Emerging biomarkers for improving pregnancy planning in multiple sclerosis

Patient disability, relapse rate, and age are used for family planning in multiple sclerosis (MS). However, the need for more accurate biomarkers is widely recognized. We aimed to explore the influence of age on neurofilament light chain (sNfL), which reflects acute inflammation; glial fibrillary ac...

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Published inFrontiers in neurology Vol. 15; p. 1292296
Main Authors Cuello, Juan Pablo, Meldaña Rivera, Ariana, Monreal, Enric, Gómez Lozano, Ana, García Cano, Ana Maria, García Domínguez, Jose Manuel, Fernández Velasco, José Ignacio, Costa-Frossard França, Lucienne, Goicochea, Haydee, Higueras, Yolanda, De León-Luis, Juan Antonio, Sainz De La Maza, Susana, Villarrubia, Noelia, Arribas Gómez, Ignacio, Ruiz Perez, Irene, Martinez Ginés, Maria Luisa, Villar, Luisa María
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 15.02.2024
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ISSN1664-2295
1664-2295
DOI10.3389/fneur.2024.1292296

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Abstract Patient disability, relapse rate, and age are used for family planning in multiple sclerosis (MS). However, the need for more accurate biomarkers is widely recognized. We aimed to explore the influence of age on neurofilament light chain (sNfL), which reflects acute inflammation; glial fibrillary acidic protein (GFAP), associated with disability progression independent of relapses; and anti-Müllerian hormone (AMH), reflecting ovarian reserve, to provide a tailored family planning strategy. This case-control study included 95 MS patients and 61 healthy control women (HCW). sNfL and GFAP levels were measured using a sensitive single-molecule array assay. AMH levels were measured by the automated Elecsys Anti-Müllerian Hormone Assay. We observed no significant differences in AMH values between MS patients and the control group within any of the age-matched categories. Age exhibited a negative correlation with AMH values in both groups, as expected. Nevertheless, our findings suggest a slight tendency toward reduced ovarian reserve in MS patients (rho MS patients = -0.67, < 0.0001; rho HCW = -0.43, = 0.0006). Interestingly, among the 76 MS participants under 40 years old, we identified ten individuals (13.1%) with AMH levels below 0.7 ng/ml, indicative of a low ovarian reserve, and an additional six individuals (7.8%) with AMH levels between 0.7 ng/ml and 0.9 ng/ml, suggesting a potential risk of premature ovarian failure. Conversely, sNfL and GFAP levels in the MS group exhibited high variability but showed no significant association with age intervals. We found no significant differences in AMH, sNfL or GFAP values between MS patients and the control group within any of the age-matched categories. The assessment of AMH, sNFL and GFAP levels at MS onset facilitates personalized therapeutic and family planning strategies for childbearing-age women.
AbstractList Patient disability, relapse rate, and age are used for family planning in multiple sclerosis (MS). However, the need for more accurate biomarkers is widely recognized. We aimed to explore the influence of age on neurofilament light chain (sNfL), which reflects acute inflammation; glial fibrillary acidic protein (GFAP), associated with disability progression independent of relapses; and anti-Müllerian hormone (AMH), reflecting ovarian reserve, to provide a tailored family planning strategy.BackgroundPatient disability, relapse rate, and age are used for family planning in multiple sclerosis (MS). However, the need for more accurate biomarkers is widely recognized. We aimed to explore the influence of age on neurofilament light chain (sNfL), which reflects acute inflammation; glial fibrillary acidic protein (GFAP), associated with disability progression independent of relapses; and anti-Müllerian hormone (AMH), reflecting ovarian reserve, to provide a tailored family planning strategy.This case-control study included 95 MS patients and 61 healthy control women (HCW). sNfL and GFAP levels were measured using a sensitive single-molecule array assay. AMH levels were measured by the automated Elecsys® Anti-Müllerian Hormone Assay.MethodsThis case-control study included 95 MS patients and 61 healthy control women (HCW). sNfL and GFAP levels were measured using a sensitive single-molecule array assay. AMH levels were measured by the automated Elecsys® Anti-Müllerian Hormone Assay.We observed no significant differences in AMH values between MS patients and the control group within any of the age-matched categories. Age exhibited a negative correlation with AMH values in both groups, as expected. Nevertheless, our findings suggest a slight tendency toward reduced ovarian reserve in MS patients (rho MS patients = -0.67, p < 0.0001; rho HCW = -0.43, p = 0.0006). Interestingly, among the 76 MS participants under 40 years old, we identified ten individuals (13.1%) with AMH levels below 0.7 ng/ml, indicative of a low ovarian reserve, and an additional six individuals (7.8%) with AMH levels between 0.7 ng/ml and 0.9 ng/ml, suggesting a potential risk of premature ovarian failure. Conversely, sNfL and GFAP levels in the MS group exhibited high variability but showed no significant association with age intervals.ResultsWe observed no significant differences in AMH values between MS