Epidemiological trends and burden of mortality from HIV/AIDS and multidrug-resistant tuberculosis without extensive drug-resistance across Africa: A global burden of disease analysis (1990–2021)

IF 2 Q3 INFECTIOUS DISEASES
Ibrahim Khalil , Noshin Anjum Tasmi , Md.Imran Hossain , Mst.Mahmuda Akter
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引用次数: 0

Abstract

Background

HIV/AIDS and multidrug-resistant tuberculosis (MDR-TB, non-extensively drug-resistant) together cause significant mortality in Africa, home to 67% of the 39 million people living with HIV globally and 2.5 million TB cases in 2022. This study analyzes Global Burden of Disease (GBD) 2021 data to quantify temporal trends and mortality burdens of HIV/AIDS and MDR-TB across African subregions from 1990 to 2021, focusing on regional and gender-specific patterns.

Methods

Age-standardized mortality rates (ASMR) per 100,000 population for HIV/AIDS and MDR-TB were extracted from GBD 2021 for the African Union (Central, Eastern, Northern, Southern, Western subregions), stratified by gender. Joinpoint regression (Joinpoint Regression Program, version 5.0.2) calculated Annual Percent Change (APC) and Average Annual Percent Change (AAPC) with 95 % CIs and p-values (p < 0.05 for significance). Weighted Bayesian Information Criterion and permutation testing identified up to six joinpoints. This method fits piecewise log-linear models, pinpointing inflection points (joinpoints) where statistically significant changes occur. Sensitivity analyses ensured robustness, adhering to GBD protocols.

Results

From 1990 to 2021, the African Union exhibited varied trends in age-standardized mortality rates (ASMR) for HIV/AIDS and multidrug-resistant tuberculosis (MDR-TB). Overall, mortality trends showed a non-significant average annual percent change (AAPC) of 1.9526 % (95 % CI: −1.7682, 6.3941; p = 0.278344), reflecting a complex epidemic trajectory. Early in the period (1990–1999), mortality surged dramatically, with annual percent changes (APCs) peaking at 99.81 % (1990–1992) due to limited treatment access. A turning point emerged around 2003, with declines becoming prominent from 2006 onward. The most substantial reductions occurred between 2006 and 2014, with an APC of (−10.3478 %; 95 % CI: −11.0939, −9.8873; p < 0.000001), driven by expanded antiretroviral therapy (ART) and improved diagnostics. Gender-specific patterns revealed steeper declines for females, particularly in Southern Africa (2007–2014, APC: −12.97 %), compared to males (2007–2013, APC: −11.36 %), highlighting the impact of targeted interventions for women. Regionally, Southern Africa bore the highest burden, with early increases (1990–1993, APC: 105.55 %) but significant declines post-2007 (APC: −11.95 %). Central Africa saw notable reductions after 2016 (APC: −15.75 %), while Northern Africa experienced a rising trend: AAPC 3.5641 % (95 % CI: 0.6866, 7.0452; p = 0.014397); driven by early spikes (1990–1992, APC: 38.89 %). Eastern and Western Africa showed modest declines, with APCs of −10.98 % (2004–2008) and −9.21 % (2006–2014), respectively.

