Reuters Health Information: Lower risk of hep C extrahepatic manifestations with sustained virological response
Lower risk of hep C extrahepatic manifestations with sustained virological response
Last Updated: 2017-06-28
By Will Boggs MD
NEW YORK (Reuters Health) - Patients who achieved a
sustained virological response (SVR) to interferon-based
antiviral therapy for hepatitis C virus (HCV) had a reduced risk
of extrahepatic manifestations, according to a retrospective
cohort study.
�Health care providers of HCV-infected individuals should
educate patients as to the extrahepatic benefits of treating the
infection, in addition to reduced risk of progression of liver
fibrosis and liver cancer,� Dr. Parag Mahale from National
Cancer Institute, Rockville, Maryland told Reuters Health by
email. �As direct-acting antiviral drugs have dramatically
increased the cure rates with few side effects and shorter
duration of therapy, health care providers should provide HCV
treatment as soon as possible after diagnosis to maximize these
benefits.�
Extrahepatic manifestations (EHMs) associated with chronic
HCV infection include essential mixed cryoglobulinemia, some
subtypes of B cell non-Hodgkin's lymphoma (NHL),
membranoproliferative glomerulonephritis, porphyria cutanea
tarda (PCT), and lichen planus, as well as type 2 diabetes,
coronary heart disease, and stroke.
Dr. Mahale and colleagues used data from the Department of
Veteran Affairs HCV Clinical Case Registry to study the effect
of SVR after interferon-based antiviral therapy on the risk of
these eight EHMs and 160,875 veterans who were followed for a
median 5.1 years.
Most EHMs were rare (<1 per 1000 person-years), and their
incidence was lower in the treated groups when compared with
untreated veterans, except for lichen planus, according to the
June 20th online report in Gut.
Achievement of SVR was associated with a 39% lower risk of
mixed cryoglobulinemia, a 38% lower risk of glomerulonephritis,
a 59% lower risk of PCT, a 36% lower risk of NHL, and 18% lower
risk of diabetes, and a 16% lower risk of stroke.
There was no reduction in the risk of lichen planus or
coronary heart disease in association with SVR.
Later initiation of antiviral therapy was associated with a
diminishing reduction in the risk of glomerulonephritis, NHL,
and stroke.
�All the extrahepatic manifestations that we studied have
risk factors other than HCV infection; we were not able to
adjust for these within individual participants in the study,�
Dr. Mahale said. �For example, diet, obesity, and genetic
factors play a major role in increasing the risk of diabetes
mellitus. To reduce the risk of diabetes, those factors should
be targeted, in addition to treatment of HCV.�
�Our study was conducted among U.S. war veterans, which is a
unique cohort with different risk profiles for various outcomes,
compared to the general population,� he said. �Therefore, this
study should be replicated in other populations.�
�Also, we could study only interferon-containing regimens
which are no longer the standard of care for HCV-infected
people,� Dr. Mahale said. �Hence, we recommend replication of
our study in people who received interferon-free direct-acting
antiviral therapy.�
SOURCE: http://bit.ly/2tkxUq8
Gut 2017.
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