Adropin and Preptin Levels in β-Thalassemia Major Complications in Babylon Province

Background: Thalassemia refers to a group of diseases in which one or more globin chains are produced less or not at all, causing a wide range of phenotypes from anemia to clinically asymptomatic individuals. Disturbances in the homeostasis of carbohydrates, serum lipids, and oxidative stress are th...

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Main Authors: Zinah Abbass Ali, Samar Hasan Shammar
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2024-12-01
Series:Medical Journal of Babylon
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Online Access:https://doi.org/10.4103/MJBL.MJBL_185_24
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author Zinah Abbass Ali
Samar Hasan Shammar
author_facet Zinah Abbass Ali
Samar Hasan Shammar
author_sort Zinah Abbass Ali
collection DOAJ
description Background: Thalassemia refers to a group of diseases in which one or more globin chains are produced less or not at all, causing a wide range of phenotypes from anemia to clinically asymptomatic individuals. Disturbances in the homeostasis of carbohydrates, serum lipids, and oxidative stress are the most common diseases brought on by iron overload in beta-thalassemia major (β-TM). Objective: To examine the association of biochemical parameters with β-TM complications in Babylon Province. Materials and Methods: This study involved 100 individuals, separated into two groups: 50 subjects and 50 controls. Commercial enzyme-linked immunosorbent assay kits were used to measure cystatin-C, ferritin, insulin, preptin, and adropin, while serum blood urea (B. urea), serum creatinine (S.Cr), and lipid profile along with fasting glucose concentration were calculated by colorimetric kit using the spectrophotometer method. Results: Serum samples were used to measure biochemical parameters of S.Cr, urea, cystatin-C, ferritin, fasting insulin, fasting glucose, adropin, preptin, and lipid profile. Adropin in the patient group of thalassemia was significantly decreased compared to the healthy controls (P < 0.001). However, preptin, cystatin-C, ferritin, B. urea, and S.Cr were elevated in the patient groups compared to the control group (P < 0.005). Also, the lipid profile, including triglycerides, cholesterol, high-density lipoprotein, low-density lipoprotein, and very low-density lipoprotein, showed significant differences between patient group of thalassemia and the control group. Conclusion: Adropin and preptin were considerable predictive markers for the development of complications in patients with β-TM.
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spelling doaj-art-2860b356017a4b86ac9e5e4431d219d02025-01-17T10:54:56ZengWolters Kluwer Medknow PublicationsMedical Journal of Babylon1812-156X2312-67602024-12-0121476677110.4103/MJBL.MJBL_185_24Adropin and Preptin Levels in β-Thalassemia Major Complications in Babylon ProvinceZinah Abbass AliSamar Hasan ShammarBackground: Thalassemia refers to a group of diseases in which one or more globin chains are produced less or not at all, causing a wide range of phenotypes from anemia to clinically asymptomatic individuals. Disturbances in the homeostasis of carbohydrates, serum lipids, and oxidative stress are the most common diseases brought on by iron overload in beta-thalassemia major (β-TM). Objective: To examine the association of biochemical parameters with β-TM complications in Babylon Province. Materials and Methods: This study involved 100 individuals, separated into two groups: 50 subjects and 50 controls. Commercial enzyme-linked immunosorbent assay kits were used to measure cystatin-C, ferritin, insulin, preptin, and adropin, while serum blood urea (B. urea), serum creatinine (S.Cr), and lipid profile along with fasting glucose concentration were calculated by colorimetric kit using the spectrophotometer method. Results: Serum samples were used to measure biochemical parameters of S.Cr, urea, cystatin-C, ferritin, fasting insulin, fasting glucose, adropin, preptin, and lipid profile. Adropin in the patient group of thalassemia was significantly decreased compared to the healthy controls (P < 0.001). However, preptin, cystatin-C, ferritin, B. urea, and S.Cr were elevated in the patient groups compared to the control group (P < 0.005). Also, the lipid profile, including triglycerides, cholesterol, high-density lipoprotein, low-density lipoprotein, and very low-density lipoprotein, showed significant differences between patient group of thalassemia and the control group. Conclusion: Adropin and preptin were considerable predictive markers for the development of complications in patients with β-TM.https://doi.org/10.4103/MJBL.MJBL_185_24adropinβ-thalassemia majorcreatininepreptinurea
spellingShingle Zinah Abbass Ali
Samar Hasan Shammar
Adropin and Preptin Levels in β-Thalassemia Major Complications in Babylon Province
Medical Journal of Babylon
adropin
β-thalassemia major
creatinine
preptin
urea
title Adropin and Preptin Levels in β-Thalassemia Major Complications in Babylon Province
title_full Adropin and Preptin Levels in β-Thalassemia Major Complications in Babylon Province
title_fullStr Adropin and Preptin Levels in β-Thalassemia Major Complications in Babylon Province
title_full_unstemmed Adropin and Preptin Levels in β-Thalassemia Major Complications in Babylon Province
title_short Adropin and Preptin Levels in β-Thalassemia Major Complications in Babylon Province
title_sort adropin and preptin levels in β thalassemia major complications in babylon province
topic adropin
β-thalassemia major
creatinine
preptin
urea
url https://doi.org/10.4103/MJBL.MJBL_185_24
work_keys_str_mv AT zinahabbassali adropinandpreptinlevelsinbthalassemiamajorcomplicationsinbabylonprovince
AT samarhasanshammar adropinandpreptinlevelsinbthalassemiamajorcomplicationsinbabylonprovince