E-ISSN 1658-8088 | ISSN 1658-807X
 

Original Article
Online Published: 08 Feb 2023
 


Erythropoietin resistance in patients with regular hemodialysis in Sohag university hospital

Nagwa S. Ahmed, Aida A Mahmoud, Nayel Abd Elhamed Zaki, Amera A. Genedy.


Abstract
Background: A definite anemia [hemoglobin (HB) 10-12 g/dl] or the need for significantly higher Erythropoietin (EPO) dosages of epoetin alfa are symptoms of EPO resistance, respectively. The recommended restorative goal is to maintain HB levels between 11 and 12 g/dl. Fe deficiency, concurrent inflammation, inadequate dialysis, hyperparathyroidism, hemolysis, vitamin B12, and folate deficiency are the main causes of EPO resistance. The objective of this study was to evaluate patients who receive frequent hemodialysis for EPO resistance.
Methods: This study was performed at Sohag University Hospital on 50 hemodialysis patients compared to 40 healthy adult subjects from June 2021 to January 2022. Serum EPO was analyzed by enzyme-linked immunosorbent assay and Angiotensin Converting Enzyme (ACE) rs1799752 polymorphism was assessed using the Genomic TaqMan genotyping test.
Results: This study found insignificant relation between EPO Resistance Index (ERI) and diverse ACE genotype groups and para thyroid hormone. A further significant direct proportional relationship was found between ERI and Ferritin. EPO and parathyroid hormone did not show any significant relationship.
Conclusion: Considering the non-critical connection between ERI and our components, it is vital to enhance the treatment of anemic patients with chronic kidney diseases to recognize the potential causes of resistance and ponder other variables for resistance before proposing an expanded EPO-stimulating agent administration.

Key words: Erythropoietin, hemodialysis, erythropoietin resistance index, erythropoietin stimulating agents.


 
ARTICLE TOOLS
Abstract
PDF Fulltext
How to cite this articleHow to cite this article
Citation Tools
Related Records
 Articles by Nagwa S. Ahmed
Articles by Aida A Mahmoud
Articles by Nayel Abd Elhamed Zaki
Articles by Amera A. Genedy
on Google
on Google Scholar


How to Cite this Article
Pubmed Style

Ahmed NS, Mahmoud AA, Zaki NAE, Genedy AA. Erythropoietin resistance in patients with regular hemodialysis in Sohag university hospital. JBCGenetics. 2023; 6(1): 14-21. doi:10.24911/JBCGenetics/183-1670609060


Web Style

Ahmed NS, Mahmoud AA, Zaki NAE, Genedy AA. Erythropoietin resistance in patients with regular hemodialysis in Sohag university hospital. https://www.jbcgenetics.com/?mno=93421 [Access: November 14, 2024]. doi:10.24911/JBCGenetics/183-1670609060


AMA (American Medical Association) Style

Ahmed NS, Mahmoud AA, Zaki NAE, Genedy AA. Erythropoietin resistance in patients with regular hemodialysis in Sohag university hospital. JBCGenetics. 2023; 6(1): 14-21. doi:10.24911/JBCGenetics/183-1670609060



Vancouver/ICMJE Style

Ahmed NS, Mahmoud AA, Zaki NAE, Genedy AA. Erythropoietin resistance in patients with regular hemodialysis in Sohag university hospital. JBCGenetics. (2023), [cited November 14, 2024]; 6(1): 14-21. doi:10.24911/JBCGenetics/183-1670609060



Harvard Style

Ahmed, N. S., Mahmoud, . A. A., Zaki, . N. A. E. & Genedy, . A. A. (2023) Erythropoietin resistance in patients with regular hemodialysis in Sohag university hospital. JBCGenetics, 6 (1), 14-21. doi:10.24911/JBCGenetics/183-1670609060



Turabian Style

Ahmed, Nagwa S., Aida A Mahmoud, Nayel Abd Elhamed Zaki, and Amera A. Genedy. 2023. Erythropoietin resistance in patients with regular hemodialysis in Sohag university hospital. Journal of Biochemical and Clinical Genetics, 6 (1), 14-21. doi:10.24911/JBCGenetics/183-1670609060



Chicago Style

Ahmed, Nagwa S., Aida A Mahmoud, Nayel Abd Elhamed Zaki, and Amera A. Genedy. "Erythropoietin resistance in patients with regular hemodialysis in Sohag university hospital." Journal of Biochemical and Clinical Genetics 6 (2023), 14-21. doi:10.24911/JBCGenetics/183-1670609060



MLA (The Modern Language Association) Style

Ahmed, Nagwa S., Aida A Mahmoud, Nayel Abd Elhamed Zaki, and Amera A. Genedy. "Erythropoietin resistance in patients with regular hemodialysis in Sohag university hospital." Journal of Biochemical and Clinical Genetics 6.1 (2023), 14-21. Print. doi:10.24911/JBCGenetics/183-1670609060



APA (American Psychological Association) Style

Ahmed, N. S., Mahmoud, . A. A., Zaki, . N. A. E. & Genedy, . A. A. (2023) Erythropoietin resistance in patients with regular hemodialysis in Sohag university hospital. Journal of Biochemical and Clinical Genetics, 6 (1), 14-21. doi:10.24911/JBCGenetics/183-1670609060





