The use of methotrexate in the treatment of psoriatic arthritis is associat
ed with risk of hepatotoxicity. However, monitoring of liver-associated enz
ymes often lacks sensitivity, and guidelines for serial liver biopsies in p
soriatic arthritis are not yet well established. We performed a retrospecti
ve review of all patients with psoriatic arthritis receiving methotrexate w
ho were enrolled in the disease-modifying anti-rheumatic drug clinics (DMAR
D clinics) at the Air Force and Army hospitals in San Antonio, Texas. Infor
mation was obtained regarding methotrexate regimen, liver-associated enzyme
results, and liver biopsy results. Thirty psoriatic arthritis patients wer
e taking methotrexate in the DMARD clinics. Seventeen patients had a total
of 21 biopsies. Biopsies were performed for surveillance dictated by cumula
tive dose. Liver biopsies were graded on Roenigk scale of I-IV where I is m
ild steatosis, IT is moderate steatosis, Ma is mild fibrosis, IIIb is sever
e fibrosis, and IV is cirrhosis. Ten biopsies were grade I, 5 were grade II
, 5 were grade IIIa, I was grade IIIb, and none were grade IV.
In this very small retrospective study, regular monitoring of liver-associa
ted enzymes did not correlate with histologic deterioration in our patients
. Until prospective studies are performed, we suggest that routine liver bi
opsies are necessary to monitor for methotrexate hepatotoxicity in psoriati
c arthritis.