Shorter Telomeres and Faster Telomere Attrition in Individuals With Five Syndromic Forms of Intellectual Disability: A Systematic Review and Meta‐Analysis.
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| Title: | Shorter Telomeres and Faster Telomere Attrition in Individuals With Five Syndromic Forms of Intellectual Disability: A Systematic Review and Meta‐Analysis. |
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| Authors: | Hanley, Sarah M., Schutte, Nicola S., Bellamy, Jessica, Denham, Joshua |
| Source: | Journal of Intellectual Disability Research. Aug2025, Vol. 69 Issue 8, p641-654. 14p. |
| Subjects: | DNA analysis, Mortality risk factors, Leukocytes, Risk assessment, Cri-du-chat syndrome, Meta-analysis, Descriptive statistics, Intellectual disabilities, Systematic reviews, MEDLINE, Chronic diseases, Diseases, Online information services, Confidence intervals, Longevity, Active aging |
| Abstract: | Background: People with intellectual disability suffer complex challenges due to adaptive functioning limitations, high rates of chronic diseases and shortened lifespans compared with the general population. Telomere shortening is a hallmark of ageing, and short telomeres are linked to neurological disorders. The main objective of this systematic review and meta‐analysis was to identify any differences in telomere length and the rate of telomere attrition in leukocytes and fibroblasts from people with intellectual disability and controls. Methods: PubMed, Scopus and ScienceDirect were searched. Articles that compared telomere length in individuals with intellectual disability to apparently healthy age‐matched controls were included. Risk of bias was assessed using the AXIS tool and data were analysed using CMA. Results: Fifteen studies comprised of 17 comparisons provided data and were included in meta‐analyses. Compared with healthy controls (N = 481), people with intellectual disability (N = 366) from a known genetic syndrome (Cri du chat, Down, Hoyeraal–Hreidarsson, Williams or Nicolaides–Baraitser) possessed shorter leukocyte telomeres (SMD: −0.853 [95% CI: −1.622 to −0.084], p = 0.03). Similarly, relative to controls (N = 16), people with syndromic intellectual disability (N = 21) possessed shorter fibroblast telomeres (−1.389 [−2.179 to −0.599], p = 0.001). Furthermore, people with syndromic forms of intellectual disability also demonstrated a faster rate (2.09‐fold) of telomere shortening. Conclusions: Consistent with epidemiological findings on mortality and morbidity risk, people with syndromic intellectual disability appear to undergo a faster rate of biological ageing compared to the general population. These findings emphasise the need for healthy ageing lifestyle (i.e., exercise and stress management) and therapeutic interventions for people with syndromic intellectual disability. [ABSTRACT FROM AUTHOR] |
| Copyright of Journal of Intellectual Disability Research is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Psychology and Behavioral Sciences Collection |
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| Header | DbId: pbh DbLabel: Psychology and Behavioral Sciences Collection An: 186527212 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Shorter Telomeres and Faster Telomere Attrition in Individuals With Five Syndromic Forms of Intellectual Disability: A Systematic Review and Meta‐Analysis. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Hanley%2C+Sarah M%2E%22">Hanley, Sarah M.</searchLink><br /><searchLink fieldCode="AR" term="%22Schutte%2C+Nicola S%2E%22">Schutte, Nicola S.</searchLink><br /><searchLink fieldCode="AR" term="%22Bellamy%2C+Jessica%22">Bellamy, Jessica</searchLink><br /><searchLink fieldCode="AR" term="%22Denham%2C+Joshua%22">Denham, Joshua</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Journal+of+Intellectual+Disability+Research%22">Journal of Intellectual Disability Research</searchLink>. Aug2025, Vol. 69 Issue 8, p641-654. 