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本文引用的文献

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Am J Clin Nutr. 2009 Oct;90(4):993-1001. doi: 10.3945/ajcn.2008.27402. Epub 2009 Aug 26.
2
Grade of adiposity affects the impact of fat mass on resting energy expenditure in women.肥胖程度会影响女性体内脂肪量对静息能量消耗的影响。
Br J Nutr. 2009 Feb;101(4):474-7. doi: 10.1017/s0007114508020357.
3
Considerations regarding the genetics of obesity.关于肥胖遗传学的思考
Obesity (Silver Spring). 2008 Dec;16 Suppl 3(Suppl 3):S33-9. doi: 10.1038/oby.2008.514.
4
No evidence of mass dependency of specific organ metabolic rate in healthy humans.在健康人体中,没有证据表明特定器官代谢率存在质量依赖性。
Am J Clin Nutr. 2008 Oct;88(4):1004-9. doi: 10.1093/ajcn/88.4.1004.
5
Lower metabolic rate in individuals heterozygous for either a frameshift or a functional missense MC4R variant.对于移码或功能性错义MC4R变体的杂合个体,其代谢率较低。
Diabetes. 2008 Dec;57(12):3267-72. doi: 10.2337/db08-0577. Epub 2008 Oct 3.
6
The obese without cardiometabolic risk factor clustering and the normal weight with cardiometabolic risk factor clustering: prevalence and correlates of 2 phenotypes among the US population (NHANES 1999-2004).无心血管代谢危险因素聚集的肥胖人群与有心血管代谢危险因素聚集的正常体重人群:美国人群(1999 - 2004年美国国家健康与营养检查调查)中两种表型的患病率及其相关因素
Arch Intern Med. 2008 Aug 11;168(15):1617-24. doi: 10.1001/archinte.168.15.1617.
7
Identification and characterization of metabolically benign obesity in humans.人类代谢性良性肥胖的识别与特征分析。
Arch Intern Med. 2008 Aug 11;168(15):1609-16. doi: 10.1001/archinte.168.15.1609.
8
Lipid droplets: FSP27 knockout enhances their sizzle.脂滴:FSP27基因敲除增强了它们的活性。
J Clin Invest. 2008 Aug;118(8):2693-6. doi: 10.1172/JCI36554.
9
Familial influences and obesity-associated metabolic risk factors contribute to the variation in resting energy expenditure: the Kiel Obesity Prevention Study.家族影响和肥胖相关的代谢危险因素导致静息能量消耗的差异:基尔肥胖预防研究。
Am J Clin Nutr. 2008 Jun;87(6):1695-701. doi: 10.1093/ajcn/87.6.1695.
10
Cardiovascular risk assessment in the metabolic syndrome: results from the Prospective Cardiovascular Munster (PROCAM) Study.代谢综合征中的心血管风险评估:来自明斯特前瞻性心血管研究(PROCAM)的结果。
Int J Obes (Lond). 2008 May;32 Suppl 2:S11-6. doi: 10.1038/ijo.2008.29.

“功能性”身体成分:区分良性肥胖和非良性肥胖。

'Functional' body composition: differentiating between benign and non-benign obesity.

作者信息

Müller Manfred J, Bosy-Westphal Anja, Heller Martin

机构信息

Institut für Humanernährung und Lebensmittelkunde, Agrar- und Ernährungswissenschaftliche Fakultät, Christian-Albrechts-Universität, Düsternbrooker Weg 17-19, D-24105 Kiel, Germany.

出版信息

F1000 Biol Rep. 2009 Oct 14;1:75. doi: 10.3410/B1-75.

DOI:10.3410/B1-75
PMID:20948613
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2948251/
Abstract

Recent body composition analyses, together with assessments of insulin resistance, aerobic fitness, and intima-media thickness of the common carotid artery, have shown that metabolically-benign obese subjects have a similar BMI, waist circumference, and subcutaneous abdominal fat compared with non-metabolically-benign obese subjects. Research has suggested that 25-30% of the obese population do not need either treatment or prevention of secondary disorders. Therefore, assessment of functional body composition should replace nutritional status-based risk assessments (such as the body mass index) in both metabolic research and clinical decision making. The concept of 'functional' body composition gives us a more sophisticated view on nutritional status, metabolism, endocrinology, and diseases. Knowledge of detailed body composition enables characterization of biomedical traits which will give functional evidence relating genetic variants.

摘要

最近的身体成分分析,连同对胰岛素抵抗、有氧适能以及颈总动脉内膜中层厚度的评估表明,代谢良性肥胖受试者与非代谢良性肥胖受试者相比,具有相似的体重指数、腰围和腹部皮下脂肪。研究表明,25%至30%的肥胖人群既不需要治疗也不需要预防继发性疾病。因此,在代谢研究和临床决策中,功能性身体成分评估应取代基于营养状况的风险评估(如体重指数)。“功能性”身体成分的概念使我们对营养状况、代谢、内分泌学和疾病有了更深入的认识。详细的身体成分知识能够对生物医学特征进行表征,从而为基因变异提供功能证据。