Skip to main content
PLOS Global Public Health logoLink to PLOS Global Public Health
. 2022 Mar 25;2(3):e0000137. doi: 10.1371/journal.pgph.0000137

Predict the incidence of Guillain Barré Syndrome and arbovirus infection in Mexico, 2014–2019

Lumumba Arriaga-Nieto 1, Porfirio Felipe Hernández-Bautista 2, Alfonso Vallejos-Parás 1,*, Concepción Grajales-Muñiz 2, Teresita Rojas-Mendoza 2, David Alejandro Cabrera-Gaytán 3, Israel Grijalva-Otero 4, Bernardo Cacho-Díaz 5, Leticia Jaimes-Betancourt 6, Rosario Padilla-Velazquez 1, Gabriel Valle-Alvarado 1, Yadira Perez-Andrade 1, Oscar David Ovalle-Luna 1, Mónica Rivera-Mahey 1
Editor: Mathieu Nacher7
PMCID: PMC10022261  PMID: 36962143

Abstract

The Dengue (DENV), Zika (ZIKV), and Chikungunya (CHIKV) virus infections have been linked to Guillain-Barré syndrome (GBS). GBS has an estimated lethality of 4% to 8%, even with effective treatment. Mexico is considered a hyperendemic country for DENV due to the circulation of four serotypes, and the ZIKV and CHIKV viruses have also been circulating in the country. The objective of this study was to predict the number of GBS cases in relation to the cumulative incidence of ZIKV / DENV / CHIKV in Mexico from 2014 to 2019. A six-year time series ecological study was carried out from GBS cases registered in the Acute Flaccid Paralysis (AFP) Epidemiological Surveillance System (ESS), and DENV, ZIKV and CHIKV estimated cases from cases registered in the epidemiological vector-borne diseases surveillance system. The results shows that the incidence of GBS in Mexico is positively correlated with DENV and ZIKV. For every 1,000 estimated DENV cases, 1.45 GBS cases occurred on average, and for every 1,000 estimated ZIKV cases, 1.93 GBS cases occurred on average. A negative correlation between GBS and CHIKV estimated cases was found. The increase in the incidence of GBS cases in Mexico can be predicted by observing DENV and ZIKV cases through the epidemiological surveillance systems. These results can be useful in public health by providing the opportunity to improve capacities for the prevention of arbovirus diseases and for the timely procurement of supplies for the treatment of GBS.

Background

Guillain-Barré syndrome (GBS) is the most common cause of Acute Flaccid Paralysis (AFP) worldwide and is characterized by ascending weakness symmetrical with depression of muscle stretch reflexes [1]. Approximately 100,000 people develop the disorder each year worldwide [2], and the global incidence of GBS ranges from 0.6 to 4.0/100,000 people [3, 4]. About 20% of patients with GBS develop respiratory failure and require mechanical ventilation [5]. The mortality rate is estimated at 4–8% for patients with GBS even with the best medical care available [6]. In Mexico the hospital mortality rate for GBS has been documented at 10.5% [7]. The long-term impact on a patients life may go beyond their residual disability or impairment, where almost 30% of them have to make substantial changes in their daily lives after suffering from GBS [8].

The underlying causes of the GBS pathology are not yet fully understood [9, 10], However, the following factors have been described as a trigger for GBS: many infections have been linked with GBS, the most common are gastrointestinal or respiratory illnesses. Up to 70% of patients have reported an antecedent illness between one and six weeks before the presentation of GBS [11], about a third of all GBS cases are preceded by Campylobacter jejuni infection [12].

Infections by patogens like Haemophilus influenzae, influenza virus, Epstein–Barr virus, cytomegalovirus, human immunodeficiency virus, Hepatitis E virus and SARS-CoV-2 are linked with GBS [13–15]; also, several neurological manifestations, including GBS, are associated with Zika (ZIKV), Dengue (DENV) or Chikungunya (CHIKV) viruses’ infection [16–21]. Probably the most studied association between GBS and arbovirus infections is ZIKV; however, there are inconsistencies in the studies of the association between ZIKV infection and GBS [22].

Mexico is mainly characterized by a tropical and subtropical climate where dengue is endemic and the number and severity of cases have increased over the last ten years [23, 24]. Mathematical models predict that although the density of mosquitoes is decreasing in Mexico, transmission of dengue will continue because of biological factors that are optimal for the dengue virus [25].

Since laboratory confirmation of the first cases of Zika virus disease in October 2015, and up to 2019, 12,932 autochthonous cases have been identified in 29 of the 32 states of Mexico [26], and 19 cases of GBS associated with Zika have been documented [27]. Since October 2014, when the first autochthonous case of Chikungunya fever was identified and up to 2017, 11,971 Chikungunya cases have been reported in Mexico [28]. A total of 148,883 DENV cases were reported from 2014 to 2019 [29]. The objective of this study is to present a predictive model for GBS cases from DENV, CHIKV and ZIKV cases, arboviruses that circulated simultaneously in Mexico from 2014 to 2019, as proposed by some authors through Epidemiological Surveillance System (ESS) [30]. This study provides information about the association with GBS between DENV, CHIKV and ZIKV infection.

Since 2016, the Epidemiological Surveillance System for Acute Flaccid Paralysis, where the GBS is one of the diagnoses to study, was allowed to report cases in people older than 15 years due to the context of ZIKV, this change in epidemiological surveillance of GBS has been maintained up to date.

All AFP, DENV, ZIKV and CHIKV cases are mandatorily reported to the national ESS in our country. This study was carried out by the Mexican Institute of Social Security (IMSS) data; IMSS is a healthcare system that provides medical assistance to 51% of the Mexican population [31] and as part of the National Health System, also report cases to the Nacional ESS.

Methodology

Ethics statement: The present study is a part of a larger research protocol of a protocol that was accepted by the IMSS Ethics and Research Commission, Number R-2016-785-026. Since the data were obtained from epidemiological surveillance records, informed consent was not necessary, no procedure was performed outside the norms for epidemiological surveillance including patient samples for laboratory tests. All data analyzed were completely anonymous prior to study.

A population-based six-year time series ecological study was carried out using the AFP cases registered in the ESS from which GBS cases were identified. All cases of AFP are required to be reported to this ESS, and all GBS cases from 2014 to 2019 were included in the study.

The arboviruses cases in the study included all cases of DENV, ZIKV and CHIKV reported from 2014 to 2019, which were obtained by years and epidemiological weeks at the regional level at the Mexican Institute of Social Security.

In Mexico, it is mandatory to report all patients suspected of having DENV, ZIKV and CHIKV infection to the National Epidemiological Surveillance System, and a laboratory sample must be taken to confirm the diagnosis or rule out a case according to the following sampling percentages: a) 30% of non-serious dengue disease cases, 100% of cases with warning signs of severe dengue and 100% of cases with severe dengue disease; b) 10% of all CHIKV reported cases and c) 100% of ZIKV reported cases in pregnant woman and 10% of all ZIKV reported cases in the rest of the population.

