{"id":63275,"date":"2024-12-30T11:40:40","date_gmt":"2024-12-30T11:40:40","guid":{"rendered":"https:\/\/biomedpharmajournal.org\/?p=63275"},"modified":"2025-01-06T18:12:24","modified_gmt":"2025-01-06T18:12:24","slug":"prevalence-of-genital-herpes-insights-from-outpatient-clinic-patients","status":"publish","type":"post","link":"https:\/\/biomedpharmajournal.org\/staging\/vol17no4\/prevalence-of-genital-herpes-insights-from-outpatient-clinic-patients\/","title":{"rendered":"Prevalence of Genital Herpes: Insights from Outpatient Clinic Patients"},"content":{"rendered":"<p><strong>Introduction<\/strong><\/p>\n<p>Herpes simplex virus (HSV) is a double-stranded DNA genera that contains two members, HSV-1 and HSV-2 cause persistent infection with recurrent lesions <sup>1<\/sup>. It manifests as groups of vesicles on an erythematous base and is caused by DNA viruses in the Herpesviridae family. A type called HSV-1 causes mainly oral infections like herpes labialis or cold sores and another, HSV-2 mostly genital ones.<sup>2<\/sup>. The lesions of HSV-1 and HSV-2 are indistinguishable per Clinique, however, both are\u00a0primarily spread through direct contact.\u00a0After an initial infection, the virus is latent in the\u00a0spinal dorsal root ganglia that innervates the\u00a0skin of even a single dermatome <sup>3, 4<\/sup>. In all cases of recurrence, the virus travels down nerves to infected areas on or around the skin and mucous membrane where it multiplies, producing large lesions. Upon completion of each episode, the virus remains latent and does so for life.<\/p>\n<p>The health burden of HSV-2 infection differs per region, with varied associated risk factors among different populations. Almost 700 million people are living with HSV-2 worldwide and the prevalence is highest in some parts of Africa and the Americas whereas Asia has lower rates <sup>5, 6<\/sup>. The Centers for Disease Control estimates that too many people, approximately one in six sexually active adults suffer from genital herpes most of them women <sup>7<\/sup>. High rates are also observed in parts of sub-Saharan Africa, where there is a high prevalence of HIV with up to 80% of HIV-positive teenagers from South Africa being seropositive for HSV-2, as well as 20% of their corresponding healthy controls <sup>8, 9<\/sup>. The average HSV-2 seropositivity rate among antenatal clinic attendees in Africa was &gt;40%, while the prevalence was 60\u201395% amongst female sex workers, especially those from sub-Saharan districts <sup>10<\/sup>.<\/p>\n<p>HSV-2 prevalence varies markedly by individual characteristics such as gender, age, sexual behaviour, marital status, education, and race <sup>11<\/sup>.\u00a0Most incident genital herpes infections do not present as recognized clinical syndromes but rather are experienced as\u00a0subclinical or unrecognized <sup>12<\/sup>. Indeed, asymptomatic infection is perhaps the most important factor in\u00a0maintaining virus circulation; many cases of genital herpes are transmitted by individuals who have no clinical awareness of their infected status <sup>13<\/sup>. Nigeria is a country in sub-Saharan Africa where the prevalence of both HSV-2 and HIV infection is high <sup>14<\/sup>. A study in Lagos reported a 59% seroprevalence among female sex workers and one from Port Harcourt, Rivers State recorded as high as 58.9% for HSV-2 IgG antibodies <sup>15, 16<\/sup>. There is a\u00a0paucity of data on the\u00a0seroprevalence of HSV-2 in Sokoto. This study specifically investigated the seroprevalence of HSV-2 infections in febrile patients attending Specialist Hospital, Sokoto.<\/p>\n<p><strong>Materials and Methods<\/strong><\/p>\n<p>A cross-sectional study was conducted at the outpatient clinic of the Specialist Hospital, Sokoto. In order to obtain a population-representative sample blood samples were harvested from every second patient with an acute febrile episode.<\/p>\n<p><strong>Study Population<\/strong><\/p>\n<p>Patients who visited the outpatient clinic between April and August of 2023 with a fever, which was defined as a body temperature that was higher than 37 degrees Celsius, were included in the study. These individuals came from a variety of various backgrounds and represented a range of ages and genders.<\/p>\n<p><strong>Data Collection<\/strong><\/p>\n<p>Information on socio-demographic variables and probable risk factors for HSV-2 infection was collected using a semi-structured questionnaire.