A number of infectious agents have previously been suggested as risk factors for the development of Guillain-Barré syndrome (GBS), but robust epidemiologic evidence for these associations is lacking.
Methods and Findings
We conducted a nested case-control study using data from the United Kingdom General Practice Research Database between 1991 and 2001. Controls were matched to cases on general practice clinic, sex, year of birth and date of outcome diagnosis in their matched case. We found positive associations between GBS and infection with Campylobacter, Epstein-Barr virus and influenza-like illness in the previous two months, as well as evidence of a protective effect of influenza vaccination. After correction for under-ascertainment of Campylobacter infection, the excess risk of GBS following Campylobacter enteritis was 60-fold and 20% of GBS cases were attributable to this pathogen.
Our findings indicate a far greater excess risk of GBS among Campylobacter enteritis patients than previously reported by retrospective serological studies. In addition, they confirm previously suggested associations between infection due to Epstein-Barr virus infection and influenza-like illness and GBS. Finally, we report evidence of a protective effect of influenza vaccination on GBS risk, which may be mediated through protection against influenza disease, or result from a lower likelihood of vaccination among those with recent infection. Cohort studies of GBS incidence in this population would help to clarify the burden of GBS due to influenza, and any potential protective effect of influenza vaccination.
Citation: Tam CC, O'Brien SJ, Petersen I, Islam A, Hayward A, Rodrigues LC (2007) Guillain-Barré Syndrome and Preceding Infection with Campylobacter, Influenza and Epstein-Barr Virus in the General Practice Research Database. PLoS ONE2(4): e344. https://doi.org/10.1371/journal.pone.0000344
Academic Editor: Joel Montgomery, US Naval Medical Research Center Detachment/Centers for Disease Control, United States of America
Received: January 9, 2007; Accepted: March 12, 2007; Published: April 4, 2007
Copyright: © 2007 Tam et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: No external funding was received for this study.
Competing interests: The authors have declared that no competing interests exist.
Guillain-Barré syndrome (GBS) is the most common cause of acute flaccid paralysis in polio-free regions, with incidence estimated at between 0.4 and 4 per 100,000 in different settings . The disease has an autoimmune pathology; following infection, antibodies produced against pathogen surface structures cross-react with nerve ending antigens, leading to neurologic damage. Several pathogens are thought to trigger GBS, primarily Campylobacter jejuni. Numerous studies have demonstrated evidence for an association between GBS and preceding C. jejuni infection. These studies have mostly relied on serologic evidence of C. jejuni infection, reporting infection prevalences of 15% to 66% among GBS cases compared with 0% to 17% in controls –, and odds ratios between three and five , . However, serologic tests are not specific for recent C. jejuni infection. These studies are thus difficult to interpret; seropositivity could indicate recent infection, past infection, or immunity, and the distribution of these is likely to differ between seropositive cases and seropositive controls, leading to biased estimates of the Campylobacter-GBS association. A Swedish capture-recapture study reported a GBS incidence of 3.0 per 10,,000 among Campylobacter enteritis cases reported to national surveillance, 100 times the incidence of GBS in the general population . Using data from a cohort of patients presenting to primary care, we have previously estimated that for every 10,000 cases of Campylobacter enteritis, two cases of GBS occur within the two months following infection, an incidence 77 times greater than that in the general population , . Our previous studies have indicated that between nine and 14 percent of GBS cases are attributable to symptomatic Campylobacter infection , , suggesting that asymptomatic infection, or infection with other pathogens, must account for the majority of GBS cases.
Other pathogens suggested to trigger GBS include cytomegalovirus , , Epstein-Barr virus (EBV), Haemophilus influenzae , , Mycoplasma pneumoniae  and influenza –. Recent work in England using time-series methods has identified associations between numbers of weekly reports of laboratory-confirmed infections with Campylobacter, M. pneumoniae and influenza, and incidence of hospitalization for GBS in subsequent weeks . In the United States, influenza vaccination during 1976–1977 was associated with a seven-fold excess risk of GBS in the subsequent six-week period , and polio vaccination has been suggested as a risk factor for GBS in Finland and China , . A recent study in England, however, found no association between any vaccination and subsequent GBS risk .
