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Activation Ratio Correlates with IQ in Female Carriers of the FMR1 Premutation

Carriers of the FMR1 premutation (PM) allele are at risk of one or more clinical conditions referred to as FX premutation-associated conditions (FXPAC). Since the FMR1 gene is on the X chromosome, the activation ratio (AR) may impact the risk, age of onset, progression, and severity of these conditi...

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Autores principales: Protic, Dragana, Polli, Roberta, Hwang, Ye Hyun, Mendoza, Guadalupe, Hagerman, Randi, Durbin-Johnson, Blythe, Hayward, Bruce E., Usdin, Karen, Murgia, Alessandra, Tassone, Flora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341054/
https://www.ncbi.nlm.nih.gov/pubmed/37443745
http://dx.doi.org/10.3390/cells12131711
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author Protic, Dragana
Polli, Roberta
Hwang, Ye Hyun
Mendoza, Guadalupe
Hagerman, Randi
Durbin-Johnson, Blythe
Hayward, Bruce E.
Usdin, Karen
Murgia, Alessandra
Tassone, Flora
author_facet Protic, Dragana
Polli, Roberta
Hwang, Ye Hyun
Mendoza, Guadalupe
Hagerman, Randi
Durbin-Johnson, Blythe
Hayward, Bruce E.
Usdin, Karen
Murgia, Alessandra
Tassone, Flora
author_sort Protic, Dragana
collection PubMed
description Carriers of the FMR1 premutation (PM) allele are at risk of one or more clinical conditions referred to as FX premutation-associated conditions (FXPAC). Since the FMR1 gene is on the X chromosome, the activation ratio (AR) may impact the risk, age of onset, progression, and severity of these conditions. The aim of this study was to evaluate the reliability of AR measured using different approaches and to investigate potential correlations with clinical outcomes. Molecular and clinical assessments were obtained for 30 PM female participants, and AR was assessed using both Southern blot analysis (AR-Sb) and methylation PCR (AR-mPCR). Higher ARs were associated with lower FMR1 transcript levels for any given repeat length. The higher AR-Sb was significantly associated with performance, verbal, and full-scale IQ scores, confirming previous reports. However, the AR-mPCR was not significantly associated (p > 0.05) with these measures. Similarly, the odds of depression and the number of medical conditions were correlated with higher AR-Sb but not correlated with a higher AR-mPCR. This study suggests that AR-Sb may be a more reliable measure of the AR in female carriers of PM alleles. However, further studies are warranted in a larger sample size to fully evaluate the methylation status in these participants and how it may affect the clinical phenotype.
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spelling pubmed-103410542023-07-14 Activation Ratio Correlates with IQ in Female Carriers of the FMR1 Premutation Protic, Dragana Polli, Roberta Hwang, Ye Hyun Mendoza, Guadalupe Hagerman, Randi Durbin-Johnson, Blythe Hayward, Bruce E. Usdin, Karen Murgia, Alessandra Tassone, Flora Cells Article Carriers of the FMR1 premutation (PM) allele are at risk of one or more clinical conditions referred to as FX premutation-associated conditions (FXPAC). Since the FMR1 gene is on the X chromosome, the activation ratio (AR) may impact the risk, age of onset, progression, and severity of these conditions. The aim of this study was to evaluate the reliability of AR measured using different approaches and to investigate potential correlations with clinical outcomes. Molecular and clinical assessments were obtained for 30 PM female participants, and AR was assessed using both Southern blot analysis (AR-Sb) and methylation PCR (AR-mPCR). Higher ARs were associated with lower FMR1 transcript levels for any given repeat length. The higher AR-Sb was significantly associated with performance, verbal, and full-scale IQ scores, confirming previous reports. However, the AR-mPCR was not significantly associated (p > 0.05) with these measures. Similarly, the odds of depression and the number of medical conditions were correlated with higher AR-Sb but not correlated with a higher AR-mPCR. This study suggests that AR-Sb may be a more reliable measure of the AR in female carriers of PM alleles. However, further studies are warranted in a larger sample size to fully evaluate the methylation status in these participants and how it may affect the clinical phenotype. MDPI 2023-06-24 /pmc/articles/PMC10341054/ /pubmed/37443745 http://dx.doi.org/10.3390/cells12131711 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Protic, Dragana
Polli, Roberta
Hwang, Ye Hyun
Mendoza, Guadalupe
Hagerman, Randi
Durbin-Johnson, Blythe
Hayward, Bruce E.
Usdin, Karen
Murgia, Alessandra
Tassone, Flora
Activation Ratio Correlates with IQ in Female Carriers of the FMR1 Premutation
title Activation Ratio Correlates with IQ in Female Carriers of the FMR1 Premutation
title_full Activation Ratio Correlates with IQ in Female Carriers of the FMR1 Premutation
title_fullStr Activation Ratio Correlates with IQ in Female Carriers of the FMR1 Premutation
title_full_unstemmed Activation Ratio Correlates with IQ in Female Carriers of the FMR1 Premutation
title_short Activation Ratio Correlates with IQ in Female Carriers of the FMR1 Premutation
title_sort activation ratio correlates with iq in female carriers of the fmr1 premutation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341054/
https://www.ncbi.nlm.nih.gov/pubmed/37443745
http://dx.doi.org/10.3390/cells12131711
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