Molecular Mechanism Research https://ojs.as-pub.com/index.php/MMR <p><strong>ISSN: 3029-2212(Online)</strong></p> <p>Molecular Mechanism Research (MMR) is an international open-access journal dedicated to publishing articles related to molecular biology research. It serves as a platform for researchers worldwide to share innovative ideas and communicate advancements in understanding the structural components of biological organisms, as well as the physical and chemical processes involved in disease development.</p> <p>This journal covers a wide range of disciplines, including botany, medicine, and zoology, and focuses on molecular mechanisms underlying diseases. MMR welcomes various article types, including original research articles, review articles, editorials, and case reports.&nbsp;The research topics of MMR include but are not limited to:</p> <ol> <li class="show">Molecular Biology</li> <li class="show">Disease Mechanisms</li> <li class="show">Structural Biology</li> <li class="show">Biochemical Processes</li> <li class="show">Aging Mechanisms</li> <li class="show">Medicine</li> <li class="show">Zoology</li> <li class="show">Stem Cells and Regenerative Medicine</li> <li class="show">Diagnostic Techniques</li> <li class="show">Treatment Strategies</li> </ol> <p><strong>The article processing charges is $800 per article.</strong></p> en-US editorial_office@as-pub.com (Managing Editor) Sun, 28 Dec 2025 00:00:00 +0800 OJS 3.1.1.0 http://blogs.law.harvard.edu/tech/rss 60 Hemoglobin phenotypic variations among voluntary blood donors in Bangladesh: A Study on genetic screening for safe blood transfusion https://ojs.as-pub.com/index.php/MMR/article/view/10226 <p><strong>Background: </strong>Blood donation is a critical component of healthcare systems worldwide, particularly in regions with endemic diseases like malaria. Hemoglobinopathies, such as sickle cell trait (HbAS) and other variants like HbAC, can influence the safety of blood donations, particularly in malaria-endemic areas. Understanding the hemoglobin profiles of voluntary blood donors is essential for ensuring safe blood transfusions.</p> <p><strong>Objective: </strong>The objective of this study was to examine the demographic characteristics and hemoglobin phenotypes of voluntary blood donors at LSBTS, Bangladesh, with a focus on their potential impact on transfusion safety.</p> <p><strong>Methods: </strong>A total of 300 voluntary blood donors were included in the study. Demographic data including age, gender, occupation, and marital status were collected. Hemoglobin phenotypes were assessed using standard hematological methods. Donor history, including frequency of previous donations and the most recent donation year, was also recorded. Data were analyzed using descriptive statistics to identify trends and associations.</p> <p><strong>Results: </strong>Most participants (80%) exhibited the normal hemoglobin phenotype (HbAA), followed by 18% with the sickle cell trait (HbAS) and 2% with other variants (HbAC). The donor population was predominantly male (70%) and largely aged between 26 and 45 years (68%). A significant proportion (62%) were repeat donors, with 70% having donated blood in 2023. Weight distribution and hemoglobin levels showed no significant association with hemoglobin phenotypes, indicating consistent donor health across groups. These findings suggest a stable donor pool with diverse hemoglobin profiles, underscoring the importance of ongoing screening and monitoring to maintain transfusion safety.</p> <p><strong>Conclusion:</strong>&nbsp;This study highlights the predominance of HbAA among voluntary blood donors in Bangladesh, suggesting that the majority of blood donations are likely to be safe for transfusion. However, the presence of HbAS and HbAC in the donor population underscores the importance of comprehensive pre-donation screening, particularly in malaria-endemic regions. Health promotion efforts should focus on enhancing donor recruitment and retention, with targeted campaigns for younger and male populations, as well as healthcare workers.</p> Md Shafiul Azam, Firoz Reza, Nisat Sultana, Naimun Nahar, Md. Sujon Ali ##submission.copyrightStatement## https://ojs.as-pub.com/index.php/MMR/article/view/10226 Thu, 24 Jul 2025 00:00:00 +0800 Thyroid dysfunction and metabolic dysregulation: A cross-sectional study of hormonal and glycemic parameters https://ojs.as-pub.com/index.php/MMR/article/view/10227 <p><strong>Background:</strong>&nbsp;Thyroid dysfunction, encompassing hypothyroidism and hyperthyroidism, has been implicated in metabolic dysregulation, including disturbances in glucose and lipid metabolism. Given the rising global prevalence of metabolic disorders such as diabetes and dyslipidemia, understanding the interplay between thyroid hormones and metabolic health is crucial. This study aimed to investigate the association between thyroid dysfunction and metabolic parameters in a clinical population.</p> <p><strong>Methods:</strong>&nbsp;A cross-sectional study was conducted at the Diabetic Care Center, Dhaka, from January to June 2023, involving 140 adult participants. Thyroid function (TSH, FT₃, FT₄), glycemic markers (FBG, ABF, HbA1c), and lipid profiles were assessed. Statistical analyses included correlation tests and multivariate regression to evaluate relationships between thyroid and metabolic parameters.</p> <p><strong>Results: </strong>The study revealed that hypothyroid participants had significantly higher fasting blood glucose (124.7 ± 18.9 mg/dL vs. 108.3 ± 14.5 mg/dL, p &lt; 0.01), postprandial glucose (165.5 ± 25.4 mg/dL vs. 143.9 ± 20.2 mg/dL, p &lt; 0.01), and HbA1c (7.4 ± 1.3% vs. 6.5 ± 1.1%, p &lt; 0.01) compared to euthyroid individuals. Additionally, hypothyroidism was associated with elevated total cholesterol (218.6 ± 34.5 mg/dL vs. 190.4 ± 28.6 mg/dL, p &lt; 0.05) and LDL (141.7 ± 27.8 mg/dL vs. 119.5 ± 23.3 mg/dL, p &lt; 0.05), alongside reduced HDL (39.2 ± 7.3 mg/dL vs. 44.7 ± 8.9 mg/dL, p = 0.04). Hyperthyroid patients also exhibited metabolic disturbances, including higher FBG (116.1 ± 16.8 mg/dL) and triglycerides (176.5 ± 38.7 mg/dL). Correlation analysis demonstrated a significant association between TSH and HbA1c (r = 0.38, p &lt; 0.01), reinforcing the role of thyroid dysfunction in metabolic dysregulation.</p> <p><strong>Conclusion:</strong>&nbsp;Thyroid dysfunction, particularly hypothyroidism, is significantly associated with impaired glycemic control and dyslipidemia. Routine thyroid screening in metabolic disorder patients and integrated management strategies are recommended to mitigate cardiovascular and diabetic risks.</p> Pronoy Kumer Sarker, Nisat Sultana, Hafizul Islam, Md Samiul Bashir, Md. Sujon Ali ##submission.copyrightStatement## https://ojs.as-pub.com/index.php/MMR/article/view/10227 Thu, 24 Jul 2025 10:16:35 +0800