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Angiotensin II receptor blockers and gastrointestinal adverse events of resembling sprue-like enteropathy: a systematic review.

Gastroenterology report
June 1, 2019
Ayesha Kamal et al. (7 authors)
Journal ArticleReviewHuman Study
Extracted Claims (10)
InterventionDirectionEndpointPopulationDosageImpactClaim #
olmesartan
increase
gastrointestinal symptoms resembling sprue-like enteropathy
-
-
associated with
#1
ARBs
increase
enteropathy
-
-
may be a class effect for
#2
ARBs
increase
onset of symptoms
cases
2 weeks to 13 years
periods between initiation and onset of symptoms ranged from
#3
ARBs
increase
villous atrophy
cases
201 cases (92.2%)
were reported in
#4
ARBs
increase
intraepithelial lymphocytosis
cases
131 cases (60.1%)
were reported in
#5
HLA testing
increase
HLA-DQ2 or HLA-DQ8 haplotypes
patients
105 (71.4%)
had
#6
Celiac-associated antibodies testing
increase
negative results
patients
167 (98.8%)
showed
#7
Gluten exclusion from the diet
no change
symptoms of enteropathy
patients
127 (97.7%) of 130 patients
failed to relieve
#8
discontinuation of ARB
decrease
complete remission of symptoms
patients
233 (97.4%) of the 239 patients
resulted in
#9
restarting olmesartan
increase
symptoms
cases
7 cases (2.8%)
reported recurrence of
#10
Abstract

BACKGROUND: Olmesartan, an angiotensin II receptor blocker (ARB), is associated with gastrointestinal symptoms resembling sprue-like enteropathy. Some have proposed that enteropathy may be a class effect rather than olmesartan-specific. We performed a systematic review to identify literature of sprue-like enteropathy for all ARBs. METHODS: Case reports, case series and comparative studies of ARBs were searched on PubMed and Embase databases through 21 November 2018 and then assessed. RESULTS: A total of 82 case reports and case series as well as 5 comparative studies, including 248 cases, were selected and analysed. The ARBs listed in the case reports were olmesartan (233 users; 94.0%), telmisartan (5 users; 2.0%), irbesartan (4 users; 1.6%), valsartan (3 users; 1.2%), losartan (2 users; 0.8%) and eprosartan (1 user; 0.4%). The periods between ARB initiation and onset of symptoms ranged from 2 weeks to 13 years. Histologic results were reported in 218 cases, in which 201 cases (92.2%) were villous atrophy and 131 cases (60.1%) were intraepithelial lymphocytosis. Human leucocyte antigen (HLA) testing was performed in 147 patients, among whom 105 (71.4%) had HLA-DQ2 or HLA-DQ8 haplotypes. Celiac-associated antibodies were tested in 169 patients, among whom 167 (98.8%) showed negative results. Gluten exclusion from the diet failed to relieve symptoms of enteropathy in 127 (97.7%) of 130 patients with information. Complete remission of symptoms after discontinuation of ARB was reported in 233 (97.4%) of the 239 patients with information. Seven cases (2.8%) reported recurrence of symptoms after restarting olmesartan; rechallenge was not reported for the non-olmesartan ARBs. The retrospective studies conducted worldwide had inconsistent study designs (e.g. differences in periods of study and case definition) and findings. CONCLUSIONS: Although enteropathy is rare, clinicians should remain vigilant of this potential adverse event even years after medication initiation.

Study Links
PubMed ID31217979
Related Supplements
Angiotensin II receptor blockers and gastrointestinal advers... | Panacea Index