In order to better define the excess risk of GBS associated with these exposures, we undertook a nested case-control analysis in a United Kingdom-based general practice setting using data from the General Practice Research Database.
General Practice Research Database
The General Practice Research Database (GPRD) constitutes several hundred general practice clinics (GP clinics) serving a 5% representative sample of the UK population. The characteristics of this data source have been previously described . The database holds electronic records of all patients registered with participating clinics, including basic patient information (birthdate, sex, registration and de-registration dates, death date) and records of all consultations with corresponding diagnoses, preventions (e.g. immunizations, screening) and prescriptions. Approval for the study was obtained from the scientific and ethics advisory group of the GPRD.
Data from participating clinics are validated to ensure accuracy and completeness for a minimum set of variables. Data meeting minimum quality criteria are termed ‘up-to-standard’ (UTS) data and are a general indicator of the overall quality of data from a given clinic . Data from any clinic not meeting UTS criteria were excluded. We define an individual's up-to-standard follow-up time as the time during which they were registered with a clinic reporting UTS data.
GPRD diagnoses are recorded using Read or Oxmis (Oxford Medical Information Systems) codes, standardized terms used by medical practitioners to record patient outcome or management information, such as medical diagnoses, symptoms, test results and family history. We obtained information on all first consultations for GBS occurring between 1990 and 2001. A consultation is defined as any contact between a patient and the clinic services that appears in their medical records. We excluded repeat consultations. For these patients, we extracted all consultations for these infections: Campylobacter, cytomegalovirus, Epstein-Barr virus, H. influenzae, M. pneumoniae and influenza-like illness (ILI). We also included two sets of non-specific codes for infectious intestinal disease (IID) and acute respiratory infection (ARI) of unspecified aetiology. Finally, we obtained records of all influenza and polio vaccinations administered to GBS patients. A list of all diagnostic codes used is available from the authors.
Cases were defined as individuals with a first GBS consultation within their UTS follow-up time. Cases with under one year of UTS time available were excluded. We also excluded GBS consultations occurring within four months of patients' registration with their clinic or on the same day as a “new patient screening” to avoid inclusion of prevalent GBS recorded on joining a new clinic .
We randomly selected 10 controls per case, matched on GP clinic, sex, birth year (within one year for cases aged under 16 years or within five years otherwise) and GBS consultation date. We matched on the latter because the risk period for GBS following infection is short and some of the pathogens are highly seasonal. For each control, we assigned a pseudo-outcome date–the date of GBS consultation in their matched case. Controls were excluded if they had under one year of UTS time available or their pseudo-outcome date was within four months of clinic registration. Figure 1 presents details of case and control exclusions.
The risk period for GBS following infection is thought to be only a few weeks. Most GBS cases will be diagnosed in hospital emergency or neurology departments; the patient's general practitioner will be notified upon discharge, potentially several weeks or months after initial diagnosis. It is thus possible that there could be a considerable delay between a patient's initial consultation for neurological symptoms and the time when a confirmed GBS diagnosis is actually recorded. As this has implications for defining the exposure period, we first investigated the temporal relationship between infection and GBS in cases and controls. Figures 2a–f show incidences of consultation for the various infections in cases and controls by month from GBS consultation in cases. No consultations for cytomegalovirus, H. influenzae or M. pneumoniae were identified; these exposures were excluded from further analyses. From these figures, we defined the risk period as 60 days prior to GBS consultation in cases (or pseudo-outcome date in controls) and excluded individuals with incomplete UTS time during this period. If one such case was excluded, all their matched controls were excluded.
Incidence of consultation for various infections and influenza vaccination among GBS cases (open bars) and matched controls (dark bars) by time from GBS consultation in cases. X-axis - time from GBS consultation in cases or pseudo-outcome date in controls (months), y-axis - percentage of individuals consulting for infections or vaccination.
The final dataset comprised 553 cases and 5445 matched controls. We based power calculations on the ability to detect a significant difference in the prior two-month incidence of Campylobacter infection between cases and controls. We used data from a community-based cohort study of IID in England to estimate the two-month incidence of Campylobacter infection in the general population . Assuming a conservative value for the between-sets correlation coefficient of 0.2, our study had 90% power to detect a minimum odds ratio of 10 at the 0.05 significance level.