Definitions

GBS: Diagnosis was done according to the clinical criteria of Asbury and Cornblath [32].

The Pan American Health Organization (PAHO) for a suspected arbovirus case definitions were used: the 2009 definitions [33] were used for DENV; the 2016 definition [34] was used for ZIKV; and the 2011 definition [35] was used for CHIKV.

DENV suspected case: defined by a combination of ≥2 clinical findings in a febrile person who traveled to or lives in a dengue-endemic area. Clinical findings include nausea, vomiting, rash, aches and pains, a positive tourniquet test, leukopenia, and the following warning signs: abdominal pain or tenderness, persistent vomiting, clinical fluid accumulation, mucosal bleeding, lethargy, restlessness, and liver enlargement.

ZIKV suspected case: defined as a patient with cutaneous exanthema with two or more of the following signs or symptoms: fever, headache, conjunctivitis (not purulent/hyperemic), arthralgia, pruritus or retroocular pain and any epidemiological association.

CHIKV suspected case: defined as a patient with acute onset of fever and severe arthralgia or arthritis not explained by other medical conditions, and who resides or has visited epidemic or endemic areas within two weeks prior to the onset of symptoms.

A confirmed case of DENV, ZIKV or CHIKV was defined as a suspected case that was determined to be positive by viral RNA detection through real-time RT-PCR in blood serum samples taken within the first five days of clinical symptoms onset (fever or other symptoms).

Estimation of arbovirus cases: laboratory samples were not taken to confirm all DENV, ZIKV or CHIKV suspected cases; therefore, positive cases were estimated according to previous studies [36].

The positivity percent for each disease was determined by dividing the number of positive cases by the sum of positive and negative cases. The positivity was defined as the probability of suffering from DENV, ZIKV and CHIKV infection among people suspected of the disease for whom a laboratory sample was not taken. The positivity was multiplied for suspected cases of DENV, CHIKV, and ZIKV without a laboratory sample, and the result was added to the number of positive cases. The positivity was obtained per epidemiological week and state (region); therefore, the estimated cases were calculated by week and region.

Data analysis

An epidemic curve was constructed for each individual disease (GBS, DENV, ZIKV and CHIKV) from the sum of the number of cases from all the states of the country for each week from 2014 to 2019. The dengue cases were grouped and added together, regardless of the type of DENV that was clinically presented (non-severe dengue, dengue with alarm signs or severe dengue). The annual cumulative incidence of each disease was calculated using the population insured by the IMSS at the middle of each year.

To predict GBS and arboviruses, an interrupted time series analysis was carried out through a segmented linear regression [37] using the weekly number of GBS cases as the dependent variable and the weekly arbovirus cases as the independent variables. For linear regression, the DENV, CHIKV, and ZIKV cases were divided by 1,000 to facilitate the interpretation of the results.

The number of weekly cases of GBS and arboviruses were calculated from the date of the onset of symptoms.

The multicollinearity of the variables was analyzed using the variance inflation factor (VIF) and tolerance; VIF values less than 10 and tolerance values greater than 0.10 were used as indicators that the explanatory variables had no multicollinearity in the model [38].

Results

A total of 1,698 cases of GBS were diagnosed during the studied period, during that time 168,979 DENV, 42,548 ZIKV, and 30,651 CHIKV cases were estimated (Table 1).

Table 1. Number of cases and cumulative incidence rate* of GBS, DENV, CHIKV and ZIKV, Mexico IMSS 2014–2019.

Disease 2014 2015 2016 2017 2018 2019
Cases CIR Cases CIR Cases CIR Cases CIR Cases CIR Cases CIR
GBS 181 0.42 127 0.29 342 0.78 306 0.64 300 0.61 442 0.87
DENV 30,684 70.80 30,839 69.76 19,913 45.13 16,467 34.68 11,065 22.48 60,011 117.59
ZIKV 0 0.00 20 0.05 35,584 80.65 6,288 13.24 610 1.24 46 0.09
CHIKV 44 0.10 29,792 67.39 764 1.73 31 0.07 19 0.04 1 0.00

*CIR = Cumulative incidence rate by 100,000 people.

The GBS cases increased from 2014 to 2019 by 2.4 times, and the highest growth occurred from 2015 to 2016; The cases and incidence of DENV per year presented changes, both of increase and decrease. In 2019 there was a DENV outbreak in Mexico. The behavior of dengue fever in Mexico has been dynamic over the years, and the outbreak patterns coincide with those factors presents at the regional level [23, 39, 40], among the factors involved is the phenomenon of global warming which has expanded the vector´s habitat, the poor treatment of bodies of water that favors their growth and increases in mosquito density, migratory phenomena and human movements, which together increase the transmission possibilities [41–43].

While the epidemiological behavior has been different for CHIKV and ZIKV diseases, incidences decreased over time after the Chikungunya national outbreak in 2015 and the Zika national outbreak in 2016, respectively, the years when the highest number of cases were recorded Fig 1.

Fig 1. Epidemic curve of GBS and arbovirus cases in Mexico, IMSS 2014–2019.

Fig 1

In Fig 1, the average mean of GBS cases before 2016 were 2.93 cases and after that year, 6.68 cases, with an average weekly increase of 77.8%.

Given that the three arboviruses are transmitted by the same vector and therefore circulate at the same time in Mexico, a correlation analysis was performed for these diseases and GBS: the results showed a positive correlation for CHIKV with DENV, DENV with ZIKV, DENV with GBS and ZIKV with GBS, and a negative correlation for CHIKV with GBS.

The results from the collinearity analyses performed for the three arboviruses indicated that a linear regression could be used to correlate arboviruses with GBS.

Segmented linear regression showed that GBS cases were related to the arboviruses with an adjusted R-squared value of 0.408 and a statistical significance of <0.0001. (Table 2).

Table 2. Interrupted time series analysis, segmented linear regression of GBS cases and arboviruses cases, 2014–2019.

  Non-standardized coefficients Standardized coefficients Sig. 95% confidence interval for B Collinearity statistics
  B Error Desv. Beta Lower limit Upper limit Tolerance VIF
(Constat) 2.496 0.331   <0.0001 1.845 3.147    
CHIKV/1000 -1.457 0.650 -0.113 0.026 -2.736 -0.179 0.742 1.349
DENV/1000 1.452 0.197 0.328 <0.0001 1.065 1.840 0.963 1.038
ZIKV/1000 1.925 0.393 0.220 <0.0001 1.152 2.698 0.938 1.067
Since 2016 year 3.048 0.379 0.411 <0.0001 2.302 3.795 0.727 1.376

Because we used a time-segmented model of GBS cases, we have two equations that can be used to estimate the number of GBS cases from the number of arbovirus cases and significant coefficients for the estimated cases of DENV, ZIKV, and CHIKV:

  1. Number of GBS cases before 2016 = 2.5 + (1.45 * (estimated number of DEN cases*1,000)) + (1.93 * (estimated number of ZVD cases*1,000))—(1.46 * (estimated number of CHIKV cases*1,000)).

