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Article

The Burden of Serious Fungal Infections in Cameroon

1
Department of Internal Medicine (Dermatology), Université des Montagnes, Bangangté P.O. Box 208, Cameroon (Central Africa)
2
National Aspergillosis Centre, Wythenshawe Hospital and The University of Manchester, Manchester M13 9PL, UK
*
Author to whom correspondence should be addressed.
J. Fungi 2018, 4(2), 44; https://doi.org/10.3390/jof4020044
Submission received: 22 February 2018 / Revised: 25 March 2018 / Accepted: 27 March 2018 / Published: 30 March 2018
(This article belongs to the Special Issue Fungal Burden in Different Countries)

Abstract

:
Fungal infections are frequent in Cameroon, and invasive fungal infections are sometimes detected, usually in HIV-infected patients. For these reasons, we have estimated the burden of fungal infections. Using published literature and population estimates for the at-risk group, we used deterministic modelling to derive national incidence and prevalence estimates for the most serious fungal diseases. HIV infection is common and an estimated 120,000 have CD4 counts <200 × 106/mL and commonly present with opportunistic infection. Oesophageal candidiasis in HIV is common, and in poorly controlled diabetics. We estimate 6720 cases of cryptococcal meningitis, 9000 of Pneumocystis pneumonia, 1800 of disseminated histoplasmosis annually complicating AIDS, and 1200 deaths from invasive aspergillosis in AIDS, but there are no data. We found that 2.4% of adults have chronic obstructive pulmonary disease (COPD) and 2.65% have asthma, with “fungal asthma” affecting 20,000. Chronic pulmonary aspergillosis probably affects about 5000 people, predominantly after tuberculosis but also with COPD and other lung diseases. Also, tinea capitis in schoolchildren is frequent. Overall, an estimated 1,236,332 people are affected by a serious fungal infection. There is an urgent need for government and clinician attention, improved laboratory facilities, fungal diagnostic tests, and competent laboratory technicians, as well as all World Health Organization (WHO)-endorsed essential antifungal drugs to be made available, as only fluconazole is registered and available in the country.

1. Introduction

Cameroon is a tropical Central African country located in the Gulf of Guinea. As in many tropical countries, infectious diseases are common and have particularly increased with the HIV epidemic, which is a huge problem in Cameroon. Although opportunistic infections occur frequently in AIDS persons, tuberculosis (TB) is the Government’s main public health concern [1]. Yet, there were nearly 30,000 estimated deaths from AIDS in 2016, a figure unchanged since 2012 and greater than in 2001. The narrow focus on TB has prevented any significant developments with respect to the other major causes of death in AIDS, namely fungal diseases, and in addition, data on the national incidence and prevalence of fungal infections are unavailable.
Limited studies and some unpublished studies record frequencies of mild superficial mycosis [2,3,4,5] or life-threatening invasive fungal infections in the HIV-infected population in Cameroon [6,7,8,9,10,11,12]. Ignorance of serious fungal infections, lack of awareness or involvement of practicing clinicians and the government, together with limited technical and structural health capabilities in Cameroon, have meant there is no register for any fungal disease. This lack of surveillance data combined with the unavailability of any non-culture diagnostic test for fungi, other than microscopy, reinforces a sense that these infections are rare or non-existent. Given that such infections are perceived to be rare, there is no call for any antifungals other than fluconazole to be made available in the country—a negative reinforcement of the absence of a problem in Cameroon.
For these reasons, here we have estimated the burden of serious fungal infections in Cameroon in the hope that highlighting the enormous gap between what is the current status quo and the likely actual situation will stimulate research, capacity development, and improved care [13].

2. Materials and Methods

In this study, we searched publications on literature in order to identify epidemiology papers reporting fungal infections frequencies from Cameroon, using PubMed. The terms used were “fungal infections in Africa”, “fungal infections in Cameroon”, and “opportunistic infections in Cameroon”.
We used the population for the at-risk group and deterministic modelling to derive national incidence and prevalence estimates for the most serious fungal diseases when data was unavailable.
We sourced the total Cameroonian population from the National Statistical Institute 2017 reports [14]. HIV/AIDS and tuberculosis prevalence were sourced from the World Health Organization (WHO) 2016 reports [15] and the Ministry of Public Health of Cameroon 2014 reports [16]. The assumptions made in estimating burden are shown in Table 1, with the pertinent references.

3. Results

3.1. Country Profile

Currently, the Cameroonian population is estimated at ~24.23 million, of whom 43.6% are aged <15 years old and 50.1% are females [14]. There are an estimated 613,731 persons living with HIV; 555,120 adults aged between 20 and 44, and 58,611 children aged <14 years old. In 2016, annual deaths from AIDS was ~29,327, and ~120,000 persons had CD4 counts <200 × 106/mL, at risk of presenting with opportunistic infections and ~240,000 not receiving (free) antiretroviral therapy (ART) [15,16]. The gross domestic product was $1033 per capita in 2016.

