دورية أكاديمية

Cortical gyrification differences between early- and late-onset obsessive-compulsive disorder: neurobiological evidence for neurodevelopmentally distinct subtypes.

التفاصيل البيبلوغرافية
العنوان: Cortical gyrification differences between early- and late-onset obsessive-compulsive disorder: neurobiological evidence for neurodevelopmentally distinct subtypes.
المؤلفون: Park I; Department of Brain and Cognitive Sciences, Seoul National University College of Natural Sciences, Seoul, Republic of Korea., Ha M; Department of Brain and Cognitive Sciences, Seoul National University College of Natural Sciences, Seoul, Republic of Korea., Kim T; Department of Bio and Brain, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea., Lho SK; Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea.; Department of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea., Moon SY; Department of Psychiatry, Hallym University Kangnam Sacred Heart Hospital, Seoul, Republic of Korea., Kim M; Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea.; Department of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea., Kwon JS; Department of Brain and Cognitive Sciences, Seoul National University College of Natural Sciences, Seoul, Republic of Korea.; Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea.; Department of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.; Institute of Human Behavioral Medicine, SNU-MRC, Seoul, Republic of Korea.
المصدر: Psychological medicine [Psychol Med] 2023 Oct; Vol. 53 (13), pp. 5976-5985. Date of Electronic Publication: 2022 Oct 19.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Cambridge University Press Country of Publication: England NLM ID: 1254142 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1469-8978 (Electronic) Linking ISSN: 00332917 NLM ISO Abbreviation: Psychol Med Subsets: MEDLINE
أسماء مطبوعة: Publication: London : Cambridge University Press
Original Publication: London, British Medical Assn.
مواضيع طبية MeSH: Obsessive-Compulsive Disorder*/diagnostic imaging , Obsessive-Compulsive Disorder*/epidemiology, Humans ; Parietal Lobe ; Brain ; Gyrus Cinguli/diagnostic imaging ; Phenotype ; Late Onset Disorders ; Magnetic Resonance Imaging
مستخلص: Background: Identifying more homogenous subtypes of patients with obsessive-compulsive disorder (OCD) using biological evidence is critical for understanding complexities of the disorder in this heterogeneous population. Age of onset serves as a useful subtyping scheme for distinguishing OCD into two subgroups that aligns with neurodevelopmental perspectives. The underlying neurobiological markers for these distinct neurodevelopmental differences can be identified by investigating gyrification changes to establish biological evidence-based homogeneous subtypes.
Methods: We compared whole-brain cortical gyrification in 84 patients with early-onset OCD, 84 patients with late-onset OCD, and 152 healthy controls (HCs) to identify potential markers for early neurodevelopmental deficits using the local gyrification index (lGI). Then, the relationships between lGI in clusters showing significant differences and performance in visuospatial memory and verbal fluency, which are considered trait-related neurocognitive impairments in OCD, were further examined in early-onset OCD patients.
Results: The early-onset OCD patients exhibited significantly greater gyrification than those with late-onset OCD patients and HCs in frontoparietal and cingulate regions, including the bilateral precentral, postcentral, precuneus, paracentral, posterior cingulate, superior frontal, and caudal anterior cingulate gyri. Moreover, impaired neurocognitive functions in early-onset OCD patients were correlated with increased gyrification.
Conclusions: Our findings provide a neurobiological marker to distinguish the OCD population into more neurodevelopmentally homogeneous subtypes, which may contribute to the understanding of the neurodevelopmental underpinnings of an etiology in early-onset OCD consistent with the accumulated phenotypic evidence of greater neurodevelopmental deficits in early-onset OCD than in late-onset OCD.
