Skip to main content
Advertisement
  • Loading metrics

Seroepidemiological investigation of COVID-19: A cross-sectional study in Jundiai, São Paulo, Brazil

  • Marília Jesus Batista ,

    Contributed equally to this work with: Marília Jesus Batista, Carolina Matteussi Lino, Carla Fabiana Tenani, Luciane Zanin, Andréa Tenório Correia da Silva, Monica Vannucci Nunes Lipay, Carolina de Lima Rossi, Jane Rodrigues Tonetti, Andréia Pinto de Souza, Fabiana Barrete de Alcântara Fredo, Evaldo Marchi

    Roles Conceptualization, Formal analysis, Methodology, Supervision, Writing – original draft, Writing – review & editing

    mariliajbatista@yahoo.com.br, mariliamota@g.fmj.br

    Affiliations Department of Community Health, Jundiai Medical School, Jundiaí, São Paulo, Brazil, Department of Health Sciences and Child Dentistry, Piracicaba Dental School, University of Campinas (UNICAMP), Piracicaba, São Paulo, Brazil

  • Carolina Matteussi Lino ,

    Contributed equally to this work with: Marília Jesus Batista, Carolina Matteussi Lino, Carla Fabiana Tenani, Luciane Zanin, Andréa Tenório Correia da Silva, Monica Vannucci Nunes Lipay, Carolina de Lima Rossi, Jane Rodrigues Tonetti, Andréia Pinto de Souza, Fabiana Barrete de Alcântara Fredo, Evaldo Marchi

    Roles Methodology, Writing – original draft, Writing – review & editing

    Affiliation Department of Health Sciences and Child Dentistry, Piracicaba Dental School, University of Campinas (UNICAMP), Piracicaba, São Paulo, Brazil

  • Carla Fabiana Tenani ,

    Contributed equally to this work with: Marília Jesus Batista, Carolina Matteussi Lino, Carla Fabiana Tenani, Luciane Zanin, Andréa Tenório Correia da Silva, Monica Vannucci Nunes Lipay, Carolina de Lima Rossi, Jane Rodrigues Tonetti, Andréia Pinto de Souza, Fabiana Barrete de Alcântara Fredo, Evaldo Marchi

    Roles Methodology, Writing – original draft, Writing – review & editing

    Affiliation Department of Health Sciences and Child Dentistry, Piracicaba Dental School, University of Campinas (UNICAMP), Piracicaba, São Paulo, Brazil

  • Luciane Zanin ,

    Contributed equally to this work with: Marília Jesus Batista, Carolina Matteussi Lino, Carla Fabiana Tenani, Luciane Zanin, Andréa Tenório Correia da Silva, Monica Vannucci Nunes Lipay, Carolina de Lima Rossi, Jane Rodrigues Tonetti, Andréia Pinto de Souza, Fabiana Barrete de Alcântara Fredo, Evaldo Marchi

    Roles Conceptualization, Methodology, Writing – review & editing

    Affiliation Department of Community Health, Jundiai Medical School, Jundiaí, São Paulo, Brazil

  • Andréa Tenório Correia da Silva ,

    Contributed equally to this work with: Marília Jesus Batista, Carolina Matteussi Lino, Carla Fabiana Tenani, Luciane Zanin, Andréa Tenório Correia da Silva, Monica Vannucci Nunes Lipay, Carolina de Lima Rossi, Jane Rodrigues Tonetti, Andréia Pinto de Souza, Fabiana Barrete de Alcântara Fredo, Evaldo Marchi

    Roles Conceptualization, Methodology, Writing – original draft, Writing – review & editing

    Affiliation Department of Community Health, Jundiai Medical School, Jundiaí, São Paulo, Brazil

  • Monica Vannucci Nunes Lipay ,

    Contributed equally to this work with: Marília Jesus Batista, Carolina Matteussi Lino, Carla Fabiana Tenani, Luciane Zanin, Andréa Tenório Correia da Silva, Monica Vannucci Nunes Lipay, Carolina de Lima Rossi, Jane Rodrigues Tonetti, Andréia Pinto de Souza, Fabiana Barrete de Alcântara Fredo, Evaldo Marchi

    Roles Conceptualization, Methodology, Writing – original draft, Writing – review & editing

    Affiliation Department of Community Health, Jundiai Medical School, Jundiaí, São Paulo, Brazil

  • Carolina de Lima Rossi ,

    Contributed equally to this work with: Marília Jesus Batista, Carolina Matteussi Lino, Carla Fabiana Tenani, Luciane Zanin, Andréa Tenório Correia da Silva, Monica Vannucci Nunes Lipay, Carolina de Lima Rossi, Jane Rodrigues Tonetti, Andréia Pinto de Souza, Fabiana Barrete de Alcântara Fredo, Evaldo Marchi

    Roles Conceptualization, Methodology, Project administration, Writing – original draft

    Affiliation Jundiaí City Hall Prefeitura Municipal de Jundiaí, Jundiaí, São Paulo, Brazil

