Article:Prevalence of asymptomatic Zika virus infection: a systematic review. (5996208)
This page is the ScienceSource HTML version of the scholarly article described at https://www.wikidata.org/wiki/Q55084346. Its title is Prevalence of asymptomatic Zika virus infection: a systematic review. and the publication date was 2018-06-01. The initial author is Michelle M Haby.
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Title: Bulletin of the World Health Organization
Prevalence of asymptomatic Zika virus infection: a systematic reviewPrévalence des infections à virus Zika asymptomatiques: revue systématiquePrevalencia de la infección asintomática del virus de Zika: una revisión sistemáticaانتشار عدوى فيروس زيكا غير المصحوب بظهور أعراض: مراجعة منهجية 无症状塞卡病毒感染的患病率：系统评审Распространенность бессимптомной инфекции, вызываемой вирусом Зика: систематический обзор
Alternative Title: Michelle M Haby et al.
Alternative Title: Asymptomatic Zika virus prevalence
- Michelle M Haby
- Mariona Pinart
- Vanessa Elias
- Ludovic Reveiz
Publication date (ppub): 6/2018
Publication date (epub): 4/2018
To conduct a systematic review to estimate the prevalence of asymptomatic Zika virus infection in the general population and in specific population groups.
We searched PubMed®, Embase® and LILACS online databases from inception to 26 January 2018. We included observational epidemiological studies where laboratory testing was used to confirm positive exposure of participants to Zika virus and in which Zika virus symptom status was also recorded. We excluded studies in which having symptoms of Zika virus was a criterion for inclusion. The main outcome assessed was percentage of all Zika virus-positive participants who were asymptomatic. We used a quality-effects approach and the double arcsine transformation for the meta-analysis.
We assessed 753 studies for inclusion, of which 23 were included in the meta-analysis, totalling 11 305 Zika virus-positive participants. The high degree of heterogeneity in the studies (I2 = 99%) suggests that the pooled prevalence of asymptomatic Zika virus-positive participants was probably not a robust estimate. Analysis based on subgroups of the population (general population, returned travellers, blood donors, adults with Guillain–Barré syndrome, pregnant women and babies with microcephaly) was not able to explain the heterogeneity. Funnel and Doi plots showed major asymmetry, suggesting selection bias or true heterogeneity.
Better-quality research is needed, using standardized methods, to determine the true prevalence of asymptomatic Zika virus and whether it varies between populations or over time.
By 25 May 2017, 48 countries and territories in the Americas had confirmed autochthonous, vector-borne transmission of Zika virus disease and 26 had reported confirmed cases of congenital syndrome associated with the infection. Symptoms are often very mild or not present. When symptomatic, the infection may include rash, fever, arthralgia and conjunctivitis. Zika virus infection during pregnancy is a cause of congenital Zika syndrome and it may also be a trigger for Guillain‒Barré syndrome.,
It has been widely reported that approximately 80% of people with Zika virus infection are asymptomatic. This statement is based on a household survey on Yap State in 2007 that has been cited in many publications on Zika virus. Among 557 residents who provided blood samples, 414 had immunoglobulin (Ig) M antibody against Zika virus and 156 of these (38%) reported an illness that met the definition for suspected Zika virus disease. However, 27 (19%) of the 143 residents who had no detectable IgM antibody against Zika virus also reported an illness that met the definition for suspected Zika virus disease. The authors concluded that, among participants who had IgM antibody against Zika virus, a total of 19% (38% minus 19%) had symptoms that were likely due to the Zika virus infection. When adjusted to the total Yap population aged 3 years or older, the authors estimated that 18% of those infected (95% confidence interval, CI: 10‒27%) had a clinical illness that was probably attributable to Zika virus. From these data we, and other authors, concluded that 82% of the population infected with Zika virus were asymptomatic.
Lack of signs and symptoms of Zika virus infection does not necessarily imply protection from potential complications, such as microcephaly in babies and Guillain‒Barré syndrome in adults. This has implications for surveillance, treatment and research efforts. For example, an analysis was conducted of pregnancies completed between 15 January and 22 September 2016, and recorded in the United States Zika pregnancy registry. Among women with laboratory evidence of Zika virus infection, there was no difference in the prevalence of birth defects in babies born to asymptomatic (16/271, 6%; 95% CI: 4–9%) or symptomatic women (10/167, 6%; 95% CI: 3–11%). Thus, if the asymptomatic pregnant women had not been included in Zika virus surveillance the 16 babies born with birth defects may not have been attributed to Zika virus.
