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  <title>DSpace Collection: The 9th International Medical Congress for Students and Young Doctors, May 12-14, 2022</title>
  <link rel="alternate" href="http://repository.usmf.md:80/handle/20.500.12710/20919" />
  <subtitle>The 9th International Medical Congress for Students and Young Doctors, May 12-14, 2022</subtitle>
  <id>http://repository.usmf.md:80/handle/20.500.12710/20919</id>
  <updated>2026-04-11T02:29:23Z</updated>
  <dc:date>2026-04-11T02:29:23Z</dc:date>
  <entry>
    <title>MedEspera 2022 : The 9th International Medical Congress for Students and Young Doctors, 12-14 May 2022 : Abstract Book</title>
    <link rel="alternate" href="http://repository.usmf.md:80/handle/20.500.12710/21396" />
    <author>
      <name />
    </author>
    <id>http://repository.usmf.md:80/handle/20.500.12710/21396</id>
    <updated>2022-07-05T11:57:26Z</updated>
    <published>2022-01-01T00:00:00Z</published>
    <summary type="text">Title: MedEspera 2022 : The 9th International Medical Congress for Students and Young Doctors, 12-14 May 2022 : Abstract Book</summary>
    <dc:date>2022-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Heart rate variability in people with personality disorders in the pain test</title>
    <link rel="alternate" href="http://repository.usmf.md:80/handle/20.500.12710/21394" />
    <author>
      <name>Ceban, Dinu</name>
    </author>
    <id>http://repository.usmf.md:80/handle/20.500.12710/21394</id>
    <updated>2022-07-05T10:29:03Z</updated>
    <published>2022-01-01T00:00:00Z</published>
    <summary type="text">Title: Heart rate variability in people with personality disorders in the pain test
Authors: Ceban, Dinu
Abstract: Introduction. The main features of each personality disorder (PD) are emotional disorders. The median&#xD;
prevalence in the population of Borderline personality disorder (BPD) was estimated at 1.6%, but may&#xD;
reach 5.9%. The increased incidence of cardiovascular disease associated with psychiatric pathologies has&#xD;
also led to increased attention to the autonomic nervous system. BPD with an increased rate of&#xD;
cardiovascular mortality, and characterized by emotional instability, is ideal for studying heart rate&#xD;
variability (HVR).&#xD;
Aim of study. The purpose of the study is to determine the autonomic changes in people with BPD by&#xD;
studying the HRV both at rest and in the pain test.&#xD;
Methods and materials. The study involved 95 people, 19 to 60 years old, using the Personality Inventory&#xD;
for DSM-5 (PID-5), all subjects were divided into 2 groups: control group (n = 64) and group of people&#xD;
with BPD (n = 32). The experimental protocol included the recording using the BIOPAC MP-36 Data&#xD;
Acquisition System of the electrocardiogram in the second standard lead in 3 functional periods: Resting&#xD;
(R) - 5 min, Pain test (pain stimulation) (PT) - 3 min and Post-pain test period (post PT) - 5 min. The&#xD;
primary data processing was performed with the help of the program Kubios HRV Standard (version 3.2.0,&#xD;
2019). The spectral analysis Fourier of the RR interval was applied and following parameters have been&#xD;
analyzed – normalized low frequency component (LFnu) and normalized high frequency component&#xD;
(HFnu).&#xD;
Results. In subjects with BPD, higher HFnu values are observed at rest, highlighting an amplified vagal&#xD;
modulation of the heart rhythm, and a lower sympathetic influence on the heart rhythm. During the pain&#xD;
test, a decrease in the vagal activity and an increase in the sympathetic activity on the heart rate were&#xD;
observed in both groups. In the post-pain test period, LFnu and HFnu values in subjects with BPD were&#xD;
reversed compared to resting period, which indicates an increase of sympathetic influences on the heart rate&#xD;
and a reduction of vagal modulatory effects. The LFnu and HFnu values in these subjects did not return to&#xD;
the initial values in the post-pain test period as they did in the control group, but, on the contrary, an increase&#xD;
