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. 2008 Sep;9(6):381–393. doi: 10.2174/138920208785699553

Table 3.

Pharmacogenetics of Sulfasalazine (SASP) in Rheumatoid Arthritis (RA)

Gene Symbol Polymorphism Effect of Polymorphism Pharmacogenetics References
NAT2 NAT2*4 Increased activity of NAT2 enzyme Decreased concentrations of SASP intermediates [75]
(wildtype) (fast acetylator status) Less prone to toxicities from SASP
NAT2*5A Decreased activity of NAT2 enzyme Increased concentrations of SASP intermediates [76, 77]
T341C,C481T (slow acetylator status) More prone to toxicities from SASP
NAT2*5B Decreased activity of NAT2 enzyme Increased concentrations of SASP intermediates [76, 77]
T341C,C481T,A803G (slow acetylator status) More prone to toxicities from SASP
NAT2*5C Decreased activity of NAT2 enzyme Increased concentrations of SASP intermediates [76, 77]
T341C,A803G (slow acetylator status) More prone to toxicities from SASP
NAT2*6 Decreased activity of NAT2 enzyme Increased concentrations of SASP intermediates [76, 77]
C282T,G590A (slow acetylator status) More prone to toxicities from SASP
NAT2*7 Decreased activity of NAT2 enzyme Increased concentrations of SASP intermediates [76, 77]
C282T,G857A (slow acetylator status) More prone to toxicities from SASP

NAT2 = N-acetyltransferase 2.