Hypertension can be considered as a progressive ischaemic syndrome interest
ing micro- and macrovasculature.
In hypertensives it is possible to observe a link between an increase in pe
ripheral resistance and blood viscosity, and a decrease in red blood cell (
RBC) deformability.
It is important to underline the link between the increase of blood viscosi
ty, the decrease of RBC deformability and the cytosolic calcium level, whic
h is related to the ischaemic syndrome in hypertension.
The aim of this study was to evaluate the level of Ca++ and its possible co
rrelation with hemorheological patterns during arterial hypertension.
Two groups were studied: Group 1 consisted of 18 mild hypertensives (11 mal
es and 7 pre-menopausal females, aged 39 +/- 3 years). This group was of me
dium risk according to WHO and ISH (1999) with no other pathologies apart f
rom peripheral occlusive arterial disease II stage type A. Group 2 was made
up of 14 healthy subjects (9 males and 5 females, aged 34 +/- 4 years). Th
e intraerythrocytic cytosolic calcium was evaluated using a fluorescent mar
ker FURA 2/AM (Calbiochem).
The following hemorheological parameters were also assessed using the new L
aser assisted Optical Rotational Red Cell Analyzer (LORCA) according to the
Hardeman method (1994): RBC deformability - Elongation Index (EI), RBC agg
regability - aggregation half time (t(1/2)).
The data obtained showed that compared to the control group the hypertensiv
es had a significantly higher level of intraerythrocytic cytosolic calcium
(p < 0.01), plus a significant decrease in EI and t(1/2) evaluated using LO
RCA.
We also observed a significant correlation (p < 0.01) between an increase i
n Ca++ and a decrease in EI in the hypertensive patients.
Moreover our study revealed a significant correlation between the increase
in intraerythrocytic Ca++ and the t(1/2) decrease.
The evaluation of the hemorheological patterns and cytosolic calcium could
explain the impairment in peripheral perfusion and oxygenation in hypertens
ive patients and could provide a good model for a better evaluation and tre
atment of microvasculature perfusion in subjects with essential and complic
ated hypertension.