Redefining Metabolic Syndrome as a Fat Storage Condition Based on Studies of Comparative Physiology

被引:53
作者
Johnson, Richard J. [1 ]
Stenvinkel, Peter [2 ]
Martin, Sandra L. [3 ]
Jani, Alkesh [1 ,4 ]
Sanchez-Lozada, Laura Gabriela [1 ]
Hill, James O. [5 ]
Lanaspa, Miguel A. [1 ]
机构
[1] Univ Colorado Denver, Div Renal Dis & Hypertens, Aurora, CO USA
[2] Karolinska Univ Hosp, Div Renal Dis, Stockholm, Sweden
[3] Univ Colorado, Dept Cell & Dev Biol, Colorado Springs, CO 80907 USA
[4] Cardiol Univ, Lab Nefrol Anexo Invest, Dept Pediat, Mexico City, DF, Mexico
[5] Univ Colorado Denver, Anschutz Hlth & Wellness Ctr, Dept Pediat, Aurora, CO USA
关键词
SUGAR-SWEETENED BEVERAGES; SERUM URIC-ACID; MAMMALIAN HIBERNATION; DIABETES-MELLITUS; THRIFTY GENOTYPES; SEX-HORMONES; WEIGHT-GAIN; OBESITY; RISK; FRUCTOSE;
D O I
10.1002/oby.20026
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: The metabolic syndrome refers to a constellation of signs including abdominal obesity, elevated serum triglycerides, low HDL-cholesterol, elevated blood pressure, and insulin resistance. Today approximately one third of the adult population has the metabolic syndrome. While there is little doubt that the signs constituting the metabolic syndrome frequently cluster, much controversy exists over the definition, pathogenesis, or clinical utility. Design and Methods: Here we present evidence from the field of comparative physiology that the metabolic syndrome is similar to the biological process that animals engage to store fat in preparation for periods of food shortage. Results: We propose that the metabolic syndrome be changed to fat storage condition to more clearly align with its etiology. Obesity in humans is likely the consequences of both genetic predisposition (driven in part by thrifty genes) and environment. Recent studies suggest that the loss of the uricase gene may be one factor that predisposes humans to obesity today. Conclusion: Understanding the process animals engage to switch from a lean insulin-sensitive to an obese insulin-resistant state may provide novel insights into the cause of obesity and diabetes in humans, and unique opportunities for reversing their pathology.
引用
收藏
页码:659 / 664
页数:6
相关论文
共 83 条
[41]  
Klaassen M, 1996, J EXP BIOL, V199, P57
[42]   Association Between Serum Uric Acid and Development of Type 2 Diabetes [J].
Kodama, Satoru ;
Saito, Kazumi ;
Yachi, Yoko ;
Asumi, Mihoko ;
Sugawara, Ayumi ;
Totsuka, Kumiko ;
Saito, Aki ;
Sone, Hirohito .
DIABETES CARE, 2009, 32 (09) :1737-1742
[43]   SEED DISPERSAL IN FLOOD-PLAIN FORESTS OF AMAZONIA [J].
KUBITZKI, K ;
ZIBURSKI, A .
BIOTROPICA, 1994, 26 (01) :30-43
[44]  
Lanaspa M, SEM NEPHROL IN PRESS
[45]  
Lanaspa MA., 2012, J Biol Chem
[46]  
Lanaspa MA, 2012, PLOS ONE, V7, DOI [10.1371/journal.pone.0047948, 10.1371/journal.pone.0048801]
[47]   Relationship between uric acid and hepatic steatosis among Koreans [J].
Lee, K. .
DIABETES & METABOLISM, 2009, 35 (06) :447-451
[48]   Sugar-Sweetened Beverages and Risk of Metabolic Syndrome and Type 2 Diabetes [J].
Malik, Vasanti S. ;
Popkin, Barry M. ;
Bray, George A. ;
Despres, Jean-Pierre ;
Willett, Walter C. ;
Hu, Frank B. .
DIABETES CARE, 2010, 33 (11) :2477-2483
[49]   Sugar-Sweetened Beverages, Obesity, Type 2 Diabetes Mellitus, and Cardiovascular Disease Risk [J].
Malik, Vasanti S. ;
Popkin, Barry M. ;
Bray, George A. ;
Despres, Jean-Pierre ;
Hu, Frank B. .
CIRCULATION, 2010, 121 (11) :1356-1364
[50]   Mammalian hibernation: a naturally reversible model for insulin resistance in man? [J].
Martin, Sandra L. .
DIABETES & VASCULAR DISEASE RESEARCH, 2008, 5 (02) :76-81