Literature DB >> 23974768

New medications for obesity management: changing the landscape of obesity treatment.

Nadia Boulghassoul-Pietrzykowska1, Jennifer Franceschelli, Christopher Still.   

Abstract

PURPOSE OF REVIEW: Despite being one of the most prevalent chronic diseases, obesity was not recognized as such until very recently. Although linked to ubiquitous diseases like diabetes, hypertension, coronary artery disease, obstructive sleep apnea, and many others, targeted treatments are few. Diet, exercise, and behavior modification are the pillars of weight loss. When they alone do not achieve the required weight reduction, medications may be used for patients with a BMI above 30 or above 27 if obesity-related comorbidities are present. The spectrum of pharmacologic agents aimed at obesity treatment will be reviewed. RECENT
FINDINGS: Two medications, phentermine and orlistat, have been the only agents approved many years ago and now still standing. Others have come and gone, removed from the market by the Food and Drug Administration (FDA) because of harmful side-effects. However, in the last few years, new drugs have started to emerge. Since 2012, two new medications phentermine-topiramate extended-release combination and lorcaserin have been FDA approved, while at least one more, naltrexone SR/bupropion SR combination is expected to be re-evaluated by the FDA in 2014.
SUMMARY: Treating obesity is crucial as it will ultimately result in the prevention of many related chronic diseases and will decrease morbidity and mortality. Weight loss medications are a valuable part of the clinician's toolbox in the treatment of obesity and should be used when appropriate. Having a variety of medications would be a great asset to accommodate various patients' needs and pre-existing medical conditions.

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Year:  2013        PMID: 23974768     DOI: 10.1097/01.med.0000433059.78485.fa

Source DB:  PubMed          Journal:  Curr Opin Endocrinol Diabetes Obes        ISSN: 1752-296X            Impact factor:   3.243


  5 in total

1.  Chemical inhibition of fatty acid absorption and cellular uptake limits lipotoxic cell death.

Authors:  Constance Ahowesso; Paul N Black; Nipun Saini; David Montefusco; Jessica Chekal; Chrysa Malosh; Craig W Lindsley; Shaun R Stauffer; Concetta C DiRusso
Journal:  Biochem Pharmacol       Date:  2015-09-21       Impact factor: 5.858

2.  Design, Synthesis, and Biological Evaluation of a Novel Series of 4-Guanidinobenzoate Derivatives as Enteropeptidase Inhibitors with Low Systemic Exposure for the Treatment of Obesity.

Authors:  Zenichi Ikeda; Keiko Kakegawa; Fumiaki Kikuchi; Sachiko Itono; Hideyuki Oki; Hiroaki Yashiro; Hideyuki Hiyoshi; Kazue Tsuchimori; Kenichi Hamagami; Masanori Watanabe; Masako Sasaki; Youko Ishihara; Kimio Tohyama; Tomoyuki Kitazaki; Tsuyoshi Maekawa; Minoru Sasaki
Journal:  J Med Chem       Date:  2022-06-10       Impact factor: 8.039

3.  Fatty Acid Transport Proteins: Targeting FATP2 as a Gatekeeper Involved in the Transport of Exogenous Fatty Acids.

Authors:  Paul N Black; Constance Ahowesso; David Montefusco; Nipun Saini; Concetta C DiRusso
Journal:  Medchemcomm       Date:  2016-02-19       Impact factor: 3.597

Review 4.  Naltrexone sustained-release/bupropion sustained-release for the management of obesity: review of the data to date.

Authors:  Assumpta Caixàs; Lara Albert; Ismael Capel; Mercedes Rigla
Journal:  Drug Des Devel Ther       Date:  2014-09-18       Impact factor: 4.162

5.  A direct tissue-grafting approach to increasing endogenous brown fat.

Authors:  Nicole R Blumenfeld; Hwan June Kang; Anna Fenzl; Ziwei Song; Janice J Chung; Ranjodh Singh; Roshawn Johnson; Ayse Karakecili; Jun B Feranil; Ninna S Rossen; Vivian Zhang; Sahir Jaggi; Bret McCarty; Steven Bessler; Gary J Schwartz; Robert Grant; Judith Korner; Florian W Kiefer; Brian M Gillette; Samuel K Sia
Journal:  Sci Rep       Date:  2018-05-21       Impact factor: 4.379

  5 in total

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