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Am. J. Trop. Med. Hyg., 69(4), 2003, pp. 447-449
Copyright © 2003 by The American Society of Tropical Medicine and Hygiene

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MOTHER-TO-CHILD TRANSMISSION OF HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 IN RELATION TO THE SEASON IN YAOUNDE, CAMEROON

AHIDJO AYOUBA, ERIC NERRIENET, ELISABETH MENU, MARCEL MONNY LOBÉ, JOCELYN THONNON, ROBERT J. I. LEKE, FRANÇOISE BARRÉ-SINOUSSI, PAUL MARTIN, AND PATRICK CUNIN FOR THE YAOUNDE MTCT GROUP*
Centre Pasteur du Cameroun, Yaounde, Cameroon; Centre Mère-Enfant, Fondation Chantal Biya, Yaounde, Cameroon; Unité de Biologie des Rétrovirus, Institut Pasteur, Paris, France; Unité 131, Institut de la Santé et de la Recherche Médicale, Clamart, France; Hôpital Central de Yaounde, Yaounde, Cameroon


ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 METHODS
 RESULTS
 REFERENCES
 
A public health program to prevent mother-to-child transmission (MTCT) of human immunodeficiency virus type 1 (HIV-1) by treatment with nevirapine has been ongoing in Yaounde, Cameroon since January 2000. After 24 months, plasma samples from 119 children born to HIV-1-positive mothers were tested for HIV-1 RNA between six and eight weeks after birth. Thirteen (10.9%) tested positive (95% confidence interval = 5.2–16.7%). Risk factors associated with MTCT in this study were maternal viral load (P < 0.05), low birth weight ({chi}2 for trend =8.78, P =0.01), and birth during the second half of the year. A high correlation was repeatedly observed between rainfall in a given month and the risk of MTCT of HIV-1 in children born three months later (r = 0.634, P < 0.001). Although we cannot rule out other tropical infections related to the rainy season, the role of malaria is highly suspected since the interval of three months we observed between the peaks of rainfall and the rate of transmission is consistent with the Plasmodium life cycle.


INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
METHODS
 RESULTS
 REFERENCES
 
In 1997 in Yaounde, Cameroon, the seroprevalence of human immunodeficiency virus (HIV) in a cohort of pregnant women was 4.2%. In 2001, The National AIDS Committee in Cameroon reported an HIV seroprevalence of 11% in pregnant women. Despite the existence of efficient prophylactic interventions to reduce mother-to-child transmission (MTCT) of HIV-1, no intervention was implemented in Cameroon until the year 2000. The main reasons were the costs and complexities of these interventions. However, the HIV-NET 012 clinical trial in Kampala, Uganda that provided single-dose nevirapine to mothers and their children has given new hope to developing countries in their fight against the spread of HIV-1.1

Since January 2000, we have implemented a Public Health Pilot Program using nevirapine for the reduction of MTCT of HIV-1 in Yaounde. We performed early diagnosis of HIV-1 infection in infants at 6–8 weeks of age to evaluate the efficacy of this intervention. In this report, we provide information on risk factors associated with MTCT of HIV-1 in our setting, in which the season of birth appeared as the most significant risk factor.


METHODS
TOP
 ABSTRACT
 INTRODUCTION
 METHODS
RESULTS
 REFERENCES
 
Voluntary counseling and testing for HIV were offered to pregnant women during their first visit at an antenatal clinic. Before entering the study, women provided informed consent at the counseling stage. The program was conducted under the auspices of the Cameroon Health Authorities and was reviewed and approved by the Cameroon National Ethical Committee. Women diagnosed as HIV-1 positive were given one dose (200 mg) of nevirapine at the beginning of labor and children were given one dose (2 mg/kg) within the first 72 hours after birth. Formula feeding was recommended, but not provided, in agreement with national health policy. Early diagnosis for HIV-1 infection in children was performed by the detection of viral RNA in plasma samples using a quantification assay (b-DNA technique; Bayer Diagnostics, Paris, France) between six and eight weeks after birth.

Proportions were compared with the Pearson chi-square test, and the dose effect was analyzed by the chi-square test for trend. Means were compared by the analysis of variance or the Kruskal-Wallis test if the variances differed. For logistic regression, the descendant stepwise method was used. All variables were initially introduced with a P value < 0.25. Data collection and analysis were performed using Epi Info software, version 6.04d (Centers for Disease Control and Prevention, Atlanta, GA) with its logistic regression module.


RESULTS
TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
REFERENCES
 
After 24 months, 119 children were tested at the age of 6–8 weeks. Seventeen (14.3%) were breastfed. Among the 119 children tested, 13 (10.9%) were HIV-1 positive (95% confidence interval [CI] = 5.2–16.7%).

