TY - JOUR
T1 - Effects of naloxegol on whole gut transit in opioid-naïve healthy subjects receiving codeine
T2 - A randomized, controlled trial
AU - Halawi, H.
AU - Vijayvargiya, P.
AU - Busciglio, I.
AU - Oduyebo, I.
AU - Khemani, D.
AU - Ryks, M.
AU - Rhoten, D.
AU - Burton, D.
AU - Szarka, L. A.
AU - Acosta, A.
AU - Camilleri, M.
N1 - Publisher Copyright:
© 2018 John Wiley & Sons Ltd
PY - 2018/5
Y1 - 2018/5
N2 - Background: Nausea, vomiting, and constipation (OIC) are common adverse effects of acute or chronic opioid use. Naloxegol (25 mg) is an approved peripherally active mu-opiate opioid receptor antagonist. Aim: To compare the effects on pan-gut transit of treatment with codeine, naloxegol, or combination in healthy volunteers. Methods: We conducted a randomized, double-blind, placebo-controlled, single-center, parallel-group study in 72 healthy opioid-naïve adults, randomized to: codeine (30 mg q.i.d.), naloxegol (25 mg daily), codeine and naloxegol, or matching placebo. During 3 days of treatment, we measured gastric emptying (GE) T 1/2 , colonic filling at 6 hours (CF6), colonic geometric center at 24 and 48 hours, and ascending colon emptying (ACE) T 1/2 . Key Results: Participants were 59.7% women, median BMI 25.0 kg/m 2 , and median age 33.8 years. Codeine significantly retarded GE T 1/2, CF6, overall colonic transit, and ACE T 1/2 . There was significant difference (P =.026) in GE T 1/2 between codeine (144.0 min [IQR 110.5-238.6]) and naloxegol (95.5 min [89.1-135.4]). There was a significant overall group difference in CF6 (P =.023), with significant difference (P =.019) between codeine (11.0% [0.0-45.0]) and naloxegol (51% [18.8-76.2]). However, no significant differences were found between codeine-treated participants concomitantly receiving placebo or naloxegol. Conclusions and Inferences: Short-term administration of naloxegol (25 mg) in healthy, opioid-naïve volunteers does not reverse the retardation of gastric, small bowel, or colonic transit induced by acute administration of codeine. Further studies with naloxegol at higher dose are warranted to assess the ability to reverse the retardation of transit caused by acute administration of codeine in opioid-naïve subjects.
AB - Background: Nausea, vomiting, and constipation (OIC) are common adverse effects of acute or chronic opioid use. Naloxegol (25 mg) is an approved peripherally active mu-opiate opioid receptor antagonist. Aim: To compare the effects on pan-gut transit of treatment with codeine, naloxegol, or combination in healthy volunteers. Methods: We conducted a randomized, double-blind, placebo-controlled, single-center, parallel-group study in 72 healthy opioid-naïve adults, randomized to: codeine (30 mg q.i.d.), naloxegol (25 mg daily), codeine and naloxegol, or matching placebo. During 3 days of treatment, we measured gastric emptying (GE) T 1/2 , colonic filling at 6 hours (CF6), colonic geometric center at 24 and 48 hours, and ascending colon emptying (ACE) T 1/2 . Key Results: Participants were 59.7% women, median BMI 25.0 kg/m 2 , and median age 33.8 years. Codeine significantly retarded GE T 1/2, CF6, overall colonic transit, and ACE T 1/2 . There was significant difference (P =.026) in GE T 1/2 between codeine (144.0 min [IQR 110.5-238.6]) and naloxegol (95.5 min [89.1-135.4]). There was a significant overall group difference in CF6 (P =.023), with significant difference (P =.019) between codeine (11.0% [0.0-45.0]) and naloxegol (51% [18.8-76.2]). However, no significant differences were found between codeine-treated participants concomitantly receiving placebo or naloxegol. Conclusions and Inferences: Short-term administration of naloxegol (25 mg) in healthy, opioid-naïve volunteers does not reverse the retardation of gastric, small bowel, or colonic transit induced by acute administration of codeine. Further studies with naloxegol at higher dose are warranted to assess the ability to reverse the retardation of transit caused by acute administration of codeine in opioid-naïve subjects.
KW - PAMORA
KW - codeine
KW - constipation
KW - gastroparesis
KW - opioid
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U2 - 10.1111/nmo.13298
DO - 10.1111/nmo.13298
M3 - Article
C2 - 29405492
AN - SCOPUS:85041626972
SN - 1350-1925
VL - 30
JO - Neurogastroenterology and Motility
JF - Neurogastroenterology and Motility
IS - 5
M1 - e13298
ER -