“…A genetics study is planned in a subgroup of patients after they receive obeticholic acid for 3 years. Assessments of safety and side effects included adverse events, laboratory variables, a visual-analogue scale for pruritus, 21 the 5-D pruritus questionnaire (measuring the degree, duration, direction [improvement or worsening], disability [effect on daily activities], and distribution of itching), 22 dual energy x-ray absorptiometry (DEXA), electrocardiography, physical examination, and vital signs. A post hoc analysis to assess the correlation between the autotaxin level and the severity of patient-reported pruritus was also performed.…”