  • Jane Rodrigues Tonetti ,

    Contributed equally to this work with: Marília Jesus Batista, Carolina Matteussi Lino, Carla Fabiana Tenani, Luciane Zanin, Andréa Tenório Correia da Silva, Monica Vannucci Nunes Lipay, Carolina de Lima Rossi, Jane Rodrigues Tonetti, Andréia Pinto de Souza, Fabiana Barrete de Alcântara Fredo, Evaldo Marchi

    Roles Conceptualization, Project administration, Supervision, Writing – original draft

    Affiliation Jundiaí City Hall Prefeitura Municipal de Jundiaí, Jundiaí, São Paulo, Brazil

  • Andréia Pinto de Souza ,

    Contributed equally to this work with: Marília Jesus Batista, Carolina Matteussi Lino, Carla Fabiana Tenani, Luciane Zanin, Andréa Tenório Correia da Silva, Monica Vannucci Nunes Lipay, Carolina de Lima Rossi, Jane Rodrigues Tonetti, Andréia Pinto de Souza, Fabiana Barrete de Alcântara Fredo, Evaldo Marchi

    Roles Supervision, Validation, Writing – original draft

    Affiliation Jundiaí City Hall Prefeitura Municipal de Jundiaí, Jundiaí, São Paulo, Brazil

  • Fabiana Barrete de Alcântara Fredo ,

    Contributed equally to this work with: Marília Jesus Batista, Carolina Matteussi Lino, Carla Fabiana Tenani, Luciane Zanin, Andréa Tenório Correia da Silva, Monica Vannucci Nunes Lipay, Carolina de Lima Rossi, Jane Rodrigues Tonetti, Andréia Pinto de Souza, Fabiana Barrete de Alcântara Fredo, Evaldo Marchi

    Roles Conceptualization, Methodology, Validation, Writing – original draft

    Affiliation Jundiaí City Hall Prefeitura Municipal de Jundiaí, Jundiaí, São Paulo, Brazil

  • Evaldo Marchi

    Contributed equally to this work with: Marília Jesus Batista, Carolina Matteussi Lino, Carla Fabiana Tenani, Luciane Zanin, Andréa Tenório Correia da Silva, Monica Vannucci Nunes Lipay, Carolina de Lima Rossi, Jane Rodrigues Tonetti, Andréia Pinto de Souza, Fabiana Barrete de Alcântara Fredo, Evaldo Marchi

    Roles Supervision, Validation, Writing – original draft, Writing – review & editing

    Affiliation Department of Community Health, Jundiai Medical School, Jundiaí, São Paulo, Brazil

Abstract

The dramatic increase in the number of COVID-19 cases has been a threat to global health and a challenge for health systems. Estimating the prevalence of infection in the population is essential to provide support for action planning. Within this scenario, the aim of the present study was to analyze the seroprevalence and associated factors of COVID-19 Jundiaí, São Paulo, Brazil. This cross-sectional study was conducted from June 1st to June 19th, 2020. The participants were patients with respiratory symptoms who sought Primary Care Units (UBS) (n = 1,181) and subjects recruited from randomly selected households by probability sampling (n = 3,065), as screening strategy. All participants, in both phases, were submitted to SARS-CoV-2 rapid antigen tests (IgG and IgM) and responded to a questionnaire including sociodemographic characteristics based on Behavioural Insights for COVID-19. Total seroprevalence (positive/negative) was the outcome and the independent variables were sociodemographic variables, health behavior and signs/symptoms. The chi-squared test was used for association analysis (p<0.05) and variables with p<0.20 were entered into the logistic regression model (p<0.05). A total of 1,181 subjects from the UBS and 3,065 from the selected households participated in the study. The seroprevalence was 30.8% in the UBS and 3.1% in the households. The adjusted logistic regression identified that lower educational level (OR 2.68; 95%CI 1.59–4.54), household member testing positive (OR 1.67; 95%CI 1.16–2.39), presence of anosmia (OR 3.68, 95%CI 2.56–5.28) and seeking UBS (OR 3.76; 95%CI 2.08–6.82) was risk factors to test positive for SARS-CoV-2. Estimating the seroprevalence in the population was important to know the disease extension that was higher than the notified cases. These results showed socioeconomic aspects associated with COVID-19 even adjusted by symptoms. Populational epidemiologic studies that investigate the associated factors of COVID-19 are relevant to plan strategies to control the pandemic.

Introduction

In December 2019, a novel type of human coronavirus denominated SARS-CoV-2 was identified in Wuhan, China, which spread quickly around the globe and led the World Health Organization (WHO) to declare the disease caused by it–COVID-19 –a pandemic on March 11, 2020 [13]. In Brazil, the first case of infection of the COVID-19 was detected in February 2020; on 15 March 2022, 20,928,008 cases and 584,421 deaths had been reported in the country, with the southeastern region accounting for the largest number of cases, with 39.03% of cases and 47.75% of deaths [4]. At the beginning, the city of São Paulo—capital of the State of São Paulo—was the epicenter but SARS-CoV-2 virus spread rapidly to the interior municipalities [5] such as Jundiaí/SP, located 57 kilometers away from the city of São Paulo. The first two COVID-19 cases in the city of Jundiaí were confirmed in March 2020 and the first death in April 2020. Currently (15 March 2022), the municipality has more than 74,000 confirmed cases, 1,760 of whom had died [6]. Jundiai was in 12th position in the COVID-19 ranking of the State of São Paulo, which has 645 municipalities, and is the 15th in the population size.