in the dynamics of the sympathetic influence was registered, even compared to the pain test period.&#xD;
Conclusion. The results present an increased vagal modulation in subjects with BPD at rest, which is&#xD;
reduced during pain stimulation and does not return rapidly to the initial value after removing the pain&#xD;
stimulus. This could be the proof of the inertia of autonomic influences in these subjects, which is in&#xD;
concordance with the results of the studies in the research papers regarding HRV.</summary>
    <dc:date>2022-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Glycated albumin – a better glycemic control marker than HbA1c in pregnancy and gestational diabetes mellitus</title>
    <link rel="alternate" href="http://repository.usmf.md:80/handle/20.500.12710/21393" />
    <author>
      <name>Bolocan, Valeria</name>
    </author>
    <id>http://repository.usmf.md:80/handle/20.500.12710/21393</id>
    <updated>2022-07-05T10:25:06Z</updated>
    <published>2022-01-01T00:00:00Z</published>
    <summary type="text">Title: Glycated albumin – a better glycemic control marker than HbA1c in pregnancy and gestational diabetes mellitus
Authors: Bolocan, Valeria
Abstract: Introduction. Since glycation of various proteins is increased in diabetes, glycated proteins can be used as&#xD;
glycemic control indicators. Despite being the gold standard of glycemic control, HbA1c does not precisely&#xD;
reflect the actual status of glycemic control in some conditions including pregnancy and gestational diabetes&#xD;
mellitus (GDM). In comparison, glycated albumin (GA) more accurately reflects changes in plasma glucose&#xD;
because it is not affected by variable haemoglobin concentrations and modified erythrocyte life span that&#xD;
naturally occur in pregnancy.&#xD;
Aim of study. Hyperglycemia that develops during pregnancy and disappears after giving birth is now&#xD;
recognized as a special type of diabetes, called GDM. GDM is a common medical complication of&#xD;
pregnancy, and the prevalence of undiagnosed hyperglycemia and even the incidence of diabetes in young&#xD;
women is constantly increasing. Therefore, new glycemic control markers are being investigated in order&#xD;
to ensure a good quality of diabetes care before, during and after pregnancy.&#xD;
Methods and materials. To achieve the proposed goal, a synthesis of the literature published from 2009&#xD;
until 2021 has been made, using 11 bibliographic sources, including electronic libraries like PubMed,&#xD;
Medscape, Diabetes Care and Diabetologia.&#xD;
Results. Normally, erythropoietin and erythrocyte production is increased during normal pregnancy, which&#xD;
contributes to the understanding of the increased erythropoiesis on the one hand, and reduced haemoglobin&#xD;
concentration on the other hand. All of those explain the reduced life span of the erythrocytes that will&#xD;
determine a decrease in HbA1c values. Besides, in the first trimester there is a lower pre- and postprandial&#xD;
blood glucose values, which also causes a decrease in the percentage of HbA1c. Instead, in the third&#xD;
trimester there is an increase in the postprandial blood glucose values, which determines an increase in&#xD;
HbA1c. These assertions suggest that, in order to ensure an optimal glycemic control, it is mandatory to&#xD;
use HbA1c references specific for each trimester. Compared with HbA1c, GA reflects the short-term status&#xD;
of glycemic control (around 2-3 weeks). Additionally, GA reflects postprandial plasma glucose more&#xD;
accurately than HbA1c, which is important for the evaluation of plasma glucose level at a time point closer&#xD;
to the time of consultation with the physician. Moreover, as it has already been mentioned, GA does not&#xD;
interfere with increased erythropoiesis and erythrocyte life span, the states present in pregnancy.&#xD;
Conclusion. Poor glycemic control can be associated with a higher incidence of perinatal maternal-infant&#xD;
complications. Regardless of its major clinical importance, HbA1c is not suitable for monitoring glycemic&#xD;