Multivariate analysis showed that the risk factors significantly associated with MTCT of HIV-1 in this study were maternal viral load, low birth weight, and birth during the second half of the year. Female sex, which was associated with infection in univariate analysis, was a confounding factor of birth weight in logistic regression. The parity and CD4 cell counts of the pregnant women before delivery were not statistically significant risk factors. Maternal viral load during pregnancy was determined for 52 of the 118 mothers who delivered (one mother delivered twins). Six of the 52 children were infected and 46 were uninfected. There was no MTCT of HIV-1 when the maternal viral load was less than 5,000 copies/mL (Table 1Go). The average maternal viral loads values for transmitting and non-transmitting mothers were 185,125 copies/mL (range = 7,157 to > 500,000) and 40,435 copies/mL (range = < 50 to 300,702), respectively (Table 1Go). The difference in viral loads between the transmitting and non-transmitting mothers was statistically significant (P < 0.05).


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TABLE 1
Risk factors for mother-to-child transmission of human immunodeficiency virus type 1 among 119 pregnant women in Yaounde, Cameroon, 2000–2002*
 
The rate of infected children increased when the birth weight decreased: 0% (0 of 29) for children weighing more than 3.5 kg, 9.6% (5 of 52) for those weighing between 3 kg and 3.5 kg, and 23.5% (8 of 34) for those weighing less than 3 kg ({chi}2 for trend = 8.78, P = 0.01).

Moreover, children born between January and June were less at risk of being infected than those born between July and December: 0% (0 of 51) versus 19.1% (13 of 68); P < 0.001. Pluviometry (rainfall) data were obtained from the provincial delegation for meteorology for the Central Province (Yaounde) of Cameroon. The rate of infected children dramatically increased with the monthly rainfall recorded three months before birth (Table 1Go). A strong correlation was observed between rainfall in a given month and the rate ofinfected children born three months later (r = 0.634, P < 0.001) (Figure 1Go). In 2000, the three peaks of rainfall were followed by three peaks of MTCT of HIV-1, and in 2001 the two peaks of rainfall were followed by two peaks of transmission, with the same interval of three months.



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  		    FIGURE 1. Pluviometry (rainfall) data and rate of mother-to-child transmission (MTCT) of human immunodeficiency virus type 1 (HIV-1) in the Yaounde, Cameroon Public Health Program setting over a 24-month period.

 
Logistic regression (viral load excluded) showed that two variables remained statistically significant: low birth weight (odds ratio [OR] = 5.2, 95% CI = 1.7–16.0) and birth during the second half of the year (OR = 112.2, 95% CI = 4.1–3,103.6).

These data suggest that a pathology related to the rainy season might enhance the risk of MTCT of HIV-1. The interval of three months observed between the peaks of rainfall and the rate of transmission is consistent with the Plasmodium life cycle. Furthermore, one of the consequences of malaria infection in pregnant women is the low birth weight of newborns.2 Moreover, an interaction between placental malaria and HIV infection has been reported.3 A change in the cytokine profile in malaria-infected placentae, especially an increase in tumor necrosis factor-{alpha}, could favor HIV-1 replication.4 These arguments suggest that malaria is the likely pathology related to the rainy season that results in an increase of risk of in utero MTCT of HIV-1. Thus, the efficacy of nevirapine in preventing transmission at delivery would be partially obscured in the second half of the year. We are currently conducting prospective studies on malaria parasites within the placenta. However, we cannot rule out the possibility of another tropical infection related to the rainy season that may also enhance the risk of MTCT of HIV-1. The occurrence of other infections during pregnancy is also being investigated.

In Cameroon, every pregnant woman is given anti-malarial prophylaxis at her first visit to an antenatal clinic. Retrospective studies are ongoing to investigate compliance with chemoprophylaxis. Unfortunately, in Yaounde, strains of P. falcifarum are highly resistant to several antimalarial drugs that are compatible with pregnancy.5

For obvious reasons of public health, a similar analysis should be performed in areas where malaria is highly endemic to confirm the correlation between the rainy season and the increase risk of MTCT of HIV-1, as well as the potential role of malaria as a risk factor. This observation has already been reported in The Gambia in a cohort of HIV-1-positive pregnant women who had no preventive antiretroviral therapy against MTCT of HIV-1.6

In conclusion, appropriate measures should be taken as soon as possible if our data are confirmed in other areas. We are currently investigating other pathologies affecting pregnant women in our program that could also be related to the rainy season.