3.2. Serious Fungal Infections

Table 2 shows our estimates of the most serious fungal infections in Cameroon. We have not added sensitivity analyses, because the basis for the estimates themselves is mostly inferred from data from other countries, and more precise local estimates are desirable before more sophisticated modeling is done.

3.2.1. Pulmonary Conditions and Infections

In 2015, ~25,975 people were notified as infected by TB, 16,000 of them also with HIV-infection and 54% of these in receipt of free ART [15]. We assumed that only those with pulmonary TB who survived 12 months would develop chronic pulmonary aspergillosis, an estimated 19,762 people. The prevalence of chronic obstructive pulmonary disease (COPD) was 2.4% in adults (over 19) based on published studies in Yaoundé in HIV-positive and -negative adults [30,31], and at risk of chronic pulmonary aspergillosis. It was estimated that 25% of COPD patients are admitted to hospital per year and are at risk of invasive aspergillosis. The estimated number of adults with clinical asthma is 385,260 (2.65%) [31], and 2.5% of asthmatics develop allergic bronchopulmonary asthma (ABPA). Assuming that about 10% of adults have severe asthma (38,526), we assumed that severe asthma with fungal sensitization (SAFS) was present in 33% of these patients. ABPA and SAFS together are called “fungal asthma”, and over 20,000 adults suffer from this. Cystic fibrosis has not been not reported in Cameroon.
Concerning aspergillosis, estimates of the annual incidence of invasive aspergillosis (IA) were made [32]. About 1175 IA cases (leukaemia, lymphoma, and COPD) were anticipated, not including those complicating lung cancer or HIV. As over 4% of patients with AIDS who die are found to have IA at autopsy (consistently in Italy over 18 years) [33], it is possible that another 1200 IA cases occur each year, but data are lacking from Africa and so are not included.
Chronic pulmonary aspergillosis (CPA) annual incidence was estimated as previously (1265 cases) with a 5-year-period prevalence of 4983 (assuming 80% of cases occur after TB) [23]. These estimates are broadly (qualitatively) supported by a recent cross-sectional study from Nigeria [24]. A recent Cameroonian study in Yaoundé recorded 20 cases of complex pulmonary aspergilloma in three years (2012–2015) in immunocompetent patients with a past history of TB, which were treated surgically, confirming that CPA occurs in Cameroon [25]. In addition, 8844 patients with ABPA complicating asthma in adults were expected and 11,675 cases of SAFS. Other less severe forms of aspergillosis were not estimated, including rhinosinusitis, onychomycosis [34], or otitis externa.

3.2.2. Opportunistic Fungal Infections Complicating HIV Infection

Opportunistic fungal infections are common in HIV-infected persons in Cameroon, but are not well documented. Pneumocystis pneumonia (PCP) was estimated at an annual rate of 7.5% in those with CD4 counts <200 × 106/mL. Although national data is unavailable, reports of high frequency in cross-sectional studies attest to endemicity in Cameroon. Nkinin and colleagues reported 82% positivity to P. jirovecii antibody using ELISA on 349 randomly collected serum samples in 2009 (50% from HIV positive people) [6]; Riebold and Enoh found that 31.6% of patients in 2014 were colonized with P. jirovecii by PCR detection of induced sputum, most of them being HIV-infected [7]. Our estimate could be an underestimate therefore.
Cryptococcal meningitis (CM) was estimated to occur at a rate of 11% over 2 years in patients with CD4 counts <200 × 106/mL (6720 cases). Reports from 2012 to 2015 showed various prevalence figures from 9.9% to 28.1% in slightly different HIV populations [8,9,10]. Our annual incidence estimate is higher than that of Rajasingham et al., (n = 3602), which was based on a prevalence of 6.1% of cryptococcal antigenaemia in those with CD4 counts <100 × 106/mL [35].
Disseminated histoplasmosis (DH) was estimated to occur at an annual rate of 1.5% in HIV patients with CD4 counts <200 × 106/mL, which means that ~1800 patients probably have this life-threatening, and probably fatal, infection each year. National data on this fungal infection is unavailable. However, a Cameroonian study reported in 2015 a prevalence of 13% of DH due to Histoplasma capsulatum var. capsulatum (Hcc) in HIV-infected persons [11]. The same author previously detected three cases of DH in HIV-infected persons: the first case was due to Histoplasma capsulatum var. duboisii (Hcd), successfully treated with boluses of fluconazole, the two other patients being Hcc histoplasmosis and detected post-mortem on skin biopsy and on peripheral blood smear [36,37]. Nonetheless, a recent publication recorded a total of 15 cases of both Hcc (9/15) and Hcd (6/15) histoplasmosis in Cameroon, HIV-positive persons being more numerous (12/15) than negative patients (3/15) [38].
Oesophageal candidiasis is a frequent problem in HIV patients and was estimated to occur in at least 43,300 people each year (177/100,000). More common is oropharyngeal candidiasis, estimated in 108,000 HIV-infected patients. In addition to this large number of cases, a local report from 2015 found 23.5% of poorly controlled diabetics to have oropharyngeal candidiasis [39]. We do not have a good denominator for diabetes in Cameroon, or what proportion are poorly controlled.