<\/p>\n<p><strong>Sample Collection and Processing<\/strong><\/p>\n<p>As part of the experiment, a laboratory technologist extracted three to four millilitres of venous blood from each participant and placed it in EDTA vials. After that, the samples were centrifuged at a speed of 2,500 revolutions per minute for five minutes to separate the plasma, which was then kept at a temperature of -20 degrees Celsius until it was analysed.<\/p>\n<p><strong>Sample Analysis<\/strong><\/p>\n<p>Plasma samples were used for enzyme-linked immunosorbent assay (ELISA) kits purchased from Diagnostic Automation (Cortez Diagnostics Inc. USA) as per the manufacturer&#8217;s instructions. In both of human plasma, the assay detected IgG antibodies specific for HSV-2.<\/p>\n<p><strong>Assay Procedure<\/strong><\/p>\n<p>A 96-well plate was prepared by adding a dilution of the negative control, the positive control, the calibrator, and each plasma sample, each of which was 100\u03bcL in volume. Additionally, one well was reserved as a reagent blank from the experiment. After thirty minutes of incubation at room temperature, the plate was washed three times before beginning the next step. After that, 100 microlitres of enzyme conjugate was introduced into every well, placed in an incubator at room temperature for 15 minutes, and then washed once more. Following this, 100 microlitres of TMB substrate was introduced onto the plate, and it was then left to incubate for a further 15 minutes. The reaction was terminated by adding 100 microlitres of 2M hydrochloric acid, and the optical density (OD) was measured over five minutes using an ELISA plate reader at a wavelength of 450 nm.<\/p>\n<p><strong>Calculation and Interpretation of Results<\/strong><\/p>\n<p>The cutoff optical density (OD) value was determined by multiplying the OD of the calibrator by a factor (f) specified on the calibrator vial (f = 0.5). The IgG index for each sample was then calculated by dividing its OD value by this cutoff. An IgG index of \u2264 0.90 was classified as seronegative, while an index between 0.91 and 0.99 was considered equivocal, necessitating retesting. In contrast, an IgG index of \u2265 1.00 was regarded as seropositive.<\/p>\n<p><strong>Data Analysis<\/strong><\/p>\n<p>SPSS software version 16.0 (SPSS Inc., Chicago, USA) was used for statistical analysis. To assess for associations between variables, multivariate regression analysis was conducted with a 95% confidence interval. Statistical significance was considered at a p-value of \u2264 0.05.<\/p>\n<p><strong>Results<\/strong><\/p>\n<p>A total of 184 plasma samples obtained from febrile patients were evaluated for HSV-2 IgG, and 100 (54.3%) were positive as determined by inhibition assay. three-quarters (95% CI = 80.6\u201391.4) were aged between 18\u201337 years, with the age group 23\u201327 years most commonly affected at 31.5% (58\/184). HSV-1 IgG was detected in all age cohorts, with the fewest numbers detected in individuals aged \u226453 years (n = 6). All six of the patients, aged 43 to 47, tested positive for the virus. The seroprevalence of HSV-2 IgG did not differ significantly by age (p = 0.729) (Table 1). It includes more females (122\/184) than males (62\/184). Of women, 66.3% (122\/184) were enrolled with fever, nearly twofold compared with men. Men had a higher prevalence of HSV-2 IgG than women (67.7%, 42\/62 vs. 47.5%, 58 \/122, P &lt; 0.0001). Although seroprevalence between groups was not significantly different (p = 0.066), male patients were 2.3 times more likely to be infected with HSV-2 than females (OR 2.317; CI 95% = 0.937-5.730).<\/p>\n<p>Occupational status Majority of the patients attending the Specialist Hospital, Sokoto are married 110\/184 (60.1%). On the other hand, a significantly higher proportion of HSV-2 IgG seropositivity (65%, 52\/80) was recorded among single individuals than for married ones (48.3%; 54 out of 112); however, this difference did not reach a\u00a0statistical significance level via chi-square test, p =.141). Employed patients had the highest seroprevalence of HSV-2 IgG (68.2%, 30\/44) and self-employed individuals recorded the\u00a0lowest prevalence rate (55.1%, 54\/98), but there was no statistically significant difference between all occupations groups adjusted for an age variable.