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Association Between Low-Density Lipoprotein Cholesterol-Lowering Genetic Variants and Risk of Type 2 Diabetes: A Meta-analysis.低密度脂蛋白胆固醇降低基因变异与2型糖尿病风险的关联:一项荟萃分析。
JAMA. 2016 Oct 4;316(13):1383-1391. doi: 10.1001/jama.2016.14568.
2
Diabetes mellitus and hypertension: a dual threat.糖尿病与高血压:双重威胁。
Curr Opin Cardiol. 2016 Jul;31(4):402-9. doi: 10.1097/HCO.0000000000000297.
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Sex differences in the effect of HbA1c-defined diabetes on a wide range of cardiovascular disease risk factors.糖化血红蛋白(HbA1c)定义的糖尿病对多种心血管疾病危险因素影响的性别差异。
Ann Med. 2016;48(1-2):34-41. doi: 10.3109/07853890.2015.1127406. Epub 2016 Jan 13.
4
Sex Differences in the Cardiovascular Consequences of Diabetes Mellitus: A Scientific Statement From the American Heart Association.糖尿病心血管后果的性别差异:美国心脏协会的科学声明
Circulation. 2015 Dec 22;132(25):2424-47. doi: 10.1161/CIR.0000000000000343. Epub 2015 Dec 7.
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Prevalence of type 1 and type 2 diabetes among children and adolescents from 2001 to 2009.2001 年至 2009 年期间儿童和青少年 1 型和 2 型糖尿病的患病率。
JAMA. 2014 May 7;311(17):1778-86. doi: 10.1001/jama.2014.3201.
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Multiple chronic conditions: diabetes associated with comorbidity and shared risk factors using CDC WEAT and SAS analytic tools.多种慢性病:使用疾病控制与预防中心的加权事件分析工具(WEAT)和SAS分析工具分析与合并症及共同风险因素相关的糖尿病
J Prim Care Community Health. 2014 Apr 1;5(2):112-21. doi: 10.1177/2150131913503347. Epub 2013 Sep 10.
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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.
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Dyslipidemia in type 2 diabetes: prevalence, pathophysiology, and management.2 型糖尿病患者的血脂异常:患病率、病理生理学和管理。
Drugs. 2013 Mar;73(4):327-39. doi: 10.1007/s40265-013-0023-5.
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Prevalence of metabolic syndrome and gender differences.代谢综合征的患病率及性别差异。
Bioinformation. 2012;8(13):613-6. doi: 10.6026/97320630008613. Epub 2012 Jul 6.
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Chronic kidney disease, diabetes mellitus and cardiovascular disease: risks and commonalities.慢性肾脏病、糖尿病和心血管疾病:风险与共性
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收缩压和低密度脂蛋白胆固醇对 2 型糖尿病的性别差异影响:博加卢萨心脏研究的生命历程数据。

Differential sex effects of systolic blood pressure and low-density lipoprotein cholesterol on type 2 diabetes: Life course data from the Bogalusa Heart Study.

机构信息

Department of Epidemiology, Tulane School of Public Health and Tropical Medicine, Tulane University School of Medicine, New Orleans, Louisiana, USA.

Department of Endocrinology, Tulane University School of Medicine, New Orleans, Louisiana, USA.

出版信息

J Diabetes. 2018 Jun;10(6):449-457. doi: 10.1111/1753-0407.12543. Epub 2017 Apr 6.

DOI:10.1111/1753-0407.12543
PMID:28239958
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5572556/
Abstract

BACKGROUND

There may be sex-specific cardiometabolic mechanisms early in life that affect the development of type 2 diabetes mellitus (T2DM) through mid-adulthood. However, few studies have examined whether early life course interactions between cardiometabolic risk factors and sex are associated with incident T2DM.

METHODS

This study followed 7725 children (3834 [49.6%] females, 3891 [50.4%] males) from the Bogalusa Heart Study through mid-adulthood to examine whether low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), body mass index (BMI), or systolic blood pressure (SBP) differentially affect the risk of T2DM for females versus males. Potential sex interactions were tested after adjusting for age, race, triglycerides, smoking, follow-up time, puberty stage, use of birth control, and enrollment year.

RESULTS

Mean (± SD) age at baseline was 9.4 ± 3.5 years. There were 176 cases of T2DM (cumulative incidence = 2.3%) during a median follow-up of 9.1 years. In females versus males, LDL-C and SBP were differentially associated with T2DM (P ≤ 0.001 and P = 0.017, respectively). The relationships of BMI and HDL-C with T2DM were non-differential between females and males (P = 0.79 and P = 0.27, respectively).

CONCLUSIONS

This study is the first to show evidence of sex-specific differential effects of LDL-C and SBP on the risk of T2DM from childhood to adulthood. Greater LDL-C places girls at disproportionally higher risk of T2DM as women, whereas greater SBP differentially exposes boys to a greater risk of T2DM as men. Additional studies within existing child cohorts are needed to confirm and investigate the mechanisms underlying these differential effects.

摘要

背景

生命早期可能存在性别特异性的心脏代谢机制,这些机制会影响成年中期 2 型糖尿病(T2DM)的发展。然而,很少有研究探讨心脏代谢危险因素与性别的早期生命历程相互作用是否与 T2DM 的发生有关。

方法

本研究通过中期随访,对博加卢萨心脏研究中的 7725 名儿童(女性 3834 名[49.6%],男性 3891 名[50.4%])进行了研究,以检验低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)、体重指数(BMI)或收缩压(SBP)是否会对女性和男性的 T2DM 风险产生不同影响。在调整年龄、种族、甘油三酯、吸烟、随访时间、青春期阶段、避孕药使用和入组年份后,对潜在的性别交互作用进行了检验。

结果

基线时的平均(±SD)年龄为 9.4±3.5 岁。中位随访 9.1 年后,共发生 176 例 T2DM(累积发病率为 2.3%)。与男性相比,女性的 LDL-C 和 SBP 与 T2DM 呈不同相关(P≤0.001 和 P=0.017)。BMI 和 HDL-C 与 T2DM 的关系在女性和男性之间无差异(P=0.79 和 P=0.27)。

结论

本研究首次证明 LDL-C 和 SBP 对女性和男性 T2DM 风险的影响存在性别特异性差异。较高的 LDL-C 使女孩在成年女性中罹患 T2DM 的风险不成比例地升高,而较高的 SBP 则使男孩在成年男性中罹患 T2DM 的风险升高。需要在现有儿童队列中进行更多研究以证实和探讨这些差异作用的机制。