3.2.3. Other Fungal Infections

Data was not found on candidaemia, candida peritonitis, or other forms of invasive candidiasis, and so we have estimated annual incidences of 5/100,000 and 0.75/100,000, based on other countries [18,19]. Likewise, we did not find any report on recurrent vulvovaginal candidiasis from Cameroon, although it is present, and so we used a 6% proportion of women aged between 5 and 50 as a prevalence estimate. This translates to nearly 350,000 women (2845/100,000) mostly without any underlying disease.
Fungal keratitis was not recorded.
Mucormycosis was estimated 0.2/100,000. Only five cases (one basidiobolomycosis) were reported in 1992 [40]. Data on chromoblastomycosis and mycetoma was not found.
Tinea capitis in schoolchildren is possibly the largest burden of significant superficial fungal infections, with frequencies from 31 to 66% [2,3,4]. Our estimate is that ~721,000 children have tinea capitis, a rate of 3240/100,000. Onychomycosis was also found at high rate (51%) especially in diabetic patients [5].

4. Discussion

In this study, we attempt to highlight the burden of serious fungal infections in Cameroon.
Aspergillosis is poorly reported and infrequently diagnosed in this country. Assuming the endemicity of TB, which is considered as the main opportunistic AIDS-defining infection and the main cause of death in AIDS persons in Cameroon [41], high frequencies of post-TB aspergillosis are expected as in other endemic sub-Saharan African countries for TB [42,43,44,45,46]. Surprisingly, only one Cameroonian publication recording 20 cases of complex pulmonary aspergilloma in immunocompetent patients has been published [25]. This contrasts with our estimate of nearly 5000 cases. No other forms of aspergillosis were reported, including invasive aspergillosis. The rarity of publications may be explained by ignorance or lack of awareness of practicians who could misdiagnose aspergillosis as TB given the similarities of clinical symptoms (cough and bloody sputum, dyspnea, and weight loss) and on thoracic imaging (nodules, cavities, and infiltrates), leading probably to presumptive antituberculosis treatment. Fever is uncommon with aspergillosis but more common with TB. The lack of efficient laboratory methods for diagnosis of aspergillosis (microscopy or culture on tissue biopsy, or IgG antibody response to Aspergillus spp.) is also a major factor in under-diagnosis. Moreover, asymptomatic patients are never encountered in sub-Saharan African countries, patients attending hospital only when they feel their lives are threatened. Many patients thus die without a definite diagnosis of aspergillosis. As no antifungals are available in Cameroon that are effective for aspergillosis (itraconazole, voriconazole, amphotericin B, or echinocandins), we must estimate that all those with invasive disease die and most of those with CPA also die.
Histoplasmosis is underreported in Cameroon. This may be explained by ignorance or lack of awareness or involvement of medical practitioners, almost no laboratory diagnostic facilities other than microscopy, and no qualified laboratory technicians. However, both Hcc and Hcd histoplasmosis coexist in Cameroon as in other sub-Saharan African countries, occurring either in HIV-infected or -negative patients, with various clinical presentations but presumably a fatal outcome in patients with deep immunosuppression especially due to HIV infection [38,47,48]. It is therefore noteworthy that sub-Saharan African clinicians should think of histoplasmosis in case of a sudden occurrence of poor general condition with CD4 T cells count <100/mm3 in HIV-infected patients [49]; or in a patient suspected of tuberculosis with negative sputum on bacteriology examination, and treated with effective antituberculosis drugs without clinical improvement [36,50]; or in case of a prolonged fever occurring in a HIV+ person or a person of unknown HIV serology status [37,51,52,53,54]. Unfortunately, fluconazole (which is the only available antifungal treatment) is a sub-optimal therapy for disseminated (and other forms) histoplasmosis, itraconazole and amphotericin being more effective (but unavailable in this country).
CM is frequently reported with high frequencies in HIV-infected patients [9,10,12], given the cheap routine means of diagnosis (direct detection with India ink and culture equipment). Meanwhile, its real national prevalence is unknown as a consequence of a lack of research, out-of-pocket payments that prevents patients from consulting at hospitals, lack of any infection-monitoring program, and routine treatment of AIDS patients with fluconazole. Our estimate is two-fold higher than another recent estimate [12]. This needs further work to clarify.
As in parts of sub-Saharan African countries, the prevalence of PCP is unknown in the general population or underestimated, owing to the high rate of death in AIDS persons and in children aged <1 year, the lack of suitable diagnostics practices, and commonly administered cotrimoxazole prophylaxis in HIV-infected persons [27,28]. Not all PCP cases are “classical” and many have co-infections, so it is highly likely that many hospitalized AIDS patients have PCP that is not diagnosed or empirically treated.
Superficial fungal infections in Cameroon are dominated by an extraordinarily high prevalence of tinea capitis, especially in school-age children, as in other sub-Saharan African countries [2,3,4,55]. Even so, it is still underestimated as the diagnosis is usually clinically documented, mycology examination being reserved only for research studies. So, many cases of scaly scalp in infants or in adults, and many girls with braided hair are not accounted for, while they could have been detected as genuine (and infectious) cases on mycology examination [2,3].
Oropharyngeal candidiasis occurs commonly in patients with advanced HIV infection or other immunosuppressive conditions. However, its prevalence cannot be established with certainty in the whole population in Cameroon, given the lack of data. Oesophageal candidiasis is probably common but not often definitively diagnosed as there is a lack of endoscopy. Estimates for other serious fungal infections including candida peritonitis and candidaemia are certainly preliminary and we are unable to make any estimate of fungal keratitis, chromoblastomycosis, or mycetoma.