<\/p>\n<p><strong>Table 1: Seroprevalence of HSV-2 about age among patients presenting with fever at the Specialist Hospital, Sokoto<\/strong><\/p>\n<table style=\"width: 95%;\" border=\"1\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr>\n<td style=\"text-align: center; width: 25%;\" width=\"25%\"><strong>Age group (years)<\/strong><\/td>\n<td style=\"text-align: center; width: 10%;\" width=\"10%\"><strong>Total<\/strong><\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\"><strong>Positive (%)<\/strong><\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\"><strong>Negative (%)<\/strong><\/td>\n<td style=\"text-align: center; width: 21%;\" rowspan=\"2\" width=\"21%\"><strong><em>p-value<\/em><\/strong><\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center; width: 25%;\" width=\"25%\"><\/td>\n<td style=\"text-align: center; width: 10%;\" width=\"10%\"><\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\"><\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\"><\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center; width: 25%;\" width=\"25%\">18\u201322<\/td>\n<td style=\"text-align: center; width: 10%;\" width=\"10%\">22<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">26(59.1)<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">18(40.9)<\/td>\n<td style=\"text-align: center; width: 21%;\" rowspan=\"7\" width=\"21%\"><em>p = 0.729<\/em><\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center; width: 25%;\" width=\"25%\">23\u201327<\/td>\n<td style=\"text-align: center; width: 10%;\" width=\"10%\">58<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">30(51.7)<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">28(48.3)<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center; width: 25%;\" width=\"25%\">28\u201332<\/td>\n<td style=\"text-align: center; width: 10%;\" width=\"10%\">42<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">22(52.4)<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">20(47.6)<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center; width: 25%;\" width=\"25%\">33- 37<\/td>\n<td style=\"text-align: center; width: 10%;\" width=\"10%\">14<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">6(42.9)<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">8(57.1)<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center; width: 25%;\" width=\"25%\">38\u201342<\/td>\n<td style=\"text-align: center; width: 10%;\" width=\"10%\">14<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">8(57.1)<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">6(42.9)<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center; width: 25%;\" width=\"25%\">43\u201347<\/td>\n<td style=\"text-align: center; width: 10%;\" width=\"10%\">6<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">6(100.0)<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">0(0)<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center; width: 25%;\" width=\"25%\">48\u201352<\/td>\n<td style=\"text-align: center; width: 10%;\" width=\"10%\">4<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">2(50.0)<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">2(50.0)<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center; width: 25%;\" width=\"25%\">\u00a0\u00a0\u00a0\u00a0 \u2265 53<\/td>\n<td style=\"text-align: center; width: 10%;\" width=\"10%\">2<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">0(0)<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\">2(100.0)<\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\"><\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: center; width: 25%;\" width=\"25%\"><strong>Total<\/strong><\/td>\n<td style=\"text-align: center; width: 10%;\" width=\"10%\"><strong>184<\/strong><\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\"><strong>100(54.3)<\/strong><\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\"><strong>84(45.7)<\/strong><\/td>\n<td style=\"text-align: center; width: 21%;\" width=\"21%\"><strong>\u00a0<\/strong><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<table style=\"width: 575px; height: 183px; margin-top: 20px;\" border=\"0\">\n<tbody>\n<tr>\n<td class=\"rowlight\" style=\"width: 175px;\"><img decoding=\"async\" class=\"alignnone size-thumbnail wp-image-63278\" src=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2025\/01\/Vol17No4_Pre_Ahm_Fig1-150x150.jpg\" alt=\"\" width=\"150\" height=\"150\" srcset=\"https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2025\/01\/Vol17No4_Pre_Ahm_Fig1-150x150.jpg 150w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2025\/01\/Vol17No4_Pre_Ahm_Fig1-250x250.jpg 250w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2025\/01\/Vol17No4_Pre_Ahm_Fig1-256x256.jpg 256w, https:\/\/biomedpharmajournal.org\/staging\/wp-content\/uploads\/2025\/01\/Vol17No4_Pre_Ahm_Fig1.jpg 718w\" sizes=\"(max-width: 150px) 100vw, 150px\" \/><\/td>\n<td class=\"rowdark\"><strong>Figure 