Marzena Walasek
Research Subjects
Marzena Walasek has a total of 20 co-authors. Here are the top co-authors by number of shared publications:
- Agnieszka Polecka
Department of Cardiology and Internal Medicine with Cardiac Intensive Care Unit, Doctoral School of the Medical University of Bialystok, Medical University of Bialystok, Poland
2 shared publications - Ewa Olszewska
Department of Otolaryngology, Sleep Apnea Surgery Center, Medical University of Bialystok, 15-276 Bialystok, Poland
2 shared publications - Piotr Fiedorczuk
Department of Otolaryngology, Medical University of Bialystok, 15-089 Bialystok, Poland
2 shared publications - Agnieszka Kulczyńska-Przybik
Department of Neurodegeneration Diagnostics, Medical University of Bialystok, 15-089 Bialystok, Poland
1 shared publication Agnieszka Perko
1 shared publication- Andrzej Sieśkiewicz
Department of Otolaryngology, Medical University of Bialystok, Poland
1 shared publication
Latest Publications
- Open Access
- 24 December 2025
- Published by RS Global Sp. z O.O. in International Journal of Innovative Technologies in Social Science
- Vol. 2 (4(48))
EFFECTS OF PHYSICAL ACTIVITY ON CHILDREN’S DEVELOPMENT – A REVIEW
Introduction: Physical activity is vital for the holistic development of children, benefiting physical, cognitive, social, and emotional domains. Engaging in regular physical activities from an early age fosters a healthy body, emotional and social well-being, and cognitive development. Aim: This study explores the diverse benefits of physical activity on childhood development, focusing on physical health, cognitive functions, social skills, and emotional well-being. Materials and Methods: A comprehensive literature review was conducted, analyzing existing research on the impact of physical activity on various aspects of childhood development. Searches were performed across databases such as PubMed and Google Scholar using keywords like "childhood physical activity" and "childhood sport." Results: Physical activity promotes healthy growth, enhances cardiovascular and musculoskeletal health, and helps maintain a healthy weight, reducing obesity risks. It improves memory, attention, and executive functions, contributing to better academic performance. Socially, it fosters peer relationships, enhances social skills, and cultivates leadership qualities. Emotionally, it aids in emotional regulation, boosts self-esteem, and reduces anxiety and depression. Discussion: The findings highlight the multifaceted benefits of physical activity on children's development, corroborating existing literature. Despite robust evidence, limitations such as reliance on self-reported data and cross-sectional study designs constrain causal inferences. Future research should use objective measures and longitudinal approaches, considering interactions with diet, sleep, and lifestyle factors. Conclusion: Physical activity significantly benefits childhood development across physical, cognitive, social, and emotional domains. Addressing limitations in existing research will enhance the understanding and application of physical activity in promoting holistic child development.
- 24 December 2025
- Published by RS Global Sp. z O.O. in International Journal of Innovative Technologies in Social Science
- Vol. 2 (4(48))
Open AccessEFFECTS OF PHYSICAL ACTIVITY ON CHILDREN’S DEVELOPMENT – A REVIEW
Introduction: Physical activity is vital for the holistic development of children, benefiting physical, cognitive, social, and emotional domains. Engaging in regular physical activities from an early age fosters a healthy body, emotional and social well-being, and cognitive development. Aim: This study explores the diverse benefits of physical activity on childhood development, focusing on physical health, cognitive functions, social skills, and emotional well-being. Materials and Methods: A comprehensive literature review was conducted, analyzing existing research on the impact of physical activity on various aspects of childhood development. Searches were performed across databases such as PubMed and Google Scholar using keywords like "childhood physical activity" and "childhood sport." Results: Physical activity promotes healthy growth, enhances cardiovascular and musculoskeletal health, and helps maintain a healthy weight, reducing obesity risks. It improves memory, attention, and executive functions, contributing to better academic performance. Socially, it fosters peer relationships, enhances social skills, and cultivates leadership qualities. Emotionally, it aids in emotional regulation, boosts self-esteem, and reduces anxiety and depression. Discussion: The findings highlight the multifaceted benefits of physical activity on children's development, corroborating existing literature. Despite robust evidence, limitations such as reliance on self-reported data and cross-sectional study designs constrain causal inferences. Future research should use objective measures and longitudinal approaches, considering interactions with diet, sleep, and lifestyle factors. Conclusion: Physical activity significantly benefits childhood development across physical, cognitive, social, and emotional domains. Addressing limitations in existing research will enhance the understanding and application of physical activity in promoting holistic child development.