The dramatic increase in the number of cases and deaths due to the SARS COV-2 has become a threat to global health and a challenge for health systems because of the demand for health professionals, intensive care beds, mechanical ventilators, and personal protective equipment for professionals. In addition, the increase in cases represents a challenge for surveillance and healthcare systems and how the disease is notified in the country [79].

International organizations like the WHO, the World Federation of Public Health Associations, and the Centers for Disease Control and Prevention of the United States have developed and disseminated measures to reduce the spread of COVID-19, including hand hygiene, the use of face masks and personal protective equipment, particularly by health professionals (N95 mask, face shield, and safety glasses), and social distancing [7,1012]. Another WHO recommendation is the focus on screening, with testing and diagnosis of positive cases, in order to isolate infected individuals and to quarantine contacts [13].

Most of the studies that investigated the epidemiological profile of COVID-19 infection have focused on severe forms of the disease using data obtained from hospital admissions and notification forms [14,15]. In Brazil, a population study on the seroprevalence of COVID-19 carried out in three stages also investigated the asymptomatic population and individuals with subclinical symptoms and found a higher prevalence of the disease than that estimated by the number of cases reported at the beginning of the pandemic in the country [16]. Thus, epidemiological studies are relevant because the growing number of cases and deaths caused by COVID-19 have an impact in health systems and compromise their response capacity [16]. Population-based epidemiological studies are extremely important for estimating the prevalence of infection in the population and for identifying the frequency of cases with mild or subclinical symptoms and asymptomatic patients that did not seek a health service but could sustain the infection [13]. Seroepidemiological surveys using WHO standards are therefore of paramount importance to identify infected individuals and associated factors in order to support measures necessary for the treatment and definition of strategies for preventing and combating COVID-19 disease [17].

Within this context, the aim of the present study was to investigate the prevalence of COVID-19 seropositivity and the factors associated with it in the municipality of Jundiai, São Paulo, Brazil, before the introduction of the vaccine against COVID-19.

Materials and methods

Study location and design

This is a cross-sectional study conducted in the municipality of Jundiaí, State of São Paulo, Brazil, from June 1st to June 19th, 2020, as a cooperation between the Municipal Health Management and Promotion Department, and the School of Medicine of Jundiaí (FMJ). The data were collected simultaneously in two phases: at Primary Care Units (UBS in the Portuguese acronym) and at selected households (Fig 1).

thumbnail
Fig 1. Data collection procedure in studies conducted at the basic health units and households, Jundiaí, São Paulo, 2020.

The figure shows the steps of collection of the data obtained in the present study.

https://doi.org/10.1371/journal.pgph.0000460.g001

Jundiai/SP is a municipality in the state of São Paulo, Brazil. The estimated population in 2019 was 403,769 inhabitants [18]. The municipality is part of the 42 cities that belong to the Regional Department of Health III–Campinas and it is divide into seven administrative regions (Center, East, Northeast, Northwest, North, West, and South) and four health regions (regional I, regional II, regional III and regional IV), with a total of 35 health units [19]. According to the Brazilian Institute of Geography and Statistics (IBGE), the 2010 Human Development Index of the municipality was 0.822 [20], a value considered to be very high compared other Brazilian municipalities.

Sample size and sample selection

The estimated sample size for data collection at the UBS was 940 cases. This estimate was obtained assuming a prevalence of 10% among all symptomatic patients tested, an alpha of 0.05, and an odds ratio (OR) of 3.0, as well as a 95% confidence interval. Considering 20% of losses or dropouts, the final sample size was 1,175 participants.

For selection the sample, in this phase, it was calculated for each UBS a different number of participants, according to the weekly average number of rapid tests performed based in the period before the study (from April to May 2020) in order to considering the different size of the population the units attend. This data was obtained from the Health Secretary of the Municipality. The data collection at that unit was stopped when the number sample size was reached. All individuals that were scheduled at the health unit to carry out a rapid test (IgG and IgM for SARS-CoV-2) after 14 days the onset of flu-like symptoms were invited to participate of the study.

For the household phase, the estimated sample size was 1,067 households. This calculation assumed an estimated population of 400,000 inhabitants, an error margin of 3%, a prevalence of 50%, and an alpha of 5%. In this phase, 20% of losses or dropouts were also considered, resulting in a final sample of 1,333 households.

The participants were selected by probability sampling in which an updated list was first obtained from the Urban Property and Land Tax registration that contained all neighborhoods and their respective numbers of households. This list was used to calculate the initial sample size for each neighborhood–considering all neighborhoods in the municipality–with the probability being proportional to the number of households. Next, the households in each neighborhood that would compose the sample were randomly selected using Microsoft Excel (Fig 2). Due to the possibility of refusals and/or empty households, two substitutes were also drawn for each previously selected house.

thumbnail
Fig 2. Households selected for data collection, Jundiaí, São Paulo, Brazil, 2020 (n = 1,333).