14p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22DNA+analysis%22">DNA analysis</searchLink><br /><searchLink fieldCode="DE" term="%22Mortality+risk+factors%22">Mortality risk factors</searchLink><br /><searchLink fieldCode="DE" term="%22Leukocytes%22">Leukocytes</searchLink><br /><searchLink fieldCode="DE" term="%22Risk+assessment%22">Risk assessment</searchLink><br /><searchLink fieldCode="DE" term="%22Cri-du-chat+syndrome%22">Cri-du-chat syndrome</searchLink><br /><searchLink fieldCode="DE" term="%22Meta-analysis%22">Meta-analysis</searchLink><br /><searchLink fieldCode="DE" term="%22Descriptive+statistics%22">Descriptive statistics</searchLink><br /><searchLink fieldCode="DE" term="%22Intellectual+disabilities%22">Intellectual disabilities</searchLink><br /><searchLink fieldCode="DE" term="%22Systematic+reviews%22">Systematic reviews</searchLink><br /><searchLink fieldCode="DE" term="%22MEDLINE%22">MEDLINE</searchLink><br /><searchLink fieldCode="DE" term="%22Chronic+diseases%22">Chronic diseases</searchLink><br /><searchLink fieldCode="DE" term="%22Diseases%22">Diseases</searchLink><br /><searchLink fieldCode="DE" term="%22Online+information+services%22">Online information services</searchLink><br /><searchLink fieldCode="DE" term="%22Confidence+intervals%22">Confidence intervals</searchLink><br /><searchLink fieldCode="DE" term="%22Longevity%22">Longevity</searchLink><br /><searchLink fieldCode="DE" term="%22Active+aging%22">Active aging</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Background: People with intellectual disability suffer complex challenges due to adaptive functioning limitations, high rates of chronic diseases and shortened lifespans compared with the general population. Telomere shortening is a hallmark of ageing, and short telomeres are linked to neurological disorders. The main objective of this systematic review and meta‐analysis was to identify any differences in telomere length and the rate of telomere attrition in leukocytes and fibroblasts from people with intellectual disability and controls. Methods: PubMed, Scopus and ScienceDirect were searched. Articles that compared telomere length in individuals with intellectual disability to apparently healthy age‐matched controls were included. Risk of bias was assessed using the AXIS tool and data were analysed using CMA. Results: Fifteen studies comprised of 17 comparisons provided data and were included in meta‐analyses. Compared with healthy controls (N = 481), people with intellectual disability (N = 366) from a known genetic syndrome (Cri du chat, Down, Hoyeraal–Hreidarsson, Williams or Nicolaides–Baraitser) possessed shorter leukocyte telomeres (SMD: −0.853 [95% CI: −1.622 to −0.084], p = 0.03). Similarly, relative to controls (N = 16), people with syndromic intellectual disability (N = 21) possessed shorter fibroblast telomeres (−1.389 [−2.179 to −0.599], p = 0.001). Furthermore, people with syndromic forms of intellectual disability also demonstrated a faster rate (2.09‐fold) of telomere shortening. Conclusions: Consistent with epidemiological findings on mortality and morbidity risk, people with syndromic intellectual disability appear to undergo a faster rate of biological ageing compared to the general population. These findings emphasise the need for healthy ageing lifestyle (i.e., exercise and stress management) and therapeutic interventions for people with syndromic intellectual disability. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Journal of Intellectual Disability Research is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=pbh&AN=186527212 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/jir.13244 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 14 StartPage: 641 Subjects: – SubjectFull: DNA analysis Type: general – SubjectFull: Mortality risk factors Type: general – SubjectFull: Leukocytes Type: general – SubjectFull: Risk assessment Type: general – SubjectFull: Cri-du-chat syndrome Type: general – SubjectFull: Meta-analysis Type: general – SubjectFull: Descriptive statistics Type: general – SubjectFull: Intellectual disabilities Type: general – SubjectFull: Systematic reviews Type: general – SubjectFull: MEDLINE Type: general – SubjectFull: Chronic diseases Type: general – SubjectFull: Diseases Type: general – SubjectFull: Online information services Type: general – SubjectFull: Confidence intervals Type: general – SubjectFull: Longevity Type: general – SubjectFull: Active aging Type: general Titles: – TitleFull: Shorter Telomeres and Faster Telomere Attrition in Individuals With Five Syndromic Forms of Intellectual Disability: A Systematic Review and Meta‐Analysis. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Hanley, Sarah M. – PersonEntity: Name: NameFull: Schutte, Nicola S. – PersonEntity: Name: NameFull: Bellamy, Jessica – PersonEntity: Name: NameFull: Denham, Joshua IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: Aug2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 09642633 Numbering: – Type: volume Value: 69 – Type: issue Value: 8 Titles: – TitleFull: Journal of Intellectual Disability Research Type: main |
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