5. Conclusions

Although fungal infections are frequent in Cameroon, it is currently not possible to estimate their frequencies with certainty in the absence of good diagnostics, registers reporting well-documented data or prospective surveys. Practitioners should be involved and more aware of fungal infections in general and particularly on health-threatening diseases, in order to provide good clinical care. They urgently need government attention, improved laboratory facilities, fungal diagnostic tests, and competent laboratory technicians, as well as all the WHO-endorsed essential antifungal drugs to be made available, as only fluconazole is registered and available in the country.

Acknowledgments

This study did not receive any financial support and the authors have not received funds for covering the publication of this article. No funds were received for open access publication.

Author Contributions

Both authors contributed to this manuscript, but it is noteworthy that David W. Denning estimated the frequency rates of diseases and fungal infections, added articles and improved Christine E. Mandengue’s English writing.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Directives Nationales de Prévention et de Prise en Charge du VIH au Cameroun, 2014–2017. Available online: https://aidsfree.usaid.gov (accessed on 12 December 2017).
  2. Koueke, P.; Ebenye, E. Les teignes scolaires à Yaoundé. Med. Afr. Noire 1981, 28, 115–121. [Google Scholar]
  3. Tassa Kayem, F.M. Etude des teignes scolaires à l’Ecole Evangélique de Mfétom de Bangangté, Cameroun. Ph.D. Thesis, Université des Montagnes, Bangangté, Cameroon, 16 November 2013. [Google Scholar]
  4. Kechia, F.A.; Kouotou, E.A.; Nkoa, T.; Nweze, E.I.; Fokoua, D.C.M.; Fosso, S.; Somo Moyou, R. Epidemiology of tinea capitis among school-age children in Meiganga, Cameroon. J. Mycol. Med. 2014, 24, 129–134. [Google Scholar] [CrossRef] [PubMed]
  5. Eba, M.; Njunda, A.L.; Mouliom, R.N.; Kwenti, E.T.; Fuh, A.N.; Nchanji, G.T.; Atashili, J. Onychomycosis in diabetic patients in Fako Division of Cameroon: Prevalence, causative agents, associated factors and antifungal sensitivity patterns. BMC Res. Notes 2016, 9, 494. [Google Scholar] [CrossRef] [PubMed]
  6. Nkinin, S.W.; Dalyb, K.R.; Walzerb, P.D.; Ndzid, E.S.; Asonganyie, T.; Respaldizaf, N.; Medranof, F.J.; Kaneshiro, E.S. Evidence for high prevalence of Pneumocystis jirovecii exposure among Cameroonians. Acta Trop. 2009, 112, 219–224. [Google Scholar] [CrossRef] [PubMed]
  7. Riebold, D.; Enoh, D.O.; Kinge, T.N.; Akam, W.; Bumah, M.K.; Russow, K.; Klammt, S.; Loebermann, M.; Fritzsche, C.; Eyong, J.E.; et al. Pneumocystis jirovecii colonisation in HIV-positive and HIV-negative subjects in Cameroon. Trop. Med. Int. Health 2014, 19, 643–655. [Google Scholar] [CrossRef] [PubMed]
  8. Dzoyem, J.P.; Kechia, F.; Ngaba, G.P.; Lunga, P.K.; Lohoue, P.J. Prevalence of cryptococcosis among HIV-infected patients in Yaoundé, Cameroon. Afr. Health Sci. 2012, 12, 129–133. [Google Scholar] [CrossRef] [PubMed]
  9. Luma, H.N.; Tchaleu, B.C.N.; Temfack, E.; Doualla, M.S.; Ndenga, D.P.N.; Mapoure, Y.N.; Njamnshi, A.K.; Djientcheu, V. HIV-Associated Central Nervous System Disease in Patients Admitted at the Douala General Hospital between 2004 and 2009: A Retrospective Study. AIDS Res. Treat. 2013. [Google Scholar] [CrossRef] [PubMed]
  10. Kammalac Ngouana, T.; Dongtsa, J.; Kouanfack, C.; Tonfack, C.; Fomena, S.; Mallié, M.; Delaporte, E.; Boyom, F.F.; Bertout, S. Cryptoccocal meningitis in Yaoundé (Cameroon) HIV infected patients: Diagnosis, frequency and Cryptococcus neoformans isolates susceptibility study to fluconazole. J. Mycol. Med. 2015, 25, 11–16. [Google Scholar] [CrossRef] [PubMed]