The map shows the division of the municipality into neighborhoods and the distribution of the households randomly selected for the study. The base layer of the map is available in the Brazilian Institute of Geography and Statistics: https://www.ibge.gov.br/geociencias/organizacao-do-territorio/malhas-territoriais/15774-malhas.html?edicao=30138&t=downloads.

https://doi.org/10.1371/journal.pgph.0000460.g002

Inclusion criteria for both phases (UBS and households) were individuals who were residents in Jundiaí, signing the free informed consent form, having more than 18 years old. Having no symptoms at moment of the study. The exclusion criteria were subjects under the influence of alcohol and/or toxic substances that prevented them from completing the questionnaire were excluded.

Data collection

The health professionals were trained for application of the rapid tests. All members of the data collection teams participated of a training for the questionnaire and study design by the researchers during face-to-face-meetings and online, with a workload of 16 hours.

Data from UBS participants were collected at the health unit, when the patient scheduled at health unit to carry out a rapid test (14 days after the onset of flu symptoms). A person trained to applying the study’s questionnaire invited the patient to participate of the study and answering the questions, upon consenting to participate, and collected the result of the test (positive or negative).

Ten teams collected the data from the households. These teams consisted of a higher health professional (responsible for carrying out the rapid tests), a community health agent, and two medicine and/or nursing interns, with access to vehicles with sufficient space for organizing the material and carrying out the rapid tests.

In order to reach the sample size (n = 1,330), each team from the 10, received a spreadsheet with 133 households for invitation of the participants. Up to five rapid tests could be performed per household and one of the residents of legal age (more than 18 years old) was selected to answer the questionnaire. If there were more than five residents, the subjects to be tested were random selected by enumerating each resident. If they agreed to participate, elderly residents and individuals with risk comorbidities were automatically selected for the tests (because age and comorbidities are risk factors for severe COVID-19). If the result was positive, the participant was referred to a health service. In case of refusals and/or empty households, the team should go to the substitute-selected household, in the same location. All data on absences, substitutions and refusals were recorded to calculate the non-response rate.

In both phases–UBS and household–Vyttra Smart Test COVID-19 rapid tests were used for determination of the seroprevalence (sensitivity of 88.7% for IgM and 91.4% for IgG; specificity of 89.1% for IgM and 94.0% for IgG) [21]. These tests enable the qualitative and differential detection of SARS-CoV-2 IgM and IgG antibodies in serum, plasma or blood. The blood sample was obtained by fingerstick, and the test was performed according to manufacturer recommendation. In addition, the participants answered a questionnaire composed of 48 questions divided into five blocks: sociodemographic data (18 questions); symptoms, comorbidity and use of health services (13 questions); knowledge of the participant about the disease (5 questions); health behavior (9 questions) and the participant’s perceived impact of the pandemic (3 questions). The questionnaire was applied with the aid of a tablet. The instrument was based on the Behavioural Insights for COVID-19 tool recommended by the WHO [22]. It should be noted that all team members were properly dressed and the material for testing was stored in accordance with WHO recommendations [23].

Variables

The dependent variable was the presence of a positive rapid test result for COVID-19 (IgG and/or IgM), considering adjustment for the test location (UBS or household) based on the different sampling strategies.

The following independent variables were considered: (i) sociodemographic (age [13–17, 18–39, 40–59, 60 years or more], sex [female, male], self-reported race/skin color [white, mixed-race, black, yellow], educational level [illiterate, elementary school, high school, higher education, postgraduation], income in minimum wages [up to 1, 1 to 2, 2 to 3, 3 to 4, 5 or more, no income]); (ii) behavioral (routine affected by the pandemic [routine remained the same or routine was affected by the pandemic, leaving home only for essential needs], adherence to preventive measures [adhered to the use of mask, hand sanitizer and social distancing, did not adhere, or household members did not adhere], adherence to social distance [adhered to social distancing or did not adhere] and report of positive cases among household members [yes or no]); (iii) signs and symptoms (presence of signs and symptoms at the time of the test [yes or no], type of sign and symptom [yes or no for each sign or symptom]: fever, cough, runny nose, headache, body aches, tiredness, diarrhea, sore throat, shortness of breath/dyspnea, anosmia, taste disorders, nail lesions, and skin alterations).

The categories 13 to 17 years (age), yellow skin (skin color), and illiterate (educational level) of the sociodemographic variable were excluded from the bivariate and logistic regression analyses because of the small number of participants in these categories.

Statistical analysis

First, the data were submitted to descriptive analysis to calculate the frequency and percentage of responses. Next, bivariate analysis (Chi-square and Fisher’s exact test) was performed to compare the sample in the UBS and the households, and to evaluate the association between the outcome and the independent variables. For logistic regression, four blocks containing variables that showed p<0.20 in bivariate analysis were elaborated: 1) socioeconomic–age, income, skin color, and educational level; 2) test location–UBS or household; 3) behavior–routine affected by the pandemic, adherence to social isolation, and household member with a positive test; 4) symptoms–fever, tiredness, taste disorders, anosmia, shortness of breath/dyspnea, and sore throat. The final model was obtained by adjusting the blocks. The analyses were performed using SPSS 20.0 and a level of significance of 5% was adopted.