- Open Access
- 10 June 2024
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 13 (12) , 3394
A Case Study of a Rare Disease (Fructosemia) Diagnosed in a Patient with Abdominal Pain
Hereditary fructose intolerance is a rare genetic disorder that is inherited in an autosomal recessive manner, with mutations sometimes occurring spontaneously. Consuming fructose triggers biochemical abnormalities, disrupting liver processes like glycogenolysis and gluconeogenesis. Recent studies have revealed elevated intrahepatic fat levels in affected individuals. Symptoms include aversion to fructose-containing foods, hypoglycemia, liver and kidney dysfunction, and growth delays, with severe cases leading to liver enlargement, fatty liver disease, kidney failure, and life-threatening hypoglycemia. In this case study, we present a 20-month-old child with symptoms including difficulty passing stool, abdominal rigidity, abdominal pain with bloating and hypoglycemia. Initial clinical findings revealed elevated liver enzymes, a mildly enlarged hyperechoic liver, hypercholesterolemia, and borderline alpha-fetoprotein values. Diagnostic assessments identified hereditary fructose intolerance (HFI) with pathogenic variants in the ALDOB gene, along with a diagnosis of celiac disease. Genetic testing of the parents revealed carrier status for pathological aldolase B genes. This case underscores the importance of comprehensive clinical evaluation and genetic testing in pediatric patients with complex metabolic presentations.
- 10 June 2024
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 13 (12) , 3394
Open AccessA Case Study of a Rare Disease (Fructosemia) Diagnosed in a Patient with Abdominal Pain
Hereditary fructose intolerance is a rare genetic disorder that is inherited in an autosomal recessive manner, with mutations sometimes occurring spontaneously. Consuming fructose triggers biochemical abnormalities, disrupting liver processes like glycogenolysis and gluconeogenesis. Recent studies have revealed elevated intrahepatic fat levels in affected individuals. Symptoms include aversion to fructose-containing foods, hypoglycemia, liver and kidney dysfunction, and growth delays, with severe cases leading to liver enlargement, fatty liver disease, kidney failure, and life-threatening hypoglycemia. In this case study, we present a 20-month-old child with symptoms including difficulty passing stool, abdominal rigidity, abdominal pain with bloating and hypoglycemia. Initial clinical findings revealed elevated liver enzymes, a mildly enlarged hyperechoic liver, hypercholesterolemia, and borderline alpha-fetoprotein values. Diagnostic assessments identified hereditary fructose intolerance (HFI) with pathogenic variants in the ALDOB gene, along with a diagnosis of celiac disease. Genetic testing of the parents revealed carrier status for pathological aldolase B genes. This case underscores the importance of comprehensive clinical evaluation and genetic testing in pediatric patients with complex metabolic presentations.
- Open Access
- 27 December 2023
- Published by Akademia Medycznych i Społecznych Nauk Stosowanych in Acta Elbingensia
- Vol. 50 (1) , 1-6
Impact of COVID-19 pandemic on the diagnosis of patients with laryngeal cancer
Introduction: Patients’ access to public healthcare has been limited during the COVID-19 pandemic. The psychological factor – the fear of patients and medical staff of infection, especially before the introduction of vaccinations – had also a negative impact on the diagnostic and therapeutic procedures.Aim: The aim of the study was to assess the impact of the COVID-19 pandemic on the degree of advancement of laryngeal cancer in patients referring for diagnosis and treatment to a IV-level clinical referral hospital.Material and methods: The medical documentation of patients presenting to IVth level reference clinical hospital was retrospectively analyzed in pre-, during and post-pandemic period of time. The total number of patients presenting to the emergency department (ED), inclusive of those receiving otolaryngological consultation, patients diagnosed with laryngeal cancer and advancement stage of disease was assessed. Additionally the comprehensive count of diagnostic and therapeutic procedures pertaining to the larynx and trachea, during the three above mentioned periods of time was performed.Results and discussion: The study revealed a significant decrease in the number of patients presenting to the ED during the pandemic, with a more pronounced drop among otolaryngological patients. The number of patients with laryngeal tumor treated in our hospital as well as the number of laryngeal diagnostic and therapeutic procedures remained stable throughout analysed periods of time. During pandemic period significant drop of patients with early-stage (T1) laryngeal cancers was observed.Conclusions: Despite maintained surgical activity in level IV reference hospital, fewer patients with early stage of laryngeal cancer (T1) were diagnosed and treated during pandemic.