  2. Number of GBS cases since 2016 = 5.5 + (1.45 * (estimated number of DEN cases*1,000)) + (1.93 * (estimated number of ZVD cases*1,000))—(1.46 * (estimated number of CHIKV cases*1,000)).

In the equations, the constant is 2.5 cases/week before 2016 and 5.5 cases/week since 2016, the change in the notification policy in 2016 increased GBS notification by 3 cases/week, therefore, it must be considered a βo value equal a 5.5 in the equation for that period (2016 to 2019).

The interpretation of the results is that in the period studied there were 2.5 cases of GBS every week before the year 2016 and 5.5 cases of GBS every week since 2016, that were not explained by the DENV, CHIKV and ZIKV estimated cases.

GBS cases increase weekly on average by 1.45 per 1000 estimated cases of DENV; They also increase on average by 1.93 cases per 1000 estimated cases of ZIKV; and decrease on average by 1.46 cases per 1000 estimated cases of CHIKV.

Fig 2 shows the cases predicted by the linear regression model with an R squared = 0.415 and statistical significance of p = 0.000 through the Ljung-Box Q test.

Fig 2. Epidemic curve of GBS model observed and predicted cases and arbovirus cases in Mexico, IMSS 2014–2019.

Fig 2

When finding a negative result for CHIKV in the model, we decided to perform a segmented linear regression only using the independent variable CHIKV, as a GBS dependent variable and using as segmentation time before the year 2016, which as can be seen in the graphical epidemic curve (Fig 1), is the period where more cases of CHIKV were reported, finding the following:

R squared = 0.016, B = -0.589 (-1.499–0.321), p = 0.202 not statistically significant. This finding is consistent with the global model presented where the correlation of CHIKV and SGB was negative.

Discussion

A population-based study was performed where the number of DENV, CHIKV and ZIKV cases were correlated with the number of GBS cases to predict the incidence of GBS cases. In our results the estimated incidence of GBS associated to ZIKV cases is 10 times greater to that published in an ecological study on the American continent, where 2 (0.5–4.5) GBS cases were estimated for every 10,000 ZIKV cases; Nevertheless, the frequency of reported suspect Zika cases varied substantially and the notification was highly uncertain in that study [44]. The relationship between ZIKV infection and GBS is probably the arbovirus infection most studied since the WHO concluded in 2016 that ZIKV infection is a trigger for GBS [45]. In our study, the incidence of GBS increased from 0.3 to 0.8 per 100,000 inhabitants/year from 2015 to 2016, which is equivalent to a 2.6-fold increase. Other Latin American countries (LAC) reported an increase in the cumulative incidence of GBS during the ZIKV epidemic; the incidence of GBS increased 4.4 times in Martinique from 2.12 to 9.35 per 100,000 and by 2.1 times in Puerto Rico from 1.7 to 3.5 per 100,000 inhabitants [46]. In LAC, the incidence of GBS increased 2.6-fold during ZIKV flare-ups and 1.9-fold during CHIKV flare-ups compared to previously reported incidence rates.

An ecological study carried out in Brazil revealed that a rapid increase in the number of hospitalizations for GBS followed the introduction of ZIKV and CHIKV in 2015, where the average number of hospitalizations increased by 45% compared to that from 2008 to 2014 [47]. In another more complex case-control study in Mexico, an association was found between acute ZIKV infection and GBS with an odds ratio of 8.04 (95% CI, 0.89–73.01); p = 0.047 [24]. However, a meta-analysis revealed that ZIKV outbreaks were not consecutive to GBS outbreaks; because only one analytical study included in the analysis indicated an association between the two types of outbreaks, the result for the association in the meta-analysis was 1.57 (95% CI 0.56–2.86) [22].

The association between DENV infection and GBS is rare [24], and it has been estimated that less than 10% of dengue cases develop neurological disorders, including GBS [48, 49]. From our results, we have estimated that for every 1,000 cases of DENV, 1.45 cases of GBS increases. The yearly distribution of GBS and DENV are not the same; specifically, GBS has a low annual frequency and is most prevalent during summer, whereas DENV has a high annual frequency. An ecological study conducted in Hong Kong found a weak correlation between GBS and meteorological factors (17%) [50].

Studies have related the presence of IgM antibodies to CHIKV with GBS [17]; however, it has been difficult to quantitatively estimate the incidence of CHIKV infection with neurological diseases. In the present study, no positive relationship was detected between CHIKV infection and GBS; The study of the relationship between Chikungunya and GBS has been complex, since, in the populations where it has been studied, there exist endemic circulation of DENV, ZIKV and CHIKV. The use of IgM and IgG antibodies reflects a previous infection with CHIKV, a complexity resulting from their transmission dynamics, and more integrative studies are needed investigating the combination of ZIKV, DENV, and CHIKV viruses and using a variety of approaches to answer questions related to the risk posed by these arboviruses [51]. In our study we include symptomatic cases of CHIKV; asymptomatic cases can be at least 47%, more than those included in this study [52]. In the studies that have used PCR to detect CHIKV infection, they have had a low number of samples to associate CHIKV and GBS [53]

Our model indicates that, before 2016 there were 2.5 cases of GBS per week and, from 2016, 5.5 cases of GBS per week that do not correlate to arboviruses; this indicates that there are different etiologies of GBS, probably the most studied infection by Campylobacter jejuni infection [12] and there is evidence that GBS cases in the pediatric population in Mexico have a relationship with this bacterium [54].

The prediction of a mathematical model indicate that even with a decrease in the density of mosquitoes in Mexico, transmission will continue because of optimal biological factors for DENV [25]. This model could be used to estimate the number of GBS cases from the burden of DENV and other vector-borne diseases.

The following limitations of the study should be considered: 1) The study was not designed to measure a causal relationship; due to the nature of the data, an exposure-disease relationship cannot be assumed, where the exposure must precede the onset of the disease [55].

Neither analyze demographic factors, such as the age or sex of the patients, although it has been shown that older patients and males have a higher incidence of GBS. 2) This is an ecological study, so its interpretation should not be at the individual level in order to not to fall into an ecological fallacy. 3) Note that coinfection between arboviruses was not analyzed, given that arbovirus cases were analyzed independently of each other; However, it is not yet known if the coinfection impacts clinical disease [56], but it has been described that GBS patients with laboratory evidence of both a recent ZIKV and CHIKV infection had a longer duration of hospitalization, were admitted to the ICU, and intubated significantly more frequently than the other patients with GBS [21].