Currently, with the exception of asymptomatic pregnant women, only people with suspected infection (i.e. symptomatic) generally undergo laboratory testing for Zika virus infection as part of national surveillance efforts. Thus, the true prevalence of infection and related complications is likely to be underestimated and biased towards those who seek care or develop a viral disease in response to infection. Knowing the prevalence of asymptomatic Zika virus infection is important for assessing the effectiveness and cost‒effectiveness of interventions, including vaccines, to prevent or treat infection. The prevalence is also needed for decision-making about the value of scaling-up surveillance efforts.
The aim of the current review was to estimate the prevalence of asymptomatic Zika virus infection in the general population and in specific population groups from observational epidemiological studies.
We used systematic review methods, including a meta-analysis., We registered the protocol on the International prospective register of systematic reviews (CRD42017059342) and followed the Preferred Reporting Items for Systematic Reviews and Meta-Analysis statement for reporting.
We included general or specific population-based studies of participants of all ages and from any country: pregnant women, newborns and infants, children, adults, newborns with congenital abnormalities, and adults with Guillain‒Barré syndrome and other neurological diseases.
We included studies if exposure to Zika virus was identified, using molecular or serological methods. We used the Pan American Health Organization (PAHO),World Health Organization (WHO) guidelines for laboratory testing wherever possible., For a confirmed case these guidelines require: (i) presence of ribonucleic acid or Zika virus antigen in any specimen (serum, urine, saliva, tissue or whole blood) tested by reverse-transcriptase polymerase chain reaction method; or (ii) positive anti-Zika virus IgM antibodies and plaque reduction neutralization test for Zika virus titres ≥ 20 and four or more times higher than for other flaviviruses; and exclusion of other flavivirus; or (iii) in autopsy specimens, detection of the viral genome (in fresh or paraffin tissue) by molecular techniques, or detection by immunohistochemistry. In practice, this definition was often not used in studies, especially in earlier research. We therefore included studies using alternative definitions for positive laboratory testing if the definition was clearly stated. One alternative definition was the PAHO‒WHO guideline for probable cases: presence of Zika IgM antibodies, with no evidence of infection with other flaviviruses.
We defined the primary outcome measure as percentage of all Zika virus-positive participants who were asymptomatic at the time of laboratory testing, or within 7 to 10 days of testing. The denominator was all participants who were Zika virus-positive. For the numerator, the PAHO‒WHO guidelines for signs and symptoms were used wherever possible, which require patients to have rash (usually pruritic and maculopapular) with two or more of the following signs or symptoms: fever, usually < 38.5 °C; conjunctivitis (non-purulent/hyperemic); arthralgia; myalgia; and/or periarticular oedema. In practice, not all studies used the PAHO‒WHO definition and we included studies using alternative definitions for symptoms if a clear definition was provided. Asymptomatic Zika virus-positive participants were those with no symptoms or with symptoms that did not meet the definition used for the particular study.
We included cross-sectional seroprevalence studies, cohort studies of pregnant women, cohort studies of newborns and infants, case‒control studies of Guillain‒Barré syndrome and other neurological diseases, case‒control studies of microcephaly and case series with at least 20 participants. The cut-off value of 20 participants for case series was chosen as a reasonable minimum number for which prevalence data can be reported. A cross-sectional seroprevalence study in the general population is the most appropriate design to determine the prevalence of asymptomatic Zika virus infection. However, to make use of the limited information that was available, we chose to include other study designs and other populations. Published and completed unpublished studies were eligible for inclusion. Data from ongoing studies were also eligible for inclusion when results from a representative sample were available.
Publications in English, French, Spanish or Portuguese were included. There was no restriction on year of publication.
We excluded studies in which having symptoms of Zika virus was a criterion for inclusion of participants in the study. This is because it would give a biased value for percentage asymptomatic of 100% solely due to the inclusion criteria. We also excluded studies where the percentage of participants who were asymptomatic could not be determined.
