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ISSN 2155-6113
Journal of AIDS & Clinical Research

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Clinical and Epidemiological Differences between Women and Men with HIV Infection in Mexico

Mata-Marín José Antonio1, Chaparro-Sánchez Alberto1*, Hernández-López Juan Carlos2, Huerta-García Gloria3, Domínguez-Hermosillo Juan Carlos1 and Cruz-Domínguez Pilar2

1Infectious Diseases Department, Hospital de Infectología, “La Raza” National Medical Center, IMSS, Mexico

2Internal Medicine Department, Hospital de Especialidades, “La Raza” National Medical Center, IMSS, Mexico

3Pediatric Infectious Diseases Department, Hospital de Pediatría, “Siglo XXI” National Medical Center, IMSS, Mexico

*Corresponding Author:
Dr. Alberto Chaparro Sánchez
Instituto Mexicano del Seguro Social, Hospital de Infectología
Centro Médico Nacional “La Raza”
Serisy Jacarandas s/n colonia la Raza
Del. Azcapotzalco, México, DF, CP. 02990
Tel: 57825900; ext 23924
E-mail: [email protected]

Received date: December 03, 2015; Accepted date: February 24, 2016; Published date: March 04, 2016

Citation: Antonio MMJ, Alberto CS, Carlos HLJ, Gloria HG, Carlos DHJ, et al. (2016) Clinical and Epidemiological Differences between Women and Men with HIV Infection in Mexico. J AIDS Clin Res 7:551. doi:10.4172/2155-6113.1000551

Copyright: © 2016 Antonio MMJ, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Objective: To evaluate the differences in gender for epidemiological, immunological, and virological outcomes at baseline, and response after 24 weeks of antiretroviral therapy in patients treated at the Hospital de Infectología “La Raza” National Medical Center.

Methods: We reviewed the medical records from March to August 2014 of outpatients who started treatment in our clinic; 65 women and 138 men in a cross-sectional study. Descriptive results are summarized using the median and 25th-75th interquartile range (IQR). Baseline differences were tested using Fisher’s exact test and the Chi-squared test. Analyses of continuous variables were performed using the Mann-Whitney U test.

Results: Similar proportions of women and men were found in the following factors: living in metropolitan area, age <40 years, economic household income source, baseline CD4+ ≤ 200 cells/μL, CD4+ ≥200 cells/μL at week 24, HIV-1 RNA ≤50 copies/mL at week 24, and opportunistic infections. Women are more usually married than men (75% vs. 10%, p<0.001); men with a higher academic degree (34% vs. 9%, p<0.001); men with an onset of sexual activity <20 years (85% vs. 79%, p=0.26); women with ≤4 sexual partners (92.3% vs. 26.3%, p<0.001); women with children (92% vs. 20%, p<0.001); men with some addiction (29% vs. 10%, p=0.04); women with baseline HIV-1 RNA viral load >100,000 copies/mL (37% vs. 54%, p=0.020); and women with virological treatment failure (10.8% vs. 2.2%, p=0.008).

Conclusion: Compared with men, mostly women showed adverse epidemiological and clinical conditions that made women more vulnerable to transmission through heterosexual activity, and more frequently present virological failure.


HIV; CD4 cell count; Viral load; Gender differences; Women; Outcome, Women with HIV


In 2014, the Joint United Nations Programme on HIV/AIDS (UNAIDS) estimated a global prevalence of 35.3 million people with human immunodeficiency virus (HIV) infection. The prevalence of women with HIV is increasing: data from the USA estimate an increase from 7% in 1985 to 27% in 2007 [1]. The latest estimates indicate that 147,137 people are living with HIV in Mexico [2]. In Mexico, the prevalence in women is estimated to be18%, with a female:male prevalence ratio of approximately 1:4. The predominant mode of male transmission is via men who have sex with men, but for women the heterosexual transmission rate is around 90% [3]. Recent studies estimate an increase in the prevalence of women with HIV infection in rural areas in Mexico [4,5].

Access to diagnosis, tests, and treatment has been unequal between genders, and factors associated with this are the lack of transport [6], childcare, lack of time [7], and economic factors [8], all making women more vulnerable to HIV infection, care approach, loss of followup and virologic failure. Studies in other countries have shown that men initiate treatment at later stages of the disease compared with women [9-11]. The impact of an early initiation of antiretroviral therapy (ART) in reducing mortality has been documented [12-14]. In the UK, it was found that women with HIV infection now have an increase in life expectancy compared with men [15]. A similar situation was found in Latin America, in a retrospective study in Buenos Aires, where men who initiated ART were in more advanced stages of the disease than women: 59.8% vs. 40.2% [16]. Other reports have suggested a more vulnerable situation for infection of women insome countries, such as having a lower educational level than men [17-19]. Moreover, the sexual behavior of men confers a risk factor for women, whereas the main risk factor for HIV infection in women is to be married to an HIV-positive partner [20]. The widespread use of ART worldwide has decreased the overall mortality considerably [21,22], even in populations with low resources. Adherence to treatment and an undetectable HIV RNA viral load (VL) are important predictors of mortality but there are gender differences that make these endpoints difficult to achieve in vulnerable populations [23]. Kumarasamy et al. evaluated the response to ART according to gender and found a better immune response in women than in men, who had a 20% increased risk of death at 24 and 36 months of treatment [24].

