The hypertrophic amygdala shape associated with anxiety in patients with primary dysmenorrhea during pain-free phase: insight from surface-based shape analysis.
The hypertrophic amygdala shape associated with anxiety in patients with primary dysmenorrhea during pain-free phase: insight from surface-based shape analysis.
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DOI:
10.1007/s11682-022-00664-3
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发表时间:
2022-10
影响因子:
3.2
通讯作者:
Yang, Jie
中科院分区:
文献类型:
--
作者:
Yu, Siyi;Wei, Wei;Liu, Liying;Guo, Xiaoli;Shen, Zhifu;Tian, Jin;Zeng, Fang;Liang, Fanrong;Yang, Jie
Primary dysmenorrhea (PDM) is highly associated with mood symptoms. However, the neuropathology of these comorbidities is unclear. In the present study, we aimed to investigate the structural changes in the amygdala of patients with PDM during the pain-free phase using a surface-based shape analysis. Forty-three PDM patients and forty healthy controls were recruited in the study, and all participants underwent structural magnetic resonance imaging scans during their periovulatory phase. FMRIB’s Integrated Registration and Segmentation Tool (FIRST) was employed to assess the subcortical volumetric and surface alterations in patients with PDM. Moreover, correlation and mediation analyses were used to detect the clinical significance of the subcortical morphometry alteration. PDM patients showed hypertrophic alteration of the amygdala in the left superficial nuclei and right basolateral and superficial nuclei but not for the whole amygdala volume. The hypertrophic amygdala was associated with disease duration, pain severity and anxiety symptoms during the menstrual period. Furthermore, the hypertrophic left amygdala could mediate the association between disease duration and anxiety severity. The results of the current study demonstrated that the localized amygdala shape hypertrophy was present in PDM patients even in the pain-free phase. In addition, the mediator role of the hypertrophic amygdala indicates the potential target of amygdala for anxiety treatment in PDM treatment in the pain-free phase. The online version contains supplementary material available at 10.1007/s11682-022-00664-3.
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影响因子:
4.8
作者:
Gutman BA;van Erp TGM;Alpert K;Ching CRK;Isaev D;Ragothaman A;Jahanshad N;Saremi A;Zavaliangos-Petropulu A;Glahn DC;Shen L;Cong S;Alnaes D;Andreassen OA;Doan NT;Westlye LT;Kochunov P;Satterthwaite TD;Wolf DH;Huang AJ;Kessler C;Weideman A;Nguyen D;Mueller BA;Faziola L;Potkin SG;Preda A;Mathalon DH;Bustillo J;Calhoun V;Ford JM;Walton E;Ehrlich S;Ducci G;Banaj N;Piras F;Piras F;Spalletta G;Canales-Rodríguez EJ;Fuentes-Claramonte P;Pomarol-Clotet E;Radua J;Salvador R;Sarró S;Dickie EW;Voineskos A;Tordesillas-Gutiérrez D;Crespo-Facorro B;Setién-Suero E;van Son JM;Borgwardt S;Schönborn-Harrisberger F;Morris D;Donohoe G;Holleran L;Cannon D;McDonald C;Corvin A;Gill M;Filho GB;Rosa PGP;Serpa MH;Zanetti MV;Lebedeva I;Kaleda V;Tomyshev A;Crow T;James A;Cervenka S;Sellgren CM;Fatouros-Bergman H;Agartz I;Howells F;Stein DJ;Temmingh H;Uhlmann A;de Zubicaray GI;McMahon KL;Wright M;Cobia D;Csernansky JG;Thompson PM;Turner JA;Wang L
通讯作者:
Wang L
影响因子:
5.7
作者:
Patenaude, Brian;Smith, Stephen M.;Kennedy, David N.;Jenkinson, Mark
通讯作者:
Jenkinson, Mark
影响因子:
4.8
作者:
Morey, Rajendra A.;Selgrade, Elizabeth S.;Wagner, Henry Ryan, II;Huettel, Scott A.;Wang, Lihong;McCarthy, Gregory
通讯作者:
McCarthy, Gregory
影响因子:
5.7
作者:
Morey RA;Petty CM;Xu Y;Hayes JP;Wagner HR 2nd;Lewis DV;LaBar KS;Styner M;McCarthy G
通讯作者:
McCarthy G
影响因子:
2.6
作者:
Pessoa L
通讯作者:
Pessoa L