Katelyn J Rittenhouse, Margaret P Kasaro, M Bridget Spelke, Yuri V Sebastião, Humphrey Mwape, Kenneth Chanda, Nelly Mandona, Ntazana Sindano, Stephen R Cole, Elizabeth M Stringer, Bellington Vwalika, Jeffrey S A Stringer
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The exposure of interest was maternal HIV infection, and the primary outcome was preeclampsia, defined as 1) new-onset (at or after 20 weeks of gestation) hypertension (systolic blood pressure [BP] 140 mm Hg or higher or diastolic BP 90 mm Hg or higher) with concurrent proteinuria (1+ or higher), 2) new onset proteinuria (1+ or higher) in participants with chronic hypertension in the absence of urinary tract infection, or 3) diagnosis of severe preeclampsia. We defined severe preeclampsia as 1) new-onset severe-range BP (systolic 160 mm Hg or higher or diastolic 110 mm Hg or higher), 2) eclamptic seizure, or 3) clinician-initiated preterm delivery (before 37 weeks of gestation) for preeclampsia. Using marginal standardization (parametric g-formula), we estimated the risk of preeclampsia associated with HIV infection. Antiretroviral therapy (ART) exposure and HIV disease severity (viral load, CD4 counts) were assessed as effect modifiers.</p><p><strong>Results: </strong>Of 4,078 women included in the combined cohort, 186 (4.6%) were diagnosed with preeclampsia, including 43 (2.7%) of 1,590 women with HIV infection and 143 (5.8%) of 2,488 women without HIV infection. Of those with HIV infection, 73.2% were on prepregnancy ART, and 56.7% had an undetectable viral load at study enrollment (median 15 weeks). In analyses standardizing for maternal age, nulliparity, and calendar time of enrollment, HIV infection was associated with lower preeclampsia risk (relative risk 0.42; 95% CI, 0.26-0.59; risk difference -3.5%; 95% CI, -4.9 to -2.1). This reduced risk persisted when stratifying by prepregnancy ART exposure, detectable viral load, and CD4 count at enrollment; findings were similar when applying the more stringent definition of severe preeclampsia.</p><p><strong>Conclusion: </strong>In this well-phenotyped cohort, women with HIV infection were less likely to have preeclampsia compared with those without HIV infection.</p>","PeriodicalId":19483,"journal":{"name":"Obstetrics and gynecology","volume":" ","pages":""},"PeriodicalIF":5.7000,"publicationDate":"2025-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Maternal Human Immunodeficiency Virus and Preeclampsia Among a Combined Cohort of Zambian Women.\",\"authors\":\"Katelyn J Rittenhouse, Margaret P Kasaro, M Bridget Spelke, Yuri V Sebastião, Humphrey Mwape, Kenneth Chanda, Nelly Mandona, Ntazana Sindano, Stephen R Cole, Elizabeth M Stringer, Bellington Vwalika, Jeffrey S A Stringer\",\"doi\":\"10.1097/AOG.0000000000005970\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To evaluate the association between maternal HIV infection and preeclampsia. We hypothesized that maternal HIV infection would be associated with a lower risk of preeclampsia, potentially due to HIV-related immunomodulatory effects.</p><p><strong>Methods: </strong>We combined participants from one observational cohort and two randomized trials conducted at the same facilities in Lusaka, Zambia between 2015 and 2022. The exposure of interest was maternal HIV infection, and the primary outcome was preeclampsia, defined as 1) new-onset (at or after 20 weeks of gestation) hypertension (systolic blood pressure [BP] 140 mm Hg or higher or diastolic BP 90 mm Hg or higher) with concurrent proteinuria (1+ or higher), 2) new onset proteinuria (1+ or higher) in participants with chronic hypertension in the absence of urinary tract infection, or 3) diagnosis of severe preeclampsia. We defined severe preeclampsia as 1) new-onset severe-range BP (systolic 160 mm Hg or higher or diastolic 110 mm Hg or higher), 2) eclamptic seizure, or 3) clinician-initiated preterm delivery (before 37 weeks of gestation) for preeclampsia. Using marginal standardization (parametric g-formula), we estimated the risk of preeclampsia associated with HIV infection. Antiretroviral therapy (ART) exposure and HIV disease severity (viral load, CD4 counts) were assessed as effect modifiers.</p><p><strong>Results: </strong>Of 4,078 women included in the combined cohort, 186 (4.6%) were diagnosed with preeclampsia, including 43 (2.7%) of 1,590 women with HIV infection and 143 (5.8%) of 2,488 women without HIV infection. Of those with HIV infection, 73.2% were on prepregnancy ART, and 56.7% had an undetectable viral load at study enrollment (median 15 weeks). In analyses standardizing for maternal age, nulliparity, and calendar time of enrollment, HIV infection was associated with lower preeclampsia risk (relative risk 0.42; 95% CI, 0.26-0.59; risk difference -3.5%; 95% CI, -4.9 to -2.1). 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引用次数: 0