  11. Mandengue, C.E.; Ngandjio, A.; Atangana, P.J.A. Histoplasmosis in HIV-Infected Persons, Yaoundé, Cameroon. Emerg. Infect. Dis. 2015, 21, 2094–2096. [Google Scholar] [CrossRef] [PubMed]
  12. Molloy, S.F.; Chiller, T.; Greene, G.S.; Burry, J.; Govender, N.P.; Kanyama, C.; Mfinanga, S.; Lesikari, S.; Mapoure, Y.N.; Kouanfack, C.; et al. Cryptococcal meningitis: A neglected NTD? PLoS Negl. Trop. Dis. 2017, 11, E0005575. [Google Scholar] [CrossRef] [PubMed]
  13. Cole, D.C.; Govender, N.P.; Chakrabarti, A.; Sacarlal, J.; Denning, DW. Improvement of fungal disease identification and management: Combined health systems and public health approaches. Lancet Infect. Dis. 2017. [Google Scholar] [CrossRef]
  14. Cameroon Population. 2017. Available online: http://countrymeters.info/fr/ (accessed on 12 December 2017).
  15. Tuberculosis Profile, Cameroon. 2016. Available online: http://www.who/tb/data (accessed on 12 December 2017).
  16. Plan Stratégique National de Lutte contre le VIH, le SIDA et les IST 2014–2017. Available online: www.childrenandaids (accessed on 12 December 2017).
  17. Smith, E.; Orholm, M. Trends and patterns of opportunistic diseases in Danish AIDS patients 1980–1990. Scand. J. Infect. Dis. 1990, 22, 665–672. [Google Scholar] [CrossRef] [PubMed]
  18. Arendrup, M.C. Epidemiology of invasive candidiasis. Curr. Opin. Crit. Care 2010, 16, 445–452. [Google Scholar] [CrossRef] [PubMed]
  19. Montravers, P.; Mira, J.-P.; Gagneux, J.-P.; Leroy, O.; Lorhtolary, O.; AmarCand study group. Multicentre study of antifungal strategies and outcome of Candida spp. peritonitis in intensive-care units. Clin. Microbiol. Infect. 2011, 17, 1061–1067. [Google Scholar] [CrossRef] [PubMed]
  20. Denning, D.W.; Kneale, M.; Rautemaa-Richardson, R.; Sobel, J.D. Global burden of recurrent vulvovaginal candidiasis. Lancet Infect. Dis. 2018, in press. [Google Scholar]
  21. Denning, D.W.; Pleuvry, A.; Cole, D.C. Global burden of ABPA in adults with asthma and its complication chronic pulmonary aspergillosis. Med. Mycol. 2013, 51, 361–370. [Google Scholar] [CrossRef] [PubMed]
  22. Denning, D.W.; Pashley, C.; Hartl, D.; Wardlaw, A.; Godet, C.; Del Giacco, S.; Delhaes, L.; Sergejeva, S. Fungal allergy in asthma–state of the art and research needs. Clin. Transl. Allergy 2014, 4, 14. [Google Scholar] [CrossRef] [PubMed]
  23. Denning, D.W.; Pleuvry, A.; Cole, D.C. Global burden of chronic pulmonary aspergillosis as a sequel to pulmonary tuberculosis. Bull. World Health Organ. 2011, 89, 864–872. [Google Scholar] [CrossRef] [PubMed]
  24. Oladele, R.O.; Irurhe, N.K.; Foden, P.; Akanmu, A.S.; Gbaja-Biamila, T.; Nwosu, A.; Ekundayo, H.A.; Ogunsola, F.T.; Richardson, M.D.; Denning, D.W. Chronic pulmonary aspergillosis as a cause of smear-negative TB and/or TB treatment failure in Nigerians. Int. J. Tuberc. Lung Dis. 2017, 21, 1056–1061. [Google Scholar] [CrossRef] [PubMed]
  25. Ngo Nonga, B.; Bang, G.A.; Jemea, B.; Savom, E.; Pefura, Y.; Ngahane, M.; Ze, J.J. Complex pulmonary aspergilloma: Surgical challenges in a third world setting. Surg. Res. Pract. 2018, 2018, 6570741. [Google Scholar] [CrossRef]
  26. Lortholary, O.; Gangneux, J.P.; Sitbon, K.; Lebeau, B.; de Monbrison, F.; Le Strat, Y.; Coignard, B.; Dromer, F.; Bretagne, S. French Mycosis Study Group. Epidemiological trends in invasive aspergillosis in France: The SAIF network (2005–2007). Clin. Microbiol. Infect. 2011, 17, 1882–1889. [Google Scholar] [CrossRef] [PubMed]