Conclusions

The study highlights significant progress in reducing HIV/AIDS and MDR-TB mortality across Africa from 1990 to 2021, largely due to expanded access to antiretroviral therapy (ART), advanced diagnostics like GeneXpert, and global health initiatives such as PEPFAR and the Global Fund. However, persistent regional disparities, with Northern Africa showing rising mortality trends and Southern Africa bearing the highest burden, underscore the need for tailored interventions. Females experienced more pronounced mortality declines in certain periods, particularly in Southern Africa, likely due to targeted interventions like PMTCT, while males showed slightly less progress overall, potentially due to factors like occupational exposures or lower ART adherence. Limitations include reliance on modeled GBD data and lack of subnational granularity.
非洲各地艾滋病毒/艾滋病和无广泛耐药性的耐多药结核病的流行病学趋势和死亡率负担:全球疾病负担分析(1990-2021年)
艾滋病毒/艾滋病和耐多药结核病(MDR-TB,非广泛耐药结核病)共同在非洲造成重大死亡率,在全球3900万艾滋病毒感染者中,非洲占67%,到2022年结核病病例将达到250万。本研究分析了全球疾病负担(GBD) 2021数据,以量化1990年至2021年非洲分区域艾滋病毒/艾滋病和耐多药结核病的时间趋势和死亡负担,重点关注区域和性别特定模式。方法从非洲联盟(中部、东部、北部、南部和西部次区域)GBD 2021中提取按性别分层的每10万人艾滋病毒/艾滋病和耐多药结核病的标准化死亡率(ASMR)。Joinpoint回归(Joinpoint regression Program, version 5.0.2)计算年度变化百分比(APC)和平均年度变化百分比(AAPC), 95% ci和p值(p <; 0.05为显著性)。加权贝叶斯信息准则和排列测试识别出多达6个连接点。该方法拟合分段对数线性模型,精确定位统计上发生重大变化的拐点(连接点)。敏感性分析确保了鲁棒性,符合GBD协议。从1990年到2021年,非洲联盟在艾滋病毒/艾滋病和耐多药结核病(MDR-TB)的年龄标准化死亡率(ASMR)方面表现出不同的趋势。总体而言,死亡率趋势显示平均年百分比变化(AAPC)为1.9526% (95% CI: - 1.7682, 6.3941; p = 0.278344),无显著性,反映了复杂的流行轨迹。在该时期早期(1990-1999年),死亡率急剧上升,由于治疗机会有限,年百分比变化(APCs)达到99.81%的峰值(1990-1992年)。转折点出现在2003年左右,从2006年开始,衰退变得明显。在扩大抗逆转录病毒治疗(ART)和改进诊断的推动下,2006年至2014年期间,APC (- 10.3478%; 95% CI: - 11.0939, - 9.8873; p < 0.000001)下降幅度最大。与男性(2007-2013年,APC: - 11.36%)相比,女性(2007-2014年,APC: - 12.97%)的下降幅度更大,这凸显了有针对性的干预措施对女性的影响。从区域来看,南部非洲的负担最重,早期有所增加(1990-1993年,APC: 105.55%),但2007年后显著下降(APC: - 11.95%)。中非在2016年之后出现了显著的下降(APC: - 15.75%),而北非则呈现上升趋势:AAPC为3.5641% (95% CI: 0.6866, 7.0452; p = 0.014397);受早期峰值驱动(1990-1992年,APC: 38.89%)。东非和西非略有下降,apc分别为- 10.98%(2004-2008年)和- 9.21%(2006-2014年)。该研究强调了1990年至2021年期间非洲在降低艾滋病毒/艾滋病和耐多药结核病死亡率方面取得的重大进展,这主要归功于抗逆转录病毒治疗(ART)的扩大获得、GeneXpert等先进诊断方法以及PEPFAR和全球基金等全球卫生倡议。然而,持续存在的区域差异,北非显示出死亡率上升的趋势,南部非洲负担最重,突出表明需要采取有针对性的干预措施。在某些时期,特别是在南部非洲,女性的死亡率下降更为明显,这可能是由于预防母婴传播等有针对性的干预措施,而男性的总体进展略少,可能是由于职业暴露或较低的抗逆转录病毒治疗依从性等因素。限制包括依赖GBD模型数据和缺乏次国家粒度。
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来源期刊
Journal of Clinical Tuberculosis and Other Mycobacterial Diseases
Journal of Clinical Tuberculosis and Other Mycobacterial Diseases Medicine-Pulmonary and Respiratory Medicine
CiteScore
4.00
自引率
5.00%
发文量
44
审稿时长
30 weeks
期刊介绍: Journal of Clinical Tuberculosis and Mycobacterial Diseases aims to provide a forum for clinically relevant articles on all aspects of tuberculosis and other mycobacterial infections, including (but not limited to) epidemiology, clinical investigation, transmission, diagnosis, treatment, drug-resistance and public policy, and encourages the submission of clinical studies, thematic reviews and case reports. Journal of Clinical Tuberculosis and Mycobacterial Diseases is an Open Access publication.
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