The study was approved by the Research Ethics Committee of the School of Medicine of Jundiaí on May 21, 2020, under number 4.040.674 (Ethical Clearance Certificate: 31748920.1.0000.5412). The data were collected after the participants had signed the free informed consent form (ICF).

Results

The data collection at the UBS included 1,181 subjects with respiratory symptoms who sought the health units for a consultation and rapid test for COVID-19. The seroprevalence found was 30.8%. Among the diagnosed subjects who answered the questionnaire, there was a predominance of women (63.7%), subjects with self-reported white skin color (67.2%), and subjects aged 18 to 39 years (52.8%).

In the household data collection step, 1,260 households were included, totaling 3,065 tested participants. The seroprevalence evidenced at this stage was 3.1% among all subjects tested. In each of the participating households, one resident was selected to apply the characterization instrument, totaling 1251 respondents. There was a higher prevalence of asymptomatic participants (97.2%), women (64.3%) and subjects with self-reported white skin color (72.3%). Regarding age, most participants were between 40 and 59 years old (39.7%). The age group over 60 years accounted for 33.1% (Table 1).

thumbnail
Table 1. Sociodemographic characteristics of the participants in the basic health unit and household samples of the seroepidemiological survey, Jundiai, São Paulo, June 1st to June 19th 2020 (n = 2,432).

https://doi.org/10.1371/journal.pgph.0000460.t001

The bivariate analysis between the test result and the independent variables showed an association between a positive result and age, skin color, educational level, adoption of social isolation, a positive result among household members and the presence of signs and symptoms. Regarding signs and symptoms, an association was observed between positive cases and tiredness, sore throat, anosmia, and taste disorders (Table 2).

thumbnail
Table 2. Bivariate analysis between the sociodemographic profile of the participants and the result of the serological test performed in the UBS and households, Jundiaí, 2020.

https://doi.org/10.1371/journal.pgph.0000460.t002

The final model obtained by adjusted logistic regression showed that participants with elementary and high school, as well as younger adults, had a higher risk to test positive for SARS-CoV-2. Despite significance in the behavioral block, adherence to social isolation was no longer significant in the final model. Regarding the type of sign and symptom, association was observed for anosmia and an inverse association for shortness of breath/dyspnea (Table 3).

thumbnail
Table 3. Logistic regression of sociodemographic factors, behavioral factors, signs, and symptoms of the participant undergoing serological testing in the UBS and households, Jundiaí, 2020.

https://doi.org/10.1371/journal.pgph.0000460.t003

Discussion

The prevalence of positive cases was higher among participants who sought the UBS than among participants from the selected households. The factors associated with seroprevalence (positive result) included education up to elementary school compared to higher education, a household member testing positive, anosmia (loss of smell), and seeking a UBS with symptoms. The present data demonstrate the importance of extensive testing, screening the population, not only consider the symptomatic who looking for health service, but also among asymptomatic, with subclinical or mild condition. Also, is important to verify associated factors that may help to identify the most prevalent group with the COVID-19 infection.

In Brazil, the spread of COVID-19 began in large capitals, where the SARS-CoV-2 virus spread from central regions to peripheral neighborhoods. Then, the displacement of the infected population between metropolises and into the interior of the states, including due to the health infrastructure, contributed to the internalization of the virus and the involvement of all strata of the population [5,24]. This internalization was identified in Jundiai, which showed an increase in the number of cases, reaching its peak in June 2020 and a heterogeneous distribution of cases, with a concentration in peripheral regions [25].

The seroprevalence identified in the present study showed that the presence of antibodies against SARS-CoV-2 was higher among the group in UBS because they were symptomatic individuals compared to individuals who were asymptomatic, in a probabilistic sample design, justifying the association with participants who sought care at the health services (UBS). These results allow us to observe that the prevalence among individuals who present signs and symptoms of the COVID-19 is higher compared to individuals who present no or very mild symptoms [26].

Among the households group it was evidenced that the presence of antibodies against SARS-CoV-2 corroborated with what was found in a serological survey carried out at national level [27] which observed, in both stages carried out, that seroprevalence increased from 1.9% to 3.1%. Comparing with the Northeast State (Maranhão) that found the prevalence of antibodies against SARS-CoV-2 of 40, 4% in the first phase of the study and 38.1% in its second phase, the present study results are lower [28]. A literature review carried out in 2020 also noted the presence of antibodies against SARS-CoV-2 among asymptomatic individuals in Iceland (43%) and Italy (41,1%) [29]. Despite the difference in methods between the studies, these data emphasize the importance of investigating the seroprevalence between the asymptomatic, because they may present a relevant percentage in the population and, may transmit the disease due the lack to diagnosis by the health services.

