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对刚果民主共和国儿童的乙型肝炎病毒感染情况进行特征分析,以为消除工作提供信息。

Characterizing hepatitis B virus infection in children in the Democratic Republic of Congo to inform elimination efforts.

作者信息

Morgan C E, Powers K A, Edwards J K, Devkota U, Biju S, Lin F C, Schmitz J L, Cloherty G, Muwonga J, Mboyo A, Tshiamala P, Kashamuka M M, Tshefu A, Emch M, Yotebieng M, Becker-Dreps S, Parr J B, Thompson P

机构信息

Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC, USA.

University of North Carolina, Chapel Hill, NC, USA.

出版信息

medRxiv. 2024 Jun 13:2024.06.12.24308840. doi: 10.1101/2024.06.12.24308840.

DOI:10.1101/2024.06.12.24308840
PMID:38947057
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11213086/
Abstract

OBJECTIVE

Despite global reductions in hepatitis B virus (HBV) prevalence, an estimated 6.2 million children are infected, two-thirds of whom live in the WHO Africa region. We sought to characterize childhood HBV to inform elimination efforts in the Democratic Republic of Congo (DRC), one of the largest and most populous African countries.

METHODS

Using the most recent (2013-14) nationally representative Demographic and Health Survey in the DRC, we analyzed HBV surface antigen (HBsAg) on dried blood spots and associated survey data from children aged 6-59 months. We estimated HBsAg-positivity prevalence nationally, regionally, and by potential correlates of infection. We evaluated spatial variation in HBsAg-positivity prevalence, overall and by age, sex, and vaccination status.

FINDINGS

Using data from 5,679 children, we found national HBsAg-positivity prevalence was 1.3% (95% CI: 0.9%-1.7%), but ranged from 0.0% in DRC's capital city province, Kinshasa, to 5.6% in northwestern Sud-Ubangi Province. Prevalence among boys (1.8%, 95% CI: 1.2%-2.7%) was double that among girls (0.7%, 95%CI: 0.4%-1.3%). Tetanus antibody-negativity, rurality, and lower household wealth were also significantly associated with higher HBsAg-positivity prevalence. We observed no difference in prevalence by age. Children had higher HBsAg-positivity odds if living with ≥1 HBsAg-positive adult household member (OR: 2.3, 95%CI: 0.7-7.8), particularly an HBsAg-positive mother (OR: 7.2, 95%CI:1.6-32.2).

CONCLUSION

In the largest national survey of HBV among children and household contacts in the DRC, we found that childhood HBV prevalence was 10-60 times the global target of 0.1%. We highlight specific regions and populations for further investigation and focused prevention efforts.

摘要

目的

尽管全球乙肝病毒(HBV)感染率有所下降,但估计仍有620万儿童受到感染,其中三分之二生活在世界卫生组织非洲区域。我们试图对儿童HBV感染情况进行特征描述,以为非洲最大且人口最多的国家之一刚果民主共和国(DRC)的消除工作提供信息。

方法

利用刚果民主共和国最近(2013 - 14年)具有全国代表性的人口与健康调查,我们分析了6至59个月儿童干血斑上的HBV表面抗原(HBsAg)以及相关调查数据。我们估计了全国、区域以及按感染潜在相关因素划分的HBsAg阳性率。我们评估了HBsAg阳性率在总体上以及按年龄、性别和疫苗接种状况的空间变异。

研究结果

利用5679名儿童的数据,我们发现全国HBsAg阳性率为1.3%(95%置信区间:0.9% - 1.7%),但在刚果民主共和国首都金沙萨省为0.0%,在西北乌班吉省为5.6%。男孩的感染率(1.8%,95%置信区间:1.2% - 2.7%)是女孩(0.7%,95%置信区间:0.4% - 1.3%)的两倍。破伤风抗体阴性、农村地区以及家庭财富较低也与较高的HBsAg阳性率显著相关。我们未观察到感染率随年龄的差异。如果儿童与≥1名HBsAg阳性成年家庭成员同住,其HBsAg阳性几率更高(比值比:2.3,95%置信区间:0.7 - 7.8),尤其是与HBsAg阳性母亲同住(比值比:7.2,95%置信区间:1.6 - 32.2)。

结论

在刚果民主共和国针对儿童及家庭接触者进行的最大规模全国性HBV调查中,我们发现儿童HBV感染率是全球0.1%目标的10至60倍。我们强调了需进一步调查的特定区域和人群,并集中开展预防工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18fe/11213086/d40eec3deb27/nihpp-2024.06.12.24308840v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18fe/11213086/61c6e433b62d/nihpp-2024.06.12.24308840v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18fe/11213086/f45efbe46fca/nihpp-2024.06.12.24308840v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18fe/11213086/5d7095184005/nihpp-2024.06.12.24308840v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18fe/11213086/d40eec3deb27/nihpp-2024.06.12.24308840v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18fe/11213086/61c6e433b62d/nihpp-2024.06.12.24308840v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18fe/11213086/f45efbe46fca/nihpp-2024.06.12.24308840v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18fe/11213086/5d7095184005/nihpp-2024.06.12.24308840v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18fe/11213086/d40eec3deb27/nihpp-2024.06.12.24308840v1-f0004.jpg

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