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      Association of Short-term Change in Leukocyte Telomere Length With Cortical Thickness and Outcomes of Mental Training Among Healthy Adults : A Randomized Clinical Trial

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          Key Points

          Question

          Is naturally occurring short-term change in leukocyte telomere length related to structural plasticity of the brain, and can telomere length be influenced through mental training?

          Findings

          In this randomized clinical trial of 298 healthy adults, the mental training intervention did not affect leukocyte telomere length. Naturally occurring change in leukocyte telomere length over 3 consecutive 3-month intervals was significantly associated with cortical thickness change in the left precuneus extending to the posterior cingulate cortex.

          Meaning

          This study provides the first evidence to date for an association between short-term change in leukocyte telomere length and brain structure, suggesting that these processes may be mechanistically linked; the mental training used did not influence leukocyte telomere length of healthy, middle-aged adults.

          Abstract

          Importance

          Telomere length is associated with the development of age-related diseases and structural differences in multiple brain regions. It remains unclear, however, whether change in telomere length is linked to brain structure change, and to what extent telomere length can be influenced through mental training.

          Objectives

          To assess the dynamic associations between leukocyte telomere length (LTL) and cortical thickness (CT), and to determine whether LTL is affected by a longitudinal contemplative mental training intervention.

          Design, Setting, and Participants

          An open-label efficacy trial of three 3-month mental training modules with healthy, meditation-naive adults was conducted. Data on LTL and CT were collected 4 times over 9 months between April 22, 2013, and March 31, 2015, as part of the ReSource Project. Data analysis was performed between September 23, 2016, and June 21, 2019. Of 1582 eligible individuals, 943 declined to participate; 362 were randomly selected for participation and assigned to training or retest control cohorts, with demographic characteristics matched. The retest control cohorts underwent all testing but no training. Intention-to-treat analysis was performed.

          Interventions

          Training cohort participants completed 3 modules cultivating interoception and attention (Presence), compassion (Affect), or perspective taking (Perspective).

          Main Outcomes and Measures

          Change in LTL and CT.

          Results

          Of the 362 individuals randomized, 30 participants dropped out before study initiation (initial sample, 332). Data were available for analysis of the training intervention in 298 participants (n = 222 training; n = 76 retest control) (175 women [58.7%]; mean [SD] age, 40.5 [9.3] years). The training modules had no effect on LTL. In 699 observations from all 298 participants, mean estimated changes in the relative ratios of telomere repeat copy number to single-copy gene (T/S) were for no training, 0.004 (95% CI, −0.010 to 0.018); Presence, −0.007 (95% CI, −0.025 to 0.011); Affect, −0.005 (95% CI, −0.019 to 0.010); and Perspective, −0.001 (95% CI, −0.017 to 0.016). Cortical thickness change data were analyzed in 167 observations from 67 retest control participants (37 women [55.2%], mean [SD] age, 39.6 [9.0] years). In this retest control cohort subsample, naturally occurring LTL change was related to CT change in the left precuneus extending to the posterior cingulate cortex (mean t 161 = 3.22; P < .001; r = 0.246). At the individual participant level, leukocyte telomere shortening as well as lengthening were observed. Leukocyte telomere shortening was related to cortical thinning ( t 77 = 2.38; P = .01; r = 0.262), and leukocyte telomere lengthening was related to cortical thickening ( t 77 = 2.42; P = .009; r = 0.266). All analyses controlled for age, sex, and body mass index.

          Conclusions and Relevance

          The findings of this trial indicate an association between short-term change in LTL and concomitant change in plasticity of the left precuneus extending to the posterior cingulate cortex. This result contributes to the evidence that LTL changes more dynamically on the individual level than previously thought. Further studies are needed to determine potential long-term implications of such change in relation to cellular aging and the development of neurodegenerative disorders. No effect of contemplative mental training was noted in what may be, to date, the longest intervention with healthy adults.

          Trial Registration

          ClinicalTrials.gov identifier: NCT01833104

          Abstract

          This randomized clinical trial examines the effect of mental attention training on leukocyte telomere length and cortical thickness among healthy adults.

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          Most cited references48

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          • Article: not found

          Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies.

          Choosing the appropriate neuroimaging phenotype is critical to successfully identify genes that influence brain structure or function. While neuroimaging methods provide numerous potential phenotypes, their role for imaging genetics studies is unclear. Here we examine the relationship between brain volume, grey matter volume, cortical thickness and surface area, from a genetic standpoint. Four hundred and eighty-six individuals from randomly ascertained extended pedigrees with high-quality T1-weighted neuroanatomic MRI images participated in the study. Surface-based and voxel-based representations of brain structure were derived, using automated methods, and these measurements were analysed using a variance-components method to identify the heritability of these traits and their genetic correlations. All neuroanatomic traits were significantly influenced by genetic factors. Cortical thickness and surface area measurements were found to be genetically and phenotypically independent. While both thickness and area influenced volume measurements of cortical grey matter, volume was more closely related to surface area than cortical thickness. This trend was observed for both the volume-based and surface-based techniques. The results suggest that surface area and cortical thickness measurements should be considered separately and preferred over gray matter volumes for imaging genetic studies. Copyright 2009 Elsevier Inc. All rights reserved.
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            Normal age-related brain morphometric changes: nonuniformity across cortical thickness, surface area and gray matter volume?

