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Clin Diabetes. 2015 Apr;33(2):97-111. doi: 10.2337/diaclin.33.2.97.
3
Metabolic syndrome in premenopausal and postmenopausal women with type 2 diabetes: loss of protective effects of premenopausal status.绝经前和绝经后2型糖尿病女性的代谢综合征:绝经前状态保护作用的丧失
J Diabetes Metab Disord. 2014 Nov 23;13(1):102. doi: 10.1186/s40200-014-0102-5. eCollection 2014.
4
Ledipasvir and sofosbuvir for untreated HCV genotype 1 infection.来迪派韦索磷布韦片与索磷布韦联用治疗初治的 HCV 基因 1 型感染。
N Engl J Med. 2014 May 15;370(20):1889-98. doi: 10.1056/NEJMoa1402454. Epub 2014 Apr 11.
5
Non-alcoholic fatty liver disease and its associated risk factors in Brazilian postmenopausal women.巴西绝经后女性的非酒精性脂肪性肝病及其相关风险因素。
Climacteric. 2014 Aug;17(4):465-71. doi: 10.3109/13697137.2014.881353. Epub 2014 Feb 11.
6
Sex differences in the metabolic syndrome: implications for cardiovascular health in women.性别差异与代谢综合征:对女性心血管健康的影响。
Clin Chem. 2014 Jan;60(1):44-52. doi: 10.1373/clinchem.2013.202549. Epub 2013 Nov 19.
7
Incidence of metabolic syndrome over 9 years follow-up; the importance of sex differences in the role of insulin resistance and other risk factors.9 年随访代谢综合征的发病率;胰岛素抵抗和其他危险因素作用中性别差异的重要性。
PLoS One. 2013 Sep 27;8(9):e76304. doi: 10.1371/journal.pone.0076304. eCollection 2013.
8
Estrogen: a master regulator of bioenergetic systems in the brain and body.雌激素:大脑和身体生物能量系统的主要调节因子。
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9
Metabolic syndrome and menopause.代谢综合征与更年期
J Diabetes Metab Disord. 2013 Jan 3;12(1):1. doi: 10.1186/2251-6581-12-1.
10
Insulin sensitivity and variability in hepatitis C virus infection using direct measurement.使用直接测量法评估丙型肝炎病毒感染患者的胰岛素敏感性和变异性。
Dig Dis Sci. 2013 Apr;58(4):1141-8. doi: 10.1007/s10620-012-2438-3. Epub 2012 Oct 21.

性别和绝经状态对慢性丙型肝炎感染患者代谢参数的影响。

Impact of gender and menopausal status on metabolic parameters in chronic hepatitis C infection.

作者信息

Gonzales C A, Bacchetti P, Khalili M

机构信息

Department of Medicine, University of California San Francisco, San Francisco, CA, USA.

Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA, USA.

出版信息

J Viral Hepat. 2016 Mar;23(3):232-9. doi: 10.1111/jvh.12487. Epub 2015 Nov 10.

DOI:10.1111/jvh.12487
PMID:26554398
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4809676/
Abstract

Hepatitis C infection (HCV) and menopause are associated with insulin resistance (IR), and IR accelerates HCV-induced liver disease. The relationship between menopause and IR has not been studied in this population. This study aimed to assess the impact of menopause on IR and metabolic syndrome in HCV. One hundred and three (69 men, 16 premenopausal, 18 postmenopausal women) noncirrhotic, nondiabetic HCV-infected adults underwent IR measurement via steady-state plasma glucose during a 240-min insulin suppression test. Metabolic syndrome was defined by at least three of five standard laboratory/clinical criteria. The patient characteristics were as follows: mean age 48 years, waist circumference 94.4 ± 12.4 cm and 37.9% Caucasian. SSPG was higher in postmenopausal than premenopausal women or men (mean difference 18, 95% CI -41 to 76 and 35, 95% CI -3 to 72 mg/dL; respectively). After adjusting for waist circumference, female gender, nonwhite race and triglycerides were positively associated and high-density lipoprotein negatively associated with steady-state plasma glucose. Compared to men, both pre- (Coef 48, 95% CI 12-84) and postmenopausal women (Coef 49, 95% CI 17-82) had higher steady-state plasma glucose. Compared to premenopausal women, men (OR 2.0, 95% CI 0.38-10.2) and postmenopausal women (OR 2.9, 95% CI 0.46-18.8) had higher odds of metabolic syndrome, but this was statistically nonsignificant. Both liver inflammation (OR 7.9) and nonwhite race (OR 6.9) were associated with metabolic syndrome. We conclude that women are at inc-reased risk for IR in HCV. There may also be an increased risk of metabolic syndrome postmenopause. Along with lifestyle modification and weight loss, women with metabolic abnormalities represent an especially at-risk group warranting HCV treatment to prevent adverse metabolic outcomes.

摘要

丙型肝炎病毒感染(HCV)与绝经均与胰岛素抵抗(IR)相关,且IR会加速HCV诱发的肝脏疾病。在这一人群中,绝经与IR之间的关系尚未得到研究。本研究旨在评估绝经对HCV患者IR及代谢综合征的影响。103名(69名男性、16名绝经前女性、18名绝经后女性)非肝硬化、非糖尿病的HCV感染成年人在240分钟胰岛素抑制试验期间通过稳态血糖测量IR。代谢综合征由五项标准实验室/临床标准中的至少三项来定义。患者特征如下:平均年龄48岁,腰围94.4±12.4厘米,37.9%为白种人。绝经后女性的稳态血糖高于绝经前女性或男性(平均差异分别为18,95%CI -41至76;35,95%CI -3至72毫克/分升)。在校正腰围后,女性性别、非白种人种族与甘油三酯与稳态血糖呈正相关,高密度脂蛋白与稳态血糖呈负相关。与男性相比,绝经前(系数48,95%CI 12 - 84)和绝经后女性(系数49,95%CI 17 - 82)的稳态血糖更高。与绝经前女性相比,男性(OR 2.0,95%CI 0.38 - 10.2)和绝经后女性(OR 2.9,95%CI 0.46 - 18.8)患代谢综合征的几率更高,但这在统计学上无显著意义。肝脏炎症(OR 7.9)和非白种人种族(OR 6.9)均与代谢综合征相关。我们得出结论,HCV女性患者发生IR的风险增加。绝经后发生代谢综合征的风险可能也会增加。除生活方式改变和减重外,有代谢异常的女性是特别高危的群体,需要进行HCV治疗以预防不良代谢结局。