Matches in SemOpenAlex for { <https://semopenalex.org/work/W4220858332> ?p ?o ?g. }
- W4220858332 endingPage "129" @default.
- W4220858332 startingPage "115" @default.
- W4220858332 abstract "Objective: Stress system dysregulation is considered to have an important role in the aetiology of paediatric functional neurological (conversion) disorder. This study examined salivary cortisol and α-amylase awakening responses in children with functional neurological disorder to determine activation patterns of the hypothalamic–pituitary–adrenal axis and sympathetic system. A healthy cortisol awakening response involves a robust increase in cortisol within 30 minutes of awakening. Alpha-amylase awakening response is variable in children. Methods: Cortisol and α-amylase were measured in saliva from 32 patients with functional neurological disorder (26 girls and 6 boys, aged 11.3−16.1 years) and 31 healthy controls (23 girls and 8 boys, aged 8.6–17.7 years). Saliva samples were collected using a Salivette sampling device at two time points – upon awakening and 30 minutes after awakening. Results: Patients with functional neurological disorder showed a decrease in cortisol awakening response (–4 nmol.min/L) and controls showed an increase (107 nmol.min/L), t(55) = –.4.6, p < 0.001. Within the functional neurological disorder group, 57% showed an attenuated cortisol awakening response and 43% showed an obliterated/reversed cortisol awakening response: Cortisol awakening response was negatively correlated with adverse childhood experiences, r(58) = –0.6, p = 0.002, and subjective distress (total Depression Anxiety and Stress Scales score), r(58) = –0.4, p = 0.050. In controls, cortisol awakening response showed no correlation with adverse childhood experiences and a positive correlation with subjective distress, r(56) = 0.4, p = 0.023. Total cortisol remained similar between the functional neurological disorder and control group. No significant differences were observed between the functional neurological disorder and control group in any of the α-amylase analyses. Discussion: The results suggest dysregulation of the hypothalamic–pituitary–adrenal axis in children with functional neurological disorder. Hypothalamic–pituitary–adrenal dysregulation in children with functional neurological disorder may contribute to comorbid symptoms of fatigue, sleep disturbance and subjective loss of well-being because circadian rhythms and energy metabolism are disrupted. Hypothalamic–pituitary–adrenal dysregulation – and changes in glucocorticoid (cortisol) signalling at the molecular level – may also contribute to increased vulnerability for functional neurological disorder symptoms because of epigenetically mediated changes to neural networks implicated in functional neurological disorder." @default.
- W4220858332 created "2022-04-03" @default.
- W4220858332 creator A5014203432 @default.
- W4220858332 creator A5035310415 @default.
- W4220858332 creator A5054364706 @default.
- W4220858332 date "2022-03-17" @default.
- W4220858332 modified "2023-10-01" @default.
- W4220858332 title "Cortisol and α-amylase awakening response in children and adolescents with functional neurological (conversion) disorder" @default.
- W4220858332 cites W1577078797 @default.
- W4220858332 cites W1584609572 @default.
- W4220858332 cites W1616879063 @default.
- W4220858332 cites W1979667536 @default.
- W4220858332 cites W1982309822 @default.
- W4220858332 cites W1989439371 @default.
- W4220858332 cites W2000150063 @default.
- W4220858332 cites W2004745276 @default.
- W4220858332 cites W2026806581 @default.
- W4220858332 cites W2040791789 @default.
- W4220858332 cites W2045776180 @default.
- W4220858332 cites W2049621745 @default.
- W4220858332 cites W2084728844 @default.
- W4220858332 cites W2090419130 @default.
- W4220858332 cites W2097971265 @default.
- W4220858332 cites W2100512026 @default.
- W4220858332 cites W2116839388 @default.
- W4220858332 cites W2120252262 @default.
- W4220858332 cites W2120345522 @default.
- W4220858332 cites W2124948190 @default.
- W4220858332 cites W2126429845 @default.
- W4220858332 cites W2129676942 @default.
- W4220858332 cites W2145734985 @default.
- W4220858332 cites W2154881642 @default.
- W4220858332 cites W2156579478 @default.
- W4220858332 cites W2167823111 @default.
- W4220858332 cites W2264087504 @default.
- W4220858332 cites W2287523226 @default.
- W4220858332 cites W2334787351 @default.
- W4220858332 cites W2346274114 @default.
- W4220858332 cites W2601561130 @default.
- W4220858332 cites W2606520198 @default.
- W4220858332 cites W2610419495 @default.
- W4220858332 cites W2612662388 @default.
- W4220858332 cites W2751563067 @default.
- W4220858332 cites W2765649113 @default.
- W4220858332 cites W2768179289 @default.
- W4220858332 cites W2807602731 @default.
- W4220858332 cites W2898233098 @default.
- W4220858332 cites W2920870682 @default.
- W4220858332 cites W2989158469 @default.
- W4220858332 cites W2998342169 @default.
- W4220858332 cites W3006600978 @default.
- W4220858332 cites W3007767275 @default.
- W4220858332 cites W3018951806 @default.
- W4220858332 cites W3036162709 @default.
- W4220858332 cites W3080642094 @default.
- W4220858332 cites W3095777033 @default.
- W4220858332 cites W3125426344 @default.
- W4220858332 cites W3134671848 @default.
- W4220858332 cites W3135528090 @default.
- W4220858332 cites W3165445259 @default.
- W4220858332 cites W3190720570 @default.
- W4220858332 cites W3197189497 @default.
- W4220858332 cites W3200964895 @default.
- W4220858332 cites W3208513901 @default.
- W4220858332 cites W4200218054 @default.
- W4220858332 cites W4220726024 @default.
- W4220858332 cites W4220762285 @default.
- W4220858332 cites W4225861566 @default.
- W4220858332 cites W4247665917 @default.
- W4220858332 cites W4254839559 @default.
- W4220858332 doi "https://doi.org/10.1177/00048674221082520" @default.
- W4220858332 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35297291" @default.
- W4220858332 hasPublicationYear "2022" @default.
- W4220858332 type Work @default.
- W4220858332 citedByCount "7" @default.
- W4220858332 countsByYear W42208583322022 @default.
- W4220858332 countsByYear W42208583322023 @default.
- W4220858332 crossrefType "journal-article" @default.
- W4220858332 hasAuthorship W4220858332A5014203432 @default.
- W4220858332 hasAuthorship W4220858332A5035310415 @default.
- W4220858332 hasAuthorship W4220858332A5054364706 @default.
- W4220858332 hasConcept C118552586 @default.
- W4220858332 hasConcept C126322002 @default.
- W4220858332 hasConcept C134018914 @default.
- W4220858332 hasConcept C139719470 @default.
- W4220858332 hasConcept C15744967 @default.
- W4220858332 hasConcept C162324750 @default.
- W4220858332 hasConcept C2776867660 @default.
- W4220858332 hasConcept C2778709874 @default.
- W4220858332 hasConcept C2779146795 @default.
- W4220858332 hasConcept C504460877 @default.
- W4220858332 hasConcept C558461103 @default.
- W4220858332 hasConcept C62913699 @default.
- W4220858332 hasConcept C71315377 @default.
- W4220858332 hasConcept C71924100 @default.
- W4220858332 hasConceptScore W4220858332C118552586 @default.
- W4220858332 hasConceptScore W4220858332C126322002 @default.
- W4220858332 hasConceptScore W4220858332C134018914 @default.