It is worth mentioning that, considering a population of 418,000 inhabitants in Jundiaí/SP, there were 9,008 seropositive cases, i.e., approximately three times the number of notifications to the Epidemiological Surveillance during the study period (2,951 cases). This difference between seroprevalence and notifications has also been identified in Rio Grande do Sul by the EPICOVID project, in which the number of people in whom antibodies were detected was 6 times greater than that of notified cases [30]. Within this context, population-based studies allow to estimate the real extent of infection and also demonstrate the importance of population testing, especially for identifying asymptomatic conditions or individuals with subclinical symptoms.

In the present study, the age profile found in the population consisted of an economically active group, and this result is similar to that found in the national seroepidemiological survey conducted by the University of Pelotas [27], with a higher prevalence among adults aged 20 to 59 years, however, was different from the profile found in a Brazilian study using national data [31] which identified a higher prevalence of positive cases among men with a mean age of 59 years. This difference may be due to the design of the study that used data of notified cases, which may correspond to the profile of more severe patients, excluding mild cases of COVID-19. This fact highlights the importance of population studies since younger people are considered an important group for contamination and transmission of the disease.

Another important sociodemographic aspect found was the higher seroprevalence was found among subjects with lower education, corroborating a study carried out in the United States, which, in addition to years of schooling, that study also reported an association with black skin color [32]. It is noteworthy that the present study also identified, in the bivariate analysis, black skin color as an associated factor; however, this variable lost significance after adjusting for the other factors in the logistic regression. This information indicates that, although COVID-19 affects all strata of the population, aspects of inequity must be highlighted with can also be related to people who have difficulty in social distancing and who need to leave home to go to work are more exposed. This reality also points to an important fact which deserve attention for health policies, because is described the current economic crisis that has been the largest since the Second World War, with millions of unemployed individuals and people in poverty [33]. In this way, public policies are needed to expand the opportunities of those who were economically more affected by the pandemic, considering that these individuals are also more exposed to infection and other diseases and put the population at risk [33].

In the present study, the prevalence of seropositivity was higher among participants with a familiar contact that tested positive. According to a study carried out in households in China, the household transmission rate was 16.3%, with age and spousal relationship being risk factors [34]. Contact with an infected individual increases the risk of infection and social distancing is therefore an important preventive measure [1012]. Quarantine of positive patients since the onset of symptoms is effective in preventing transmission and the occurrence of new cases.

Among the participants who tested positive, the anosmia was one of the associated factors identified in the present study, even, after adjusting the logistic regression models. However, anosmia appeared as a protective factor for the most severe forms of infection. The report of shortness of breath/dyspnea was identified as a protective factor, however, after adjusting the model with other regression factors, there was no significance in the present study. Other study carried out in primary care services in the region of Tarragona [35] identified anosmia as a protective factor for the critical outcome of the infection and dyspnea was associated with the risk of developing more severe forms of the disease, the inverse association we have found in the present study, probably this difference could be attribute to disease levels, mild and severe [35]. It is noteworthy that, from the present study, it was not possible to identify which variant of SARS-CoV-2 was circulating to be associated with the symptom of anosmia.

The behavior variables studied as social distance and use of masks were associated in bivariate analyses but didn’t remain after adjusted, considering the importance of sociodemographic factors associated with the COVID-19 in the present study. However, it is important to emphasize that these measures are essential to contain the pandemic [7].

This study was the result of cooperation between a teaching institution and the city hall, reinforcing the idea that the integration of scientific knowledge, health services and health management is necessary to achieve good public health outcomes in SUS [36]. Effective testing strategies are very important to efficiently utilize the tests and resources provided by the government for the detection and control of the coronavirus, in addition to providing results for a poorly studied population.

One limitation of this seroepidemiological survey was the difficult of training the teams for data collection and application of the tests in the pandemic context. The training of the volunteers in the application of the questionnaire and use of the app was a way to overcome this barrier. Other limitation was the different study design for sample selection in both groups, that contribute with the greater positivity in symptomatic individuals who seek the health service. Other important point to highlight is the sensitivity and specificity of the rapid test, that depends on the period of the onset symptoms, and it is not clear if the antibody tests are able to detect lower antibody levels likely seen with milder and asymptomatic COVID‐19 disease, which represents a challenge to screening the population [26].

Besides the limitation found, screening COVID-19 infection it was very important to plan measures of mitigation the pandemic, and rapid tests are easy and fast to apply and to obtain the result, making possible in populational studies to comprehend the extension of the infection in the location. However, the results should be interpreted carefully based on diagnostic method chosen.

This study contributed to the understanding of the seroprevalence of SARS-CoV-2, that was higher among symptomatic and asymptomatic individuals and to the identification of the epidemiological profile of the disease, as well as health behaviors related to the pandemic. Sociodemographic factors were associated with being positive for antibodies, and anosmia and having familiar who tested positive. Extensive COVID-19 testing is recommended as a preventive strategy. We highlight the importance of studies such as the present one that are representative of the population and that investigate factors associated with infection so that more accurate and comprehensive strategies can be implemented.