摘要
目的:探讨母体HIV感染与子痫前期的关系。我们假设母体HIV感染可能与较低的子痫前期风险相关,这可能是由于HIV相关的免疫调节作用。方法:我们结合了2015年至2022年在赞比亚卢萨卡同一设施进行的一个观察队列和两个随机试验的参与者。感兴趣的暴露是母体HIV感染,主要结局是子痫前期,定义为1)新发(妊娠20周或20周后)高血压(收缩压[BP] 140 mm Hg或更高或舒张压90 mm Hg或更高)并发蛋白尿(1+或更高),2)无尿路感染的慢性高血压参与者新发蛋白尿(1+或更高),或3)诊断为严重子痫前期。我们将重度先兆子痫定义为:1)新发重度血压(收缩期160毫米汞柱或更高或舒张期110毫米汞柱或更高),2)子痫性发作,或3)临床引发的早产(妊娠37周前)。使用边际标准化(参数g公式),我们估计与HIV感染相关的先兆子痫的风险。抗逆转录病毒治疗(ART)暴露和艾滋病毒疾病严重程度(病毒载量,CD4计数)被评估为效果调节剂。结果:在纳入联合队列的4078名女性中,186名(4.6%)被诊断为子痫前期,其中包括1590名感染HIV的女性中的43名(2.7%)和2488名未感染HIV的女性中的143名(5.8%)。在艾滋病毒感染者中,73.2%的人接受了孕前抗逆转录病毒治疗,56.7%的人在研究入组时(中位15周)的病毒载量无法检测到。在对产妇年龄、未生育和入组日历时间进行标准化分析时,HIV感染与较低的子痫前期风险相关(相对风险0.42;95% ci, 0.26-0.59;风险差-3.5%;95% CI, -4.9至-2.1)。当通过孕前ART暴露、可检测的病毒载量和入组时CD4计数进行分层时,这种降低的风险仍然存在;当应用更严格的重度子痫前期定义时,结果相似。结论:在这个表型良好的队列中,与未感染艾滋病毒的妇女相比,感染艾滋病毒的妇女患先兆子痫的可能性较低。
Maternal Human Immunodeficiency Virus and Preeclampsia Among a Combined Cohort of Zambian Women.
Objective: To evaluate the association between maternal HIV infection and preeclampsia. We hypothesized that maternal HIV infection would be associated with a lower risk of preeclampsia, potentially due to HIV-related immunomodulatory effects.
Methods: We combined participants from one observational cohort and two randomized trials conducted at the same facilities in Lusaka, Zambia between 2015 and 2022. The exposure of interest was maternal HIV infection, and the primary outcome was preeclampsia, defined as 1) new-onset (at or after 20 weeks of gestation) hypertension (systolic blood pressure [BP] 140 mm Hg or higher or diastolic BP 90 mm Hg or higher) with concurrent proteinuria (1+ or higher), 2) new onset proteinuria (1+ or higher) in participants with chronic hypertension in the absence of urinary tract infection, or 3) diagnosis of severe preeclampsia. We defined severe preeclampsia as 1) new-onset severe-range BP (systolic 160 mm Hg or higher or diastolic 110 mm Hg or higher), 2) eclamptic seizure, or 3) clinician-initiated preterm delivery (before 37 weeks of gestation) for preeclampsia. Using marginal standardization (parametric g-formula), we estimated the risk of preeclampsia associated with HIV infection. Antiretroviral therapy (ART) exposure and HIV disease severity (viral load, CD4 counts) were assessed as effect modifiers.
Results: Of 4,078 women included in the combined cohort, 186 (4.6%) were diagnosed with preeclampsia, including 43 (2.7%) of 1,590 women with HIV infection and 143 (5.8%) of 2,488 women without HIV infection. Of those with HIV infection, 73.2% were on prepregnancy ART, and 56.7% had an undetectable viral load at study enrollment (median 15 weeks). In analyses standardizing for maternal age, nulliparity, and calendar time of enrollment, HIV infection was associated with lower preeclampsia risk (relative risk 0.42; 95% CI, 0.26-0.59; risk difference -3.5%; 95% CI, -4.9 to -2.1). This reduced risk persisted when stratifying by prepregnancy ART exposure, detectable viral load, and CD4 count at enrollment; findings were similar when applying the more stringent definition of severe preeclampsia.
Conclusion: In this well-phenotyped cohort, women with HIV infection were less likely to have preeclampsia compared with those without HIV infection.
期刊介绍:
"Obstetrics & Gynecology," affectionately known as "The Green Journal," is the official publication of the American College of Obstetricians and Gynecologists (ACOG). Since its inception in 1953, the journal has been dedicated to advancing the clinical practice of obstetrics and gynecology, as well as related fields. The journal's mission is to promote excellence in these areas by publishing a diverse range of articles that cover translational and clinical topics.
"Obstetrics & Gynecology" provides a platform for the dissemination of evidence-based research, clinical guidelines, and expert opinions that are essential for the continuous improvement of women's health care. The journal's content is designed to inform and educate obstetricians, gynecologists, and other healthcare professionals, ensuring that they stay abreast of the latest developments and best practices in their field.