control in pregnant women with diabetes and GDM. It has become clear that GA, another indicator of&#xD;
glycemic control, is not influenced by the limitations of HbA1c and therefore might be a better indicator of&#xD;
glycemic control in patients with GDM and pregnant women with diabetes mellitus. However, further largepopulation studies are necessary in order to confirm these findings.</summary>
    <dc:date>2022-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Gene therapy in some genetic diseases</title>
    <link rel="alternate" href="http://repository.usmf.md:80/handle/20.500.12710/21391" />
    <author>
      <name>Junbei, Mircea</name>
    </author>
    <id>http://repository.usmf.md:80/handle/20.500.12710/21391</id>
    <updated>2022-07-05T10:20:46Z</updated>
    <published>2022-01-01T00:00:00Z</published>
    <summary type="text">Title: Gene therapy in some genetic diseases
Authors: Junbei, Mircea
Abstract: Introduction. Gene therapy it's a complex of methods that treats at least 10% of the approximately 9,000&#xD;
genetic diseases recorded. Genetic diseases involve all dysfunctions that include deficiencies, absence or&#xD;
surplus of certain genetic information. Gene therapy is a complex of treatments that comes to complete the&#xD;
deficiency or lack of genes indispensable for the proper living of patients with an active disease. Gene&#xD;
therapy is a relatively young field and thus an expensive one in production, therefor today some of the drugs&#xD;
(for ex.: Nusinersen, Zolgensma, etc.) can reach from 325 thousand $ to 725 thousand $ a year, any target&#xD;
disease of gene therapy that has a huge degree of specificity and personalization. Approved treatments with&#xD;
a considerable degree of success are: Duchene amyotrophy (DMD), spinal muscular dystrophy (SMA),&#xD;
central nervous system cancer - glioblastoma; and also some therapies that need to be approved for&#xD;
treatment: various forms of hemophilia, Wiskott-Aldrich syndrome, diabetic retinopathy, corneal&#xD;
neovascularization, cancer, etc.&#xD;
Aim of study. Gene therapy techniques include the direct introduction of substituents into the intercellular&#xD;
space in the body through viral vectors - in-vivo such as: adeno-associated, adenoviral, retroviral, lentiviral&#xD;
vectors, etc. as well as non-viral vectors, for example: CRISPR-Cas9, introduction of plasmids, techniques&#xD;
such as: exon skipping, antisense oligonucleotides, also ex-vivo techniques such as introducing of modified&#xD;
cells, like CAR T. Some obstacles have already been overcome, for example the immune response has been&#xD;
partially resolved, enough to achieve the treatment, by combining it with immunomodulatory treatment&#xD;
with corticosteroids. Individualized forms, such as the degree in a spinal amyodistrophy type I-IV&#xD;
manifestation, are already coordinated with the amount of gene 2 copy.&#xD;
Methods and materials. The paper was based on a review of the literature, using textbooks and articles&#xD;
published in electronic sources recognized by the international medical community as: PubMed, NEJM,&#xD;
NCBI, GeneCards. Also, two clinical cases of two children suffering from Duchenne progressive muscular&#xD;
dystrophy and belt-shaped muscular dystrophy that could benefit from gene therapy in the Republic of&#xD;
Moldova were described.&#xD;
Results. During the study it was observed that gene therapy has widely started to be used in various&#xD;
diseases: cardiovascular, neuromuscular, oncology, ophthalmology, etc. Disappointing that in both clinical&#xD;
cases, costs of treatment are too high for the patients, this remains to be the main obstacle.&#xD;
Conclusion. Gene therapy has a promising future in solving incurable diseases, by proposing a new way&#xD;
of treatment through the involvement in genetic pathophysiology and creation of cells. This encourages&#xD;
medical scientists to include new diseases in research and develop new ways, more accessible to production.</summary>
    <dc:date>2022-01-01T00:00:00Z</dc:date>
  </entry>
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