We have no scientific information on the clinical and epidemiological characteristics and differences between men and women infected with HIV and receiving ART in Mexico. The aim of this study was to evaluate the differences in epidemiological, immunological, and virological outcome at baseline and response with respect to gender after 24 weeks of ART in patients treated at the Hospital de Infectología “La Raza” National Medical Center, a tertiary-level infectious diseases care hospital in Mexico City.



We conducted a cross-sectional study at our institution from March to August 2014. A non-probabilistic sample was done with the files analized.


Eligible patients needed to be >16 years old of age with an HIV- 1 infection confirmed by enzyme-linked immunosorbent assay and western blotting, and being treated with ART in our HIV clinic. Patients were invited to participate by completing a questionnaire. All participants were outpatients who started treatment in our clinic and whose medical records were used to collect information about sociodemographic characteristics, CD4+ cell count, HIV-1 RNA VL, blood chemistry, liver function tests, and blood cell counts at the first visit. Our hospital institutional review board and ethics committee reviewed and approved this study (reference number R-2014-3502- 139).

Measurements and procedures

Data were collected from medical records regarding demographic factors for each gender: age, educational level, area of residence, household income source, number of children, heterosexual or homosexual activities, age at the onset of sexual activity, numbers of sexual partners, any illicit drug use, history of opportunistic infections, hepatitis serology, baseline CD4+ cell count, baseline CD4+ cell count of <200 cell/μL, baseline HIV-1 RNA VL, baseline HIV-1 RNA VL of >100,000 copies/mL, and CD4+ cell count and HIV-1 RNA VL at week 24 of treatment. Virological failure was defined as an HIV-1 RNA VL of >200 copies/mL in two separate consecutive samples once HIV was undetectable, or an HIV-1 RNA VL of >200 copies/mL at week 24 after the initiation of ART.

Statistical analysis

Analyses were performed using IBM SPSS software (version 20.0; IBM Corp, Armonk, NY, USA). The Kolmogorov-Smirnov test was used to determine the normality of sample distributions. Descriptive results are summarized using the median and 25th-75th interquartile range (IQR). Baseline differences regarding categorical variables were tested using Fisher’s exact test and the Chi-squared test. Analyses of continuous variables were performed using the Mann-Whitney U test.


We included 203 patients, 65 of whom were women. The median age of the women was 35 years (IQR27-42), and 13 (20%) were >50 years old. The median age of the men was 33 (IQR 27-43) years old, and 18 (13%) were >50 years old. Most patients started treatment with tenofovir/emtricitabine (TDF/FTC) plus efavirenz (EFV); abacavir/ lamivudine (ABC/3TC) plus EFV; TDF/FTC plus atazanavir/ritonavir (ATV/r); or ABC/3TC plus ATV/r.

More women than men were living in metropolitan areas (64%vs. 52%). Some differences were found in the marital status where more of women are married compared with men (75% vs. 10%; p<0.001). Men had a higher educational level than women (34% vs. 9%; p<0.001). More women had ≤4 sexual partners than men (92% vs. 26%; p<0.001). More women had children compared with men (92% vs. 19%; p<0.001) and more men had some drug addictions compared with women (29% vs. 10%; p=0.04).

A baseline CD4+ cell count of ≤200 cells/μL was found in 53% of women compared with 50% of men. The median baseline HIV- 1 RNA VL was 44,000 copies/mL (IQR 25078-233,722) in women versus126,765 copies/mL (IQR 46,372-343,215) in men, and women had fewer opportunistic infections than men (20% vs. 30%).

Other differences were found such as a lower median CD4+ cell count at week 24 of treatment in women (289 vs. 358; p=0.061). Women had a lower rate of reaching an HIV-1 RNA VL of <50 copies/mL at 24 weeks (80% vs. 90%; p=0.028), and a higher proportion of women than men had virological failure (10% vs. 2%; p=0.008) (Tables 1 and 2).

Characteristics Women(n=65) Men(n=138) p value
ge (y), median (IQR) 35 (27–42) 33 (27–43) 0.562
ge >50 years old, n (%) 13 (20) 18 (13) 0.199
Living in metropolitan area,n (%) 41 (63) 71 (52) 0.120
University study, n (%) 6 (9) 48 (34) <0.001
Married status, n (%) 49 (75) 14 (10) <0.001
Children, n (%) 60 (92) 27 (20) <0.001
Current drug user, n (%) 7 (10) 40 (29) 0.004
ge in y at the onset of sexual activity, median (IQR) 18 (16–19) 18 (16–19) 0.690
Onset of sexual activity£20 years old, n (%) 51 (79) 117 (85) 0.266
Number of sexual partners, median (IQR) 2 (1–3) 8(4–20) <0.001
Sexual partners £4, n (%) 60 (92) 36 (26) <0.001
Sexual transmission, n (%) 63 (97%) 137 (99%) 0.19
Other transmission, n (%) 2 (3%) 1 (1%) 0.19
Opportunistic infections at the beginning, n(%) 13 (20) 41 (30) 0.230

Table 1: Epidemiological characteristics.

