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本文引用的文献

1
2 years of calorie restriction and cardiometabolic risk (CALERIE): exploratory outcomes of a multicentre, phase 2, randomised controlled trial.热量限制与心脏代谢风险持续 2 年(CALERIE):一项多中心、2 期、随机对照试验的探索性结果。
Lancet Diabetes Endocrinol. 2019 Sep;7(9):673-683. doi: 10.1016/S2213-8587(19)30151-2. Epub 2019 Jul 11.
2
Sex differences in the response to dietary restriction in rodents.啮齿动物对饮食限制反应的性别差异。
Curr Opin Physiol. 2018 Dec;6:28-34. doi: 10.1016/j.cophys.2018.03.008. Epub 2018 Mar 27.
3
Sex Differences in Nonalcoholic Fatty Liver Disease: State of the Art and Identification of Research Gaps.非酒精性脂肪性肝病的性别差异:现状与研究空白的识别。
Hepatology. 2019 Oct;70(4):1457-1469. doi: 10.1002/hep.30626. Epub 2019 Sep 23.
4
The peculiar aging of human liver: A geroscience perspective within transplant context.人类肝脏的特殊衰老:移植背景下的老年科学视角。
Ageing Res Rev. 2019 May;51:24-34. doi: 10.1016/j.arr.2019.02.002. Epub 2019 Feb 14.
5
Long-term effects of increased protein intake after weight loss on intrahepatic lipid content and implications for insulin sensitivity: a PREVIEW study.减肥后增加蛋白质摄入对肝内脂质含量的长期影响及其对胰岛素敏感性的影响:PREVIEW 研究。
Am J Physiol Endocrinol Metab. 2018 Nov 1;315(5):E885-E891. doi: 10.1152/ajpendo.00162.2018. Epub 2018 Aug 7.
6
Significant improvement in cardiometabolic health in healthy nonobese individuals during caloric restriction-induced weight loss and weight loss maintenance.热量限制引起的体重减轻及其维持过程中,健康非肥胖个体的心血代谢健康得到显著改善。
Am J Physiol Endocrinol Metab. 2018 Apr 1;314(4):E396-E405. doi: 10.1152/ajpendo.00261.2017. Epub 2017 Dec 12.
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Guidelines on the management of abnormal liver blood tests.肝脏血液检查异常的管理指南。
Gut. 2018 Jan;67(1):6-19. doi: 10.1136/gutjnl-2017-314924. Epub 2017 Nov 9.
8
Body fat distribution, in particular visceral fat, is associated with cardiometabolic risk factors in obese women.身体脂肪分布,尤其是内脏脂肪,与肥胖女性的心血管代谢危险因素相关。
PLoS One. 2017 Sep 28;12(9):e0185403. doi: 10.1371/journal.pone.0185403. eCollection 2017.
9
Dietary Composition Independent of Weight Loss in the Management of Non-Alcoholic Fatty Liver Disease.饮食组成与非酒精性脂肪性肝病管理中的体重减轻无关。
Nutrients. 2017 Jul 26;9(8):800. doi: 10.3390/nu9080800.
10
Body Fat Distribution and the Risk of Incident Metabolic Syndrome: A Longitudinal Cohort Study.体脂肪分布与代谢综合征发病风险:一项纵向队列研究。
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两年热量限制对肝脏生物标志物的影响:CALERIE 2期随机对照试验的结果

Effect of 2 years of calorie restriction on liver biomarkers: results from the CALERIE phase 2 randomized controlled trial.

作者信息

Dorling James L, Ravussin Eric, Redman Leanne M, Bhapkar Manju, Huffman Kim M, Racette Susan B, Das Sai K, Apolzan John W, Kraus William E, Höchsmann Christoph, Martin Corby K

机构信息

Pennington Biomedical Research Center, 6400 Perkins Rd., Baton Rouge, LA, 70808, USA.

Duke University School of Medicine, Durham, NC, USA.

出版信息

Eur J Nutr. 2021 Apr;60(3):1633-1643. doi: 10.1007/s00394-020-02361-7. Epub 2020 Aug 14.

DOI:10.1007/s00394-020-02361-7
PMID:32803412
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7882001/
Abstract

PURPOSE

Calorie restriction (CR) is an effective treatment for obesity-related liver and metabolic disease. However, CR studies in individuals without obesity are needed to see if CR could delay disease onset. Liver biomarkers indicate hepatic health and are linked to cardiometabolic disease. Our aim was to examine the effects of a 2-year CR intervention on liver biomarkers in healthy individuals without obesity.

METHODS

The Comprehensive Assessment of Long-term Effects of Reducing Intake of Energy (CALERIE) study was a 2-year randomized controlled trial. Overall, 218 participants (body mass index: 25.1 ± 1.7 kg/m) were enrolled into a control group (n = 75) that ate ad libitum (AL), or a CR group (n = 143) that aimed to decrease energy intake by 25%. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), gamma-glutamyl transferase (GGT), and bilirubin were measured during the trial.

RESULTS

At month 24, relative to the AL group, ALP (- 7 ± 1 IU/L; P < 0.01) and GGT (- 0.11 ± 0.04 log IU/L; P = 0.02) decreased and bilirubin increased (0.21 ± 0.06 log mg/dL; P < 0.01) in the CR group; no between-group differences in ALT (- 1 ± 1 IU/L; P > 0.99) or AST (2 ± 2 IU/L; P = 0.68) were revealed. However, sex-by-treatment-by-time interactions (P < 0.01) were observed, with CR (vs. control) inducing reduced ALT and GGT and increased AST in men only (P ≤ 0.02).

CONCLUSIONS

In metabolically healthy individuals without obesity, 2 years of CR improves several liver biomarkers, with potentially greater improvements in men. These data suggest that sustained CR may improve long-term liver and metabolic disease risk in healthy adults.

TRIAL REGISTRATION

Clinicaltrials.gov (NCT00427193). Registered January 2007.

摘要

目的

热量限制(CR)是治疗肥胖相关肝脏和代谢疾病的有效方法。然而,需要对非肥胖个体进行CR研究,以确定CR是否能延缓疾病发作。肝脏生物标志物可指示肝脏健康状况,并与心脏代谢疾病相关。我们的目的是研究为期2年的CR干预对非肥胖健康个体肝脏生物标志物的影响。

方法

能量摄入减少长期效应综合评估(CALERIE)研究是一项为期2年的随机对照试验。共有218名参与者(体重指数:25.1±1.7kg/m²)被纳入自由进食(AL)的对照组(n = 75)或旨在将能量摄入减少25%的CR组(n = 143)。在试验期间测量了丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)、碱性磷酸酶(ALP)、γ-谷氨酰转移酶(GGT)和胆红素。

结果

在第24个月时,与AL组相比,CR组的ALP(-7±1IU/L;P<0.01)和GGT(-0.11±0.04logIU/L;P = 0.02)降低,胆红素升高(0.21±0.06logmg/dL;P<0.01);未发现ALT(-1±1IU/L;P>0.99)或AST(2±2IU/L;P = 0.68)的组间差异。然而,观察到性别×治疗×时间的交互作用(P<0.01),CR(与对照组相比)仅在男性中导致ALT和GGT降低,AST升高(P≤0.02)。

结论

在非肥胖的代谢健康个体中,2年的CR可改善多种肝脏生物标志物,男性的改善可能更大。这些数据表明,持续的CR可能会降低健康成年人患长期肝脏和代谢疾病的风险。

试验注册

Clinicaltrials.gov(NCT00427193)。2007年1月注册。