अमूर्त
Epidemiology and effect of a new variant (from alpha to delta strains) of SARS-COV-2 for children and adults.
Bibigul Doltayeva*, Altynshash Kushkarova, Parkhat Utepov, Sara Yeskerova, Akmaral Zhumadilova
Background: Several clinical studies have demonstrated that arterial stiffness is an early indicator of cardiovascular events. Our study aimed to detect the potential cardiovascular changes using arterial stiffness parameters and compare these changes with echocardiographic aortic stiffness parameters in cancer patients treated with cardio toxic chemotherapeutics. Methods and Results: Our study is a prospective case-control study. A total of 70 subjects between the ages of 18 and 50 years were included into our study. 30 of them were newly diagnosed cancer patients and 40 were age and sex matched control group. Baseline oscillometric arterial and echocardiographic aortic stiffness parameters were measured in all patients. In cancer patients, all of these parameters were measured again one month after chemotherapy protocol was completed. Mean age of the cancer patients was 41.4 ± 5.9 years and mean age of the control group was 39.6 ± 6.6 years (p=0.258). Before chemotherapy, arterial and aortic stiffness parameters were similar between the study and the control groups. After chemotherapy, oscillometric pulse wave velocity parameter increased compared to the control group and to the pre-chemotherapy values (p=0.004 and p<0.001, respectively). After chemotherapy, augmentation index parameter increased compared to the control group (p=0.013). On the other hand, no difference was detected between the groups in terms of echocardiographic aortic stiffness parameters. Conclusion: In newly diagnosed cancer patients treated with cardio toxic chemotherapeutics, considerable impairment occurs in some of the oscillometric arterial stiffness parameters while there is no substantial effect on echocardiographic aortic stiffness. Arterial stiffness parameters in these patients might be useful in evaluating subclinical cardiovascular damage.