Baseline characteristics Women (n=65) Men (n=138) p value
CD4+ cells/mL, median (IQR) 175 (130–221) 203 (148–244) 0.605
CD4+<200 cells/mL, n (%) 35 (53) 69 (50) 0.535
HIV-1 RNA VL, copies/mL, median (IQR) 44,000
HIV-1 RNA VL >100,000 copies/mL, n (%) 24 (37) 75 (54) 0.020
Variables at week 24
CD4+cells/mL, median (IQR) 289 (192–437) 358 (216–519) 0.061
HIV-1 RNA VL copies/mL, median (IQR) 40 (19–205) 78 (19–402) 0.33
HIV-1RNA VL <50 copies/mL, n (%) 52 (80) 124 (90) 0.028
Withdrawal because of adverse events, n (%) 4 (6) 3 (2) 0.147
Virological failure, n (%) 7 (10) 3 (2) 0.008
Interruption for other causes, n (%) 2 (3) 8 (6) 0.403

Table 2: Virological and immunological characteristics at baseline and after 24 weeks of ART.


Significant differences were found between women and men with HIV infection in terms of epidemiological, clinical, and virological characteristics. Compared with men, women were more usually married, had a lower educational level, fewer sexual partners, and more usually had children. In addition, women had a baseline level of CD4+ cell count similar to men but with a lower baseline HIV-1 RNA viral load level. Finally, women were more likely than men to show virological failure after 24 weeks of ART.

These characteristics of men and women with HIV infections are similar to those observed in other studies worldwide, namely women are more vulnerable and have lower socioeconomic profiles than men [1]. The psychosocial burden for women infected with HIV/AIDS is greater than their physical burden, because it will hamper their survival and can cause emotional and mental health problems and poor medication adherence [25]. A study at the John Hopkins HIV clinic reported that 54% of women with HIV/AIDS were also diagnosed with psychopathologies: 20% suffered from severe depression; 18% had adjustment disorders; and 74% had a substance abuse disorder [26]. Mental and emotional disorders, and especially depression in people with HIV/AIDS, might affect medication adherence leading to virological failure [27].

Similar to our study, in a multinational clinical trial, women had a lower HIV-1 RNA viral load than men; in contrast, the same study showed that women presented with a higher CD4+ cell count than men [25]. However, in our study, we did not find this difference.

Women in our study were more likely than men to have children; in other studies, the primary caregiver of children and the number of children have been associated with poor virological outcome [28,29].

One study carried out in Colombia, a country with sociodemographic similarities with Mexico, found that 43% of the women showed low adherence to treatment and 80% were classified as having a low social status [30]. Most of the variables in the social position survey had a significant effect on low adherence, including low socioeconomic status (odds ratio, OR=2.26; 95% confidence interval, CI=1.2-4.04) and an educational level of high school or less (OR = 2.850;95% CI=1.625- 5.000). However, unlike our study, they found that sociodemographic variables and clinical variables that did not have a significant effect on adherence included being solely responsible for the family income, having children, and living with children with or without a partner.

Our results are similar to those of some clinical trials that found a higher frequency of virological failure in women [29-31]. Univariate analysis of factors associated with nonadherence, antiretroviral discontinuation, and poor virological response were being the primary caregiver for children, being unemployed, having a low educational level, and having transportation difficulties. The major sex-based differences in responses might have been caused by higher discontinuation rates in women in those studies. However, a study in Spain showed a similar response in both sexes [32].

The limitations of the current study did not allow us to compare epidemiological and clinical characteristics in certain groups, such as infected heterosexual couples, or to compare variables and infer risk factors for vulnerability to infection. Because of the small sample size, we were not able to compare between ART regimens or between some factors such as women living in rural areas compared with those living in metropolitan areas. In addition, we could not evaluate the impact of unemployment, because we retrieved our data from clinical charts. In spite of these study limitations, we obtained relevant information about differences between women and men in our Mexican population. A prospective multicenter study should be developed to evaluate these data further and to obtain more epidemiological and clinical information on vulnerable characteristics among women with HIV infection.

In conclusion, these Mexican women showed differences in epidemiological and clinical characteristics that could have had an impact on their virological and immunological responses to ART. Improving women’s adherence to HIV/AIDS treatment in Mexico would require eliminating barriers to the national health care system and comprehensive health care services, and implementing programs that take into account women’s role as maternal caregivers. Our findings underscore the need to integrate social determinants of health associated with gender inequality and social position when analyzing treatment response.


We would like to thank all the physicians that were involved with the follow up of the patients and to all the patient’s families because of their trust and patience.


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  1. Mathew
    Posted on Oct 20 2016 at 7:55 pm
    The work, in itself, is interesting and well written but few modifications will enhance the quality of the proposed research.

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