Obesity Therapy: How and Why?

被引:35
作者
Paccosi, Sara [1 ]
Cresci, Barbara [2 ]
Pala, Laura [2 ]
Rotella, Carlo Maria [2 ,3 ]
Parenti, Astrid [1 ]
机构
[1] Univ Florence, Dept Hlth Sci, Clin Pharmacol & Oncol Sect, Florence, Italy
[2] Careggi Univ Hosp, Diabetol, Florence, Italy
[3] Univ Florence, Endocrine Unit, Dept Biomed Clin & Expt Sci, Florence, Italy
关键词
Obesity; type-2; diabetes; pharmacology; action-mechanism; self-medication; dietary supplements; BODY-WEIGHT; DIETARY-SUPPLEMENTS; LIPASE INHIBITOR; GLYCEMIC CONTROL; ORLISTAT; OVERWEIGHT; RELEASE; TETRAHYDROLIPSTATIN; METAANALYSIS; SAFETY;
D O I
10.2174/0929867326666190124121725
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Obesity represents the second preventable mortality cause worldwide, and is very often associated with type 2 Diabetes Mellitus (T2DM). The first line treatment is lifestyle modification to weiv,ht-loss, but for those who fail to achieve the goal or have difficulty in maintaining achieved results, pharmacological treatment is needed. Few drugs are available today, because of their side effects. Objective: We aim to review actual pharmacological management of obese patients, highlighting differences between Food and Drug Administration- and European Medicine Agency-approved molecules, and pointing out self-medications readily obtainable and widely distributed. Methods: Papers on obesity, weight loss, pharmacotherapy, self- medication and diet-aid products were selected using Medline. Research articles, systematic reviews, clinical trials and meta-analyses were screened. Results: Anti-obesity drugs with central mechanisms, such as phentennine and lorcaserin, are available in USA, but not in Europe. Phenterminehopiramate and naltrexone/bupropion combinations are now available, even though the former is still under investigation from EMA. Orlistat, with peripheral mechanisms, represents the only drug approved for weight reduction in adolescents. Liraglutide has been approved at higher dose for obesity. Anti-obesity drugs, readily obtainable from the internet, include crude-drug products and supplements for which there is often a lack of compliance to national regulatory standards. Conclusions: Mechanisms of weight loss drugs include the reduction of energy intake or the increase in energy expenditure and sense of satiety as well as the decrease of hunger or the reduction in calories absorption. Few drugs are approved, and differences exist between USA and Europe. Moreover, herbal medicines and supplements often sold on the internet and widely used by obese patients, present a risk of adverse effects.
引用
收藏
页码:174 / 186
页数:13
相关论文
共 82 条
  • [11] Circulating dendritic cell number and intracellular TNF-α production in women with type 2 diabetes
    Blank, Sally E.
    Johnson, Emily Carolyn
    Weeks, Debra K.
    Wysham, Carol H.
    [J]. ACTA DIABETOLOGICA, 2012, 49 : S25 - S32
  • [13] Why Do We Need Drugs to Treat the Patient with Obesity?
    Bray, George A.
    [J]. OBESITY, 2013, 21 (05) : 893 - 899
  • [14] Iodine excess
    Buergi, Hans
    [J]. BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM, 2010, 24 (01) : 107 - 115
  • [15] A functional neuroimaging review of obesity, appetitive hormones and ingestive behavior
    Burger, Kyle S.
    Berner, Laura A.
    [J]. PHYSIOLOGY & BEHAVIOR, 2014, 136 : 121 - 127
  • [16] Potential Risks Associated with the Use of Herbal Anti-Obesity Products
    Chan, Thomas Y. K.
    [J]. DRUG SAFETY, 2009, 32 (06) : 453 - 456
  • [17] Chen Y, 2016, DRUG DISCOV THER, V10, P62, DOI 10.5582/ddt.2016.01014
  • [18] Safety of antiobesity drugs
    Cheung, Bernard Man Yung
    Cheung, Tommy Tsang
    Samaranayake, Nithushi Rajitha
    [J]. THERAPEUTIC ADVANCES IN DRUG SAFETY, 2013, 4 (04) : 171 - 181
  • [19] Four experimental stimulants found in sports and weight loss supplements: 2-amino-6-methylheptane (octodrine), 1,4-dimethylamylamine (1,4-DMAA), 1,3-dimethylamylamine (1,3-DMAA) and 1,3-dimethylbutylamine (1,3-DMBA)
    Cohen, Pieter A.
    Travis, John C.
    Keizers, Peter H. J.
    Deuster, Patricia
    Venhuis, Bastiaan J.
    [J]. CLINICAL TOXICOLOGY, 2018, 56 (06) : 421 - 426
  • [20] Cuzzolaro M, 2016, CLIN MANAGEMENT OVER, P103