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APOE Gene polymorphism among Jordanian Alzheimer’s patients with relation to lipid profile

OBJECTIVES: To investigate the frequencies of the apolipoprotein E (APOE) alleles and genotypes and study their relationship with the lipid profile in Jordanian patients with late-onset Alzheimer’s disease (AD). METHODS: This case-control study was carried out on 71 Jordanian individuals: 38 patient...

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Autores principales: Shafagoj, Yanal A., Naffa, Randa G., El-Khateeb, Mohammed S., Abdulla, Yazeed L., Al-qaddoumi, Aseem A., Khatib, Faisal A., AL-Motassem, Yousef F., Al-Khateeb, Eman M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Riyadh : Armed Forces Hospital 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751906/
https://www.ncbi.nlm.nih.gov/pubmed/29455218
http://dx.doi.org/10.17712/nsj.2018.1.20170169
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author Shafagoj, Yanal A.
Naffa, Randa G.
El-Khateeb, Mohammed S.
Abdulla, Yazeed L.
Al-qaddoumi, Aseem A.
Khatib, Faisal A.
AL-Motassem, Yousef F.
Al-Khateeb, Eman M.
author_facet Shafagoj, Yanal A.
Naffa, Randa G.
El-Khateeb, Mohammed S.
Abdulla, Yazeed L.
Al-qaddoumi, Aseem A.
Khatib, Faisal A.
AL-Motassem, Yousef F.
Al-Khateeb, Eman M.
author_sort Shafagoj, Yanal A.
collection PubMed
description OBJECTIVES: To investigate the frequencies of the apolipoprotein E (APOE) alleles and genotypes and study their relationship with the lipid profile in Jordanian patients with late-onset Alzheimer’s disease (AD). METHODS: This case-control study was carried out on 71 Jordanian individuals: 38 patients with late-onset AD (age ≥65 years) and 33 age-matched healthy controls. All participants were recruited from senior homes and Jordan University Hospital, Amman, Jordan between January 2010 and December 2013. Each sample was examined for APOE’s 3 major isoforms (e2, e3, e4) using the polymerase chain reaction technique (PCR) followed by the sequencing technique. In addition, samples were screened for lipid profiles (total cholesterol (TC), high-density lipoprotein (HDL), lower-density lipoprotein (LDL), and triglyceride (TG) levels. RESULTS: The e3/e4 genotype and e4 allele prevalence were higher in AD patients compared to healthy controls (26.3% vs. 3.0%, p=0.03 and 15.8% vs. 4.5%, p=0.03; respectively). In the AD group, the e2 carriers showed the lowest levels of total and LDL cholesterol, and the e4 carriers showed the highest levels of total and LDL cholesterol, although the difference was not statistically significant (p>0.05). CONCLUSION: APOE-e4 frequency was almost 4 times higher in the AD group compared to the control group, and this difference was statistically significant. A trend that was observed in the AD group regarding the lipid profile and e2 and e4 carriers requires further investigation using a larger sample size.
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spelling pubmed-67519062021-02-17 APOE Gene polymorphism among Jordanian Alzheimer’s patients with relation to lipid profile Shafagoj, Yanal A. Naffa, Randa G. El-Khateeb, Mohammed S. Abdulla, Yazeed L. Al-qaddoumi, Aseem A. Khatib, Faisal A. AL-Motassem, Yousef F. Al-Khateeb, Eman M. Neurosciences (Riyadh) Original Article OBJECTIVES: To investigate the frequencies of the apolipoprotein E (APOE) alleles and genotypes and study their relationship with the lipid profile in Jordanian patients with late-onset Alzheimer’s disease (AD). METHODS: This case-control study was carried out on 71 Jordanian individuals: 38 patients with late-onset AD (age ≥65 years) and 33 age-matched healthy controls. All participants were recruited from senior homes and Jordan University Hospital, Amman, Jordan between January 2010 and December 2013. Each sample was examined for APOE’s 3 major isoforms (e2, e3, e4) using the polymerase chain reaction technique (PCR) followed by the sequencing technique. In addition, samples were screened for lipid profiles (total cholesterol (TC), high-density lipoprotein (HDL), lower-density lipoprotein (LDL), and triglyceride (TG) levels. RESULTS: The e3/e4 genotype and e4 allele prevalence were higher in AD patients compared to healthy controls (26.3% vs. 3.0%, p=0.03 and 15.8% vs. 4.5%, p=0.03; respectively). In the AD group, the e2 carriers showed the lowest levels of total and LDL cholesterol, and the e4 carriers showed the highest levels of total and LDL cholesterol, although the difference was not statistically significant (p>0.05). CONCLUSION: APOE-e4 frequency was almost 4 times higher in the AD group compared to the control group, and this difference was statistically significant. A trend that was observed in the AD group regarding the lipid profile and e2 and e4 carriers requires further investigation using a larger sample size. Riyadh : Armed Forces Hospital 2018-01 /pmc/articles/PMC6751906/ /pubmed/29455218 http://dx.doi.org/10.17712/nsj.2018.1.20170169 Text en Copyright: © Neurosciences http://creativecommons.org/licenses/by-nc/3.0/ Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work.
spellingShingle Original Article
Shafagoj, Yanal A.
Naffa, Randa G.
El-Khateeb, Mohammed S.
Abdulla, Yazeed L.
Al-qaddoumi, Aseem A.
Khatib, Faisal A.
AL-Motassem, Yousef F.
Al-Khateeb, Eman M.
APOE Gene polymorphism among Jordanian Alzheimer’s patients with relation to lipid profile
title APOE Gene polymorphism among Jordanian Alzheimer’s patients with relation to lipid profile
title_full APOE Gene polymorphism among Jordanian Alzheimer’s patients with relation to lipid profile
title_fullStr APOE Gene polymorphism among Jordanian Alzheimer’s patients with relation to lipid profile
title_full_unstemmed APOE Gene polymorphism among Jordanian Alzheimer’s patients with relation to lipid profile
title_short APOE Gene polymorphism among Jordanian Alzheimer’s patients with relation to lipid profile
title_sort apoe gene polymorphism among jordanian alzheimer’s patients with relation to lipid profile
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751906/
https://www.ncbi.nlm.nih.gov/pubmed/29455218
http://dx.doi.org/10.17712/nsj.2018.1.20170169
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