References: BMC Med. 2013 Sep 12;11:201. (PMID: 24228940)
Trends Neurosci. 2013 May;36(5):275-84. (PMID: 23415112)
Nat Neurosci. 2019 Jun;22(6):992-999. (PMID: 31086316)
Nature. 1997 Jan 23;385(6614):313-8. (PMID: 9002514)
J Psychiatry Neurosci. 2019 Nov 25;45(4):234-242. (PMID: 31765115)
Psychol Med. 2013 May;43(5):1081-91. (PMID: 22935427)
Cereb Cortex. 1995 Jan-Feb;5(1):56-63. (PMID: 7719130)
Am J Psychiatry. 2001 Jan;158(1):137-9. (PMID: 11136649)
Biol Psychiatry. 1998 May 1;43(9):623-40. (PMID: 9582996)
World J Psychiatry. 2012 Dec 22;2(6):86-90. (PMID: 24175173)
J Psychiatr Res. 2002 Jul-Aug;36(4):257-65. (PMID: 12191630)
PLoS One. 2014 Jan 28;9(1):e85663. (PMID: 24489665)
Am J Psychiatry. 2016 Sep 9;174(1):60-69. (PMID: 27609241)
J Psychiatr Res. 2012 Sep;46(9):1161-8. (PMID: 22770508)
Nature. 2022 Mar;603(7902):654-660. (PMID: 35296861)
Clin Psychol Rev. 2011 Nov;31(7):1083-100. (PMID: 21820387)
Cogn Neuropsychiatry. 2015;20(2):128-43. (PMID: 25420427)
Brain Cogn. 2010 Feb;72(1):36-45. (PMID: 19942335)
Eur Child Adolesc Psychiatry. 2010 Apr;19(4):365-70. (PMID: 19763663)
Arch Gen Psychiatry. 1989 Nov;46(11):1006-11. (PMID: 2684084)
Int J Neuropsychopharmacol. 2011 Jun;14(5):606-17. (PMID: 21232166)
Prog Neuropsychopharmacol Biol Psychiatry. 2008 Aug 1;32(6):1574-9. (PMID: 18582524)
Arch Gen Psychiatry. 1989 Apr;46(4):335-41. (PMID: 2930330)
Compr Psychiatry. 2000 Sep-Oct;41(5):373-9. (PMID: 11011834)
Psychiatr Genet. 2019 Dec;29(6):211-219. (PMID: 31625982)
Psychol Med. 2014 Apr;44(6):1121-30. (PMID: 23866289)
Anat Embryol (Berl). 1988;179(2):173-9. (PMID: 3232854)
Trends Cogn Sci. 2012 Jan;16(1):43-51. (PMID: 22138231)
Depress Anxiety. 2010 Jun;27(6):507-27. (PMID: 20217853)
Proc Natl Acad Sci U S A. 2000 Sep 26;97(20):11050-5. (PMID: 10984517)
J Neurol Neurosurg Psychiatry. 1960 Feb;23:56-62. (PMID: 14399272)
IEEE Trans Med Imaging. 2008 Feb;27(2):161-70. (PMID: 18334438)
Eur Arch Psychiatry Clin Neurosci. 2010 Sep;260(6):455-64. (PMID: 20112027)
J Neuropsychiatry Clin Neurosci. 2005 Spring;17(2):208-13. (PMID: 15939975)
J Int Neuropsychol Soc. 2007 Jan;13(1):30-7. (PMID: 17166301)
Psychol Med. 2017 Apr;47(6):1053-1061. (PMID: 27938423)
Clin Psychol Rev. 2008 Dec;28(8):1310-25. (PMID: 18701199)
J Psychiatr Res. 2003 Mar-Apr;37(2):127-33. (PMID: 12842166)
Psychiatry Clin Neurosci. 2005 Oct;59(5):539-45. (PMID: 16194255)
Neurosci Lett. 2009 Oct 16;464(1):62-6. (PMID: 19666084)
PLoS One. 2014 Sep 09;9(9):e106768. (PMID: 25203441)
Am J Psychiatry. 2014 Apr;171(4):395-7. (PMID: 24687194)
Eur Psychiatry. 2008 Apr;23(3):187-94. (PMID: 18329252)
Neuroimage Clin. 2021;30:102686. (PMID: 34215156)
Br J Med Psychol. 1959;32(1):50-5. (PMID: 13638508)
J Am Acad Child Adolesc Psychiatry. 1998 Apr;37(4):420-7. (PMID: 9549963)
Cereb Cortex. 2005 Dec;15(12):1900-13. (PMID: 15758198)
J Affect Disord. 2012 Feb;136(3):498-504. (PMID: 22119088)
Psychoneuroendocrinology. 2017 Dec;86:45-52. (PMID: 28915380)
Neurosci Biobehav Rev. 2009 Jun;33(6):818-30. (PMID: 19428494)
J Psychiatry Neurosci. 2009 Nov;34(6):443-9. (PMID: 19949720)
فهرسة مساهمة: Keywords: Cortical folding; gyrification; neurodevelopment; obsessive–compulsive disorder; onset age; subtypes; verbal fluency; visuospatial memory
تواريخ الأحداث: Date Created: 20221019 Date Completed: 20231023 Latest Revision: 20231025
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC10520599
DOI: 10.1017/S0033291722003129
PMID: 36259417
قاعدة البيانات: MEDLINE