The search strategy and keywords used are shown in Box 1. The titles and abstracts of these references were checked by one author against the inclusion criteria. Additional published articles were also identified through separate manual searches of PubMed® and revision of Zika virus article alerts by another author. The full text of any potentially relevant papers were checked by a second author and disagreements resolved by discussion and consultation with a third author. Papers excluded after review by a second reviewer and discussions between reviewers were detailed in a table, together with the reason for their exclusion. We also made contact (by email or in-person at key Zika virus meetings) with known research groups conducting cross-sectional studies of Zika virus. These groups were identified through the PAHO‒WHO Zika virus research platform, which includes research protocols that detail ongoing research related to the virus.Box 1
Search strategy for the systematic review of the prevalence of asymptomatic Zika virus infection
We searched PubMed®, Embase® and LILACS online databases from inception to date of search (4 November 2016, updated 7 March 2017 and 26 January 2018) using the term “zika” as text word for PubMed® and LILACS and “zika” as keyword (zika.mp) for Embase® (Ovid). References were imported into EndNote version X7 reference management software (Clarivate Analytics, Philadelphia, United States of America). The search was then limited using the terms: (cohort OR case control OR case-control OR series OR prospective OR retrospective OR longitudinal OR cross-sectional OR cross sectional OR observational OR transversal OR seroprevalence OR prevalence OR asymptomatic) in any field and then checked for duplicates.
We extracted qualitative information into a Word version 14 table and quantitative data into an Excel version 14 spreadsheet (Microsoft Corporation, Redmond, USA). One author extracted the data and another author checked it: disagreements were resolved by discussion and consultation with a third author where necessary. We extracted the following data: country of study; region within the country; study design (cross-sectional, cohort, case‒control, case series); population (all ages, pregnant women, newborns and infants, newborns with congenital abnormalities, adults, adults with Guillain‒Barré syndrome); age range; period of study; definition of Zika virus positive according to laboratory tests; definition of symptomatic and asymptomatic Zika virus; preferential recruitment of participants with symptoms (yes/no); sample size calculation; and comments.
Quantitative data extracted included: response rate; total number of participants; total number classified as Zika virus positive; number of Zika virus-positive participants classified as symptomatic and as asymptomatic; and percentage of the total sample who were symptomatic at time of recruitment. For the cohort studies we used Zika virus-positive status at any time during the pregnancy (for studies of pregnant women) or any time during the study (for studies of newborns and infants). We extracted quantitative data for relevant subgroups where the data and sample size allowed, including for population subgroups and different definitions of Zika virus exposure.
The quality of the included studies was assessed independently by two authors using the critical appraisal checklist for prevalence studies, developed by The Joanna Briggs Institute. This tool includes the same dimensions as the Assessing Risk of Bias in Prevalence Studies tool, but was considered more useful for this review as it is applicable to a variety of study designs. The Joanna Briggs Institute tool also includes extra items related to sample size and subgroups. Disagreements were resolved by discussion and consultation with a third author where necessary.
We summarized the findings from the included studies in numerical and narrative tables. We conducted quality-effects meta-analysis using MetaXL version 5.3 (Ersatz, EpiGear International, Sunrise Beach, Australia) and the double arcsine transformation of prevalence.– We assessed heterogeneity using the Q and I2 statistics. We used Doi plots and the Luis Furuya‒Kanamori index to evaluate the presence of small-study effects, where asymmetry can indicate publication or other biases. A symmetrical mountain-like plot with values of the Luis Furuya-Kanamori index within ± 1 indicates no asymmetry; between ± 1 and ± 2 indicates minor asymmetry; and exceeding ± 2 suggests major asymmetry. Due to the high degree of heterogeneity in the results, we also checked whether the heterogeneity could be explained by population subgroups. The number of included studies was insufficient for testing multiple subgroups. We also tested the sensitivity of the results to excluding the largest study and to using the actual sample figure, rather than the population estimate reported by the authors that accounts for symptoms not attributable to Zika virus infection.
