ALEXITHYMIA, BURDEN AND EMOTIONAL STATE IN ALS\u2019 CAREGIVERS

Introduction: Living with a progressively disease such as Amyotrophic lateral sclerosis (ALS) has a strong impact on the people affected and on their relatives, who have to tackle the demanding duties of caring for and assisting them (Tramonti et al., 2014). Although an extensive literature documents the levels of distress among caregivers of patients with progressive illness, less attention has been directed to determinants of caregiver mood and emotional regulation (Rabkin et al., 2009). In particular, there are not studies that assess the role of alexithymia in ALS. We evaluated the relationship between alexithymia and burden, and psychopatological symptoms in ALS\u2019caregivers. Methods: 17 ALS\u2019caregivers were tested with the following instruments: Toronto Alexithymia Scale-20 (TAS20); Hospital Anxiety and Depression Scale (HADS); Caregiver Burden Inventory (CBI). Results: 9 (53%) caregivers suffered from alexithymia (M=58; SD=6.2), while 8 individuals (47%) were not alexithymic (M=41.25; SD=8.31). We showed a positive correlation between total alexithymia score (TAS20-Tot) and depression (HADS-D; \u3c1= 0.575, p<0.01) and emotional burden (CBI-E; \u3c1=0.581, p<0.01). We found positive associations between TAS20 Difficulty Identifying Feelings subscale (TAS20-DIF) and anxiety (HADS-A; \u3c1=0.505, p<0.05), and HADS-D (\u3c1=0.679, p<0.05), and CBI-E (\u3c1=0.672, p<0.01). TAS20 Difficulty Describing Feelings subscale (TAS20-DDF) correlated with HADS-D (\u3c1=0.508, p<0.05) and CBI-E (\u3c1=0.747, p