Does sex hormone treatment reverse the sex-dependent stress regulation? A longitudinal study on hypothalamus–pituitary–adrenal (HPA) axis activity in transgender individuals

Author(s):  
Fuss J ◽  
Claro L ◽  
Ising M ◽  
Biedermann SV ◽  
Wiedemann K ◽  
...  
2008 ◽  
Author(s):  
Robina Khan ◽  
Katja Bertsch ◽  
Ewald Naumann ◽  
Menno R. Kruk ◽  
Patrick Britz ◽  
...  
Keyword(s):  
Hpa Axis ◽  

2004 ◽  
Vol 36 (05) ◽  
Author(s):  
D Eser ◽  
P Zwanzger ◽  
S Aicher ◽  
C Schüle ◽  
TC Baghai ◽  
...  

2017 ◽  
Vol 14 (4) ◽  
pp. e163-e164
Author(s):  
A.D. Fisher ◽  
G. Castellini ◽  
J. Ristori ◽  
H. Casale ◽  
E. Cassioli ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Behzad S. Khorashad ◽  
Amirhossein Manzouri ◽  
Jamie D. Feusner ◽  
Ivanka Savic

AbstractReferrals for gender dysphoria (GD), characterized by a distressful incongruence between gender identity and at-birth assigned sex, are steadily increasing. The underlying neurobiology, and the mechanisms of the often-beneficial cross-sex hormone treatment are unknown. Here, we test hypothesis that own body perception networks (incorporated in the default mode network—DMN, and partly in the salience network—SN), are different in trans-compared with cis-gender persons. We also investigate whether these networks change with cross-sex hormone treatment. Forty transmen (TrM) and 25 transwomen (TrW) were scanned before and after cross-sex hormone institution. We used our own developed Body Morph test (BM), to assess the perception of own body as self. Fifteen cisgender persons were controls. Within and between-group differences in functional connectivity were calculated using independent components analysis within the DMN, SN, and motor network (a control network). Pretreatment, TrM and TrW scored lower “self” on the BM test than controls. Their functional connections were weaker in the anterior cingulate-, mesial prefrontal-cortex (mPFC), precuneus, the left angular gyrus, and superior parietal cortex of the DMN, and ACC in the SN “Self” identification and connectivity in the mPFC in both TrM and TrW increased from scan 1 to 2, and at scan 2 no group differences remained. The neurobiological underpinnings of GD seem subserved by cerebral structures composing major parts of the DMN.


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