Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome

被引:3
|
作者
Ge, Ruiyang [1 ,2 ]
Ching, Christopher R. K. [3 ]
Bassett, Anne S. [4 ,5 ,6 ,7 ]
Kushan, Leila [8 ]
Antshel, Kevin M. [9 ]
van Amelsvoort, Therese [10 ]
Bakker, Geor [10 ]
Butcher, Nancy J. [7 ,11 ]
Campbell, Linda E. [12 ]
Chow, Eva W. C. [4 ,7 ]
Craig, Michael [13 ,14 ]
Crossley, Nicolas A. [15 ]
Cunningham, Adam [16 ]
Daly, Eileen [13 ]
Doherty, Joanne L. [16 ,17 ]
Durdle, Courtney A. [18 ,19 ]
Emanuel, Beverly S. [20 ,21 ]
Fiksinski, Ania [22 ,23 ]
Forsyth, Jennifer K. [8 ,24 ]
Fremont, Wanda [25 ]
Goodrich-Hunsaker, Naomi J. [18 ,26 ]
Gudbrandsen, Maria [13 ,27 ]
Gur, Raquel E. [28 ]
Jalbrzikowski, Maria [29 ,30 ]
Kates, Wendy R. [25 ]
Lin, Amy [8 ,31 ]
Linden, David E. J. [16 ]
Mccabe, Kathryn L. [12 ,18 ]
McDonald-McGinn, Donna [21 ,32 ,33 ]
Moss, Hayley [16 ]
Murphy, Declan G. [13 ,34 ]
Murphy, Kieran C. [35 ]
Owen, Michael J. [16 ]
Villalon-Reina, Julio E. [3 ]
Repetto, Gabriela M. [36 ]
Roalf, David R. [37 ]
Ruparel, Kosha [37 ]
Schmitt, J. Eric [38 ]
Schuite-Koops, Sanne [39 ]
Angkustsiri, Kathleen [18 ]
Sun, Daqiang [8 ]
Vajdi, Ariana [8 ,40 ]
van den Bree, Marianne [16 ]
Vorstman, Jacob [7 ,41 ]
Thompson, Paul M. [42 ]
Vila-Rodriguez, Fidel [1 ,2 ,43 ]
Bearden, Carrie E. [8 ]
机构
[1] Univ British Columbia, Dept Psychiat, Vancouver, BC, Canada
[2] Univ British Columbia, Djavad Mowafaghian Ctr Brain Hlth, Vancouver, BC, Canada
[3] Univ Southern Calif, Imaging Genet Ctr, Los Angeles, CA 90007 USA
[4] Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON, Canada
[5] Univ Hlth Network, Toronto Gen Hosp Res Inst, Dept Psychiat, Dept Med,Dalglish Family 22q Clin, Toronto, ON, Canada
[6] Campbell Family Mental Hlth Res Inst, Ctr Addict & Mental Hlth, Toronto, ON, Canada
[7] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[8] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Dept Psychiat & Biobehav Sci, Los Angeles, CA USA
[9] Syracuse Univ, Dept Psychol, Syracuse, NY USA
[10] Maastricht Univ, Dept Psychiat & Neuropsychol, Maastricht, Netherlands
[11] Hosp Sick Children, Child Hlth Evaluat Sci, Toronto, ON, Canada
[12] Univ Newcastle, Sch Psychol Sci, Callaghan, Australia
[13] Kings Coll London, Dept Forens & Neurodev Sci, Sackler Inst Translat Neurodev, Inst Psychiat Psychol & Neurosci, London, England
[14] Bethlem Royal & Maudsley Hosp, Beckenham, Kent, England
[15] Periodista Pontificia Univ Catol Chile, Santiago, Chile
[16] Cardiff Univ, MRC Ctr Neuropsychiat Genet & Genom, Div Psychol Med & Clin Neurosci, Cardiff, Wales
[17] Cardiff Univ, Cardiff Univ Brain Res Imaging Ctr CUBRIC, Sch Psychol, Cardiff, Wales
[18] UC Davis MIND Inst, Davis, CA USA
[19] UC Santa Barbara, Dept Psychol & Brain Sci, Santa Barbara, CA USA
[20] Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA USA
[21] Univ Penn, Perelman Sch Med, Dept Pediat, Philadelphia, PA USA
[22] Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, Dept Pediat, Utrecht, Netherlands
[23] Maastricht Univ, Dept Psychiat & Neuropsychol, Sch Mental Hlth & Neurosci MHeNS, Maastricht, Netherlands
[24] Univ Washington, Dept Psychol, Seattle, WA USA
[25] State Univ New York Upstate Med Univ, Dept Psychiat & Behav Sci, Syracuse, NY 13210 USA
[26] Univ Utah, Dept Neurol, Salt Lake City, UT USA
[27] Univ Roehampton, Sch Psychol, Psychol, London, England
[28] Univ Penn, Childrens Hosp Philadelphia, Perelman Sch Med, Dept Radiol, Philadelphia, PA USA
[29] Harvard Med Sch, Dept Psychiat, Boston, MA USA
[30] Boston Childrens Hosp, Dept Psychiat & Behav Sci, Boston, MA USA
[31] UCLA, Sch Med, Los Angeles, CA USA
[32] Childrens Hosp Philadelphia, 22q & You Ctr, Clin Genet Ctr, Div Human Genet, Philadelphia, PA 19104 USA