  27. De Armas Rodríguez, Y.; Wissmann, G.; Müller, A.L.; Pederiva, M.A.; Brum, M.C.; Brackmann, R.L.; Capó De Paz, V.; Calderón, E.J. Pneumocystis jirovecii pneumonia in developing countries. Parasite 2011, 18, 219–228. [Google Scholar] [CrossRef] [PubMed]
  28. Wasserman, S.; Engel, M.E.; Griesel, R.; Mendelson, M. Burden of Pneumocystis pneumonia in HIV-infected adults in sub-Saharan Africa: A systematic review and meta-analysis. BMC Infect. Dis. 2016, 16, 482. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  29. Lofgren, S.M.; Kirsch, E.J.; Maro, V.P.; Morrissey, A.B.; Msuya, L.J.; Kinabo, G.D.; Saganda, W.; Diefenthal, H.C.; Ramadhani, H.O.; Wheat, L.J.; et al. Histoplasmosis among hospitalized febrile patients in northern Tanzania. Trans. R. Soc. Trop. Med. Hyg. 2012, 106, 504–507. [Google Scholar] [CrossRef] [PubMed]
  30. Pefura-Yone, E.W.; Fodjeu, G.; Kengne, A.P.; Roche, N.; Kuaban, C. Prevalence and determinants of chronic obstructive pulmonary disease in HIV infected patients in an African country with low level of tobacco smoking. Respir. Med. 2015, 109, 247–254. [Google Scholar] [CrossRef] [PubMed]
  31. Pefura-Yone, E.W.; Kengne, A.P.; Dodo Balkissou, A.; Magne-Fotso, C.G.; Ngo-Yonga, M.; Boulleys-Nana, J.R.; Efe-de-Melingui, N.R. Prevalence of obstructive lung disease in an African country using definitions from different international guidelines: A community based cross-sectional survey. BMC Res. Notes 2016, 9, 124. [Google Scholar] [CrossRef] [PubMed]
  32. Mandengue, C.; Denning, D.W. Estimation of the burden of serious mycoses in Cameroon. In Proceedings of the European Congress of Clinical Microbiology and Infectious Diseases, Vienna, Austria, 22–25 April 2017. [Google Scholar]
  33. Antinori, S.; Nebuloni, M.; Magni, C.; Fasan, M.; Adorni, F.; Viola, A.; Corbellino, M.; Galli, M.; Vago, G.; Parravicini, C.; et al. Trends in the Postmortem Diagnosis of Opportunisti Invasive Fungal Infections in Patients With AIDS: A Retrospective Study of 1630 Autopsies Performed Between 1984 and 2002. Am. J. Clin. Pathol. 2009, 132, 221–227. [Google Scholar] [CrossRef] [PubMed]
  34. Bongomin, F.; Batac, C.R.; Richardson, M.D.; Denning, D.W. A review of Onychomycosis due to Aspergillus species: Mycology and Epidemiology. Mycopathologia 2017. [Google Scholar] [CrossRef] [PubMed]
  35. Rajasingham, R.; Smith, R.M.; Park, B.J.; Jarvis, J.N.; Denning, D.W.; Govender, N.P.; Loyse, A.; Boulware, D.R. Estimation of the global burden of HIV-Associated cryptococcal meningitis. Lancet. Infect. Dis. 2017, 17, 873–881. [Google Scholar] [CrossRef]
  36. Mandengue, C.E.; Lindou, J.; Mandeng, N.; Takuefou, B.; Nouedoui, C.; Atangana, P.; Fonkoua, M.C. Fatal miliary tuberculosis in an HIV-infected Cameroon woman: Disseminated histoplasmosis due to Histoplasma capsulatum capsulatum. Med. Trop. 2011, 71, 615–617. (In French) [Google Scholar]
  37. Mandengue Ebenye, C. A case of disseminated histoplasmosis detected in peripheral blood smear staining revealing AIDS at terminal phase in female patient from Cameroon. Case Rep. Med. 2012, 2012, 215207. [Google Scholar] [CrossRef]
  38. Oladele, R.O.; Ayanlowo, O.O.; Richardson, M.D.; Denning, D.W. Histoplasmosis in Africa: An emerging or a neglected disease? PLOS Negl. Trop. Dis. 2018, 12. [Google Scholar] [CrossRef] [PubMed]
  39. Bissong, M.; Azodo, C.C.; Agbor, M.A.; Nkuo-Akenji, T.; Fon, P.N. Oral Health Status of diabetes mellitus patients in Southwest Cameroon. Odontostomatol. Trop. 2015, 38, 49–57. [Google Scholar] [PubMed]