We identified a total of 960 records from database searches and another 12 records through other sources (Fig. 1). No unpublished or in-process studies were identified. After screening, we assessed 64 full-text articles for eligibility (Fig. 1) and excluded 36 articles– for various reasons (Table 1). No studies were excluded due to language restrictions. A total of 23 studies from 28 articles met the inclusion criteria for the review (Table 2; available at: http://www.who.int/bulletin/volumes/96/6/17-201541).,,–Fig. 1
Flow diagram of selection of articles for the systematic review of the prevalence of asymptomatic Zika virus infection
a Further restrictions were applied using Endnote reference management software (Clarivate Analytics, Philadelphia, United States of America; Box 1).Table 1
Reasons for exclusion of studies from the systematic review of the prevalence of asymptomatic Zika virus infection
PCR: polymerase chain reaction.Table 2
Characteristics of studies included in the systematic review of the prevalence of asymptomatic Zika virus infection
|Study, author and year of primary referencea||Country or territory||Population||Study design||Definition of Zika virus positive||Definition of symptomatic Zika virus||Risk of bias scoreb|
|Duffy et al., 20094||Federated States of Micronesia (Yap State)||General population||Cross-sectional||Evidence of recent infection: positive for IgM antibody against Zika virus by ELISA in serum||Defined as acute onset of generalized macular or papular rash, arthritis or arthralgia, or non-purulent conjunctivitis||8|
|Musso et al., 201455,56||French Polynesia||Blood donors||Cross-sectional||Positive to Zika virus nucleic acid test in serum by real-time RT–PCRc||Not defined. Blood donors who were Zika-virus positive were telephoned and asked about “Zika fever-like syndrome” (rash, conjunctivitis, arthralgia) after their donation||7|
|Adams et al., 201657||USA (Puerto Rico)||Pregnant women||Case series (surveillance)||Confirmed case: positive by RT–PCR in blood or urine. Presumptive case: positive Zika virus IgM by ELISA and negative dengue virus IgM by ELISA, or positive Zika virus by MAC-ELISA in a pregnant woman||Not defined||5|
|Araujo et al., 201658||Brazil (metropolitan region of Recife)||Cases: neonates with microcephaly.Controls: live neonates without microcephaly, with no brain abnormalities or birth defects||Case–control||Positive by RT–PCR or IgM serum test of mothers and neonates||Not defined. Presence of maternal rash was reported||8|
|Cao-Lormeau et al., 201659||French Polynesia||Cases: adults with Guillain–Barré syndrome.(Controls: excluded because no data on Zika symptoms were reported)||Case–control||Presence in serum of PRNT antibodies for Zika virus and anti-Zika virus IgG or IgM||Not defined. Described as recent history of viral syndrome before onset of neurological symptoms. Participants’ most commonly reported rash, arthralgia and fever||9|
|Dasgupta et al., 201660||USA||Travellers;d pregnant women travellersd||Case series (surveillance)||Confirmed case: detection of Zika virus RNA by RT–PCR or; anti-Zika IgM antibodies by ELISA with neutralizing antibody titres against Zika virus, at levels ≥ 4-fold higher than those against dengue virus||Defined as at least one of the following: fever, rash, arthralgia, or conjunctivitis||5|
|de Laval et al., 201661||French Guiana||Travellersd||Cohort||Confirmed case: viral RNA detected by real-time PCR in blood or urine, or Zika virus IgM antibodies and neutralizing antibodies found in serum. Malaria excluded by thin and thick blood smears; dengue and chikungunya viruses excluded by blood real-time PCR||Not defined. All participants had cutaneous rash or other symptoms||3|
|Díaz-Menéndez et al., 201662,63||Spain (Madrid; one hospital)||Travellersd||Case series||Confirmed case: positive microneutralization antibodies and/or positive RT–PCR for RNA in urine, blood, semen or amniotic fluide||Not defined. Participants had one or more of: temperature > 38 °C, maculopapular rash, arthralgia, red eyes or headache||6|
|Leal et al., 201664||Brazil (Pernambuco; one hospital)||Babies with microcephaly||Case series||Positive by Zika virus-specific IgM capture ELISA in cerebrospinal fluid||Not defined. Presence and timing of maternal rash during pregnancy was reported||4|
|Pacheco et al., 201665||Colombia||Babies with possible microcephaly||Case series (surveillance)||Positive for Zika virus RNA in serum using RT–PCR and negative for syphilis, toxoplasmosis, other agents, rubella, cytomegalovirus and herpes virus tests, and normal karyotypes||Defined as fever and rash, plus at least one of the following symptoms: nonpurulent conjunctivitis, headache, pruritus, arthralgia, myalgia or malaise||6|
|Parra et al., 201666||Colombia (Cucuta, Medellín, Neiva, Barranquilla and Cali; six hospitals)||Adults with Guillain–Barré syndrome||Case series||Definite case: positive for Zika virus RNA in blood, cerebrospinal fluid or urine by RT–PCR. Probable case: positive ELISA for antiflavivirus antibodies in cerebrospinal fluid, serum or both, but negative RT–PCR for Zika virus and for the four dengue virus serotypes||Defined as onset of systemic symptoms by Pan American Health Organization case definition||6|