- 27 December 2023
- Published by Akademia Medycznych i Społecznych Nauk Stosowanych in Acta Elbingensia
- Vol. 50 (1) , 1-6
Open AccessImpact of COVID-19 pandemic on the diagnosis of patients with laryngeal cancer
Introduction: Patients’ access to public healthcare has been limited during the COVID-19 pandemic. The psychological factor – the fear of patients and medical staff of infection, especially before the introduction of vaccinations – had also a negative impact on the diagnostic and therapeutic procedures.Aim: The aim of the study was to assess the impact of the COVID-19 pandemic on the degree of advancement of laryngeal cancer in patients referring for diagnosis and treatment to a IV-level clinical referral hospital.Material and methods: The medical documentation of patients presenting to IVth level reference clinical hospital was retrospectively analyzed in pre-, during and post-pandemic period of time. The total number of patients presenting to the emergency department (ED), inclusive of those receiving otolaryngological consultation, patients diagnosed with laryngeal cancer and advancement stage of disease was assessed. Additionally the comprehensive count of diagnostic and therapeutic procedures pertaining to the larynx and trachea, during the three above mentioned periods of time was performed.Results and discussion: The study revealed a significant decrease in the number of patients presenting to the ED during the pandemic, with a more pronounced drop among otolaryngological patients. The number of patients with laryngeal tumor treated in our hospital as well as the number of laryngeal diagnostic and therapeutic procedures remained stable throughout analysed periods of time. During pandemic period significant drop of patients with early-stage (T1) laryngeal cancers was observed.Conclusions: Despite maintained surgical activity in level IV reference hospital, fewer patients with early stage of laryngeal cancer (T1) were diagnosed and treated during pandemic.
- Open Access
- 9 September 2023
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 24 (18) , 13875
Investigating the Role of Serum and Plasma IL-6, IL-8, IL-10, TNF-alpha, CRP, and S100B Concentrations in Obstructive Sleep Apnea Diagnosis
Obstructive sleep apnea (OSA) is a prevalent and underdiagnosed condition associated with cardiovascular diseases, depression, accidents, and stroke. There is an increasing need for alternative diagnostic tools beyond overnight sleep studies that measure the Apnea/Hypopnea Index (AHI). In this single-center, case-control study, we evaluated serum and plasma concentrations of IL-6, IL-8, IL-10, TNF-α, CRP, and S100B in 80 subjects, including 52 OSA patients (27 moderate [15 ≤ AHI ˂ 30], 25 severe [AHI ≥ 30]) and 28 non-OSA controls (AHI 0-5). Participants with OSA showed approximately 2 times higher median concentrations of CRP in plasma, and IL-6 in serum, as well as 1.3 to 1.7 times higher concentrations of TNF-α and IL-8 in plasma compared with the control group. Receiver Operator Characteristic (ROC) curve analysis was performed to evaluate the predictive capabilities of these serum and plasma biomarkers in distinguishing between the OSA and control groups, revealing varying sensitivity and specificity. In summary, in this study, serum and plasma biomarkers CRP, S100B, IL-6, TNF-α, and IL-8 have been shown to be elevated in patients with OSA, correlated positively with disease severity, age, and BMI. These results support the potential role of these biomarkers in diagnosing OSA, supplementing traditional methods such as overnight sleep studies.