  40. Michel, G.; Ravisse, P.; Lohoue-Petmy, J.; Steinmetz, J.P.; Winter, C.; Mbakop, A.; Ave, P.; Ruffaud, M.A. 5 new cases of entomophthoromycosis observed in Cameroon. Role of immunofluorescence in their diagnosis. Bull. Soc. Pathol. Exot. 1992, 85, 10–16. [Google Scholar] [PubMed]
  41. Mbuagbaw, J.; Jingi, A.M.; Noubiap, J.J.N.; Kaze, A.D.; Nansseu, J.R.N.; Bigna, J.J.R.; Wawo Yonta, E.; Ngu Blackett, K. Patterns and trends in mortality among HIV-infected and HIV-uninfected patients in a major Internal Medicine Unit in Yaoundé, Cameroon: A retrospective cohort study. J. R. Soc. Med. Open 2016, 7. [Google Scholar] [CrossRef] [PubMed]
  42. Oladele, R.O.; Denning, D.W. Burden of Serious Fungal Infection in Nigeria. West Afr. J. Med. 2014, 33, 107–114. [Google Scholar] [PubMed]
  43. Chakaya, J.; Kirenga, B.; Getahun, H. Long term complications after completion of pulmonary tuberculosis treatment: A quest for a public health approach. J. Clin. Tuberc. Other Mycobact. Dis. 2016, 3, 10–12. [Google Scholar] [CrossRef]
  44. Guto, J.A.; Bii, C.C.; Denning, D.W. Estimated burden of fungal infections in Kenya. J. Infect. Dev. Ctries. 2016, 10, 777–784. [Google Scholar] [CrossRef] [PubMed]
  45. Badiane, A.S.; Ndiaye, D.; Denning, D.W. Burden of fungal infections in Senegal. Mycoses 2015, 58, 63–69. [Google Scholar] [CrossRef] [PubMed]
  46. Faini, D.; Maokola, W.; Furrer, H.; Battegay, C.H.M.; Tanner, M.; Denning, D.W.; Letangaini, E. Burden of serious fungal infections in Tanzania. Mycoses 2015, 58, 70–79. [Google Scholar] [CrossRef] [PubMed]
  47. Gugnani, H.C.; Mutoe-Okafor, F. African histoplasmosis: A review. Rev. Iberoam. Micol. 1997, 14, 155–159. [Google Scholar] [PubMed]
  48. Loulergue, P.; Bastides, F.; Baudouin, V.; Chandenier, J.; Mariani-Kurkdjian, P.; Dupont, B.; Viard, J.P.; Dromer, F.; Lortholary, O. Literature review and case histories of Histoplasma capsulatum var duboisii infections in HIV-infected patients. Emerg. Infect. Dis. 2007, 13, 1647–1652. [Google Scholar] [CrossRef] [PubMed]
  49. El Guedj, M.; Couppie, P.; Pradinaud, R.; Aznar, C.; Carme, B.; Clity, E.; Farge, D. Histoplasmose à Histoplasma capsulatum capsulatum et infection à VIH. Rev. Med. Int. 2000, 21, 408–415. [Google Scholar] [CrossRef]
  50. Ouattara, B.; Kadjo, K.; Sanogo, S.; Koffi, K.; Niamkey, E.; Beda, Y. Histoplasmose à Histoplasma capsulatum: À propos d’un cas observé dans le service de médecine interne du CHU de Treichville (Abidjan). Bull. Soc. Pathol. Exot. 1998, 91, 158–159. [Google Scholar]
  51. Gangat, N.; Lin, Y.; Elkin, P.L. A 68-Year-old man with fatigue, fever, and weight loss. Mayo Clin. Proc. 2005, 80, 939–942. [Google Scholar] [CrossRef] [PubMed]
  52. Carme, B. Histoplasmose dépistée sur frottis sanguin révélatrice d’un SIDA en phase terminale. Med. Trop. 2011, 71, 347. [Google Scholar]
  53. Zyrek-Betts, J.; Donabedian, H.; Booth, R. A 49-year-old man with AIDS, fever, and weight loss. Lab. Med. 2006, 37, 536–538. [Google Scholar] [CrossRef]
  54. Updesh, M.; Sachdeva, S.; Das, R. Peripheral smear discloses histoplasmosis. Blood 2010, 115, 3653. [Google Scholar] [CrossRef] [PubMed]
  55. Moto, J.N.; Muthini Maingi, J.; Kebira Nyamache, A. Prevalence of tinea capitis in school going children from Mathare, informal settlement in Nairobi, Kenya. BMC Res. Notes 2015, 8, 274. [Google Scholar] [CrossRef] [PubMed]
Table 1. Assumptions made in assessing burden.
Table 1. Assumptions made in assessing burden.
DiseaseUnderlying Disease(s)Incidence/Prevalence Used to Estimate BurdenCommentsReference