Acknowledgments

The authors thank the entire team of the Jundiaí City Hall, especially Luiz Fernando A. Machado, Tiago Texera, Fauzia A. A. Raiza, Ana Cláudia Marques B. Diaz, José Antônio Parimoschi, Roberto Araújo (in memoriam), Daniela Ap. Paganini, Örjan Olsén, Maria Carolina G. Zara, Felipe Risso, Daniela T. Zito, and Maria do Carmo Possidente. We also thank the teams of the health units and the students of Jundiai Medical School, Campo Limpo Paulista University Center and Anchieta University Center who participated in the data collection.

References

  1. 1. Dierz L, Horve PF, Coil DA, Fretz M, Eisen JA, Wymelenberg KVD. 2019 novel coronavirus (COVID-19) pandemic: built environment considerations to reduce transmission. mSphere. 2020; 5: e00245–20. pmid:32265315
  2. 2. Zhao S, Musa SS, Lin Q, Ran J, Yang G, Wang W, et al. Estimating the unreported number of novel coronavirus (2019-nCoV) cases in China in the first half of January 2020: a data-driven modelling analysis of the early outbreak. J Clin Med. 2020; 9 (2): 388. pmid:32024089
  3. 3. Organização Pan-Americana de Saúde. OMS afirma que COVID-19 é agora caracterizada como pandemia. 2020. https://www.paho.org/bra/index.php?option=com_content&view=article&id=6120:oms-afirma-que-Covid-19-e-agora-caracterizada-como-pandemia&Itemid=812.
  4. 4. Brasil. Ministério da Saúde. Painel Coronavírus 2020. https://covid.saude.gov.br/.
  5. 5. Nicolelis MAL, Raimundo RLG, Peixoto OS, Andreazzi CS. The impact of super spreader cities, highways, and intensive care availability in the early stages of the COVID 19 epidemic in Brazil. Sci Rep. 2021; 1: 13001. https://doi.org/10.1038/s41598-021-92263-3.
  6. 6. Prefeitura de Jundiaí. Boletim Epidemiológico–Novo Coronavírus. 2020. https://jundiai.sp.gov.br/coronavirus/.
  7. 7. Walker PGT, Whittaker C, Watson O, Baguelin M, Ainslie KEC, Bhatia S, et al. The Global Impact of COVID-19 and Strategies for Mitigation and Suppression. WHO Collaborating Centre for Infectious Disease Modelling, MRC Centre for Global Infectious Disease Analysis, Abdul Latif Jameel Institute for Disease and Emergency Analytics, Imperial College London. 2020.
  8. 8. Weston S, Frieman MB. COVID-19: Knowns, Unknowns, and Questions. mSphere. 2020; 5(2): e00203–20. pmid:32188753
  9. 9. Lana LM, Coelho FC, Gomes MFC, Cruz OG, Bastos LS, Villela DAM et al. The novel coronavirus (SARS-CoV-2) emergency and the role of timely and effective national health surveillance. Cad. Saúde Pública. 2020; 36(3): e00019620. pmid:32187288
  10. 10. World Health Organization. Novel Coronavirus (2019-nCoV): situation report 11–31 January 2020. 2020. https://www.who.int/docs/default-source/coronaviruse/situation-reports/20200131-sitrep-11-ncov.pdf?sfvrsn=de7c0f7_4.
  11. 11. Merchant RM, Lurie N. Social Media and Emergency Preparedness in Response to Novel Coronavirus. JAMA. 2020; 323(20):2011–2012. pmid:32202611
  12. 12. Nussbaumer-Streit B, Mayr V, Dobrescu AI, Chapman A, Persad E, Klerings I et al. Quarantine alone or in combination with other public health measures to control COVID-19: a rapid review. Cochrane Database Syst Rev. 2020; 4(4):CD013574. pmid:32267544
  13. 13. World Health Organization. Population-based age-stratified seroepidemiological investigation protocol for COVID-19 virus infection version, 17March 2020. https://www.who.int/publications-detail/population-based-age-stratified-seroepidemiological-investigation-protocol-for-covid-19-virus-infection.
  14. 14. Teich VD, Klajner S, Almeida FAS, Dantas ACB, Laselva CR, Torritesi MG et al. Epidemiologic and clinical features of patients with COVID-19 in Brazil. Einstein. 2020;18:eAO6022. pmid:32813760
  15. 15. Ranzani OT, Bastos LSL, Gelli JGM, Marchesi JF, Baião F, Hamacher S et al. Characterisation of the first 250,000 hospital admissions for COVID-19 in Brazil: a retrospective analysis of nationwide data. Lancet Respir Med. 2021 Apr;9(4):407–418. pmid:33460571
  16. 16. Hallal PC, Horta BL, Barros AJD, Dellagostin OA, Hartwig FP, Pellanda LC et al. Trends in the prevalence of COVID-19 infection in Rio Grande do Sul, Brazil: repeated serological surveys. Ciênc. saúde coletiva. 2020; 25 (suppl 1): 2395–2401. pmid:32520284