patients and the control group within any of the age-matched categories. Age exhibited a negative correlation with AMH values in both groups, as expected. Nevertheless, our findings suggest a slight tendency toward reduced ovarian reserve in MS patients (rho MS patients = -0.67, p < 0.0001; rho HCW = -0.43, p = 0.0006). Interestingly, among the 76 MS participants under 40 years old, we identified ten individuals (13.1%) with AMH levels below 0.7 ng/ml, indicative of a low ovarian reserve, and an additional six individuals (7.8%) with AMH levels between 0.7 ng/ml and 0.9 ng/ml, suggesting a potential risk of premature ovarian failure. Conversely, sNfL and GFAP levels in the MS group exhibited high variability but showed no significant association with age intervals.We found no significant differences in AMH, sNfL or GFAP values between MS patients and the control group within any of the age-matched categories. The assessment of AMH, sNFL and GFAP levels at MS onset facilitates personalized therapeutic and family planning strategies for childbearing-age women.ConclusionWe found no significant differences in AMH, sNfL or GFAP values between MS patients and the control group within any of the age-matched categories. The assessment of AMH, sNFL and GFAP levels at MS onset facilitates personalized therapeutic and family planning strategies for childbearing-age women.
Patient disability, relapse rate, and age are used for family planning in multiple sclerosis (MS). However, the need for more accurate biomarkers is widely recognized. We aimed to explore the influence of age on neurofilament light chain (sNfL), which reflects acute inflammation; glial fibrillary acidic protein (GFAP), associated with disability progression independent of relapses; and anti-Müllerian hormone (AMH), reflecting ovarian reserve, to provide a tailored family planning strategy. This case-control study included 95 MS patients and 61 healthy control women (HCW). sNfL and GFAP levels were measured using a sensitive single-molecule array assay. AMH levels were measured by the automated Elecsys Anti-Müllerian Hormone Assay. We observed no significant differences in AMH values between MS patients and the control group within any of the age-matched categories. Age exhibited a negative correlation with AMH values in both groups, as expected. Nevertheless, our findings suggest a slight tendency toward reduced ovarian reserve in MS patients (rho MS patients = -0.67, < 0.0001; rho HCW = -0.43, = 0.0006). Interestingly, among the 76 MS participants under 40 years old, we identified ten individuals (13.1%) with AMH levels below 0.7 ng/ml, indicative of a low ovarian reserve, and an additional six individuals (7.8%) with AMH levels between 0.7 ng/ml and 0.9 ng/ml, suggesting a potential risk of premature ovarian failure. Conversely, sNfL and GFAP levels in the MS group exhibited high variability but showed no significant association with age intervals. We found no significant differences in AMH, sNfL or GFAP values between MS patients and the control group within any of the age-matched categories. The assessment of AMH, sNFL and GFAP levels at MS onset facilitates personalized therapeutic and family planning strategies for childbearing-age women.
A case-control study comprising 95 multiple sclerosis patients and 61 healthy control women. Evaluating Anti-Müllerian hormone, Neurofilament light-chain, and Glial Fibrillary Acidic Protein at disease onset enables personalized therapeutic and family planning strategies.
BackgroundPatient disability, relapse rate, and age are used for family planning in multiple sclerosis (MS). However, the need for more accurate biomarkers is widely recognized. We aimed to explore the influence of age on neurofilament light chain (sNfL), which reflects acute inflammation; glial fibrillary acidic protein (GFAP), associated with disability progression independent of relapses; and anti-Müllerian hormone (AMH), reflecting ovarian reserve, to provide a tailored family planning strategy.MethodsThis case-control study included 95 MS patients and 61 healthy control women (HCW). sNfL and GFAP levels were measured using a sensitive single-molecule array assay. AMH levels were measured by the automated Elecsys® Anti-Müllerian Hormone Assay.ResultsWe observed no significant differences in AMH values between MS patients and the control group within any of the age-matched categories. Age exhibited a negative correlation with AMH values in both groups, as expected. Nevertheless, our findings suggest a slight tendency toward reduced ovarian reserve in MS patients (rho MS patients = −0.67, p < 0.0001; rho HCW = −0.43, p = 0.0006). Interestingly, among the 76 MS participants under 40 years old, we identified ten individuals (13.1%) with AMH levels below 0.7 ng/ml, indicative of a low ovarian reserve, and an additional six individuals (7.8%) with AMH levels between 0.7 ng/ml and 0.9 ng/ml, suggesting a potential risk of premature ovarian failure. Conversely, sNfL and GFAP levels in the MS group exhibited high variability but showed no significant association with age intervals.ConclusionWe found no significant differences in AMH, sNfL or GFAP values between MS patients and the control group within any of the age-matched categories. The assessment of AMH, sNFL and GFAP levels at MS onset facilitates personalized therapeutic and family planning strategies for childbearing-age women.