4) The GBS clinical variant was not considered in this study, all cases regardless of the type of variant were included in the analysis. The clinical phenotype of GBS associated with ZIKV infection reported in literature is generally a sensorimotor demyelinating GBS with frequent facial palsy and a severe disease course often necessitating ICU admittance [57].

5) A surveillance bias exists because surveillance of GBS was reinforced by the identification of autochthonous cases of ZIKV by allowing the notification of GBS in people older than 15 years, since it was very specific for the search for flaccid paralysis in search of poliomyelitis.

Conclusions

Our results in this study indicate a positive relationship between ZIKV and DENV with GBS; thus, in the face of abrupt increases in these diseases, it is recommended that incidences of GBS in Mexico be monitored and the health system be prepared to care for these cases.

Data Availability

All data are available from the public repository database in: https://figshare.com/articles/dataset/Predict_the_incidence_of_Guillain_Barr_Syndrome_and_Arbovirus_Infection_in_Mexico_2014-2019/17082470.

Funding Statement

The author(s) received no specific funding for this work.

References

  • 1.Yuki N, Hartung HP. Guillain-Barré syndrome. N Engl J Med. 2012. Jun 14;366(24):2294–304. doi: 10.1056/NEJMra1114525 Erratum in: N Engl J Med. 2012 Oct 25;367(17):1673. [DOI] [PubMed] [Google Scholar]
  • 2.Willison HJ, Jacobs BC, van Doorn PA. Guillain-Barré syndrome. Lancet. 2016. Aug 13;388(10045):717–27. doi: 10.1016/S0140-6736(16)00339-1 Epub 2016 Mar 2. [DOI] [PubMed] [Google Scholar]
  • 3.Dimachkie M. M., & Barohn R. J. (2013). Guillain-Barré syndrome and variants. Neurologic clinics, 31(2), 491–510. doi: 10.1016/j.ncl.2013.01.005 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Shahrizaila N, Lehmann HC, Kuwabara S. Guillain-Barré syndrome. Lancet. 2021. Mar 27;397(10280):1214–1228. doi: 10.1016/S0140-6736(21)00517-1 Epub 2021 Feb 26. [DOI] [PubMed] [Google Scholar]
  • 5.Leonhard SE, Mandarakas MR, Gondim FAA, Bateman K, Ferreira MLB, Cornblath DR, et al. Diagnosis and management of Guillain–Barré syndrome in ten steps. Nature Reviews Neurology. 2019;15(11):671–83. doi: 10.1038/s41582-019-0250-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.van den Berg B, Bunschoten C, van Doorn PA, Jacobs BC. Mortality in Guillain-Barre syndrome. Neurology. 2013 Apr 30;80(18):1650–4. doi: 10.1212/WNL.0b013e3182904fcc Epub 2013 Apr 10. [DOI] [PubMed] [Google Scholar]
  • 7.Domínguez-Moreno R, Tolosa-Tort P, Patiño-Tamez A, Quintero-Bauman A, Collado-Frías DK, Miranda-Rodríguez MG, et al. [Mortality associated with a diagnosis of Guillain-Barré syndrome in adults of Mexican health institutions]. Revista de neurología. 2014. Jan;58(1):4–10. DOI: 10.33588/rn.5801.2013370. [DOI] [PubMed] [Google Scholar]
  • 8.Bersano A, Carpo M, Allaria S, Franciotta D, Citterio A, Nobile-Orazio E. Long term disability and social status change after Guillain-Barré syndrome. J Neurol. 2006 Feb;253(2):214–8. doi: 10.1007/s00415-005-0958-x Epub 2005 Aug 17. [DOI] [PubMed] [Google Scholar]
  • 9.Wobeto WP, Zani BB, Esteves AB da S, Marangoni MV da S, Pinatti N da S, Pedro KNS, et al. Guillain-Barre Syndrome: Case Study and Literature Review. Immunome Research. 2019;15(3):1–7. doi: 10.35248/1745-7580.19.15.172 [DOI] [Google Scholar]
  • 10.Jasti AK, Selmi C, Sarmiento-Monroy JC, Vega DA, Anaya J-M, Gershwin ME. Guillain-Barré syndrome: causes, immunopathogenic mechanisms and treatment. Expert review of clinical immunology. 2016. Nov;12(11):1175–89. doi: 10.1080/1744666X.2016.1193006 [DOI] [PubMed] [Google Scholar]
  • 11.Fokke C, van den Berg B, Drenthen J, Walgaard C, van Doorn PA, Jacobs BC. Diagnosis of Guillain-Barré syndrome and validation of Brighton criteria. Brain: a journal of neurology. 2014;137(Pt 1):33–43. doi: 10.1093/brain/awt285 [DOI] [PubMed] [Google Scholar]
  • 12.Israeli E, Agmon-Levin N, Blank M, Chapman J, Shoenfeld Y. Guillain-Barré syndrome-a classical autoimmune disease triggered by infection or vaccination. Vol. 42, Clinical Reviews in Allergy and Immunology. 2012. p. 121–30. doi: 10.1007/s12016-010-8213-3 [DOI] [PubMed] [Google Scholar]
  • 13.Jacobs BC, Rothbarth PH, van der Meché FG, Herbrink P, Schmitz PI, de Klerk MA, et al. The spectrum of antecedent infections in Guillain-Barré syndrome: a case-control study. Neurology. 1998. Oct;51(4):1110–5. doi: 10.1212/wnl.51.4.1110 [DOI] [PubMed] [Google Scholar]
  • 14.Gupta A, Paliwal VK, Garg RK. Is COVID-19-related Guillain-Barré syndrome different? Brain, Behavior, and Immunity. 2020. Jul 1; 87:177–8. doi: 10.1016/j.bbi.2020.05.051 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Stevens O, Claeys KG, Poesen K, Saegeman V, Van Damme P. Diagnostic Challenges and Clinical Characteristics of Hepatitis E Virus–Associated Guillain-Barré Syndrome. JAMA Neurology. 2017. Jan 1;74(1):26–33. doi: 10.1001/jamaneurol.2016.3541 [DOI] [PubMed] [Google Scholar]
  • 16.Broutet N, Krauer F, Riesen M, Khalakdina A, Almiron M, Aldighieri S, et al. Zika Virus as a Cause of Neurologic Disorders. New England Journal of Medicine. 2016;374(16):1506–9. doi: 10.1056/NEJMp1602708 [DOI] [PubMed] [Google Scholar]
  • 17.Mehta R, Gerardin P, de Brito CAA, Soares CN, Ferreira MLB, Solomon T. The neurological complications of chikungunya virus: A systematic review. Reviews in medical virology. 2018. May;28(3): e1978. doi: 10.1002/rmv.1978 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Verma R, Sahu R, Holla V. Neurological manifestations of dengue infection: a review. Journal of the neurological sciences. 2014. Nov;346(1–2):26–34. doi: 10.1016/j.jns.2014.08.044 [DOI] [PubMed] [Google Scholar]