1: Seroprevalence of HSV-2 with the occupational status of patients<\/strong><a href=\"https:\/\/biomedpharmajournal.org\/wp-content\/uploads\/2025\/01\/Vol17No4_Pre_Ahm_Fig1.jpg\" target=\"_blank\" rel=\"noopener\">Click here to View Figure<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Concerning knowledge of HSV-2, results showed that 91.3% (168\/184) patients did not know the virus at all and only 8.7% or n =16\/184 ever heard of genital herpes. Seventy-five percent (12\/16) of 19 who were aware had HSV-2, compared to over half of the total population at risk unaware124(88\/168), P = 0.220. Three patients had heard about HSV-2 during hospital visits, to a school lecture and 1 patient learnt from life.<\/p>\n<p>In terms of possible risk factors for HSV-2 infection, the analysis associated with HSV-2 in this study was (p&gt; 0.05). The seroprevalence of HSV-2 was found in 60% (18\/30) and 51.6% (32\/62), between patients not sexually active and those that were engaged to be sex-active, respectively-p = 0.449 Fifty-two percent (32\/61) of those with only one partner and 100% of the patient who reported multiple partners were seropositive, respectively (p =.538). Of the 10 (19.6%) patients who reported placing only partial vaginal penetration, five seroconverted within six months of potential exposure and all were positive for HSV-2 IgG at their follow-up visit; two others had been positive, to begin with, while three stayed non-reactive in both analyses.<\/p>\n<p><strong>Discussion<\/strong><\/p>\n<p>Over half (100\/184; 54.3%) of the patients presenting with fever were seropositive for HSV-2 in this study. This rate is consistent with 59% and 47.3% seroprevalence rates, found in previous Nigeria-based studies <sup>17, 18<\/sup>. This, however, is lower than the seroprevalence rates of 87% and 77.8% reported in Jos and Enugu, Nigeria respectively<sup>19, 20<\/sup>, but higher than the 16.5 % recorded from research done in the\u00a0United States <sup>21<\/sup>. The number of seropositive patients is indicative that many are probably unaware of their infection because HSV-2 infections often remain asymptomatic. They are consequently a population with increased susceptibility to HIV because HSV-2 infection can be expected. HSV-2 establishes a lifelong infection with periods of recurrent disease, leaving such patients reservoirs for the\u00a0virus. The presence of anti-HSV antibodies helps diagnose persons who are\u00a0carrying the infection. Secondly, patients co-infected with HIV might develop more frequent recurrent fevers caused by HSV-2 reactivation. These patients find it challenging to cope with this condition, which manifests in a combination of medical, psychological, and social symptoms.<\/p>\n<p>In this study, the highest seroprevalence of HSV-2 was found to be among those aged 43\u201347 years, which is to some degree like another finding in a Jos-based study as well, where participants within an age range of 51\u201360 had the highest prevalence. As observed in other countries and previous studies conducted in Nigeria, the prevalence of HSV-2 increases with age. <sup>9, 22<\/sup>. Similarly, based on research in Brazil. <sup>5<\/sup>, Croatia <sup>23<\/sup>, India <sup>24<\/sup>, Morocco, and Sri Lanka <sup>25<\/sup>, age is strongly associated with a greater prevalence of HSV-2. Moreover, the seroprevalence was found higher among males than females in this study, consistent with previous reports. This could be related to more frequent sexual activity or a higher number of sex partners among men. In contrast, other research has shown increased HSV-2 in women relative to men.<\/p>\n<p>We also found an even higher seroprevalence among single patients than married ones again, in line with studies from the United States<sup>26<\/sup>. This is the case in Kenya and Nigeria, where high sexual activity outside of marriage with a mix of one or more sex partners per month increases exposure to commercial workers<sup>27<\/sup>. Patients self-identifying as nonsexual active were more likely to be seropositive for HSV-2 than those with sexual activity; all the other patients, save one person who had several partners, tested negative. Many studies have proposed that sexual transmission of the virus occurs, and there is an association between having more sex partners and having higher HSV-2 seropositivity<sup>28-30<\/sup>. Seroconversion was higher in unprotected cases compared to those who did, contrary to previous reports on the use of protection.