The article describes the foundations of using method of using laser Doppler flowmetry in evaluation of the state of blood microcirculation system in students, future software engineers. By the method of laser Doppler flowmetry (LDF) individually-typological features of indicators of tissue blood flow in conventionally healthy adolescent students aged 17-20 years have been studied. Due to the results of research 3 types of LDF-grams have been defined: aperiodic, monotonous low amplitude, sinusoidal type with high perfusion. Among the examined students, future engineersprogrammers different frequency of appearing microcirculatory types with predominance of normoemic type with characteristic “aperiodic” LDF-gram has been found.
One of the aims of the given research is realization of one of possible variants of the solution of the problem of efficient integration of high-level information in low-level image presentation. The result of this integration is high efficiency of recognition. The advantage of such recognition is compact description of object image that considers reduced size of database and more fast-acting realization of processing. For solution of above-mentioned problems, the creation of common methodological basis for synthesis of simple computational algorithm of image preprocessing with their segmentation and formalized procedures of separate parts description with high adaptive ability on the basis of the ideas of algebraic approach to recognition problems is very actual.
The influence of metabolic, molecular genetic- and immune-inflammatory factors on the course of reparative osteogenesis and the formation of bone nonunion of long bones is investigated on the basis of computer statistical analysis and forecasting methods. It has been established that hyperhomocysteinemia, dyslipidemia and cytokine imbalance are negative regressors of the structural and functional state of bone tissue, leading to increased levels of bone resorption markers and the development of systemic and local osteoporosis. The genetic determinants of the course of reparative osteogenesis in a hypoplastic and atrophic type are the homozygous carrier of mutations MTHFR C677T or eNOS T786S, as well as a combination of both polymorphisms.