|Adhikari et al., 201767,68||USA (Dallas, Texas)||Pregnant women travellersd||Case series (screening)f||Probable case: positive by serum IgM test or real-time RT–PCR (serum or urine or both). Confirmation by serum PRNTg||Not defined. Participants’ symptoms included rash, fever, conjunctivitis and arthralgia||8|
|Aubry et al., 201769||French Polynesia||General population, including schoolchildren||Cross-sectional||Positive for Zika virus IgG in blood by recombinant antigen-based indirect ELISA (schoolchildren) or in serum by microsphere immunoassay (general population)||Not defined. Participants were asked “whether they had clinical manifestations suggestive of past Zika infection”||6|
|Flamand et al., 201770||French Guiana||Pregnant women||Cohort||Zika virus-positive by real-time RT–PCR in at least one blood or urine sample, or positive for Zika virus IgM antibodies in serum, irrespective of IgG resultsh||Defined as a clinical illness compatible with Zika virus in the 7 days before confirmation by RT–PCR or between the beginning of the outbreak and the date of laboratory diagnosis for IgM-positive cases. A compatible clinical illness was defined as at least one of the following symptoms: fever, a macular or papular rash, myalgia, arthralgia or conjunctival hyperaemia||9|
|Lozier et al., 201771||Puerto Rico||General population (within 100 m radius of the residences of 19 index cases)||Cross-sectional (household-based cluster investigations)||Current infection: detection of Zika virus nucleic acid by RT–PCR in any specimen (serum, urine or whole blood).Recent infection: detection of anti-Zika virus IgM antibody by ELISA in serum. Recent flavivirus infection: detection of both anti-Zika virus IgM and anti-dengue virus IgM antibodies by ELISA in a serum specimen, in the absence of Zika virus or dengue virus nucleic acid detection (results were a subset of recent Zika virus infection).Zika virus positivity: evidence of current or recent Zika virus or flavivirus infection||Defined as presence of rash or arthralgia||7|
|Meneses et al., 201772||Brazil||Babies with congenital Zika virus syndrome||Case seriesf||Zika virus-specific IgM tested by MAC-ELISA in cerebrospinal fluid. Positive results were followed by PRNT to confirm specificity of IgM antibodies against Zika virus and rule out cross-reactivity against other flaviviruses, including dengue||Defined as presence of symptoms related to a possible Zika virus infection during gestation: fever, maculopapular rash, arthralgia and conjunctivitis||4|
|Pomar et al., 201773,74||French Guiana (Western part)||Pregnant women.Babies with congenital Zika virus syndrome||Case series (screening)f||Positive by RT–PCR (using the RealStar® Zika kit; Altona Diagnostics GmbH, Hamburg, Germany) in blood or urine or both, or by anti-Zika virus antibody detection using an in-house (National Referral Centre) IgM and IgG antibody-capture ELISA||Not defined. Participants’ symptoms were fever, pruritus, erythema, conjunctivitis, arthralgia or myalgia||6|
|Reynolds et al., 20175,75||USA||Pregnant women||Case series (surveillance)f||Recent possible infection: based on presence of Zika virus RNA by nucleic acid test (e.g. RT–PCR) on any maternal, placental, fetal, or infant specimen (serum, urine, blood, cerebrospinal fluid, cord serum and cord blood); or serological evidence of recent Zika virus infection or recent unspecified flavivirus infection from a maternal, fetal or infant specimen (i.e. Zika virus PRNT titre ≥ 10 with positive or negative Zika virus IgM, and regardless of dengue virus PRNT titre). Infants with positive or equivocal Zika virus IgM were included, provided a confirmatory PRNT was performed on a maternal or infant specimen||Not defined||5|
|Rodo et al., 201776||Spain||Pregnant women travellersd||Case seriesf||Not defined. Reported as confirmed by RT–PCR, or probable by positive Zika virus-IgM or positive Zika virus neutralization tests (specimen type not reported)||Not defined. 13/17 symptomatic pregnant women had a rash||1|
|Rozé et al., 201777||France, Martinique||Adults with Guillain–Barré syndrome||Cohort||Recent infection: Zika virus nucleic acid detected by RT–PCR in any specimen (cerebrospinal fluid, urine and plasma); or serum antibodies to Zika virus detected by Zika virus MAC-ELISA, and negative IgM MAC-ELISA against dengue virus or positive for neutralizing antibodies against Zika virus||Not defined. Participants’ symptoms were described as “preceding arbovirus-like syndrome,” characterized by fever, headache, retro-orbital pain, nonpurulent conjunctivitis, maculopapular rash, arthralgia or myalgia||6|