Received November 4, 2002. Accepted for publication July 1, 2003.

Acknowledgments: We thank Drs. Odile Mercereau-Puijalon, Charlotte Behr, and Gérard Chaouat for helpful discussions.

Financial support: The Public Health Pilot Program was supported by the GlaxoSmithKline Foundation.

* The Yaounde MTCT Group: (National AIDS Committee) S. Koulla-Shiro, A. Njom-Nlend (Foundation Chantal Biya), M. Monny Lobé, G. Tene (Centre Pasteur du Cameroun) A. Kfutwah, Y. Foupouapounognigni, B. Njinku (Hôpital Central de Yaounde), C. Kouanfack, R. Mimbiang, C. Sonkeng, M. Tardy, C. Commeyras, C. Essomba, N. Eteki, and O. Laborde. Back

Authors’ addresses: Ahidjo Ayouba, Eric Nerrienet, and Jocelyn Thonnon, Centre Pasteur Pasteur du Cameroun, BP 1274 Yaounde, Cameroon, Telephone: 237-223-1803, Fax: 237-223-1564, E-mails: ayouba{at}pasteur.cm, nerrienet{at}pasteur.cm, and thonnon{at}pasteur.cm. Elisabeth Menu and Françoise Barré-Sinoussi, Institut Pasteur, Unité de Biologie des Rétrovirus, 25, rue du Dr Roux, 75724 Paris Cedex 15, France, Telephone: 33-1-40-61-39-69, Fax: 33-1-45-68-89-57, E-mails: emenu{at}pasteur.fr and fbarre{at}pasteur.fr. Marcel Monny Lobé, Centre Mère et Enfant, Fondation Chantal Biya, Yaounde, Cameroon, Telephone: 237-222-2000. Robert J. I. Leke, University Centre for Health Sciences, University of Yaounde I, Yaounde Cameroon, Telephone: 237-223-4020, Fax: 237-223-4451, E-mail: robert.leke{at}camnet.cm. Paul Martin, Laboratoire des Listeria, Institut Pasteur, 25, rue du Dr Roux, 75724 Paris Cedex 15, France, Telephone: 33-1-40-61-39-62, Fax: 33-1-40-61-35-67, E-mail: pmartin{at}pasteur.fr. Patrick Cunin, Hôpital Henri Mondor, 92000, Créteil, France, Telephone/Fax: 33-1-34-77-04-62, E-mail: patrickcunin{at}aol.com.


REFERENCES
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 METHODS
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  1. Guay LA, Musoke P, Fleming T, Bagenda D, Allen M, Nakabiito C, Sherman J, Bakaki P, Ducar C, Deseyve M, Emel L, Mirochnick M, Fowler MG, Mofenson L, Miotti P, Dransfield K, Bray D, Mmiro F, Jackson JB, 1999. Intrapartum and neonatal single-dose nevirapine compared with zidovudine for prevention of mother-to-child transmission of HIV-1 in Kampala, Uganda: HIVNET 012 randomised trial. Lancet354: 795–802.[ISI][Medline]
  2. Menendez C, Ordi J, Ismail R, Ventura PJ, Aponte JJ, Kahigwa E, Font F, Alonzo PL, 2000. The impact of placental malaria on gestational age and birth weight. J Infect Dis 181: 1740–1745.[ISI][Medline]
  3. Ayisi JG, van Eijk AM, ter Kuile FO, Kolczak MS, Otieno JA, Misore AO, Kager PA, Steketee RW, Nahlen BL, 2003. The effect of dual infection with HIV and malaria on pregnancy outcome in western Kenya. AIDS 17: 585–594.[ISI][Medline]
  4. Fievet N, Moussa M, Tami G, Maubert B, Cot M, Deloron P, Chaouat G, 2001. Plasmodium falcifarum induces a Th1/Th2 disequilibrium, favoring the Th1-type pathway, in the human placenta. J Infect Dis 183: 1530–1534.[ISI][Medline]
  5. Soula G, Ndounga M, Foumane V, Ollivier G, Youmba JC, Basco L, Boudin C, Same Ekobo A, Ringwald P, 2000. Bilan de la résistance de Plasmodium falciparum à la chloroquine au Cameroun et alternatives thérapeutiques. Bull Liais Doc OCEAC 33: 13–22.
  6. O’Donovan D, Ariyoshi K, Milligan P, Ota M, Yamuah L, Sarge-Njie R, Whittle H, 2000. Maternal plasma viral RNA levels determine marked differences in mother-to child transmission rates of HIV-1 and HIV-2 in the Gambia. AIDS 14: 441–448.[ISI][Medline]



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