INTRODUCTION
CThe burden of psoriatic disease is substantial and includes pruritus, pain, sleep disturbance,1 and work productivity impairment.2 However, itch as a mediator
of symptoms has been underexplored, especially since pruritus does not always correlate with disease severity. Consistent
with this hypothesis, one study recently demonstrated that sleep was not affected by disease severity,3 as measured by the PASI score, but was affected by symptoms of itching (pruritus) and obstructive sleep apnea (psoriasis patients are frequently overweight or obese, and obstructive sleep apnea is often undiagnosed in patients with insomnia).4 Zachariae et al.5 recently evaluated sleep as a mediating factor between affective pruritus severity and domains of depression, general distress, and health-related quality of life in psoriasis patients and found sleep mediated the association between pruritus severity and general distress, as measured by the Brief Symptom
Inventory.
Psoriasis patients are also known to experience substantial work presenteesim, which improves as the disease regresses.2,6,7 Given that insomnia is associated with presenteeism,8 it is important to explore potential relationships between pruritus,
sleep impairment, and work productivity activity impairment. These relationships are not well understood and are likely to be complicated, but they are critical in assessing the burden of disease and the value of therapy to patients affected by these conditions. We conducted a post hoc analysis to determine any associations between pruritus severity and the variables of sleep problems and work productivity activity impairment. We also evaluated the role of sleep quality as a possible mediator.
METHODS AND MATERIALS
Data Source
Data were from a double-blind, randomized, placebo-controlled,
phase 2 clinical trial that has been previously reported.9 Briefly, 142 adult patients with chronic moderate-to-severe plaque psoriasis (for ≥6 months prior to randomization) received
subcutaneous 10, 25, 75, or 150 mg of ixekizumab or placebo at 0 (baseline), 2, 4, 8, 12, and 16 weeks. The primary outcome was the proportion of patients with at least a 75% reduction
in the Psoriasis Area-and-Severity Index (PASI) score from baseline at 12 weeks. The PASI was also assessed at weeks 8 and 16. Neither obstructive sleep apnea nor sleeping pill usage
was exclusion criteria in this study.