Oesophageal candidiasisHIV/AIDS22% of patients with CD4 counts <200 × 106/mL and 5% of ARV-treated patients [17]
CandidaemiaMultiple hospitalized patients5/100,000 population, 33% occurring in intensive careFew patients managed in ICU currently.[18]
Candida peritonitisMajor abdominal surgery, pancreatitis50% of the ICU population with candidaemia [19]
Recurrent vaginal candidiasis (>4×/year)Pre-menopausal women6% prevalenceBased on mean self-reported disease in Europe and US, reduced by 33% because of incorrect diagnosis.[20]
Allergic bronchopulmonary aspergillosisAsthma2.5% of adults with asthmaRare in children[21]
Severe asthma with fungal sensitisationSevere asthma33% of the 10% of the most severe adult asthmatics Uncommon in children. Fungal sensitization prevalence not known for Cameroon.[22]
Chronic pulmonary aspergillosisTuberculosis (TB), COPD, prior pneumothorax, asthma, lung surgery22% of patients with a cavity of pulmonary TB survivors (22%), 2% of those without a cavity. Patients with other pulmonary conditions contribute an additional 25% of cases [23,24,25]
Invasive aspergillosisLeukaemia, lymphoma, COPD10% of acute myeloid leukaemia, an equal number of cases in all other haematological conditions + 1.3% of patients with COPD admitted to hospitalPatients with other conditions not included, including HIV/AIDS.[26]
Cryptococcal meningitisHIV/AIDS11% over 2 years in patients with CD4 counts <200 × 106/mLThe annual incidence rises as the CD4 count falls[8,9,10]
Pneumocystis pneumoniaHIV/AIDS15% over 2 years in patients with CD4 counts <200 × 106/mLCommon in children but not estimated separately. Cases in non-AIDS cases not estimated.[27,28]
HistoplasmosisHIV/AIDS1.5% over 2 years in patients with CD4 counts <200 × 106/mL [29]
Tinea capitisChildren 1–15 years8.1%The most conservative estimate is 8.1% in school aged children. There will be a slight over-estimate by including babies under 2 years.[2]
Table 2. Estimates of most severe fungal infections in Cameroon.
Table 2. Estimates of most severe fungal infections in Cameroon.
InfectionNumber of Infections per Underlying Disorder per YearRate/100 KTotal Burden
NoneHIV/AIDSRespiratoryCancer/TxICU *
Oesophageal candidiasis-43,300-?-19343,300
Candidaemia---7793345.01113
Candida peritonitis----1670.75167
Recurrent vaginal candidiasis (4×/year +)316,555----2845316,555
ABPA *--8844--408844
SAFS *--11,675--5211,675
Chronic pulmonary aspergillosis--4983--224983
Invasive aspergillosis---13410415.31175
Cryptococcal meningitis?6720-?-306720
Pneumocystis pneumonia-9000-?-409000
Histoplasmosis?1800???161800
Tinea capitis721,000----3240721,000
Total burden estimated1,037,55560,82025,5029131542-1,126,332
ICU = intensive care unit; ABPA = allergic bronchopulmonary aspergillosis; SAFS = severe asthma with fungal sensitization; * collectively called “fungal asthma”; + indicates rate per 100,000 females; ? indicates no reliable estimate possible.

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Mandengue, C.E.; Denning, D.W. The Burden of Serious Fungal Infections in Cameroon. J. Fungi 2018, 4, 44. https://doi.org/10.3390/jof4020044

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Mandengue CE, Denning DW. The Burden of Serious Fungal Infections in Cameroon. Journal of Fungi. 2018; 4(2):44. https://doi.org/10.3390/jof4020044

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Mandengue, Christine E., and David W. Denning. 2018. "The Burden of Serious Fungal Infections in Cameroon" Journal of Fungi 4, no. 2: 44. https://doi.org/10.3390/jof4020044

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