  • 19.Simon O, Billot S, Guyon D, Daures M, Descloux E, Gourinat AC, et al. Early Guillain–Barré Syndrome associated with acute dengue fever. Journal of Clinical Virology. 2016. Apr 1; 77:29–31. doi: 10.1016/j.jcv.2016.01.016 [DOI] [PubMed] [Google Scholar]
  • 20.Silva JVJ, Ludwig-Begall LF, Oliveira-Filho EF de, Oliveira RAS, Durães-Carvalho R, Lopes TRR, et al. A scoping review of Chikungunya virus infection: epidemiology, clinical characteristics, viral co-circulation complications, and control. Acta Tropica. 2018. Dec 1; 188:213–24. doi: 10.1016/j.actatropica.2018.09.003 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Leonhard SE, Halstead S, Lant SB, Militão de Albuquerque M de FP, de Brito CAA, de Albuquerque LBB, et al. Guillain-Barré syndrome during the Zika virus outbreak in Northeast Brazil: An observational cohort study. Journal of the Neurological Sciences. 2021. Jan 15;420. doi: 10.1016/j.jns.2020.117272 [DOI] [PubMed] [Google Scholar]
  • 22.Bautista LE. Zika virus infection and risk of Guillain-Barré syndrome: A meta-analysis. Journal of the neurological sciences. 2019. Aug; 403:99–105. doi: 10.1016/j.jns.2019.06.019 [DOI] [PubMed] [Google Scholar]
  • 23.Arredondo-García JL, Aguilar-López Escalera CG, Aguilar Lugo-Gerez JJ, Osnaya-Romero N, Pérez-Guillé G, Medina-Cortina H. Panorama epidemiológico de dengue en México 2000–2019. Revista Latinoamericana de Infectología Pediátrica. 2020;33(2):78–83. doi: 10.35366/94418 [DOI] [Google Scholar]
  • 24.Sahu R, Verma R, Jain A, Garg RK, Singh MK, Malhotra HS, et al. Neurologic complications in dengue virus infection: a prospective cohort study. Neurology. 2014. Oct;83(18):1601–9. doi: 10.1212/WNL.0000000000000935 [DOI] [PubMed] [Google Scholar]
  • 25.Sánchez-González G, Condé R, Moreno RN, López Vázquez PC. Prediction of dengue outbreaks in Mexico based on entomological, meteorological and demographic data. PLoS ONE. 2018;13(8). doi: 10.1371/journal.pone.0196047 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Secretaría de salud. Casos Confirmados Autóctonos de Enfermedad por Virus del Zika por Entidad Federativa. 2021;(157):4. https://www.gob.mx/cms/uploads/attachment/file/614755/CuadroCasosZikayEmb_SE04_2021.pdf. [Google Scholar]
  • 27.SINAVE/DGE/SS. Casos confirmados de Síndrome de Guillain-Barré asociado a Zika en México. Secretaría de Salud, Subsecretaría de Prevención y Promoción de la Salud, Dirección General de Epidemiología México. 2018;52(55):5337. https://www.gob.mx/cms/uploads/attachment/file/390724/ZIKA_SxGB_060218.pdf.
  • 28.PLISA Health Information Platform for the Americas. Chikungunya data PAHO. https://www3.paho.org/data/index.php/en/mnu-topics/chikv-en.html.
  • 29.Secretaría de salud. Manual de Procedimientos Estandarizados para la vigilancia epidemiológica de las enfermedades transmitidas por vector. https://epidemiologia.salud.gob.mx/gobmx/salud/documentos/manuales/36_Manual_ETV.pdf.
  • 30.Kohler A, Farez M, Heck E, Barroso FA, Bruno V. Association between neurological syndromes and Arbovirus in Buenos Aires—Relationship between Guillain Barre Syndrome, Encephalitis and Myelitis with Zika, Dengue and Chikungunya (P4.6–024). Neurology. 2019. Apr 9;92. [Google Scholar]
  • 31.Instituto Nacional de Estadística y Geografía. México 2020. https://www.inegi.org.mx/.
  • 32.Asbury AK, Cornblath DR. Assessment of current diagnostic criteria for Guillain-Barré syndrome. Annals of neurology. 1990;27 Suppl: S21–4. doi: 10.1002/ana.410270707 [DOI] [PubMed] [Google Scholar]
  • 33.Organización Panamericana de la Salud. Guías para la atención de enfermos en la región de las américas. Vol. dos, Catalogación en la Fuente, Biblioteca Sede de la OPS. 2015. 126 p. https://iris.paho.org/handle/10665.2/28232?locale-attribute=es.
  • 34.Zamai CA, Bavoso D, Rodrigues AA, Barbosa JAS. Guía para la vigilancia de la enfermedad por el virus del Zika y sus complicaciones. Vol. 3, Resma. 2016. 13–22 p. https://iris.paho.org/handle/10665.2/28234. [Google Scholar]
  • 35.Frank Hadley Collins; Preparedness and Response for Introduction in the America. Pan American Health Organization 2010. 148 p. https://iris.paho.org/bitstream/handle/10665.2/4009/chikungunyavirus.pdf?sequence=1.
  • 36.Grajales-Muñiz C, Borja-Aburto VH, Cabrera-Gaytán DA, Rojas-Mendoza T, Arriaga-Nieto L, Vallejos-Parás A. Zika virus: Epidemiological surveillance of the Mexican Institute of Social Security. Samy AM, editor. PLOS ONE. 2019. Feb 11;14(2): e0212114. doi: 10.1371/journal.pone.0212114 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Bernal JL, Cummins S, Gasparrini A. Interrupted time series regression for the evaluation of public health interventions: a tutorial. International Journal of Epidemiology. 2017. Feb 1;46(1):348–55. doi: 10.1093/ije/dyw098 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Belsley D.A.; Kuh E.; Welsch RE. Regression Diagnostics: Identifying Influential Data and Sources of Collinearity. Wiley, editor. New York, 2004. 292 p. 10.1002/jae.3950040108. [DOI] [Google Scholar]
  • 39.Abd Majid N, Muhamad Nazi N, Mohamed AF. Distribution and Spatial Pattern Analysis on Dengue Cases in Seremban District, Negeri Sembilan, Malaysia. Vol. 11, Sustainability. 2019. 10.3390/su11133572. [DOI] [Google Scholar]