Author Cuello, Juan Pablo
Monreal, Enric
García Cano, Ana Maria
Fernández Velasco, José Ignacio
Gómez Lozano, Ana
Meldaña Rivera, Ariana
Higueras, Yolanda
Sainz De La Maza, Susana
Villarrubia, Noelia
Ruiz Perez, Irene
Martinez Ginés, Maria Luisa
Costa-Frossard França, Lucienne
De León-Luis, Juan Antonio
García Domínguez, Jose Manuel
Goicochea, Haydee
Arribas Gómez, Ignacio
Villar, Luisa María
AuthorAffiliation 4 Department of Clinical Biochemistry, Hospital Universitario Ramón y Cajal , Madrid , Spain
5 Department of Immunology, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Red Española de Esclerosis Múltiple (REEM), Red de Enfermedades Inflamatorias (REI) , Madrid , Spain
7 Department of Obstetrics and Gynecology, Hospital General Universitario Gregorio Marañón , Madrid , Spain
3 Department of Neurology, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Red Española de Esclerosis Múltiple (REEM), Red de Enfermedades Inflamatorias (REI) , Madrid , Spain
1 Department of Neurology, Hospital General Universitario Gregorio Marañón , Madrid , Spain
2 Health Research Institute Gregorio Marañón , Madrid , Spain
6 Department of Public and Maternal and Child Health, School of Medicine, Complutense University of Madrid , Madrid , Spain
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Copyright © 2024 Cuello, Meldaña Rivera, Monreal, Gómez Lozano, García Cano, García Domínguez, Fernández Velasco, Costa-Frossard França, Goicochea, Higueras, De León-Luis, Sainz De La Maza, Villarrubia, Arribas Gómez, Ruiz Perez, Martinez Ginés and Villar. 2024 Cuello, Meldaña Rivera, Monreal, Gómez Lozano, García Cano, García Domínguez, Fernández Velasco, Costa-Frossard França, Goicochea, Higueras, De León-Luis, Sainz De La Maza, Villarrubia, Arribas Gómez, Ruiz Perez, Martinez Ginés and Villar
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Keywords antimüllerian hormone
Multiple sclerosis
neurofilament light chain
glial fibrillary acidic protein
pregnancy
Language English
License Copyright © 2024 Cuello, Meldaña Rivera, Monreal, Gómez Lozano, García Cano, García Domínguez, Fernández Velasco, Costa-Frossard França, Goicochea, Higueras, De León-Luis, Sainz De La Maza, Villarrubia, Arribas Gómez, Ruiz Perez, Martinez Ginés and Villar.
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Cristina Valencia-Sanchez, Mayo Clinic Arizona, United States
ORCID: Juan Antonio De León-Luis orcid.org/0000-0002-6320-2668
Maria Luisa Martinez Ginés orcid.org/0009-0005-1264-2793
Edited by: Patricia Coyle, Stony Brook University, United States
Reviewed by: Lucía Romero-Pinel, Hospital Universitari de Bellvitge, Spain
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Snippet Patient disability, relapse rate, and age are used for family planning in multiple sclerosis (MS). However, the need for more accurate biomarkers is widely...
A case-control study comprising 95 multiple sclerosis patients and 61 healthy control women. Evaluating Anti-Müllerian hormone, Neurofilament light-chain, and...
BackgroundPatient disability, relapse rate, and age are used for family planning in multiple sclerosis (MS). However, the need for more accurate biomarkers is...
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SubjectTerms antimüllerian hormone
glial fibrillary acidic protein
Multiple sclerosis
neurofilament light chain
Neurology
pregnancy
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Title Emerging biomarkers for improving pregnancy planning in multiple sclerosis
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