Cox proportional hazard-model application: time to cervical cancer screening among women living with HIV in South Africa

IF 3.1 2区 医学 Q3 IMMUNOLOGY
Marcus Hollington
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Abstract

There is an increased risk of cervical cancer among women living with HIV. While studies have long examined the association between cervical cancer among women with HIV, no study has examined the time taken for women with HIV to undergo cervical cancer screening as well as the hazard thereof in South Africa. The study used cross-sectional data from the 2016 South Africa Demographic and Health Survey. To allow for longitudinal analysis and to address the issue of right-censoring, the data were reformatted to a person-data file. The selection criteria were limited to women living with HIV (WLHIV) who had also responded to the question on cervical cancer screening. Descriptive statistics were employed to show the levels of HIV among women aged 15 and older in South Africa. Additionally, Kaplan‒Meier curves were employed to investigate the time to CCS by WLHIV in South Africa. Thereafter, an unadjusted Cox hazards regression model was employed to examine the hazard of undergoing CCS among WLHIV. Finally, it employed an adjusted model to examine the hazard of CCS among WLHIV while adjusting for other factors. Nineteen percent (n = 1,159) of the women who participated in the study tested positive for HIV. Herein, it was found that the risk of CCS among WLHIV began at the age of approximately 19 years. Thereafter, the hazard of undergoing CCS among WLHIV began to decrease at 58 years. There was a significant association between CCS and WLHIV. Additionally, several covariates were found to be significantly associated with HIV. These were race, province, area of residence, marriage, educational attainment, employment, alcohol consumption, perceived health perception, and health insurance. The hazard of CCS was lower among WLHIV compared to WLHIV who did not undergo CCS in South Africa. This puts HIV-positive women at risk of increased morbidity and mortality from potential cervical cancer and HIV comorbidity due to CCS deficits within this group. This is because they are susceptible to HPV and subsequent cervical cancer due to a compromised immune system. HIV-positive women need to routinely undergo CCS every 12 months from baseline for 3 years. Thereafter, they should undergo CCS once every 3 years to reduce their risk of developing the disease.
Cox 比例危险模型的应用:南非感染艾滋病毒妇女接受宫颈癌筛查的时间
感染艾滋病毒的妇女患宫颈癌的风险增加。虽然长期以来一直有研究探讨宫颈癌与女性艾滋病病毒感染者之间的关系,但在南非,还没有研究探讨过女性艾滋病病毒感染者接受宫颈癌筛查所需的时间及其危害。该研究使用了 2016 年南非人口与健康调查的横截面数据。为了进行纵向分析并解决右删减问题,数据被重新格式化为个人数据文件。选择标准仅限于同时回答宫颈癌筛查问题的女性艾滋病病毒感染者(WLHIV)。我们采用了描述性统计来显示南非 15 岁及以上女性的艾滋病毒感染水平。此外,还采用 Kaplan-Meier 曲线来调查南非 WLHIV 接受宫颈癌筛查的时间。然后,采用未经调整的 Cox 危险回归模型来研究 WLHIV 接受 CCS 的危险性。最后,在对其他因素进行调整的基础上,采用调整模型来检验 WLHIV 接受 CCS 的风险。在参与研究的妇女中,19%(n = 1,159 人)的艾滋病毒检测呈阳性。研究发现,WLHIV 感染 CCS 的风险始于 19 岁左右。此后,WLHIV 接受 CCS 的风险在 58 岁时开始下降。CCS与WLHIV之间存在明显的关联。此外,研究还发现几个协变量与艾滋病毒有显著关联。这些因素包括种族、省份、居住地区、婚姻、教育程度、就业、饮酒、健康感知和医疗保险。在南非,与未接受 CCS 的 WLHIV 相比,接受 CCS 的风险较低。这就使艾滋病毒呈阳性的妇女面临着因潜在的宫颈癌和艾滋病毒合并症而增加发病率和死亡率的风险,原因是这一群体的 CCS 缺陷。这是因为她们的免疫系统受损,容易感染人乳头瘤病毒,继而患上宫颈癌。艾滋病毒呈阳性的女性需要从基线开始每 12 个月定期接受一次 CCS 检查,持续 3 年。此后,她们应每 3 年接受一次 CCS 检查,以降低患病风险。
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来源期刊
Infectious Agents and Cancer
Infectious Agents and Cancer ONCOLOGY-IMMUNOLOGY
CiteScore
5.80
自引率
2.70%
发文量
54
期刊介绍: Infectious Agents and Cancer is an open access, peer-reviewed online journal that encompasses all aspects of basic, clinical, epidemiological and translational research providing an insight into the association between chronic infections and cancer. The journal welcomes submissions in the pathogen-related cancer areas and other related topics, in particular: • HPV and anogenital cancers, as well as head and neck cancers; • EBV and Burkitt lymphoma; • HCV/HBV and hepatocellular carcinoma as well as lymphoproliferative diseases; • HHV8 and Kaposi sarcoma; • HTLV and leukemia; • Cancers in Low- and Middle-income countries. The link between infection and cancer has become well established over the past 50 years, and infection-associated cancer contribute up to 16% of cancers in developed countries and 33% in less developed countries. Preventive vaccines have been developed for only two cancer-causing viruses, highlighting both the opportunity to prevent infection-associated cancers by vaccination and the gaps that remain before vaccines can be developed for other cancer-causing agents. These gaps are due to incomplete understanding of the basic biology, natural history, epidemiology of many of the pathogens that cause cancer, the mechanisms they exploit to cause cancer, and how to interrupt progression to cancer in human populations. Early diagnosis or identification of lesions at high risk of progression represent the current most critical research area of the field supported by recent advances in genomics and proteomics technologies.
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