- 9 September 2023
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 24 (18) , 13875
Open AccessInvestigating the Role of Serum and Plasma IL-6, IL-8, IL-10, TNF-alpha, CRP, and S100B Concentrations in Obstructive Sleep Apnea Diagnosis
Obstructive sleep apnea (OSA) is a prevalent and underdiagnosed condition associated with cardiovascular diseases, depression, accidents, and stroke. There is an increasing need for alternative diagnostic tools beyond overnight sleep studies that measure the Apnea/Hypopnea Index (AHI). In this single-center, case-control study, we evaluated serum and plasma concentrations of IL-6, IL-8, IL-10, TNF-α, CRP, and S100B in 80 subjects, including 52 OSA patients (27 moderate [15 ≤ AHI ˂ 30], 25 severe [AHI ≥ 30]) and 28 non-OSA controls (AHI 0-5). Participants with OSA showed approximately 2 times higher median concentrations of CRP in plasma, and IL-6 in serum, as well as 1.3 to 1.7 times higher concentrations of TNF-α and IL-8 in plasma compared with the control group. Receiver Operator Characteristic (ROC) curve analysis was performed to evaluate the predictive capabilities of these serum and plasma biomarkers in distinguishing between the OSA and control groups, revealing varying sensitivity and specificity. In summary, in this study, serum and plasma biomarkers CRP, S100B, IL-6, TNF-α, and IL-8 have been shown to be elevated in patients with OSA, correlated positively with disease severity, age, and BMI. These results support the potential role of these biomarkers in diagnosing OSA, supplementing traditional methods such as overnight sleep studies.
- Open Access
- 21 December 2022
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 12 (1) , 60
Potential Diagnostic and Monitoring Biomarkers of Obstructive Sleep Apnea–Umbrella Review of Meta-Analyses
Obstructive sleep apnea (OSA) is a prevalent, underdiagnosed disease that imposes a significant impact on the health and wellbeing of patients and a financial burden on individuals, their families, and society. Development of new methods of testing other than an overnight sleep study, such as measurement of serum or plasma biomarkers, may provide an easier diagnostic process to identify patients with OSA and allow earlier initiation of treatment, which might prevent serious comorbidities. We conducted a systematic review and quality assessment of available meta-analyses regarding potential diagnostic and monitoring biomarkers of obstructive sleep apnea. A total of 14 sets of candidate biomarkers displayed differences in levels or concentrations in OSA patients compared to non-OSA controls, and decreased after OSA treatment: CRP, IL-6, TNF-α, Il-8, HCY, ICAM-1, VCAM-1, VEGF, TC, LDLc, HDLc, TG, leptin, MDA, ALT, AST, IGF-1, adiponectin, and cortisol. This review summarizes the evidence for OSA-associated potential biomarkers and demonstrates that the quality of available studies, as measured by AMSTAR2, is often low and associated with a high risk of bias.
- 21 December 2022
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 12 (1) , 60
Open AccessPotential Diagnostic and Monitoring Biomarkers of Obstructive Sleep Apnea–Umbrella Review of Meta-Analyses
Obstructive sleep apnea (OSA) is a prevalent, underdiagnosed disease that imposes a significant impact on the health and wellbeing of patients and a financial burden on individuals, their families, and society. Development of new methods of testing other than an overnight sleep study, such as measurement of serum or plasma biomarkers, may provide an easier diagnostic process to identify patients with OSA and allow earlier initiation of treatment, which might prevent serious comorbidities. We conducted a systematic review and quality assessment of available meta-analyses regarding potential diagnostic and monitoring biomarkers of obstructive sleep apnea. A total of 14 sets of candidate biomarkers displayed differences in levels or concentrations in OSA patients compared to non-OSA controls, and decreased after OSA treatment: CRP, IL-6, TNF-α, Il-8, HCY, ICAM-1, VCAM-1, VEGF, TC, LDLc, HDLc, TG, leptin, MDA, ALT, AST, IGF-1, adiponectin, and cortisol. This review summarizes the evidence for OSA-associated potential biomarkers and demonstrates that the quality of available studies, as measured by AMSTAR2, is often low and associated with a high risk of bias.