Literature DB >> 35429263

The effect of additional acarbose on metformin-associated artificially high 18F-Fluorodeoxyglucose uptake in positron emission tomography/computed tomography.

Emre Urhan1, Emre Temizer2, Zuleyha Karaca1, Ummuhan Abdulrezzak2, Canan Sehit Kara1, Aysa Hacioglu1, Kursad Unluhizarci3.   

Abstract

AIM: Metformin causes diffuse and intense fluorodeoxyglucose (FDG) uptake more frequently in the colon and less frequently in the small intestine. In this study, we aimed to investigate the effect of simultaneous use of acarbose and metformin on FDG uptake in positron emission tomography/computed tomography (PET/CT), which has not been investigated previously.
METHODS: Totally 145 patients with a median age of 65 years (range: 18-80 years), who underwent FDG PET/CT in the Department of Nuclear Medicine of Erciyes University Medical School between 2018 and 2021, were involved in the study. The patients undergoing PET/CT were categorized as metformin plus acarbose users (group MA), metformin users (group M), and control subjects without diabetes (group C). The maximum and mean standard uptake values (SUVmax and SUVmean) of FDG uptake of the all intestine segments were measured separately.
RESULTS: The number of participants in each group was 35, 51 and 59 in group MA, group M and group C, respectively. The FDG uptake of all intestine was significantly higher in group MA and group M than in group C. The FDG uptake of ascending, transverse, descending, and sigmoid colon was significantly lower in group MA than in group M. The FDG uptake of the small intestine was not different between group MA and group M. The FDG uptake of the rectum was lower in group MA than group M and it was significant for SUVmean, but not significant for SUVmax.
CONCLUSION: The addition of acarbose to metformin therapy decreased SUV and artificially high FDG uptake in the colon and may be an alternative recommendation to discontinuing metformin in patients going to PET/CT imaging.
© 2022. Springer-Verlag Italia S.r.l., part of Springer Nature.

Entities:  

Keywords:  Acarbose; Colon; Gastrointestinal system; Glucose uptake; Metformin; Positive emisson tomography (PET)

Mesh:

Substances:

Year:  2022        PMID: 35429263     DOI: 10.1007/s00592-022-01890-3

Source DB:  PubMed          Journal:  Acta Diabetol        ISSN: 0940-5429            Impact factor:   4.280


  30 in total

1.  Metformin treatment significantly enhances intestinal glucose uptake in patients with type 2 diabetes: Results from a randomized clinical trial.

Authors:  Jukka P Koffert; Kirsi Mikkola; Kirsi A Virtanen; Anna-Maria D Andersson; Linda Faxius; Kirsti Hällsten; Mikael Heglind; Letizia Guiducci; Tam Pham; Johanna M U Silvola; Jenni Virta; Olof Eriksson; Saila P Kauhanen; Antti Saraste; Sven Enerbäck; Patricia Iozzo; Riitta Parkkola; Maria F Gomez; Pirjo Nuutila
Journal:  Diabetes Res Clin Pract       Date:  2017-07-20       Impact factor: 5.602

2.  Impact of medication discontinuation on increased intestinal FDG accumulation in diabetic patients treated with metformin.

Authors:  Jong-Ryool Oh; Ho-Chun Song; Ari Chong; Jung-Min Ha; Shin-Young Jeong; Jung-Joon Min; Hee-Seung Bom
Journal:  AJR Am J Roentgenol       Date:  2010-12       Impact factor: 3.959

3.  Finding the sweet spot for metformin in 18F-FDG-PET.

Authors:  Michael Morris; Babak Saboury; Wengen Chen; Eliot L Siegel; Bahar Dasgeb
Journal:  Nucl Med Commun       Date:  2017-10       Impact factor: 1.690

Review 4.  Metformin - a new old drug.

Authors:  Marta Patrycja Wróbel; Bogdan Marek; Dariusz Kajdaniuk; Dominika Rokicka; Aleksandra Szymborska-Kajanek; Krzysztof Strojek
Journal:  Endokrynol Pol       Date:  2017       Impact factor: 1.582

5.  Metformin may be associated with false-negative cancer detection in the gastrointestinal tract on PET/CT.

Authors:  Devin W Steenkamp; Marie E McDonnell; Sara Meibom
Journal:  Endocr Pract       Date:  2014-10       Impact factor: 3.443

6.  GLUT2 accumulation in enterocyte apical and intracellular membranes: a study in morbidly obese human subjects and ob/ob and high fat-fed mice.

Authors:  Amal Ait-Omar; Milena Monteiro-Sepulveda; Christine Poitou; Maude Le Gall; Aurélie Cotillard; Jules Gilet; Kevin Garbin; Anne Houllier; Danièle Château; Amélie Lacombe; Nicolas Veyrie; Danielle Hugol; Joan Tordjman; Christophe Magnan; Patricia Serradas; Karine Clément; Armelle Leturque; Edith Brot-Laroche
Journal:  Diabetes       Date:  2011-08-18       Impact factor: 9.461

7.  Metformin acutely lowers blood glucose levels by inhibition of intestinal glucose transport.

Authors:  Olga Horakova; Petra Kroupova; Kristina Bardova; Jana Buresova; Petra Janovska; Jan Kopecky; Martin Rossmeisl
Journal:  Sci Rep       Date:  2019-04-16       Impact factor: 4.379

8.  Association Between Colonic 18F-FDG Uptake and Glycemic Control in Patients with Diabetes Mellitus.

Authors:  Hyung Seok Chang; Soo Jeong Kim; Young Hwan Kim
Journal:  Nucl Med Mol Imaging       Date:  2020-06-17

9.  Beneficial endocrine but adverse exocrine effects of sitagliptin in the human islet amyloid polypeptide transgenic rat model of type 2 diabetes: interactions with metformin.

Authors:  Aleksey V Matveyenko; Sarah Dry; Heather I Cox; Artemis Moshtaghian; Tatyana Gurlo; Ryan Galasso; Alexandra E Butler; Peter C Butler
Journal:  Diabetes       Date:  2009-04-29       Impact factor: 9.461

10.  Mechanisms of metformin action: In and out of the gut.

Authors:  Takahiro Minamii; Munenobu Nogami; Wataru Ogawa
Journal:  J Diabetes Investig       Date:  2018-06-05       Impact factor: 4.232

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