Influence of multisystemic affection on health-related quality of life in patients with myotonic dystrophy type 1

Abstract

AimTo assess health-related quality of life (HRQoL) in patients with DM1, to identify muscular, multisystemic, central and social factors that may affect QoL and to define a DM1 patient in risk of poor QoL. Patients and methodThis cross-sectional study comprised 120 DM1 consecutive patients. The following scales were used: Multidimensional Scale of Perceived Social Support (MSPSS), Muscular Impairment Rating Scale (MIRS), battery of neuropsychological tests, acceptance of illness scale (AIS), Hamilton rating scale for depression (Ham-D), Krupp's Fatigue Severity Scale (FSS), Daytime Sleepiness Scale (DSS) and SF-36 questionnaire. ResultsHRQoL was impaired in DM1 patients in both physical and mental domains (PCS was 41.8±23.5, MCS 47.0±24.3 and total SF-36 score 45.6±24.0). The most significant factors correlating with better SF-36 total score were younger age (β=−0.45, p<0.001), shorter duration of disease (β=−0.27, p=0.001), higher education (β=0.20, p=0.009), less severe muscular weakness (β=−0.52, p<0.001), normal swallowing (β=0.22, p=0.005), absence of fainting (β=0.31, p=0.002), absence of snoring (β=0.21, p=0.036), better acceptance of disease (β=−0.17, p=0.036), lower depressiveness (β=−0.46, p=0.001), lower fatigue (β=−0.32, p=0.001), absence of cataract (β=−0.21, p=0.034), absence of kyphosis (β=0.31, p=0.004) and absence of constipation (β=0.24, p=0.016). Second linear regression analysis revealed that depressed (β=−0.38, p<0.001) and elder patients (β=−0.27, p=0.007) and as well as those with poor acceptance of illness (β=−0.21, p=0.006) were in especially higher risk of having poor HRQoL (R2=0.68). ConclusionWe identified different central, social, muscular, cardiorespiratory and other factors correlating with HRQoL. It is of great importance that most of these factors are amenable to treatment.