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  1. AU="Spano, Luana"
  2. AU="Macomb, Christopher V"
  3. AU="Cylwik, Jolanta"
  4. AU="Mirzabeigi, Parastoo"
  5. AU="Lesage, C"
  6. AU=Kim Donghyun AU=Kim Donghyun
  7. AU="Weisburd, Ben"
  8. AU="van den Berg, Linda M"
  9. AU="Kurochkina, Yu D"
  10. AU="H Cao"
  11. AU="Elias, Rui"
  12. AU="Hofstaedter, Ferdinand"
  13. AU="Ross, Ashley E"
  14. AU="Luque Alarcón, Mónica"

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  1. Artikel: Associations between circadian misalignment and telomere length in BD: an actigraphy study.

    Spano, Luana / Hennion, Vincent / Marie-Claire, Cynthia / Bellivier, Frank / Scott, Jan / Etain, Bruno

    International journal of bipolar disorders

    2022  Band 10, Heft 1, Seite(n) 14

    Abstract: Background: Life expectancy is significantly decreased in bipolar disorder (BD). This is associated with accelerated cellular aging which can be estimated by telomere length (TL). However, specific determinants of shorter TL in BD are under-explored. ... ...

    Abstract Background: Life expectancy is significantly decreased in bipolar disorder (BD). This is associated with accelerated cellular aging which can be estimated by telomere length (TL). However, specific determinants of shorter TL in BD are under-explored. This study examines whether circadian misalignment (i.e. mismatch between preferred and actual phase of circadian activity rhythms) is associated with shorter TL in BD.
    Methods: Euthymic individuals with BD (n = 101) undertook 21 consecutive days of actigraphy recording and completed the Composite Scale of Morningness (CSM) to assess phase preference for activities (chronotype). Polymerase chain reaction was used to measure TL in blood. Cluster analysis identified circadian aligned/misaligned subgroups as defined by preferred (CSM score) and actual phases of activity (actigraphically determined onset of active and inactive periods). We tested for any associations between TL and clusters, with adjustments for between-cluster differences in socio-demographic and illness factors.
    Results: We identified three clusters: an "Aligned Morning" cluster (n = 31) with preferred and actual timing of activity in the morning, an "Aligned Evening" cluster (n = 37) with preferred and actual timing of activity in the evening and a "Misaligned" cluster (n = 32) with an evening chronotype, but an earlier objective onset of active periods. After adjustment for confounders, we found that TL was significantly associated with circadian misalignment and older age.
    Conclusions: Circadian misalignment may partly explain shorter TL in BD and could contribute to accelerated aging in these individuals.
    Sprache Englisch
    Erscheinungsdatum 2022-05-27
    Erscheinungsland Germany
    Dokumenttyp Journal Article
    ZDB-ID 2732954-9
    ISSN 2194-7511
    ISSN 2194-7511
    DOI 10.1186/s40345-022-00260-w
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Telomere length and mitochondrial DNA copy number in bipolar disorder: A sibling study.

    Spano, Luana / Etain, Bruno / Laplanche, Jean-Louis / Leboyer, Marion / Gard, Sébastien / Bellivier, Frank / Marie-Claire, Cynthia

    The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry

    2022  Band 24, Heft 5, Seite(n) 449–456

    Abstract: Objectives: An accelerated cellular ageing has been observed in bipolar disorder (BD) using biomarkers such as telomere length (TL) and mitochondrial DNA copy number (mtDNAcn). Several risk factors might drive premature ageing in individuals with BD, ... ...

    Abstract Objectives: An accelerated cellular ageing has been observed in bipolar disorder (BD) using biomarkers such as telomere length (TL) and mitochondrial DNA copy number (mtDNAcn). Several risk factors might drive premature ageing in individuals with BD, including a familial predisposition. This study compared TL and mtDNAcn between individuals with BD and their (un)-affected siblings, and explored factors that may explain proband-sibling differences.
    Methods: Sixty individuals with BD and seventy-four siblings (34 affected with BD or mood disorders and 40 unaffected) were included. Quantitative polymerase chain reaction (qPCR) was used to measure TL and mtDNAcn from peripheral blood genomic DNA.
    Results: TL and mtDNAcn did not significantly differ between probands and their siblings, whatever these latter were affected or not with mood disorders. However, the correlation plots of TL or mtDNAcn in proband-sibling pairs suggested that some pairs were discordant. The within proband-sibling pairs differences for TL and mtDNAcn were not explained by differences in all tested factors.
    Conclusions: This study shows that probands with BD and their siblings are concordant for TL and mtDNAcn suggesting that they may share some environmental or genetic determinants of these two biomarkers of cellular ageing.
    Mesh-Begriff(e) Humans ; DNA, Mitochondrial/genetics ; Bipolar Disorder/genetics ; Siblings ; DNA Copy Number Variations ; Biomarkers ; Telomere/genetics
    Chemische Substanzen DNA, Mitochondrial ; Biomarkers
    Sprache Englisch
    Erscheinungsdatum 2022-10-19
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2051402-5
    ISSN 1814-1412 ; 1562-2975
    ISSN (online) 1814-1412
    ISSN 1562-2975
    DOI 10.1080/15622975.2022.2131907
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Decreased telomere length in a subgroup of young individuals with bipolar disorders: replication in the FACE-BD cohort and association with the shelterin component POT1.

