Abstract:
:Multiple sclerosis (MS) patients present several alterations related to sensing of bodily signals. However, no specific neurocognitive impairment has yet been proposed as a core deficit underlying such symptoms. We aimed to determine whether MS patients present changes in interoception-that is, the monitoring of autonomic bodily information-a process that might be related to various bodily dysfunctions. We performed two studies in 34 relapsing-remitting, early-stage MS patients and 46 controls matched for gender, age, and education. In Study 1, we evaluated the heartbeat-evoked potential (HEP), a cortical signature of interoception, via a 128-channel EEG system during a heartbeat detection task including an exteroceptive and an interoceptive condition. Then, we obtained whole-brain MRI recordings. In Study 2, participants underwent fMRI recordings during two resting-state conditions: mind wandering and interoception. In Study 1, controls exhibited greater HEP modulation during the interoceptive condition than the exteroceptive one, but no systematic differences between conditions emerged in MS patients. Patients presented atrophy in the left insula, the posterior part of the right insula, and the right anterior cingulate cortex, with abnormal associations between neurophysiological and neuroanatomical patterns. In Study 2, controls showed higher functional connectivity and degree for the interoceptive state compared with mind wandering; however, this pattern was absent in patients, who nonetheless presented greater connectivity and degree than controls during mind wandering. MS patients were characterized by atypical multimodal brain signatures of interoception. This finding opens a new agenda to examine the role of inner-signal monitoring in the body symptomatology of MS.
journal_name
Hum Brain Mappjournal_title
Human brain mappingauthors
Salamone PC,Esteves S,Sinay VJ,García-Cordero I,Abrevaya S,Couto B,Adolfi F,Martorell M,Petroni A,Yoris A,Torquati K,Alifano F,Legaz A,Cassará FP,Bruno D,Kemp AH,Herrera E,García AM,Ibáñez A,Sedeño Ldoi
10.1002/hbm.24319subject
Has Abstractpub_date
2018-12-01 00:00:00pages
4743-4754issue
12eissn
1065-9471issn
1097-0193journal_volume
39pub_type
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