|Shapiro-Mendoza et al., 201778||United States Territories and freely associated States||Pregnant women. Babies with ≥ 1 birth defect||Case series (surveillance)f||Recent possible infection: based on presence of Zika virus RNA by nucleic acid test (e.g. RT–PCR) on any maternal, placental, fetal, or infant specimen (serum, urine, blood, cerebrospinal fluid, cord serum and cord blood); or serological evidence of recent Zika virus infection or recent unspecified flavivirus infection (i.e. Zika virus PRNT titre ≥ 10 with positive or negative Zika virus IgM, and regardless of dengue virus PRNT titre). Infants with positive or equivocal Zika virus IgM were included, provided a confirmatory PRNT was performed on a maternal or infant specimen (serum, urine, and cerebrospinal fluid)i||Defined as one or more signs or symptoms consistent with Zika virus disease: acute onset of fever, rash, arthralgia or conjunctivitis||5|
|Stone et al., 201779||USA||Zika virus RNA-positive blood donors||Cohort||Blood compartments and body fluids (whole blood, plasma, urine, saliva and semen) were tested for Zika RNA by real time RT–PCR. Plasma samples were tested for Zika virus IgM and IgG antibodies (specimen type not reported)||Not defined. Participants developed “multiple Zika virus-related symptoms”||2|
|Shiu et al., 201880||USA||Pregnant women||Case series (screening)||PRNT was performed if real-time RT–PCR or IgM in serum or urine was positive. Women with non-negative Zika virus IgM, Zika virus PRNT > 10 and dengue virus PRNT < 10 were considered to be infected with Zika virus. Women with IgM-positive tests, but with PRNT results not yet available were also included||Not defined. Participants had “documented symptoms suspicious for Zika virus infection”||7|
ELISA: enzyme-linked immunosorbent assay; Ig: immunoglobulin; MAC-ELISA: IgM antibody capture enzyme-linked immunosorbent assay; RNA: ribonucleic acid; PRNT: plaque reduction neutralization test; RT–PCR: reverse transcription-polymerase chain reaction; USA: United States of America.
a If a study had more than one reference, we awarded one reference the status of primary reference.
b The risk of bias was measured using the critical appraisal checklist for prevalence studies developed by the Joanna Briggs Institute, which has a maximum score of 10. The risk of bias scores ranged from 1 to 9, with a mean score of 5.8.
c A sample was considered positive when amplification showed a cycle threshold value < 38.5. However, to avoid false-negative results due to the pooling, each minipool showing a cycle threshold value < 40 with at least one primer-probe set was controlled by individual RT–PCR. Even if the two primers-probe sets did not react with the four dengue virus serotypes, the specificity of the amplified product from two donors whose blood was Zika virus-positive by RT–PCR was controlled by sequencing.
d Travellers were those with recent travel to or from a Zika-affected area.
e A patient where the detection of RNA of Zika virus by means of a confirmed positive PCR (two positive PCRs designed with different genomic targets and similar sensitivity or in different aliquots of the same sample) was obtained, was considered as a confirmed case. The confirmation of positive cases by immunofluorescence tests requires positive results in microneutralization tests.
f The study was actually a cohort study but only the baseline data are used here.
g Serum IgM assay was performed by Dallas County Health and Human Services for specimens collected > 2 weeks after travel in asymptomatic and symptomatic pregnant women, up to 9 months after return from travel. Presumptive positive or equivocal serum IgM specimens were forwarded to the United States Centers for Disease Control and Prevention for confirmatory PRNT testing. Serum real-time RT–PCR for Zika virus RNA was performed by Dallas County Health and Human Services on any specimen collected within 4 weeks of symptom onset or within 6 weeks of return from travel. In August 2016, following release of the interim guidance for urine testing and evaluation of pregnant women, the authors implemented real-time RT–PCR testing of subsequent urine specimens for pregnant women with presumptive positive or equivocal serum IgM.
h Serology was done using an in-house MAC-ELISA (based on whole virus antigens obtained in cell culture and on hyperimmune ascitic fluid) at each trimester of pregnancy. The sensitivity of the test was evaluated in sera from 71 patients with Zika virus infection confirmed by real-time PCR between day 5 and day 20 after symptom onset, was 87% and increased to more than 98% for sera sampled after day 7 from symptoms onset. The specificity was very low in sera from people with confirmed acute dengue virus infection, but increased to more than 80% for a panel of sera-negative samples for all tested arboviruses.
i The use of PRNT for confirmation of Zika virus infection is not routinely recommended in Puerto Rico; dengue virus is endemic and cross-reactivity is likely to occur in most cases. In Puerto Rico, detection of Zika virus IgM antibodies in a pregnant woman, fetus or infant (within 48 hours after delivery) was considered sufficient to indicate recent possible Zika virus infection.