    Spano, Luana / Marie-Claire, Cynthia / Godin, Ophélia / Lebras, Apolline / Courtin, Cindie / Laplanche, Jean-Louis / Leboyer, Marion / Aouizerate, Bruno / Lefrere, Antoine / Belzeaux, Raoul / Courtet, Philippe / Olié, Emilie / Dubertret, Caroline / Schwan, Raymund / Aubin, Valérie / Roux, Paul / Polosan, Mircea / Samalin, Ludovic / Haffen, Emmanuel /
    Bellivier, Frank / Etain, Bruno

    Translational psychiatry

    2024  Band 14, Heft 1, Seite(n) 131

    Abstract: Bipolar disorder (BD) has been associated with premature cellular aging with shortened telomere length (TL) as compared to the general population. We recently identified a subgroup of young individuals with prematurely shortened TL. The aims of the ... ...

    Abstract Bipolar disorder (BD) has been associated with premature cellular aging with shortened telomere length (TL) as compared to the general population. We recently identified a subgroup of young individuals with prematurely shortened TL. The aims of the present study were to replicate this observation in a larger sample and analyze the expression levels of genes associated with age or TL in a subsample of these individuals. TL was measured on peripheral blood DNA using quantitative polymerase chain reaction in a sample of 542 individuals with BD and clustering analyses were performed. Gene expression level of 29 genes, associated with aging or with telomere maintenance, was analyzed in RNA samples from a subsample of 129 individuals. Clustering analyses identified a group of young individuals (mean age 29.64 years), with shorter TL. None of the tested clinical variables were significantly associated with this subgroup. Gene expression level analyses showed significant downregulation of MYC, POT1, and CD27 in the prematurely aged young individuals compared to the young individuals with longer TL. After adjustment only POT1 remained significantly differentially expressed between the two groups of young individuals. This study confirms the existence of a subgroup of young individuals with BD with shortened TL. The observed decrease of POT1 expression level suggests a newly described cellular mechanism in individuals with BD, that may contribute to telomere shortening.
    Mesh-Begriff(e) Adult ; Aged ; Humans ; Aging ; Aging, Premature ; Bipolar Disorder/genetics ; Shelterin Complex ; Telomere/genetics ; Telomere Shortening/genetics ; Telomere-Binding Proteins/genetics
    Chemische Substanzen POT1 protein, human ; Shelterin Complex ; Telomere-Binding Proteins
    Sprache Englisch
    Erscheinungsdatum 2024-03-01
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2609311-X
    ISSN 2158-3188 ; 2158-3188
    ISSN (online) 2158-3188
    ISSN 2158-3188
    DOI 10.1038/s41398-024-02824-z
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Accelerated aging in bipolar disorders: An exploratory study of six epigenetic clocks.

    Bourdon, Céline / Etain, Bruno / Spano, Luana / Belzeaux, Raoul / Leboyer, Marion / Delahaye-Duriez, Andrée / Ibrahim, El Chérif / Lutz, Pierre-Eric / Gard, Sébastien / Schwan, Raymund / Polosan, Mircea / Courtet, Philippe / Passerieux, Christine / Bellivier, Frank / Marie-Claire, Cynthia

    Psychiatry research

    2023  Band 327, Seite(n) 115373

    Abstract: Bipolar disorder (BD) is a chronic and severe psychiatric disorder associated with significant medical morbidity and reduced life expectancy. In this study, we assessed accelerated epigenetic aging in individuals with BD using various DNA methylation ( ... ...

    Abstract Bipolar disorder (BD) is a chronic and severe psychiatric disorder associated with significant medical morbidity and reduced life expectancy. In this study, we assessed accelerated epigenetic aging in individuals with BD using various DNA methylation (DNAm)-based markers. For this purpose, we used five epigenetic clocks (Horvath, Hannum, EN, PhenoAge, and GrimAge) and a DNAm-based telomere length clock (DNAmTL). DNAm profiles were obtained using Infinium MethylationEPIC Arrays from whole-blood samples of 184 individuals with BD. We also estimated blood cell counts based on DNAm levels for adjustment. Significant correlations between chronological age and each epigenetic age estimated using the six different clocks were observed. Following adjustment for blood cell counts, we found that the six epigenetic AgeAccels (age accelerations) were significantly associated with the body mass index. GrimAge AgeAccel was significantly associated with male sex, smoking status and childhood maltreatment. DNAmTL AgeAccel was significantly associated with smoking status. Overall, this study showed that distinct epigenetic clocks are sensitive to different aspects of aging process in BD. Further investigations with comprehensive epigenetic clock analyses and large samples are required to confirm our findings of potential determinants of an accelerated epigenetic aging in BD.
    Mesh-Begriff(e) Humans ; Male ; Bipolar Disorder/genetics ; Epigenesis, Genetic ; Aging/genetics ; DNA Methylation ; Smoking
    Sprache Englisch
    Erscheinungsdatum 2023-07-26
    Erscheinungsland Ireland
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 445361-x
    ISSN 1872-7123 ; 1872-7506 ; 0925-4927 ; 0165-1781
    ISSN (online) 1872-7123 ; 1872-7506
    ISSN 0925-4927 ; 0165-1781
    DOI 10.1016/j.psychres.2023.115373
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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