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Age-Related Macular Degeneration in Patients with Androgenetic Alopecia: Could the Monocyte/HDL Ratio Be the Link?
INTRODUCTION: Both Androgenetic alopecia (AGA) and age-related macular degeneration (AMD) shared the microinflammatory milieu and increased oxidative stress as important criteria in their pathogenesis. The monocyte/high density lipoprotein (HDL) ratio (MHR) seems to be an easy-to-calculate prognosti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mattioli 1885
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656190/ https://www.ncbi.nlm.nih.gov/pubmed/37992380 http://dx.doi.org/10.5826/dpc.1304a285 |
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author | Shams, Ghada Mohamed Saleh, Ahmed Abdel-Wahab Saeed, Ahmed Mohamed El-Damaty, Safa Nabil Abdel-Ghaffar, Amira Osama |
author_facet | Shams, Ghada Mohamed Saleh, Ahmed Abdel-Wahab Saeed, Ahmed Mohamed El-Damaty, Safa Nabil Abdel-Ghaffar, Amira Osama |
author_sort | Shams, Ghada Mohamed |
collection | PubMed |
description | INTRODUCTION: Both Androgenetic alopecia (AGA) and age-related macular degeneration (AMD) shared the microinflammatory milieu and increased oxidative stress as important criteria in their pathogenesis. The monocyte/high density lipoprotein (HDL) ratio (MHR) seems to be an easy-to-calculate prognostic marker of microinflammation. OBJECTIVES: To assess MHR in patients with AGA and its correlation to AMD in these patients, if any. METHODS: Forty patients with AGA aged 40 years or more of both sexes and 40 control subjects participated in this case-control study. General, dermatological, and ophthalmologic examination, MHR evaluation and optical coherence tomography (OCT) were performed. RESULTS: The mean MHR was significantly higher in AGA patients (6.98 ± 2.21) than in controls (3.82 ± 0.68) (P < 0.001). AMD was significantly higher in patients than controls (P < 0.001). Eighty percent of AGA patients were diagnosed with AMD versus 20% of control subjects. The presence of AMD in AGA was significantly related to the degree of severity of AGA in male patients (P = 0.02). The MHR was significantly higher in AGA patients found to have AMD (9.37 ± 1.1 and 7.01 ± 1.42 in the wet and dry type respectively) than those without AMD (P < 0.001). CONCLUSIONS: AMD may develop more frequently in those with AGA. The MHR seems to be a missing link between both conditions, and could be utilized as a potential biomarker for predicting AMD in AGA patients. |
format | Online Article Text |
id | pubmed-10656190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Mattioli 1885 |
record_format | MEDLINE/PubMed |
spelling | pubmed-106561902023-10-01 Age-Related Macular Degeneration in Patients with Androgenetic Alopecia: Could the Monocyte/HDL Ratio Be the Link? Shams, Ghada Mohamed Saleh, Ahmed Abdel-Wahab Saeed, Ahmed Mohamed El-Damaty, Safa Nabil Abdel-Ghaffar, Amira Osama Dermatol Pract Concept Original Article INTRODUCTION: Both Androgenetic alopecia (AGA) and age-related macular degeneration (AMD) shared the microinflammatory milieu and increased oxidative stress as important criteria in their pathogenesis. The monocyte/high density lipoprotein (HDL) ratio (MHR) seems to be an easy-to-calculate prognostic marker of microinflammation. OBJECTIVES: To assess MHR in patients with AGA and its correlation to AMD in these patients, if any. METHODS: Forty patients with AGA aged 40 years or more of both sexes and 40 control subjects participated in this case-control study. General, dermatological, and ophthalmologic examination, MHR evaluation and optical coherence tomography (OCT) were performed. RESULTS: The mean MHR was significantly higher in AGA patients (6.98 ± 2.21) than in controls (3.82 ± 0.68) (P < 0.001). AMD was significantly higher in patients than controls (P < 0.001). Eighty percent of AGA patients were diagnosed with AMD versus 20% of control subjects. The presence of AMD in AGA was significantly related to the degree of severity of AGA in male patients (P = 0.02). The MHR was significantly higher in AGA patients found to have AMD (9.37 ± 1.1 and 7.01 ± 1.42 in the wet and dry type respectively) than those without AMD (P < 0.001). CONCLUSIONS: AMD may develop more frequently in those with AGA. The MHR seems to be a missing link between both conditions, and could be utilized as a potential biomarker for predicting AMD in AGA patients. Mattioli 1885 2023-10-01 /pmc/articles/PMC10656190/ /pubmed/37992380 http://dx.doi.org/10.5826/dpc.1304a285 Text en ©2023 Shams et al. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (BY-NC-4.0), https://creativecommons.org/licenses/by-nc/4.0/, which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original authors and source are credited. |
spellingShingle | Original Article Shams, Ghada Mohamed Saleh, Ahmed Abdel-Wahab Saeed, Ahmed Mohamed El-Damaty, Safa Nabil Abdel-Ghaffar, Amira Osama Age-Related Macular Degeneration in Patients with Androgenetic Alopecia: Could the Monocyte/HDL Ratio Be the Link? |
title | Age-Related Macular Degeneration in Patients with Androgenetic Alopecia: Could the Monocyte/HDL Ratio Be the Link? |
title_full | Age-Related Macular Degeneration in Patients with Androgenetic Alopecia: Could the Monocyte/HDL Ratio Be the Link? |
title_fullStr | Age-Related Macular Degeneration in Patients with Androgenetic Alopecia: Could the Monocyte/HDL Ratio Be the Link? |
title_full_unstemmed | Age-Related Macular Degeneration in Patients with Androgenetic Alopecia: Could the Monocyte/HDL Ratio Be the Link? |
title_short | Age-Related Macular Degeneration in Patients with Androgenetic Alopecia: Could the Monocyte/HDL Ratio Be the Link? |
title_sort | age-related macular degeneration in patients with androgenetic alopecia: could the monocyte/hdl ratio be the link? |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656190/ https://www.ncbi.nlm.nih.gov/pubmed/37992380 http://dx.doi.org/10.5826/dpc.1304a285 |
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