  • 40.Dantés HG, Farfán-Ale JA, Sarti E. Epidemiological Trends of Dengue Disease in Mexico (2000–2011): A Systematic Literature Search and Analysis. PLOS Neglected Tropical Diseases. 2014. Nov 6;8(11): e3158. doi: 10.1371/journal.pntd.0003158 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Short EE, Caminade C, Thomas BN. Climate Change Contribution to the Emergence or Re-Emergence of Parasitic Diseases. Infectious diseases. 2017. Sep 25; 10:1178633617732296–1178633617732296. doi: 10.1177/1178633617732296 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Kesetyaningsih TW, Andarini S, Sudarto , Pramoedyo H. Determination of environmental factors affecting dengue incidence in Sleman district, yogyakarta, Indonesia. African journal of infectious diseases. 2018. Mar 7;12(1 Suppl):13–25. doi: 10.2101/Ajid.12v1S.3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Teurlai M, Menkès CE, Cavarero V, Degallier N, Descloux E, Grangeon J-P, et al. Socio-economic and Climate Factors Associated with Dengue Fever Spatial Heterogeneity: A Worked Example in New Caledonia. PLOS Neglected Tropical Diseases. 2015. Dec 1;9(12): e0004211. doi: 10.1371/journal.pntd.0004211 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Mier-Y-Teran-Romero L, Delorey MJ, Sejvar JJ, Johansson MA. Guillain-Barré syndrome risk among individuals infected with Zika virus: a multi-country assessment. ine (2018) 16:67 doi: 10.1186/s12916-018-1052-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Krauer F, Riesen M, Reveiz L, Oladapo OT, Martínez-Vega R, Porgo T V, et al. Zika Virus Infection as a Cause of Congenital Brain Abnormalities and Guillain-Barré Syndrome: Systematic Review. PLoS medicine. 2017. Jan 3;14(1): e1002203–e1002203. doi: 10.1371/journal.pmed.1002203 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Capasso A, Ompad DC, Vieira DL, Wilder-Smith A, Tozan Y. Incidence of Guillain-Barré Syndrome (GBS) in Latin America and the Caribbean before and during the 2015–2016 Zika virus epidemic: A systematic review and meta-analysis. PLoS neglected tropical diseases. 2019. Aug;13(8): e0007622. doi: 10.1371/journal.pntd.0007622 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Maria Alves Siqueira Malta J. Guillain-Barré syndrome hospitalizations in Brazil Epidemiol. Serv Saude, Brasília. 2020;29(4):2020. 10.5123/s1679-49742020000400020. [DOI] [PubMed] [Google Scholar]
  • 48.Singh H, Pannu AK, Bhalla A, Suri V, Kumari S. Dengue: Uncommon Neurological Presentations of a Common Tropical Illness. Indian journal of critical care medicine: peer-reviewed, official publication of Indian Society of Critical Care Medicine. 2019. Jun;23(6):274–5. doi: 10.5005/jp-journals-10071-23179 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Tang X, Zhao S, Chiu APY, Wang X, Yang L, He D. Analysing increasing trends of Guillain-Barré Syndrome (GBS) and dengue cases in Hong Kong using meteorological data. PLOS ONE. 2017. Dec 4;12(12): e0187830. doi: 10.1371/journal.pone.0187830 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Lebrun G, Chadda K, Reboux AH, Martinet O, Gaüzère BA. Guillain-barré syndrome after chikungunya infection. Vol. 15, Emerging Infectious Diseases. 2009. p. 495–6. doi: 10.3201/eid1503.071482 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Jones R, Kulkarni MA, Davidson TM V, Team R-LR, Talbot B. Arbovirus vectors of epidemiological concern in the Americas: A scoping review of entomological studies on Zika, dengue and chikungunya virus vectors. PLOS ONE. 2020. Feb 6;15(2): e0220753. doi: 10.1371/journal.pone.0220753 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Nakkhara P, Chongsuvivatwong V, Thammapalo S. Risk factors for symptomatic and asymptomatic chikungunya infection. Transactions of The Royal Society of Tropical Medicine and Hygiene. 2013. Dec 1;107(12):789–96. doi: 10.1093/trstmh/trt083 [DOI] [PubMed] [Google Scholar]
  • 53.Grijalva I, Grajales-Muñiz C, González-Bonilla C, Borja-Aburto VH, Paredes-Cruz M, Guerrero-Cantera J, et al. Zika and dengue but not chikungunya are associated with Guillain-Barré syndrome in Mexico: A case-control study. PLoS Negl Trop Dis. 2020. Dec 17;14(12):e0008032. doi: 10.1371/journal.pntd.0008032 PMCID: PMC7775118. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Nachamkin I, Barbosa PA, Ung H, Lobato C, Rivera AG, Rodriguez P, et al. Patterns of Guillain-Barré syndrome in children. Neurology. 2007. Oct 23;69(17):1665 LP– 1671. doi: 10.1212/01.wnl.0000265396.87983.bd [DOI] [PubMed] [Google Scholar]
  • 55.Fedak KM, Bernal A, Capshaw ZA, Gross S. Applying the Bradford Hill criteria in the 21st century: how data integration has changed causal inference in molecular epidemiology. Emerging Themes in Epidemiology. 2015. Dec 30;12(1):14. doi: 10.1186/s12982-015-0037-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Vogels CBF, Rückert C, Cavany SM, Perkins TA, Ebel GD, Grubaugh ND. Arbovirus coinfection and co-transmission: A neglected public health concern? PLOS Biology. 2019. Jan 22;17(1): e3000130. doi: 10.1371/journal.pbio.3000130 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Leonhard SE, Bresani-Salvi CC, Lyra Batista JD, Cunha S, Jacobs BC, Brito Ferreira ML, et al. Guillain-Barré syndrome related to Zika virus infection: A systematic review and meta-analysis of the clinical and electrophysiological phenotype. PLOS Neglected Tropical Diseases. 2020. Apr 27;14(4): e0008264. doi: 10.1371/journal.pntd.0008264 [DOI] [PMC free article] [PubMed] [Google Scholar]
PLOS Glob Public Health. doi: 10.1371/journal.pgph.0000137.r001

