Effect of Highly Active Antiretroviral Therapy (HAART) and Menopause on Risk of Progression of Cervical Dysplasia in Human Immune-Deficiency Virus- (HIV-) Infected Women

Kim, Suk Chul; Messing, Susan; Shah, Krupa; Luque, Amneris E.

doi:10.1155/2013/784718

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Effect of Highly Active Antiretroviral Therapy (HAART) and Menopause on Risk of Progression of Cervical Dysplasia in Human Immune-Deficiency Virus- (HIV-) Infected Women

Published Date:

Dec 18 2013

Publisher's site:

http://dx.doi.org/10.1155/2013/784718 New Site Icon

Source:

Infect Dis Obstet Gynecol. 2013; 2013.

[PDF-601.91 KB]

Details:

Personal Authors:

Kim, Suk Chul ; Messing, Susan ; Shah, Krupa ; Luque, Amneris E. ;

Keywords:

[+]

Pubmed ID:

24453469

Pubmed Central ID:

PMC3878554

Description:

More HIV-infected women are reaching older age and menopause, but there is limited information on cervical squamous intraepithelial lesions (SILs) on these women.|To assess the effect of HAART and menopause on SILs in HIV-infected women, we reviewed the results of Papanicolaou (Pap) tests obtained between 1991 and 2011 on 245 women. Progression to SILs was determined by comparing Pap test results. The association of HAART and transition to menopause on SILs was assessed using survival analysis.|Women receiving HAART had a 52% reduced risk in the progression to SILs compared to women receiving any other antiretroviral regimen or no regimen (CI: 0.33-0.70, P = 0.0001). A greater increase of CD4(+) cell counts was associated with a greater reduction on the risk of progression to SILs. Menopausal women had a 70% higher risk of progression to SILs than premenopausal women (CI: 1.11-2.62, P < 0.0001), adjusting for HIV medications, CD4(+) count, duration of HIV infection, moderation effect of menopause by age, prior IV drug use, and smoking.|HAART had a positive long-term effect on the progression to SILs. However, being younger and menopausal increases the risk of progression.

Document Type:

Journal Article

Collection(s):

CDC Public Access

Funding:

P30 AI078498/AI/NIAID NIH HHS/United States
UL1 PR024160/PR/OCPHP CDC HHS/United States

Supporting Files:

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