Serum Immunoglobulins and Complement Factors levels in in splenectomized and non splenectomized β-thalassemia major patients.

Background: Beta-thalassemia major (ß-TM) is the most common hereditary hemoglobin synthesis disorder, often requiring blood transfusions, which, along with splenectomy and iron supplementation, increases the risk of bacterial infections and alters the immune profile of affected individuals. Beta-thalassemia major (ß-TM) is the most common hereditary hemoglobin synthesis disorder, often requiring blood transfusions, which, along with splenectomy and iron supplementation, increases the risk of bacterial infections and alters the immune profile of the affected individuals. Objective: This study aimed to assess the serum concentrations of immunoglobulins (IgG, IgM and IgA) and complement components (C3 and C4) in both splenectomized and non-splenectomized ß-TM patients and; correlate these levels with ferritin, blood transfusion and iron chelation therapy. \Methods: A cross-sectional comparative study involving 100 ß-TM patients in Sana'a City-Yemen, was conducted, categorizing the participants into splenectomized and non-splenectomized groups. Sociodemographic data were collected via a structured questionnaire,, ferritin levels were assessed using the Cobas e411 method, and immunoglobulins and complement factors were quantified using the immunoturbidimetry method. Results: The results indicate that ß-TM patients who have undergone splenectomy exhibit higher serum ferritin and immunoglobulin (IgM, IgG, IgA) levels than non-splenectomized ß -TM patients, with stable C3 and a non-significant decline in C4. Additionally, significant correlations were found between IgG, IgA, blood transfusions and iron chelation therapy, whereas C3 and C4 levels were not significantly associated with these treatments. Conclusion: The findings indicated that splenectomy alters the immunological profile of ß-TM patients, although the precise mechanism underlying this alteration remains ambiguous; thus, analyzing serum immunoglobulins and complements levels may prove beneficial in assessing infection severity in these patients.

Authors

Institutions

Publication Details

Journal
مجلة جامعة صنعاء للطب والعلوم الصحية
Published
2024-12-29
DOI
https://doi.org/10.59628/jchm.v18i5.1381
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Serum Immunoglobulins and Complement Factors levels in in splenectomized and non splenectomized β-thalassemia major patients.

Ahmed Y. Al-Jaufy, Mohammed Almorish, Rana M. Al-Gahwashi
مجلة جامعة صنعاء للطب والعلوم الصحية
Hemoglobinopathies and Related Disorders
article

Serum Immunoglobulins and Complement Factors levels in in splenectomized and non splenectomized β-thalassemia major patients.

Ahmed Y. Al-Jaufy, Mohammed Almorish, Rana M. Al-Gahwashi
article en

Abstract

Background: Beta-thalassemia major (ß-TM) is the most common hereditary hemoglobin synthesis disorder, often requiring blood transfusions, which, along with splenectomy and iron supplementation, increases the risk of bacterial infections and alters the immune profile of affected individuals. Beta-thalassemia major (ß-TM) is the most common hereditary hemoglobin synthesis disorder, often requiring blood transfusions, which, along with splenectomy and iron supplementation, increases the risk of bacterial infections and alters the immune profile of the affected individuals. Objective: This study aimed to assess the serum concentrations of immunoglobulins (IgG, IgM and IgA) and complement components (C3 and C4) in both splenectomized and non-splenectomized ß-TM patients and; correlate these levels with ferritin, blood transfusion and iron chelation therapy. \Methods: A cross-sectional comparative study involving 100 ß-TM patients in Sana'a City-Yemen, was conducted, categorizing the participants into splenectomized and non-splenectomized groups. Sociodemographic data were collected via a structured questionnaire,, ferritin levels were assessed using the Cobas e411 method, and immunoglobulins and complement factors were quantified using the immunoturbidimetry method. Results: The results indicate that ß-TM patients who have undergone splenectomy exhibit higher serum ferritin and immunoglobulin (IgM, IgG, IgA) levels than non-splenectomized ß -TM patients, with stable C3 and a non-significant decline in C4. Additionally, significant correlations were found between IgG, IgA, blood transfusions and iron chelation therapy, whereas C3 and C4 levels were not significantly associated with these treatments. Conclusion: The findings indicated that splenectomy alters the immunological profile of ß-TM patients, although the precise mechanism underlying this alteration remains ambiguous; thus, analyzing serum immunoglobulins and complements levels may prove beneficial in assessing infection severity in these patients.

مجلة جامعة صنعاء للطب والعلوم الصحيةVol. 18(5)
Sana'a University (YE)
Openalex Percentile: Top 55%
Hemoglobinopathies and Related Disorders
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.