Most Viewed Articles
Most Accessed Articles

  • Frontonasal dysplasia: a review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Muhammad Arshad
    JBCGenetics. 2018; 1(2): 66-76
    » Abstract » doi: 10.24911/JBCGenetics/183-1530765389

  • The role of C-terminal tensin-like (Cten) gene in cancer metastasis
    Saleh Alghamdi, Sarah Alkwai, Mohammad Ilyas
    JBCGenetics. 2018; 1(1): 2-9
    » Abstract » doi: 10.24911/JBCGenetics/183-1531548689

  • Clinical reassessment of post-laboratory variant call format (VCF) files
    Lamia Alsubaie, Saeed Alturki, Ali Alothaim, Ahmed Alfares
    JBCGenetics. 2018; 1(1): 31-36
    » Abstract » doi: 10.24911/JBCGenetics/183-1529928114

  • Microcephalic osteodysplastic primordial dwarfism type II and Klinefelter syndrome: report of two competing growth syndromes
    AlAnoud Al-Jarbou, Afnan Al-Turki, Suha Tashkandi, Eissa A. Faqeih
    JBCGenetics. 2018; 1(1): 37-39
    » Abstract » doi: 10.24911/JBCGenetics/183-1530040885

  • Recessive ARFGEF2 mutation causes progressive microcephaly, epilepsy, and a distinct MRI pattern
    Maram Alojair, Abdulaziz Alghamdi, Kalthoum Tlili, Sateesh Maddirevula, Fowzan Sami Alkuraya, Brahim Tabarki
    JBCGenetics. 2018; 1(1): 40-42
    » Abstract » doi: 10.24911/JBCGenetics/183-1531469195

  • Most Downloaded
    Top Downloaded Articles

  • Frontonasal dysplasia: a review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Muhammad Arshad
    JBCGenetics. 2018; 1(2): 66-76
    » Abstract » doi: 10.24911/JBCGenetics/183-1530765389

  • Generation of a mouse model of Primary Hyperoxaluria Type 1 via CRISPR/Cas9 mediated gene editing
    Kimberly A Coughlan, Rajanikanth J Maganti, Andrea Frassetto, Christine M DeAntonis, meredith Wolfrom, Anne-Renee Graham, Shawn M Hillier, Steven Fortucci, Hoor Al Jandal, Sue-Jean Hong, Paloma H Giangrande, Paolo GV Martini,
    JBCGenetics. 2019; 2(1): 28-39
    » Abstract » doi: 10.24911/JBCGenetics/183-1542047633

  • Syndactyly genes and classification: a mini review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Safdar Abbas
    JBCGenetics. 2018; 1(1): 10-18
    » Abstract » doi: 10.24911/JBCGenetics/183-1532177257

  • Recessive ARFGEF2 mutation causes progressive microcephaly, epilepsy, and a distinct MRI pattern
    Maram Alojair, Abdulaziz Alghamdi, Kalthoum Tlili, Sateesh Maddirevula, Fowzan Sami Alkuraya, Brahim Tabarki
    JBCGenetics. 2018; 1(1): 40-42
    » Abstract » doi: 10.24911/JBCGenetics/183-1531469195

  • Consanguinity, awareness, and genetic disorders among female university students in Riyadh, Saudi Arabia
    Hadil Alahdal, Huda Alshanbari, Hana Saud Almazroa, Sarah Majed Alayesh, Alaa Mohammad Alrhaili, Nora Alqubi, Fai Fahad Alzamil, Reem Albassam
    JBCGenetics. 2021; 4(1): 27-34
    » Abstract » doi: 10.24911/JBCGenetics/183-1601264923

  • Most Cited Articles
    Most Cited Articles

  • Frontonasal dysplasia: a review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Muhammad Arshad
    JBCGenetics. 2018; 1(2): 66-76
    » Abstract » doi: 10.24911/JBCGenetics/183-1530765389
    Cited : 4 times [Click to see citing articles]

  • Syndactyly genes and classification: a mini review
    Muhammad Umair, Farooq Ahmad, Muhammad Bilal, Safdar Abbas
    JBCGenetics. 2018; 1(1): 10-18
    » Abstract » doi: 10.24911/JBCGenetics/183-1532177257
    Cited : 4 times [Click to see citing articles]

  • Genomics in Saudi Arabia Call for Data-Sharing Policy
    Ahmed Alfares,
    JBCGenetics. 2018; 1(2): 51-52
    » Abstract » doi: 10.24911/JBCGenetics/183-1546945268
    Cited : 4 times [Click to see citing articles]

  • Consanguinity, awareness, and genetic disorders among female university students in Riyadh, Saudi Arabia
    Hadil Alahdal, Huda Alshanbari, Hana Saud Almazroa, Sarah Majed Alayesh, Alaa Mohammad Alrhaili, Nora Alqubi, Fai Fahad Alzamil, Reem Albassam
    JBCGenetics. 2021; 4(1): 27-34
    » Abstract » doi: 10.24911/JBCGenetics/183-1601264923
    Cited : 2 times [Click to see citing articles]

  • Harel-Yoon syndrome: the first case report from Saudi Arabia
    Alaa AlAyed, Manar A. Samman, Abdul Ali Peer-Zada, Mohammed Almannai
    JBCGenetics. 2020; 3(1): 22-27
    » Abstract » doi: 10.24911/JBCGenetics/183-1585816398
    Cited : 2 times [Click to see citing articles]