients. Table 1 contains general data about patients. The study was approved by the local Ethics Committee and informed consent was obtained from the relatives of each examined individual. SONOS 4500 ultrasound system (Agilent, Andover, MA, USA) with a 3–11-MHz linear transducer was used for in vivo and in vitro ultrasonography. In vivo IMT measurements were performed in a longitudinal B-mode projection while Epigenetic phosphorylation the patient was in a supine position. IMT was determined as the distance from the leading edge of the first echogenic line to the leading edge of the second echogenic

line of the double line pattern of the far artery wall ( Fig. 2). Three measurements along a 2–3-mm portion of the vessel were performed and were averaged. IMT measurements site on the CCA were localized by the distance of 30 mm from tip of the flow divider. This landmark enabled us to reconstruct the position of the in vivo IMT measurement later during the postmortem IMT determination. Wall thickening over 2 mm was determined as plaque and excluded from further evaluation, which resulted in an important screening Y-27632 2HCl of the postmortem Trametinib price usable arterial specimens. Within 24 h after death, 4 cm of common carotid arteries (CCA) and 4 cm of the proximal segments of internal- and external carotid arteries (ICA and ECA) were removed in toto from both sides. The native vessels were filled with histological embedding material (Cryochrome Blue; Thermo Shandon, Pittsburgh, PA, USA) and a constant pressure of 100 mmHg was adjusted ( Fig. 1). The presence of ICA and ECA helped us to identify the anatomical position during the insonation

to visualize precisely the far and near arterial. Subsequently, in vitro IMT was measured in 34 CCAs as described upper using ultrasound gel during the direct contact between transducer and prepared arterial specimens. In vitro measurements were compared with in vivo IMT values ( Fig. 2). A thread has been fixed at 3 cm distance from tip of the flow divider in order to mark the exact location where in vitro IMT measurements were performed. Afterwards, filled specimens were frozen at −20 °C in a box containing embedding material, and subsequently, cut into 3 mm thick slices ( Fig. 1) as described previously [31] and [32]. Consecutive slices were photographed with a high-resolution (3040 × 2016 pixels) digital camera (FinePix S1 Pro; Fuji Photo Film Co.