<\/p>\n<p><strong>Conclusion<\/strong><\/p>\n<p>Conclusions Our results since 54.3% of\u00a0patients reacted positively in the\u00a0serology test with no signs or symptoms related to infection detected during physical examination. They are therefore silent virus carriers. HSV-2 infection was not significantly associated with the socio-demographic background and predisposing risk factors assessed in the study. The public health implications of HSV-2 in Nigeria are highlighted by the results, given that anti-HSV-2 testing is not generally available and infants would be at high risk from neonatal transmission with possible complications during delivery. Public awareness and information on genital herpes, the many ways by which it may be transmitted and its public health importance based on high seroprevalence of HSV-2 in this study is necessary. Future research should focus on whether patients with frequent fever need to be investigated for HSV-2 antibodies and such studies can reveal findings that are statistically significant if done in a larger study population. As the treatment of HSV-2 is lifelong and there is no known cure, primary prevention plays a crucial role in controlling it.<\/p>\n<p><strong>Acknowledgement<\/strong><\/p>\n<p>The author wishes to thank Zarqa University, Jodan for providing support in publishing this manuscript.<\/p>\n<p><strong>Funding Sources<\/strong><\/p>\n<p>The author(s) received no financial support for the research, authorship, and\/or publication of this article.<\/p>\n<p><strong>Conflict of Interest<\/strong><\/p>\n<p>The author(s) do not have any conflict of interest.<\/p>\n<p><strong>Data Availability Statement<\/strong><\/p>\n<p>This statement does not apply to this article.<\/p>\n<p><strong>Ethics Statement<\/strong><\/p>\n<p>The ethical approval to conduct this research was obtained from Specialist Hospital, Sokoto Research Ethics Committee (SHS\/SUB\/145\/Vol2)<\/p>\n<p><strong>Informed Consent Statement<\/strong><\/p>\n<p>Informed consent was obtained from all patients before experimentation. The protection of human subjects&#8217; privacy rights should always be maintained.<strong>\u00a0<\/strong><\/p>\n<p><strong>Clinical Trial Registration<\/strong><\/p>\n<p>This research does not involve any clinical trials<\/p>\n<p><strong>Author Contributions<\/strong><\/p>\n<p>Ahmed Subeh Alshrari: Conceptualization, Methodology, Writing \u2013 Original Draft.<\/p>\n<p>Shuaibu Abdullahi Hudu: Data Collection, Analysis, Writing \u2013 Review &amp; Editing.<\/p>\n<p>Abdulgafar Olayiwola Jimoh: Visualization, Supervision, Project Administration.<\/p>\n<p>Bahaa Mohammed Badr: Funding Acquisition, Resources, Supervision.<\/p>\n<p><strong>References<\/strong><\/p>\n<ol>\n<li>Maris AS, Tao L, Schmitz JE: Herpes simplex viruses. 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Sexually transmitted infections in the context of haematological malignancies. <em>The Lancet Haematology<\/em>. 2024;11(10):e792-802.<br \/>\n<a href=\"https:\/\/doi.org\/10.1016\/S2352-3026(24)00210-2\">CrossRef<\/a><\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>Introduction Herpes simplex virus (HSV) is a double-stranded DNA genera  [&#8230;]<\/p>\n","protected":false},"author":15,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[119],"tags":[],"class_list":["post-63275","post","type-post","status-publish","format-standard","hentry","category-vol17no4"],"_links":{"self":[{"href":"https:\/\/biomedpharmajournal.org\/staging\/wp-json\/wp\/v2\/posts\/63275","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/biomedpharmajournal.org\/staging\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/biomedpharmajournal.org\/staging\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/biomedpharmajournal.org\/staging\/wp-json\/wp\/v2\/users\/15"}],"replies":[{"embeddable":true,"href":"https:\/\/biomedpharmajournal.org\/staging\/wp-json\/wp\/v2\/comments?post=63275"}],"version-history":[{"count":5,"href":"https:\/\/biomedpharmajournal.org\/staging\/wp-json\/wp\/v2\/posts\/63275\/revisions"}],"predecessor-version":[{"id":63520,"href":"https:\/\/biomedpharmajournal.org\/staging\/wp-json\/wp\/v2\/posts\/63275\/revisions\/63520"}],"wp:attachment":[{"href":"https:\/\/biomedpharmajournal.org\/staging\/wp-json\/wp\/v2\/media?parent=63275"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/biomedpharmajournal.org\/staging\/wp-json\/wp\/v2\/categories?post=63275"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/biomedpharmajournal.org\/staging\/wp-json\/wp\/v2\/tags?post=63275"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}