Decision Letter 0

Mathieu Nacher, Julia Robinson

29 Sep 2021

PGPH-D-21-00407

Temporal Correlation Between Guillain Barré Syndrome and Arbovirus Infection in Mexico, 2014-2019.

PLOS Global Public Health

Dear Dr. Vallejos-Parás,

Thank you for submitting your manuscript to PLOS Global Public Health. After careful consideration, we feel that it has merit but does not fully meet PLOS Global Public Health’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Please submit your revised manuscript by Nov 11 2021 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at globalpubhealth@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pgph/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

We look forward to receiving your revised manuscript.

Kind regards,

Mathieu Nacher

Academic Editor

PLOS Global Public Health

Journal Requirements:

1. In your ethics statement in the manuscript, please ensure that you have discussed whether all data/samples were fully anonymized before you accessed them and/or whether the IRB or ethics committee waived the requirement for informed consent. If patients provided informed written consent to have data/samples from their medical records used in research, please include this information.

2. Please provide  separate figure files in .tif or .eps format only.  Please ensure that all files are under our size limit of 20MB.  

For more information about how to convert your figure files please see our guidelines: Once you've converted your files to .tif or .eps, please also make sure that your figures meet our format requirements

3. We have noticed that you have uploaded supporting information but you have not included a list of legends.  Please add a full list of legends for all supporting information files (including figures, table and data files) after the references list. 

4. In the online submission form, you indicated that your data will be submitted to a repository upon acceptance.  We strongly recommend all authors deposit their data before acceptance, as the process can be lengthy and hold up publication timelines. Please note that, though access restrictions are acceptable now, your entire data will need to be made freely accessible if your manuscript is accepted for publication. This policy applies to all data except where public deposition would breach compliance with the protocol approved by your research ethics board. If you are unable to adhere to our open data policy, please kindly revise your statement to explain your reasoning and we will seek the editor's input on an exemption. Please be assured that, once you have provided your new statement, the assessment of your exemption will not hold up the peer review process.

Additional Editor Comments (if provided):

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Does this manuscript meet PLOS Global Public Health’s publication criteria? Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe methodologically and ethically rigorous research with conclusions that are appropriately drawn based on the data presented.

Reviewer #1: Partly

Reviewer #2: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: I don't know

**********

3. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception. The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: No

Reviewer #2: No

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS Global Public Health does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: No

Reviewer #2: No

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The main objective of this paper is predict the incidence of Guillain-Barré Syndrome in Mexico from the incidence of Dengue, Zika and Chikungunya diseases using a linear regression model applied to national surveillance data collected between 2014 and 2019. These three arboviroses already represent a heavy burden for the population of Latin America, GBS is an added complication for both patients and health systems. The data and analysis presented in this paper is of relevance to a public health audience.

* Title and abstract

The title of the paper and the objective section of the abstract do not reflect the main objective of the study which is to predict the incidence of GBS, of public health interest, whereas correlations appear secondary when reading the whole manuscript.

The methods section of the abstract mentions a five-year analysis when a six-year analysis is presented in the paper (2014-2019).

In the results section: “The increase of incidence of GBS in Mexico is correlated with the epidemic years of DENV and ZIKV”. None of the results of the paper supports this particular claim. The linear regression or the correlations shown in the paper do not allow drawing conclusions that distinguish epidemic vs. non-epidemic years.

* Background

This introduction does not mention the different etiologies of GBS other than arboviruses (eg: Campylobacter infections). Surprisingly, the lethality figure mentioned in the abstract is not found in the background section; with a proper reference, this figure would help stressing out the importance of GBS as a health problem.

Line 73: The formulation of the objective is too vague. In my opinion the interest of the paper is the presentation of a predictive model and should be focused on it. This should also be reflected in the title of the paper.

* Methods

Case definitions and sources of data are well described.

Linear regression: Line 127 “to correlate”; the term should be changed. The objective of the model is not to study correlations but to predict the number of GBS cases for each increase in the incidence of ZKV/DENV/CHIKV. Please precise that the dependent variable is also the weekly number of GBS cases (line 127).

Please also clarify what is the date used for the cases: date of symptom onset, date of reporting?

ANOVA: Why was an ANOVA performed? It is unclear what variables were compared in the ANOVA: “weekly means and annual GBS cases”; is the variance of weekly cases of GBS compared between each year? Why?

* Results

Table 1

Please harmonize acronyms in Table 1 with the rest of the text: SGB vs GBS, DEN vs DENV, etc. The first year should be 2014 and not 2015.

There is clearly a change in the yearly number of cases of GBS before and after 2016. As mentioned in the discussion, this could be attributed to a change in the reporting policy especially in the context of ZKV epidemic and international awareness. This could be estimated with an interrupted time series analysis (ITSA, segmented linear regression) by adding to the linear regression model a step variable (0 before 2016, 1 after) to model this change in the surveillance system. The associated coefficient would estimate the before/after variation.

Line 145: I find a lack of epidemiological rigor in the way the evolution of yearly cases of GBS and arboviruses cases is presented. Especially: line 146: “the incidence and number of DEN cases doubled from 2015 and 2019” is quite misleading. Graph 1 clearly shows that each year Mexico experiences a DENV epidemic, the magnitude of which appears to decrease slightly between 2014 and 2018. Only in 2019 the epidemic was particularly big. Do the authors have any explanation for this observation?

Table2

The ANOVA shows that the yearly mean of weekly GBS cases are statistically different over the period, this result in itself is not much more informative than those shown in Table 1 and Graph 1. It clearly shows an increase between 2014-2015 and 2016-2019; another argument in favor of a change of reporting policy.

Line 168: why is this statement important? For a linear regression, only the distribution of error terms should be normal. Was this checked?

Line 163/Line 171: please be clearer about why despite positive correlations between independent variables only limited collinearity was found. The correlations presented in the appendix do not bring much added information.

Table 3

The values shown for the coefficients and associated 95%CI have too few significant numbers. Maybe a change in the unit of the independent variables (i.e.: 1000 cases instead of single case) would make the table and the equation more readable. It would also better fit the interpretation given in the discussion (lines 187 and 188).

Have you tried a simpler model using a single independent variable grouping all cases of arboviruses instead of distinguishing the diseases?

Again, I suggest trying an ITSA to explore the effect of change of policy in the reporting of GBS.

* Discussion

The constant of the model (4.2 to 5.1 cases of GBS per week in absence of arboviroses) should be discussed. So should the negative coefficient for CHIKV (cf lines 216-218).

Line 188: “This finding is very similar”, the ZIKV-associated incidence of GBS estimated in this article is 10 times greater than the mean value found in ref #21. I don’t think ‘very similar’ is appropriate.

Lines 225-228: This is unclear. What is meant by a “temporality bias”? Indeed a time lag exists between ZIKV infection and GBS onset: was it taken into account into the analysis? If not, why?

Lines 235-236: There is a clear shift before and after 2016 in the total number of GBS cases reported each year, despite the absence of Zika epidemic after 2016. A change in surveillance and reporting of GBS is a major bias and should be explored before discussing trend evolution between 2014 and 2019.

Line 233: “infected with GBS”: this phrasing is not appropriate; GBS is an auto-immune disorder that may result from an infection, but not an infectious disease in itself. Did the authors write GBS instead of ZKV?

Line 238: “DENV” should be replaced by “GBS”

Reviewer #2: Cumulative data support an association between ZIKV and GBS in some parts of the world. However, uncertainty remains regarding the association between other arbovirus cases and GBS.