We found only three cross-sectional seroprevalence studies of the general population, which are considered to be the most appropriate design to measure prevalence. These included the original study of Yap State residents, Federated States of Micronesia, conducted in 2007, a study of the general population and schoolchildren in French Polynesia conducted in 2014–2015 and a study in 2016 of the general population living near 19 index cases in San Juan, Puerto Rico. The majority of the studies were case series from population health surveillance programmes,,,,, systematic screenings of an at-risk population, or hospital-based screenings of an at-risk population.,,,,, A cohort design was used in four studies,,,, a case‒control design in two studies,, and a cross-sectional study of blood donors in one study (Table 2).
There was considerable variation in the methods of laboratory testing and the definitions of Zika virus positivity used in the studies (Table 2). Also, few studies offered a definition for symptomatic or asymptomatic. Sample sizes in studies varied from 30 to over 9000 (Table 3).Table 3
Results of the systematic review of the prevalence of asymptomatic Zika virus infection
NA: not applicable.
a If a studied had more than one reference, we awarded one reference the status of primary reference. All study references are presented in Table 1.
b These data are shown in parentheses because they do not contribute to the primary result but were used in sensitivity analyses.
Note: We searched for studies published from inception of the databases until 26 January 2018.
The risk of bias scores ranged from 1 to 9 out of a possible total of 10, with a mean score of 5.8 (Table 2). The most common limitations were: sample not clearly representative of the population (18 studies); response rate not reported, or large number of non-responders (19 studies); and not accounting for confounding factors or failure to identify subgroup differences (17 studies). The three cross-sectional seroprevalence studies of the general population had risk of bias scores between 6 and 8.
The 23 studies included a pooled number of 11 305 participants positive for Zika virus, 6921 of whom were asymptomatic. Meta-analysis showed a combined prevalence of asymptomatic Zika virus of 61.8% (95% CI: 33.0–87.1%). However, there was substantial heterogeneity (Q = 3291, P < 0.001, I2 = 99%), suggesting that the pooled prevalence is probably not a robust estimate. Analysis based on subgroups of the population (general population, returned travellers, blood donors, adults with Guillain‒Barré syndrome, pregnant women or babies with microcephaly) was not able to explain the heterogeneity (Fig. 2). There was also significant heterogeneity within all subgroups.Fig. 2
Prevalence of asymptomatic Zika virus infection in the systematic review of the literature
CI: confidence interval.
Notes: We searched for studies published from inception of the databases until 26 January 2018. The forest plot shows percentage of participants who tested positive for Zika virus and were asymptomatic. Prevalence was estimated from the quality effects model and using the double arcsine transformation of prevalence. The dotted line represents the combined prevalence found in the meta-analysis (0.62).
Both the funnel plot (Fig. 3) and Doi plot (Fig. 4) showed major asymmetry. The most likely explanations for the asymmetry are selection bias, including publication bias, or true heterogeneity in the included studies. The largest study (population-adjusted sample: 6892; actual sample: 557) had a weight of 40.7% in the meta-analysis. Excluding this study completely removed the asymmetry (Luis Furuya-Kanamori index: 0.05) but not the heterogeneity (Q = 1484.5, P < 0.001, I2 = 98%). The study’s exclusion also resulted in a substantial reduction in the pooled estimate to 45.2% (95% CI: 28.9–62.0%) and a narrowing of the confidence intervals. When the actual sample figures from this study were used instead of the population-adjusted figures the resulting pooled estimate was 46.5% (95% CI: 31.2–62.2%), with major heterogeneity (Q = 1537.1, P < 0.001, I2 = 98%) but no asymmetry (Luis Furuya-Kanamori index: −0.57).Fig. 3
Funnel plot of publication bias in the systematic review of the prevalence of asymptomatic Zika virus infection
Note: The vertical line represents the combined effect size from the fixed effect meta-analysisFig. 4
Doi plot of publication bias in the systematic review of the prevalence of asymptomatic Zika virus infection
LFK: Luis Furuya-Kanamori.
Note: The vertical line represents the combined effect size from the quality effects meta-analysis.
