Skip to main content
. Author manuscript; available in PMC: 2016 Jun 1.
Published in final edited form as: Aliment Pharmacol Ther. 2015 Mar 23;41(11):1094–1103. doi: 10.1111/apt.13175

Table 2.

Baseline factors reported to be associated with drug PK and/or clinical outcomes after anti-TNF therapy for UC

Baseline Factor Association with PK Association with outcomes
Age Inversely associated with clinical
 response to IFX 65
Sex IFX clearance faster in men37 Increased rates of clinical
 response and remission in
 females treated with GLM 23
Race White race associated with higher
 rates of GLM clinical response
23
Weight Directly associated with IFX
 volume of distribution 37
Inversely associated with
 frequency of IFX dose
 escalation in children 39
High body weight associated with
 higherIFX clearance; low body
 weight associated with low
 trough IFX levels since
 relationship between weight
 and clearance is nonlinear47
Directly associated with serum
 IFX levels in children 27
Albumin Low albuminassociated withlow
 serum IFX concentrations
 rapid clearance26,44,47
Low serum albumin associated
 with lower IFX response
 rates44, increased colectomy
 rates46, and increased
 frequency of IFX dose
 escalation in
 children39
CRP CRP inversely associated with
 IFX levels 26
CRP inversely associated with
 GLM response23
ESR High ESR associated with
 increased frequency of IFX
 dose escalation in children39
Fecal
inflammatory
markers
Fecal lactoferrin inversely
 associated with GLM
 response23
Fecal calprotectin inversely
 related to IFX response in
 ASUC38
Mayo Score Inversely associated with IFX
 levels26
Inversely associated with
 incidence of clinical remission
 after treatment with IFX or
 GLM23,28
pANCA Positive pANCA associated with
 decreased rates of clinical
 response to IFX65
TNF Mucosal TNF gene expression
 inversely associated with
 response to IFX32
Mucosal gene
expression
Panel of 5 genes (TNFRSF11B,
 STC1, PTGS2, IL13RA2 and
 IL11) predicted response to
 IFX66
Gene expression principle
 component representing UC
 molecular disturbance
 associated with non-
 response.67

IFX, infliximab; GLM, golimumab; CRP, c-reactive protein; ESR, erythrocyte sedimentation rate; pANCA, pronuclear anti-neutrophil cytoplasmic antibodies