Comparison of regional brain deficit patterns in common psychiatric and neurological disorders as revealed by big data.
Comparison of regional brain deficit patterns in common psychiatric and neurological disorders as revealed by big data.
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DOI:
10.1016/j.nicl.2021.102574
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发表时间:
2021
期刊:
影响因子:
--
通讯作者:
Hong LE
中科院分区:
文献类型:
--
作者:
Kochunov P;Ryan MC;Yang Q;Hatch KS;Zhu A;Thomopoulos SI;Jahanshad N;Schmaal L;Thompson PM;Chen S;Du X;Adhikari BM;Bruce H;Hare S;Goldwaser EL;Kvarta MD;Nichols TE;Hong LE
RVI for MDD and AD was derived based on large meta-analytical findings. RVI-MDD and AD were significantly elevated in UKBB subjects with respective illnesses. There was no elevation of RVI-MDD in subjects with AD or RVI-AD in subjects with MDD. RVI captures neuroanatomic deviation patterns. RVI is a useful biomarker for assessing similarity to neuropsychiatric illnesses. Neurological and psychiatric illnesses are associated with regional brain deficit patterns that bear unique signatures and capture illness-specific characteristics. The Regional Vulnerability Index (RVI) was developed to quantify brain similarity by comparing individual white matter microstructure, cortical gray matter thickness and subcortical gray matter structural volume measures with neuroanatomical deficit patterns derived from large-scale meta-analytic studies. We tested the specificity of the RVI approach for major depressive disorder (MDD) and Alzheimer’s disease (AD) in a large epidemiological sample of UK Biobank (UKBB) participants (N = 19,393; 9138 M/10,255F; age = 64.8 ± 7.4 years). Compared to controls free of neuropsychiatric disorders, participants with MDD (N = 2,248; 805 M/1443F; age = 63.4 ± 7.4) had significantly higher RVI-MDD values (t = 5.6, p = 1·10−8), but showed no detectable difference in RVI-AD (t = 2.0, p = 0.10). Subjects with dementia (N = 7; 4 M/3F; age = 68.6 ± 8.6 years) showed significant elevation in RVI-AD (t = 4.2, p = 3·10−5) but not RVI-MDD (t = 2.1, p = 0.10) compared to controls. Even within affective illnesses, participants with bipolar disorder (N = 54) and anxiety disorder (N = 773) showed no significant elevation in whole-brain RVI-MDD. Participants with Parkinson’s disease (N = 37) showed elevation in RVI-AD (t = 2.4, p = 0.01) while subjects with stroke (N = 247) showed no such elevation (t = 1.1, p = 0.3). In summary, we demonstrated elevation in RVI-MDD and RVI-AD measures in the respective illnesses with strong replicability that is relatively specific to the respective diagnoses. These neuroanatomic deviation patterns offer a useful biomarker for population-wide assessments of similarity to neuropsychiatric illnesses.
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影响因子:
64.8
作者:
Bycroft C;Freeman C;Petkova D;Band G;Elliott LT;Sharp K;Motyer A;Vukcevic D;Delaneau O;O'Connell J;Cortes A;Welsh S;Young A;Effingham M;McVean G;Leslie S;Allen N;Donnelly P;Marchini J
