Cargando…
Hemochromatosis Mutations, Brain Iron Imaging, and Dementia in the UK Biobank Cohort
BACKGROUND: Brain iron deposition occurs in dementia. In European ancestry populations, the HFE p.C282Y variant can cause iron overload and hemochromatosis, mostly in homozygous males. OBJECTIVE: To estimate p.C282Y associations with brain MRI features plus incident dementia diagnoses during follow-...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990419/ https://www.ncbi.nlm.nih.gov/pubmed/33427739 http://dx.doi.org/10.3233/JAD-201080 |
_version_ | 1783669068776079360 |
---|---|
author | Atkins, Janice L. Pilling, Luke C. Heales, Christine J. Savage, Sharon Kuo, Chia-Ling Kuchel, George A. Steffens, David C. Melzer, David |
author_facet | Atkins, Janice L. Pilling, Luke C. Heales, Christine J. Savage, Sharon Kuo, Chia-Ling Kuchel, George A. Steffens, David C. Melzer, David |
author_sort | Atkins, Janice L. |
collection | PubMed |
description | BACKGROUND: Brain iron deposition occurs in dementia. In European ancestry populations, the HFE p.C282Y variant can cause iron overload and hemochromatosis, mostly in homozygous males. OBJECTIVE: To estimate p.C282Y associations with brain MRI features plus incident dementia diagnoses during follow-up in a large community cohort. METHODS: UK Biobank participants with follow-up hospitalization records (mean 10.5 years). MRI in 206 p.C282Y homozygotes versus 23,349 without variants, including T2(*) measures (lower values indicating more iron). RESULTS: European ancestry participants included 2,890 p.C282Y homozygotes. Male p.C282Y homozygotes had lower T2(*) measures in areas including the putamen, thalamus, and hippocampus, compared to no HFE mutations. Incident dementia was more common in p.C282Y homozygous men (Hazard Ratio HR = 1.83; 95% CI 1.23 to 2.72, p = 0.003), as was delirium. There were no associations in homozygote women or in heterozygotes. CONCLUSION: Studies are needed of whether early iron reduction prevents or slows related brain pathologies in male HFE p.C282Y homozygotes. |
format | Online Article Text |
id | pubmed-7990419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79904192021-04-14 Hemochromatosis Mutations, Brain Iron Imaging, and Dementia in the UK Biobank Cohort Atkins, Janice L. Pilling, Luke C. Heales, Christine J. Savage, Sharon Kuo, Chia-Ling Kuchel, George A. Steffens, David C. Melzer, David J Alzheimers Dis Research Article BACKGROUND: Brain iron deposition occurs in dementia. In European ancestry populations, the HFE p.C282Y variant can cause iron overload and hemochromatosis, mostly in homozygous males. OBJECTIVE: To estimate p.C282Y associations with brain MRI features plus incident dementia diagnoses during follow-up in a large community cohort. METHODS: UK Biobank participants with follow-up hospitalization records (mean 10.5 years). MRI in 206 p.C282Y homozygotes versus 23,349 without variants, including T2(*) measures (lower values indicating more iron). RESULTS: European ancestry participants included 2,890 p.C282Y homozygotes. Male p.C282Y homozygotes had lower T2(*) measures in areas including the putamen, thalamus, and hippocampus, compared to no HFE mutations. Incident dementia was more common in p.C282Y homozygous men (Hazard Ratio HR = 1.83; 95% CI 1.23 to 2.72, p = 0.003), as was delirium. There were no associations in homozygote women or in heterozygotes. CONCLUSION: Studies are needed of whether early iron reduction prevents or slows related brain pathologies in male HFE p.C282Y homozygotes. IOS Press 2021-02-02 /pmc/articles/PMC7990419/ /pubmed/33427739 http://dx.doi.org/10.3233/JAD-201080 Text en © 2021 – The authors. Published by IOS Press https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) License (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Atkins, Janice L. Pilling, Luke C. Heales, Christine J. Savage, Sharon Kuo, Chia-Ling Kuchel, George A. Steffens, David C. Melzer, David Hemochromatosis Mutations, Brain Iron Imaging, and Dementia in the UK Biobank Cohort |
title | Hemochromatosis Mutations, Brain Iron Imaging, and Dementia in the UK Biobank Cohort |
title_full | Hemochromatosis Mutations, Brain Iron Imaging, and Dementia in the UK Biobank Cohort |
title_fullStr | Hemochromatosis Mutations, Brain Iron Imaging, and Dementia in the UK Biobank Cohort |
title_full_unstemmed | Hemochromatosis Mutations, Brain Iron Imaging, and Dementia in the UK Biobank Cohort |
title_short | Hemochromatosis Mutations, Brain Iron Imaging, and Dementia in the UK Biobank Cohort |
title_sort | hemochromatosis mutations, brain iron imaging, and dementia in the uk biobank cohort |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990419/ https://www.ncbi.nlm.nih.gov/pubmed/33427739 http://dx.doi.org/10.3233/JAD-201080 |
work_keys_str_mv | AT atkinsjanicel hemochromatosismutationsbrainironimaginganddementiaintheukbiobankcohort AT pillinglukec hemochromatosismutationsbrainironimaginganddementiaintheukbiobankcohort AT healeschristinej hemochromatosismutationsbrainironimaginganddementiaintheukbiobankcohort AT savagesharon hemochromatosismutationsbrainironimaginganddementiaintheukbiobankcohort AT kuochialing hemochromatosismutationsbrainironimaginganddementiaintheukbiobankcohort AT kuchelgeorgea hemochromatosismutationsbrainironimaginganddementiaintheukbiobankcohort AT steffensdavidc hemochromatosismutationsbrainironimaginganddementiaintheukbiobankcohort AT melzerdavid hemochromatosismutationsbrainironimaginganddementiaintheukbiobankcohort |