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Dysfunction at baseline was also associated with higher severity of certain PROs.Pretreatment dysfunction was associated with continued decline and lack of recovery of HRQoL in this patient population.
As hypothesized, HEE-EOI at baseline was also associated with worse fatigue severity, but, contrary to predictions, not disability reported at follow-up (see Table 3).
CGI-S at baseline was also associated with categorical improvement at 6 months, however with better odds for improvement in patients with low CGI-S at baseline.
Similarly, IL-4 production in supernatant of PBMC cultured with PPD at baseline was also associated with an increased risk of experiencing a decline in CD4+ cell count to < 350/μL during ART interruption (Table 2).
LEA at baseline was also associated with increased risk during follow-up of ESRD, myocardial infarction, all-cause mortality, and specifically, with mortality due to cardiovascular and infectious diseases.
Valgus alignment at baseline was also associated with a nearly fivefold increase in the odds of lateral progression; the severity of varus correlated with medial joint space loss (r = 0.52, 95% CI = 0.40 0.62 in dominant knees), and the severity of valgus correlated with subsequent lateral joint space loss (r = 0.35, 95% CI = 0.21 0.47 in dominant knees).
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Lower cognitive ability and a greater number of medications at baseline were also associated with fewer hours of HHS.
Low levels of ENRAGE at baseline were also associated with improvement in FACIT-F scores at week 14.
Higher child activity levels and lower levels of family cohesion at baseline were also associated with lower current levels of psychosocial well-being.
Higher baseline HbA1 was also associated with higher AP.
Higher baseline HbA1 was also associated with higher AP and lower SEVR multivariately.
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