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Rhinorrhea, cough and fatigue in patients taking sitagliptin 英文参考文献
Baraniuk and Jamieson Allergy, Asthma Clinical Immunology 2010, 6:8
/content/6/1/8
ALLERGY, ASTHMA CLINICAL
IMMUNOLOGY
RESEARCH
Open Access
Rhinorrhea, cough and fatigue in patients taking Research
sitagliptin
James N Baraniuk1 and Mary J Jamieson*2
Abstract
Sitagliptin is a dipeptidyl peptidase-4 (DPP IV, CD26) inhibitor indicated for treatment of Type II diabetes as a second
line therapy after metformin. We report fifteen sitagliptin intolerant patients who developed anterior and posterior
rhinorrhea, cough, dyspnea, and fatigue. Symptoms typically developed within 1 to 8 weeks of starting, and resolved
within 1 week of stopping the drug. Peak expiratory flow rates increased 34% in 8 patients who stopped sitagliptin.
Similar changes were found in 4 out of 5 persons who had confirmatory readministration. Chart review identified 17
patients who tolerated sitagliptin and had no symptomatic changes. The sitagliptin intolerant group had higher rates
of clinically diagnosed allergic rhinitis (15/15 vs. 6/18; p = 0.00005), Fishers Exact test) and angiotensin converting
enzyme inhibitor - induced cough (6/13 vs. 1/18; p = 0.012). Nasal and inhaled glucocorticoids may control the
underlying allergic inflammation and abrogate this new sitagliptin - induced pharmacological syndrome. Potential
mucosal and central nervous system mechanisms include disruption of neuropeptides and/or cytokines that rely on
DPP IV for activation or inactivation, and T cell dysfunction.
Background
gliptin induced a reproducible syndrome. When the
challenges were affirmative, we reviewed charts to iden-
tify other sitagliptin - treated subjects. We identified sita-
Sitagliptin is a selective dipeptidylpeptidase-4 (DPP IV,
CD26, EC ) inhibitor indicated for the treatment
of Type II diabetes mellitus [1]. Diabetics treated with gliptin intolerant and tolerant groups, and began an
sitagliptin (Januvia?, Merck Co., Inc., Whitehouse Sta-
tion, N.J.)
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