            Normal aging is accompanied by global as well as regional structural changes. While these age-related changes in gray matter volume have been extensively studied, less has been done using newer morphological indexes, such as cortical thickness and surface area. To this end, we analyzed structural images of 216 healthy volunteers, ranging from 18 to 87 years of age, using a surface-based automated parcellation approach. Linear regressions of age revealed a concomitant global age-related reduction in cortical thickness, surface area and volume. Cortical thickness and volume collectively confirmed the vulnerability of the prefrontal cortex, whereas in other cortical regions, such as in the parietal cortex, thickness was the only measure sensitive to the pronounced age-related atrophy. No cortical regions showed more surface area reduction than the global average. The distinction between these morphological measures may provide valuable information to dissect age-related structural changes of the brain, with each of these indexes probably reflecting specific histological changes occurring during aging. Published by Elsevier Inc.
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              • Article: not found

              Telomere shortening and mood disorders: preliminary support for a chronic stress model of accelerated aging.

              Little is known about the biological mechanisms underlying the excess medical morbidity and mortality associated with mood disorders. Substantial evidence supports abnormalities in stress-related biological systems in depression. Accelerated telomere shortening may reflect stress-related oxidative damage to cells and accelerated aging, and severe psychosocial stress has been linked to telomere shortening. We propose that chronic stress associated with mood disorders may contribute to excess vulnerability for diseases of aging such as cardiovascular disease and possibly some cancers through accelerated organismal aging. Telomere length was measured by Southern Analysis in 44 individuals with chronic mood disorders and 44 nonpsychiatrically ill age-matched control subjects. Telomere length was significantly shorter in those with mood disorders, representing as much as 10 years of accelerated aging. These results provide preliminary evidence that mood disorders are associated with accelerated aging and may suggest a novel mechanism for mood disorder-associated morbidity and mortality.
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                Author and article information

                Journal
                JAMA Netw Open
                JAMA Netw Open
                JAMA Netw Open
                JAMA Network Open
                American Medical Association
                2574-3805
                25 September 2019
                September 2019
                25 September 2019
                : 2
                : 9
                : e199687
                Affiliations
                [1 ]Research Group, “Social Stress and Family Health,” Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany
                [2 ]Institute of Systems Neuroscience, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany
                [3 ]Institute of Neuroscience and Medicine (INM-7: Brain & Behaviour), Research Centre Jülich, Jülich, Germany
                [4 ]Montreal Neurological Institute, McGill University, Montreal, Québec, Canada
                [5 ]Department of Biochemistry and Biophysics, University of California, San Francisco
                [6 ]Department of Psychiatry, University of California, San Francisco
                [7 ]Social Neuroscience Lab, Max Planck Society, Berlin, Germany
                Author notes
                Article Information
                Accepted for Publication: June 25, 2019.
                Published: September 25, 2019. doi:10.1001/jamanetworkopen.2019.9687
                Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2019 Puhlmann LMC et al. JAMA Network Open.
                Corresponding Author: Lara M. C. Puhlmann, MSc, Research Group “Social Stress and Family Health,” Max Planck Institute for Human Cognitive and Brain Sciences, Stephanstrasse, 1a, 04103 Leipzig, Germany ( puhlmann@ 123456cbs.mpg.de ).
                Author Contributions: Drs Vrtička and Singer share senior authorship. Ms Puhlmann had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
                Concept and design: Puhlmann, Valk, Engert, Epel, Singer.
                Acquisition, analysis, or interpretation of data: All authors.
                Drafting of the manuscript: Puhlmann, Engert, Vrtička.
                Critical revision of the manuscript for important intellectual content: All authors.
                Statistical analysis: Puhlmann, Valk, Vrtička.
                Obtained funding: Singer.
                Administrative, technical, or material support: Lin, Singer.
                Supervision: Valk, Engert, Epel, Vrtička, Singer.
                Conflict of Interest Disclosures: Dr Lin is a paid consultant to Telomere Diagnostics Inc, formerly Telome Health, and owns stock in the company; the company had no role in this research. Dr Singer reported receiving grants from the European Research Council during the conduct of the study. No other disclosures were reported.
                Funding/Support: Dr Singer, as principal investigator, received funding for the ReSource Project from the European Research Council under the European Community’s Seventh Framework Program (FP7/2007-2013/ERC grant agreement 205557) and from the Max Planck Society.
                Role of the Funder/Sponsor: The funding organizations had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
                Data Sharing Statement: See Supplement 3.
                Additional Contributions: We thank the members of the former Department of Social Neuroscience involved in the ReSource Project over many years, in particular all ReSource Project teachers who taught the intervention program. Astrid Ackermann, Christina Bochow, PhD, Matthias Bolz, and Sandra Zurborg, PhD, managed the large-scale longitudinal study; Hannes Niederhausen, Henrik Grunert, and Torsten Kästner provided technical support; Sylvia Tydeks and Elisabeth Murzik recruited participants; and Manuela Hofmann, Sylvie Neubert, and Nicole Pampus helped with recruitment and data collection in the ReSource Project in general. All of these contributors were under a regular contract in the Department of Social Neuroscience at the Max Planck Institute of Human Cognitive and Brain Sciences, and no additional compensation was received by any outside funding sponsor.
                Additional Information: This study forms part of the ReSource Project, headed by Tania Singer. Data for this project were collected between 2013 and 2016 at the former Department of Social Neuroscience at the Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.
                Article
                zoi190381
                10.1001/jamanetworkopen.2019.9687
                6763984
                31553468
                ea8e5823-4846-41bf-b522-e10747a64c14
                Copyright 2019 Puhlmann LMC et al. JAMA Network Open.

                This is an open access article distributed under the terms of the CC-BY License.

                History
                : 11 April 2019
                : 25 June 2019
                Categories
                Research
                Original Investigation
                Online Only
                Neurology

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