通讯作者:
Marchini J
影响因子:
11
作者:
van Erp TG;Hibar DP;Rasmussen JM;Glahn DC;Pearlson GD;Andreassen OA;Agartz I;Westlye LT;Haukvik UK;Dale AM;Melle I;Hartberg CB;Gruber O;Kraemer B;Zilles D;Donohoe G;Kelly S;McDonald C;Morris DW;Cannon DM;Corvin A;Machielsen MW;Koenders L;de Haan L;Veltman DJ;Satterthwaite TD;Wolf DH;Gur RC;Gur RE;Potkin SG;Mathalon DH;Mueller BA;Preda A;Macciardi F;Ehrlich S;Walton E;Hass J;Calhoun VD;Bockholt HJ;Sponheim SR;Shoemaker JM;van Haren NE;Hulshoff Pol HE;Ophoff RA;Kahn RS;Roiz-Santiañez R;Crespo-Facorro B;Wang L;Alpert KI;Jönsson EG;Dimitrova R;Bois C;Whalley HC;McIntosh AM;Lawrie SM;Hashimoto R;Thompson PM;Turner JA
通讯作者:
Turner JA
影响因子:
48
作者:
Kalaria, Raj N.;Maestre, Gladys E.;Arizaga, Raul;Friedland, Robert P.;Galasko, Doug;Hall, Kathleen;Luchsinger, Jose A.;Ogunniyi, Adesola;Perry, Elaine K.;Potocnik, Felix;Prince, Martin;Stewart, Robert;Wimo, Anders;Zhang, Zhen-Xin;Antuono, Piero
通讯作者:
Antuono, Piero
影响因子:
10.6
作者:
van Erp TGM;Walton E;Hibar DP;Schmaal L;Jiang W;Glahn DC;Pearlson GD;Yao N;Fukunaga M;Hashimoto R;Okada N;Yamamori H;Bustillo JR;Clark VP;Agartz I;Mueller BA;Cahn W;de Zwarte SMC;Hulshoff Pol HE;Kahn RS;Ophoff RA;van Haren NEM;Andreassen OA;Dale AM;Doan NT;Gurholt TP;Hartberg CB;Haukvik UK;Jørgensen KN;Lagerberg TV;Melle I;Westlye LT;Gruber O;Kraemer B;Richter A;Zilles D;Calhoun VD;Crespo-Facorro B;Roiz-Santiañez R;Tordesillas-Gutiérrez D;Loughland C;Carr VJ;Catts S;Cropley VL;Fullerton JM;Green MJ;Henskens FA;Jablensky A;Lenroot RK;Mowry BJ;Michie PT;Pantelis C;Quidé Y;Schall U;Scott RJ;Cairns MJ;Seal M;Tooney PA;Rasser PE;Cooper G;Shannon Weickert C;Weickert TW;Morris DW;Hong E;Kochunov P;Beard LM;Gur RE;Gur RC;Satterthwaite TD;Wolf DH;Belger A;Brown GG;Ford JM;Macciardi F;Mathalon DH;O'Leary DS;Potkin SG;Preda A;Voyvodic J;Lim KO;McEwen S;Yang F;Tan Y;Tan S;Wang Z;Fan F;Chen J;Xiang H;Tang S;Guo H;Wan P;Wei D;Bockholt HJ;Ehrlich S;Wolthusen RPF;King MD;Shoemaker JM;Sponheim SR;De Haan L;Koenders L;Machielsen MW;van Amelsvoort T;Veltman DJ;Assogna F;Banaj N;de Rossi P;Iorio M;Piras F;Spalletta G;McKenna PJ;Pomarol-Clotet E;Salvador R;Corvin A;Donohoe G;Kelly S;Whelan CD;Dickie EW;Rotenberg D;Voineskos AN;Ciufolini S;Radua J;Dazzan P;Murray R;Reis Marques T;Simmons A;Borgwardt S;Egloff L;Harrisberger F;Riecher-Rössler A;Smieskova R;Alpert KI;Wang L;Jönsson EG;Koops S;Sommer IEC;Bertolino A;Bonvino A;Di Giorgio A;Neilson E;Mayer AR;Stephen JM;Kwon JS;Yun JY;Cannon DM;McDonald C;Lebedeva I;Tomyshev AS;Akhadov T;Kaleda V;Fatouros-Bergman H;Flyckt L;Karolinska Schizophrenia Project;Busatto GF;Rosa PGP;Serpa MH;Zanetti MV;Hoschl C;Skoch A;Spaniel F;Tomecek D;Hagenaars SP;McIntosh AM;Whalley HC;Lawrie SM;Knöchel C;Oertel-Knöchel V;Stäblein M;Howells FM;Stein DJ;Temmingh HS;Uhlmann A;Lopez-Jaramillo C;Dima D;McMahon A;Faskowitz JI;Gutman BA;Jahanshad N;Thompson PM;Turner JA
通讯作者:
Turner JA
影响因子:
6.6
作者:
Kochunov, Peter;Hong, L. Elliot
通讯作者:
Hong, L. Elliot