  17. 17. Ribeiro LC, Bernardes AT. Estimate of underreporting of COVID-19 in Brazil by acute respiratory syndrome hospitalization reports. 2020. https://www.scielo.br/revistas/ress/pinstruc.htm.
  18. 18. Fundação Sistema Educacional de Análise de dados. Sistema SEADE de projeções populacionais. 2020. http://produtos.seade.gov.br/produtos/projpop/.
  19. 19. Prefeitura de Jundiaí. Divisão de regiões e abairramento oficial, Jundiaí/SP. 2017. https://jundiai.sp.gov.br/assistencia-e-desenvolvimento-social/wp-content/uploads/sites/5/2017/05/MAPA_0.1.pdf.
  20. 20. Instituto Brasileiro de Geografia e Estatística. Censo demográfico 2010. https://www.ibge.gov.br/estatisticas/sociais/saude/9662-censo-demografico-2010.html?edicao=9758&t=resultados.
  21. 21. Brasil. Ministério da Saúde. Acurácia dos testes diagnósticos registrados na ANVISA para a COVID-19. 2020. https://portalarquivos2.saude.gov.br/images/pdf/2020/June /02/AcuraciaDiagnostico-COVID19-atualizacaoC.pdf.
  22. 22. World Health Organization. Survey tool and guidance rapid, simple, flexible behavioural insights on covid-19. 2020. Available at: http://www.euro.who.int/__data/assets/pdf_file/0007/436705/COVID-19-survey-tool-and-guidance.pdf?ua=1.
  23. 23. Pan American Health Organization. Requirements and technical specifications of personal protective equipment (PPE) for the novel coronavirus (2019-ncov) in healthcare settings. 2020. Available at: https://iris.paho.org/handle/10665.2/51906?show=full.
  24. 24. Albuquerque MV, Ribeiro LHL. Desigualdade, situação geográfica e sentidos da ação na pandemia da COVID-19 no Brasil. Cad. Saúde Pública 2020; 36(12): e00208720. https://doi.org/10.1590/0102-311X00208720.
  25. 25. Lino CM, Tenani CF, Batista MJ. COVID-19 in Jundiaí/SP: temporal dynamics of notifications and spatial analysis of seroepidemiological prevalence. Rev. epidemiol. controle infecç 2021; 11(2) https://doi.org/10.17058/reci.v11i2.15903.
  26. 26. Deeks JJ, Dinnes J, Takwoingi Y, Davenport C, Spijker R, Taylor-Phillips S et al. Antibody tests for identification of current and past infection with SARS‐CoV‐2. Cochrane Database of Syst Rev. 2020; 6(6):CD013652. pmid:32584464
  27. 27. Hallal PC, Hartwig FP, Horta BL, Silveira MF, Struchiner CJ, Vidaletti LP et al. SARS-CoV-2 antibody prevalence in Brazil: results from two successive nationwide serological household surveys. Lancet Glob Health.; 8(11): e1390–e1398. pmid:32979314
  28. 28. Governo do Maranhão. Secretaria do Estado da Saúde. Prevalência de infecção pelo vírus SARS-CoV-2 no Maranhão, Brasil: Relatório Final de Pesquisa—Fase II. https://www.saude.ma.gov.br/wp-content/uploads/2020/11/Inquerito-Sorologico-Maranhao-Fase-2.pdf.
  29. 29. Oran DP, Topol EJ. Prevalence of Asymptomatic SARS-CoV-2 Infection: a narrative review. Ann Intern Med. 2020; 173(5):362–367. pmid:32491919
  30. 30. Agência Brasil. Conheça resultado do maior estudo sobre a covid-19 no Brasil. 2020. https://agenciabrasil.ebc.com.br/ saude/noticia/2020-07/conheca-resultado-maior-estudo-sobre-covid-19-no-brasil.
  31. 31. De Souza WM, Buss LF, Candido DS, Carrera JP, Li S, Zarebski AE et al. Epidemiological and clinical characteristics of the COVID-19 epidemic in Brazil. Nat Hum Behay. 2020; 4(8):856–865. pmid:32737472
  32. 32. Hawkins RB, Charles EJ, Mehaffey JH. Socio-economic status and COVID-19-related cases and fatalities. Public Health. 2020; 189:129–134. pmid:33227595
  33. 33. Pellicano E, Stears M. The hidden inequalities of COVID-19. Autism. 2020; 24(6):1309–1310. pmid:32423232
  34. 34. Li W, Zhang B, Lu J, Liu S, Chang Z, Peng C, et al. Characteristics of Household Transmission of COVID-19. Clin Infect Dis. 2020; 71(8):1943–1946. pmid:32301964
  35. 35. Vila-Corcoles A, Satue-Gracia E, Vila-Rovira A, de Diego-Cabanes C, Forcadell-Peris MJ, Ochoa-Gondar O. Development of a predictive prognostic rule for early assessment of COVID-19 patients in primary care settings. Aten Primaria. 2021; 53(9):102118. pmid:34139400
  36. 36. Hawkes S, Aulakh BK, Jadeja N, Jimenez M, Buse K, Anwar I et al. Strengthening capacity to apply health research evidence in policy making: experience from four countries. Health Policy and Plan. 2016; 31(2): 161–70. pmid:25900967