Global burden, trends and inequalities for ischaemic heart disease attributable to high fasting plasma glucose, high low-density lipoprotein cholesterol and high systolic blood pressure, 1990–2021: An analysis of the Global Burden of Disease Study 2021

IF 5.7 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Diabetes, Obesity & Metabolism Pub Date : 2025-02-17 DOI:10.1111/dom.16199
Jun-Qiao An MM, Yu-Zhi Jia MD, Xiao-Han Shi MM, Xue He MM, Jin-Xi Zhang MD, Yue-Han Ren MD, Qing-Yong He MD
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Abstract

Aims

The three key and direct risk factors for the significant health issue prevalent worldwide, ischaemic heart disease(IHD), are high fasting plasma glucose (HFPG), high low-density lipoprotein (HLDL) and high systolic blood pressure (HSBP) in metabolic syndrome (MetS). A comprehensive study is essential to present the most recent global epidemiological trends.

Methods

IHD data attributable to HFPG, HLDL and HSBP (3H) were obtained from the Global Burden of Disease Study (GBD) 2021. The absolute burden was manifested in the number of death cases and disability-adjusted life years (DALY). The relative burden was quantified through the age-standardized mortality rate (ASMR) and the age-standardized DALY rate (ASDR). Estimated annual percentage change (EAPC) was used to measure trends.

Results

HSBP caused the greatest IHD burden, followed by HLDL, which was much higher than HFPG. The IHD burden associated with HLDL and HSBP were more alike and notably different from HFPG. From 1990 to 2021, ASDR for HSBP and HLDL-related IHD generally declined, with the EAPC of −1.28 (95% CI: −1.34, −1.23) and −1.38 (95% CI: −1.44, −1.33). But the trend was less pronounced for HFPG-related IHD, with the EAPC of −0.90 (95% CI: −2.25, 0.46). The absolute burden was higher in men under 80 and peaked 5–10 years earlier than women. Compared to HSBP and HLDL, HFPG caused a significant increase in burden in low-middle and low socio-demographic index (SDI) regions. The high-middle SDI region, which originally had the highest burden, showed a clear downward trend after 2005 and was gradually overtaken by the low-middle region. Eastern Europe, Central Asia, North Africa and the Middle East had the highest burden among the regions with the same SDI level in Europe, Asia and Africa.

Conclusion

The HFPG-related IHD burden should be managed differently from HSBP and HLDL. Particular attention should be paid to men, older age groups and regions with low-middle SDI.

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1990-2021年,由高空腹血糖、高低密度脂蛋白胆固醇和高收缩压引起的缺血性心脏病的全球负担、趋势和不平等:对2021年全球疾病负担研究的分析
目的:全球范围内普遍存在的重大健康问题缺血性心脏病(IHD)的三个关键和直接危险因素是代谢综合征(MetS)中的高空腹血糖(HFPG)、高低密度脂蛋白(HLDL)和高收缩压(HSBP)。一项全面的研究对于介绍最新的全球流行病学趋势至关重要。方法:由HFPG、HLDL和HSBP (3H)引起的IHD数据来自全球疾病负担研究(GBD) 2021。绝对负担表现在死亡病例数和残疾调整生命年(DALY)上。通过年龄标准化死亡率(ASMR)和年龄标准化DALY率(ASDR)量化相对负担。估计年度百分比变化(EAPC)用于衡量趋势。结果:HSBP引起的IHD负担最大,其次是HLDL,远高于HFPG。与HLDL和HSBP相关的IHD负担更相似,与HFPG有显著差异。从1990年到2021年,HSBP和hdl相关IHD的ASDR普遍下降,EAPC分别为-1.28 (95% CI: -1.34, -1.23)和-1.38 (95% CI: -1.44, -1.33)。但hfp相关IHD的趋势不太明显,EAPC为-0.90 (95% CI: -2.25, 0.46)。80岁以下男性的绝对负担更高,比女性早5-10年达到峰值。与HSBP和HLDL相比,HFPG在中低和低社会人口指数(SDI)地区造成的负担显著增加。2005年以后,原本负担最高的中高SDI区域呈现明显的下降趋势,并逐渐被中低SDI区域所取代。在欧洲、亚洲和非洲相同SDI水平的区域中,东欧、中亚、北非和中东的负担最重。结论:hfp相关IHD负担的管理应与HSBP和HLDL不同。应特别注意男性、老年群体和中低SDI地区。
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来源期刊
Diabetes, Obesity & Metabolism
Diabetes, Obesity & Metabolism 医学-内分泌学与代谢
CiteScore
10.90
自引率
6.90%
发文量
319
审稿时长
3-8 weeks
期刊介绍: Diabetes, Obesity and Metabolism is primarily a journal of clinical and experimental pharmacology and therapeutics covering the interrelated areas of diabetes, obesity and metabolism. The journal prioritises high-quality original research that reports on the effects of new or existing therapies, including dietary, exercise and lifestyle (non-pharmacological) interventions, in any aspect of metabolic and endocrine disease, either in humans or animal and cellular systems. ‘Metabolism’ may relate to lipids, bone and drug metabolism, or broader aspects of endocrine dysfunction. Preclinical pharmacology, pharmacokinetic studies, meta-analyses and those addressing drug safety and tolerability are also highly suitable for publication in this journal. Original research may be published as a main paper or as a research letter.
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