应对人乳头瘤病毒与艾滋病毒的交叉:肯尼亚艾滋病毒感染妇女的宫颈细胞学意义。

Southern African journal of HIV medicine Pub Date : 2023-10-27 eCollection Date: 2023-01-01 DOI:10.4102/sajhivmed.v24i1.1508
James M Kangethe, Stephen Gichuhi, Eddy Odari, Jillian Pintye, Kenneth Mutai, Leila Abdullahi, Alex Maiyo, Marianne W Mureithi
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引用次数: 0

摘要

背景:高危型人乳头瘤病毒(HR-HPV)是癌症的主要病因,导致全球超过311 000人死亡,主要发生在中低收入国家。肯尼亚艾滋病毒感染者(WLHIV)面临着不成比例的HR-HPV负担。目的:我们确定了肯尼亚WLHIV患者中HR-HPV感染的流行率及其与宫颈细胞学检查结果的关系。方法:我们对在肯尼亚国家转诊医院肯雅塔国家医院(KNH)HIV护理和治疗诊所就诊的WLHIV患者进行了一项横断面研究。研究护士用细胞刷收集宫颈样本,使用Gene Xpert®分析和HPV Genotypes 14 Real TM Quant V67-100FRT进行HR-HPV基因分型。双变量分析探讨了这些关联。结果:我们招募了647名WLHIV患者(平均年龄42.8岁),其中97.2%的患者接受了抗逆转录病毒疗法(ART),79%的患者病毒载量受到抑制(血浆<50拷贝/mL)。任何和疫苗可预防的HR-HPV的患病率分别为34.6%和29.4%,其中HPV 52是最常见的基因型(13.4%)。与单次HR-HPV感染的妇女相比,患有多发性HR-HPV的妇女更有可能出现细胞学异常(34.9%对9.3%,调整后比值比[aOR]=6.2,95%置信区间[CI]:2.7-14.1,P=0.001)(53.1%vs 46.7%,aOR=2.3,95%CI:1.3-4.1,P=0.005)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Confronting the human papillomavirus-HIV intersection: Cervical cytology implications for Kenyan women living with HIV.

Confronting the human papillomavirus-HIV intersection: Cervical cytology implications for Kenyan women living with HIV.

Confronting the human papillomavirus-HIV intersection: Cervical cytology implications for Kenyan women living with HIV.

Confronting the human papillomavirus-HIV intersection: Cervical cytology implications for Kenyan women living with HIV.

Background: High-risk human papillomavirus (HR-HPV) is the primary cause of cervical cancer, leading to over 311 000 global deaths, mainly in low- and middle-income countries. Kenyan women living with HIV (WLHIV) face a disproportionate burden of HR-HPV.

Objectives: We determined the prevalence of HR-HPV infections and their association with cervical cytology findings among Kenyan WLHIV.

Method: We conducted a cross-sectional study among WLHIV attending the HIV care and treatment clinic at the Kenyatta National Hospital (KNH), Kenya's national referral hospital. Study nurses collected a cervical sample with a cytobrush for HR-HPV genotyping using Gene Xpert® assays and HPV Genotypes 14 Real-TM Quant V67-100FRT. Bivariate analysis explored the associations.

Results: We enrolled 647 WLHIV (mean age of 42.8 years), with 97.2% on antiretroviral therapy (ART) and 79% with a suppressed viral load (< 50 copies/mL plasma). The prevalence of any and vaccine-preventable HR-HPV was 34.6% and 29.4%, respectively, with HPV 52 being the most common genotype (13.4%). Among WLHIV with HR-HPV infections, 21.4% had abnormal cervical cytology. Women with multiple HR-HPV infections were more likely to have abnormal cytology compared to those with single HR-HPV infections (34.9 vs 9.3%, adjusted odds ratio [aOR] = 6.2, 95% confidence interval [CI]: 2.7-14.1, P = 0.001). Women with HR-HPV infection (single or multiple) were more likely to be on the second-line ART regimen compared to those without HR-HPV infections (53.1% vs 46.7%, aOR = 2.3, 95% CI: 1.3-4.1, P = 0.005).

Conclusion: Among WLHIV at KNH, abnormal cytology was common and more frequent among women with multiple HR-HPV infections.

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