The authors conducted a population-based study analysing a 6-year time series in Mexico (2014-2019). They assessed the correlation between Guillain-Barré syndrome cases and arboviruses cases (DENV, ZIKV, CHIKV).

The data are based on a nationwide epidemiological surveillance system of both GBS and arbovirus cases.

The methods are well explained and the results are clearly presented. The identification of arbovirus cases is well explained and clear. The gathering of data is well designed.

The authors conclude that GBS cases are positively correlated with DENV and ZIKV cases and determined the strenght of this association. On the opposite they report a negative correlation between CHIKV and GBS cases which is a matter of debate.

The authors also discuss thoroughly the limitations of their study.

The data seem robust to support the conclusions of the authors.

The manuscript is quite concise and clear and as a significant potential for publication.

However I have some remarks regarding the manuscript.

First, the statistical analysis plan need to be assessed by a times series analysis specialist to check if.

Second, the authors should strengthen what this study adds to the current knowledge about the subject. I suggest the introduction section should state more clearly what is already known about it and what remains to be studied.

Even though the manuscrit is in general comprehensive some language editing should made throughout the manuscript to gain in clarity (ex l 94-95, 118, 121-122, l 204)

Some of the results are given in the discussion section(see L 188-189) (or the abstract "For every 1,000 cases of dengue, 2 cases of GBS occurred, and for every 1,000 cases of Zika, 3 cases of GBS occurred") and should be cited in the results section because it corresponds to the main objective of the study.

L 231 231 the authors state that "there is no evidence that coinfection between DENV and ZIKV increases the risk of GBS". This point has been assessed somewhere else and should be discussed see Leonhard et al https://doi.org/10.1016/j.jns.2020.117272

The authors find a negative correlation between CHIK and GBS cases. Tis point is not really discussed after. It could be interesting because some authors found a possible association between CHIKV and GBS (see also Leonhard et al).

The time bias evoked by the authors should be discussed more thoroughly. Indeed this point limits the interpretation of the temporal correlation found here. Is the short timelapse (6-11 days) cited by the authors between arbovirus infection and GBS occurrence is really that certain?

The discussion section could be somewhat reviewed to clarify the authors’ point.

L 211 Do the authors refer to their result or to the literature?

Table 2 Do the authors refer to ANOVA of weekly means?

In the abstract the authors wrote 5-year time series whereas it is 6-year time series.

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

Do you want your identity to be public for this peer review? If you choose “no”, your identity will remain anonymous but your review may still be made public.

For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: Yes: Paul Le Turnier

**********

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLOS Glob Public Health. doi: 10.1371/journal.pgph.0000137.r003

Decision Letter 1

Mathieu Nacher

7 Jan 2022

PGPH-D-21-00407R1

Predict the incidence of Guillain Barré Syndrome and Arbovirus infection in Mexico, 2014-2019

PLOS Global Public Health

Dear Dr. Vallejos-Parás,

Thank you for submitting your manuscript to PLOS Global Public Health. After careful consideration, we feel that it has merit but does not fully meet PLOS Global Public Health’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Please submit your revised manuscript by Feb 21 2022 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at globalpubhealth@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pgph/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

We look forward to receiving your revised manuscript.

Kind regards,

Mathieu Nacher

Academic Editor

PLOS Global Public Health

Journal Requirements:

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

Additional Editor Comments (if provided):

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: (No Response)

Reviewer #2: All comments have been addressed

**********

2. Does this manuscript meet PLOS Global Public Health’s publication criteria? Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe methodologically and ethically rigorous research with conclusions that are appropriately drawn based on the data presented.

Reviewer #1: Yes

Reviewer #2: Partly

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: I don't know

**********

4. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception. The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS Global Public Health does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: No

Reviewer #2: No

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Thank you for addressing the main concerns raised during the first round of review.

General comments:

I particularly appreciate the additions brought to the introduction, and the author's effort to conduct an interrupted time series analysis. This seems a genuine improvement.

However I think the English of the manuscript needs additional proofreading before publication.

Specific comments:

- Graph 2 displays the same information as Graph 1 with a scale change and highlight of 2016 policy change. I suggest combining the two figures, especially given Graph 3 displays actual vs. modelled data.

- Line 211: the effect of 2016 policy change is missing from the equation of the model

- Line 217: the interpretation is not correct; after 2016 the notification increases by three (additional model) but is not multiplied by 3. The constant is 2.5 cases/week before 2016 and 5.5 cases/week after 2016.

- I suggest avoiding reporting zero p-values (i.e. p=0.000 in Table 1) and using p<0.0001 instead.

Reviewer #2: The authors have made significant efforts to answer the questions of both reviewers and have improved the manuscript. The conclusions are supported by the data. However, a language editing remains necessary to gain in clarity in many parts of the manuscript considering some authors' points are still hard to catch (ex l223-226, 264-270).

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

Do you want your identity to be public for this peer review? If you choose “no”, your identity will remain anonymous but your review may still be made public.

For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: Yann Lambert

Reviewer #2: Yes: Paul Le Turnier

**********

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLOS Glob Public Health. doi: 10.1371/journal.pgph.0000137.r005

Decision Letter 2

Mathieu Nacher, Julia Robinson

2 Mar 2022

Predict the incidence of Guillain Barré Syndrome and Arbovirus infection in Mexico, 2014-2019

PGPH-D-21-00407R2

Dear Mr Vallejos-Parás,

We are pleased to inform you that your manuscript 'Predict the incidence of Guillain Barré Syndrome and Arbovirus infection in Mexico, 2014-2019' has been provisionally accepted for publication in PLOS Global Public Health.

Before your manuscript can be formally accepted you will need to complete some formatting changes, which you will receive in a follow up email. A member of our team will be in touch with a set of requests.

Please note that your manuscript will not be scheduled for publication until you have made the required changes, so a swift response is appreciated.

IMPORTANT: The editorial review process is now complete. PLOS will only permit corrections to spelling, formatting or significant scientific errors from this point onwards. Requests for major changes, or any which affect the scientific understanding of your work, will cause delays to the publication date of your manuscript.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they'll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact globalpubhealth@plos.org.

Thank you again for supporting Open Access publishing; we are looking forward to publishing your work in PLOS Global Public Health.

Best regards,

Mathieu Nacher

Academic Editor

PLOS Global Public Health

***********************************************************

Reviewer Comments (if any, and for reference):

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    Attachment

    Submitted filename: response to reviews 301121.docx

    Attachment

    Submitted filename: response to reviews 220222.docx

    Data Availability Statement

    All data are available from the public repository database in: https://figshare.com/articles/dataset/Predict_the_incidence_of_Guillain_Barr_Syndrome_and_Arbovirus_Infection_in_Mexico_2014-2019/17082470.


    Articles from PLOS Global Public Health are provided here courtesy of PLOS

    RESOURCES