[33] Sapienza Univ, Dept Human Biol & Med Genet, Viale Policlin 155, I-00161 Rome, Italy
[34] South London & Maudsley Fdn NHS Trust, Behav Genet Clin, Adult Autism Serv, Behav & Dev Psychiat Clin Acad Grp, London, England
[35] Royal Coll Surgeons Ireland, Dept Psychiat, Dublin, Ireland
[36] Clin Alemana Univ Desarrollo, Fac Med, Ctr Bioet, Santiago, Chile
[37] Univ Penn, Dept Psychiat, Philadelphia, PA 19104 USA
[38] Univ Penn, Dept Radiol, Philadelphia, PA 19104 USA
[39] Univ Med Ctr Groningen, Dept Hlth Psychol, Groningen, Netherlands
[40] Kaiser Permanente Bernard J Tyson Sch Med, Pasadena, CA USA
[41] Hosp Sick Children Res Inst, Program Genet & Genome Biol, Toronto, ON, Canada
[42] Univ Southern Calif, Dept Radiol, Los Angeles, CA USA
[43] Univ British Columbia, Sch Biomed Engn, Vancouver, BC, Canada
基金
加拿大健康研究院; 英国惠康基金;
关键词
22q11 deletion syndrome; gray matter volume; magnetic resonnance imaging; source-based morphometry; LARGE-SCALE; CHILDREN; COVARIANCE; BEHAVIOR; ASSOCIATIONS; DISORDERS; NETWORKS;
D O I
10.1002/hbm.26553
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
22q11.2 deletion syndrome (22q11DS) is the most frequently occurring microdeletion in humans. It is associated with a significant impact on brain structure, including prominent reductions in gray matter volume (GMV), and neuropsychiatric manifestations, including cognitive impairment and psychosis. It is unclear whether GMV alterations in 22q11DS occur according to distinct structural patterns. Then, 783 participants (470 with 22q11DS: 51% females, mean age [SD] 18.2 [9.2]; and 313 typically developing [TD] controls: 46% females, mean age 18.0 [8.6]) from 13 datasets were included in the present study. We segmented structural T1-weighted brain MRI scans and extracted GMV images, which were then utilized in a novel source-based morphometry (SBM) pipeline (SS-Detect) to generate structural brain patterns (SBPs) that capture co-varying GMV. We investigated the impact of the 22q11.2 deletion, deletion size, intelligence quotient, and psychosis on the SBPs. Seventeen GMV-SBPs were derived, which provided spatial patterns of GMV covariance associated with a quantitative metric (i.e., loading score) for analysis. Patterns of topographically widespread differences in GMV covariance, including the cerebellum, discriminated individuals with 22q11DS from healthy controls. The spatial extents of the SBPs that revealed disparities between individuals with 22q11DS and controls were consistent with the findings of the univariate voxel-based morphometry analysis. Larger deletion size was associated with significantly lower GMV in frontal and occipital SBPs; however, history of psychosis did not show a strong relationship with these covariance patterns. 22q11DS is associated with distinct structural abnormalities captured by topographical GMV covariance patterns that include the cerebellum. Findings indicate that structural anomalies in 22q11DS manifest in a nonrandom manner and in distinct covarying anatomical patterns, rather than a diffuse global process. These SBP abnormalities converge with previously reported cortical surface area abnormalities, suggesting disturbances of early neurodevelopment as the most likely underlying mechanism. Using a novel source-based morphometry method called SS-Detect, we identified 12 structural brain patterns (SBPs) that discriminated individuals with 22q11.2 deletion syndrome from healthy controls. We further demonstrated that deletion size was related to structural covariance patterns; however, history of psychosis did not show a strong relationship with these covariance patterns.image
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页数:15
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