Although we found 23 studies for this review, the high degree of heterogeneity in the studies made it difficult to form clear conclusions as to the true prevalence of asymptomatic Zika virus infection. Furthermore, subgroup analysis by population group was unable to explain the heterogeneity. While the prevalence of asymptomatic Zika virus infection appeared to be lower in returned travellers and adults with Guillain‒Barré syndrome, this could be due to the lack of representativeness of the samples, as those with symptoms are more likely to be tested.
The large variation in prevalence of asymptomatic Zika virus infection in the general population, which ranged from 29% (95% CI: 24–24%) in schoolchildren from French Polynesia to 82% (95% CI: 81–83%) in the general population of Yap State could be due to several reasons. One possibility could be the lack of representativeness of the French Polynesia sample as the response rate was not reported. A second possibility is that the population prevalence in Yap State was overestimated due to the method of assessing symptom status, which was done retrospectively and then adjusted for the percentage unlikely to be attributable to Zika virus infection. The high degree of sensitivity of the results to the removal of this study lends supports to this possibility. A third possibility is that differences in definitions of symptoms and criteria for Zika virus infection (including the diagnostic test used) could have led to differences in prevalence estimates. This possibility is supported by the lower prevalence of asymptomatic Zika virus infection in pregnant women with confirmed recent infection than in those with possible recent infection (42% versus 63%; Table 3) in the United States. Finally, the difference could be real.
The authors of a systematic review and meta-analysis of 55 influenza virus infection studies also found considerable heterogeneity in the proportion of asymptomatic infected persons. Despite the large number of studies, the heterogeneity could not be explained by the type of influenza, the laboratory tests used to detect the virus, the year of the study, or the location of the study. For Zika virus the amount and quality of the available evidence is insufficient to provide a single estimate of the prevalence of asymptomatic infection or to determine whether the heterogeneity found in this review is real.
In relation to the heterogeneity in prevalence, comparing two included studies that presented data on completed pregnancies from the United States Zika pregnancy registry and used similar surveillance methods is important., One study in the USA found an asymptomatic Zika virus infection prevalence of 63%; this is consistent with an earlier report of 61% from the same population, suggesting little variation over time. The other study was of completed pregnancies in United States Territories (American Samoa, Puerto Rico and United States Virgin Islands) and the Federated States of Micronesia and Marshall Islands and found a prevalence of asymptomatic Zika virus infection of 38%. If the difference is real or a result of differences in ascertainment of asymptomatic Zika virus infection is difficult to know. The registry is based on surveillance systems, which depend on testing in clinical practice and which can be affected by the care-seeking behaviour of the population. This raises the issue of the ability of surveillance systems to provide unbiased results for Zika virus research questions.
Although we included population subgroups in our meta-analysis there were insufficient data to study the effect of demographic variables on the prevalence of asymptomatic Zika virus. While three of the included studies reported on age, sex or geographical differences in symptomatic infection,– clear conclusions were not possible to make.
A key strength of this review was the use of high-quality systematic review methods. Limitations of the review include the small number of studies found, especially cross-sectional seroprevalence studies, and the heterogeneity in the methods used across studies. The majority of studies included in the review were based on population health surveillance or screening programmes, rather than good-quality research studies. Furthermore, the included studies used various definitions of Zika virus positivity and rarely offered a definition for Zika virus symptom status. A variety of laboratory tests were used with varying degrees of validity, which can lead to potential misclassification error. A particular issue for Zika virus infection is the serological cross-reactivity of current IgM antibody assays with dengue virus, among other flaviviruses., The potential effect on the results is not known. In several studies there was also a bias towards inclusion of participants with symptoms due to the criteria for population surveillance or because symptomatic people are more likely to seek health care (e.g. travellers returning from Zika virus-endemic areas).
One clear finding from this review is that, given the current state of the evidence, it is not possible to give an accurate figure for the prevalence of asymptomatic Zika virus. Nor is it known whether the prevalence varies between populations or over time. Better-quality research is needed to estimate prevalence in the general population and in specific population groups. The use of standardized protocols developed by WHO and partners, particularly the protocol for the cross-sectional seroprevalence study of Zika virus infection in the general population, will be important in this regard. The protocol aims to standardize the diagnostic tests and definitions used, as well as encouraging consistent reporting., Use of the protocol will ensure results can be compared across regions and countries and help to improve the quality of the studies by minimizing bias. In this way the results of studies will better inform future public health surveillance and interventions.
Michelle Haby was contracted by the Pan American Health Organization to work on the Zika virus research platform and support Zika virus research efforts during the initial stages of this review, including study selection.
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