We created indicator variables defining whether or not an individual had consulted for each of the exposures within the 60-day risk period. An individual was allowed to contribute only one consultation per condition during this period, resulting in a set of binary exposures.
We computed univariate matched odds ratios (ORs) and 95% confidence intervals (CIs) using conditional logistic regression. With the exception of one case with influenza-like illness who also received polio vaccine within the two-month exposure period, there were no individuals with multiple exposure events (two or more infections or vaccinations, or infection and vaccination); multivariable analysis was thus not performed. For GBS patients with preceding influenza-like illness or polio vaccination, for which there were sufficient numbers, we compared the median number of GP consultations for any condition in the 12 months following GBS diagnosis with that in the 12 months prior to GBS diagnosis using the Wilcoxon signed-rank test for matched pairs. All analyses were performed using Stata version 8.0 (StataCorp, Texas).
Correction for under-ascertainment of Campylobacter infection
There is considerable under-ascertainment of infection in the GPRD: not all community Campylobacter enteritis cases present to general practice and, of those that do, only some are confirmed microbiologically. Recording of infections in patients' records may also be incomplete. The degree of under-ascertainment will vary between organisms, but is non-differential (independent of case or control status), as infection is diagnosed prior to GBS. Thus, the estimate of the OR will, on average, be biased towards the null; for a given infection incidence, the lower the ascertainment, the greater the bias . For Campylobacter enteritis, the community incidence in England is estimated at 8.7 per 1000 personyears . The incidence in the GPRD population is 0.5 per 1000 personyears. The ratio of GPRD to community incidences estimates the ascertainment probability for Campylobacter enteritis (0.058). We assume the specificity to be 1.0, as a culture-confirmed diagnosis of Campylobacter is unlikely to be false positive.
For a two-by-two table with a exposed cases, b exposed controls, c unexposed cases and d unexposed controls, the expected number of truly exposed cases is a/s, where s is the ascertainment probability. Similarly, b/s gives the expected number of truly exposed controls. By re-assigning the appropriate number of individuals from c to a and d to b, a corrected estimate of the true OR is obtained. This adjustment disregards matching and does not account for variability in ascertainment; bias could still arise if ascertainment probability is associated with the matching factors. The major factor influencing ascertainment is likely to be GP clinic, as diagnostic practices differ between clinics. We performed an OR correction by simulating 1000 matched case-control analyses in which the ascertainment probability for Campylobacter was fixed within clinics, regardless of case or control status, but allowed to vary between clinics. We assumed an underlying population of GP clinics with a true Campylobacter enteritis incidence of 8.7/1000 personyears. We then obtained GP clinic-specific incidences of Campylobacter enteritis using standard survival analysis methods similar to those in our previous GPRD study . The ratio of these to the true incidence gives a distribution of ascertainment probabilities, s, across all clinics. The logarithm of this distribution is approximately Normal with mean −3.01 and standard deviation 0.76 (data not shown). For each clinic, we randomly assigned a value of s from this distribution. Within each clinic, we calculated the probability that an unexposed case actually had prior Campylobacter infection, (a/s−a)/c, based on this value of s and conditional values of a and c from the observed results (table 1, row 1). The corresponding probability for controls was calculated using the respective values for b and d. These two probabilities were applied to unexposed individuals within clinics to randomly re-assign exposure status among cases and controls, and an OR estimate obtained by conditional logistic regression. A thousand such simulations were performed to obtain the corrected OR distribution. The median OR and central 95% range of this distribution are presented. Comparable community incidence estimates were unavailable for other organisms; correction for under-ascertainment of these was not attempted.
Population attributable fraction (PAF)
We estimated the proportion of GBS cases attributable to Campylobacter as:where p represents the Campylobacter enteritis prevalence among cases. We estimated p as the mean number of exposed cases across the 1000 simulations divided by the total number of cases.
Figures 2a–f show clearly elevated incidences of consultation for Campylobacter, EBV, ILI, IID and ARI in the two months prior to GBS consultation in cases compared with controls. No such difference is apparent for influenza vaccination.
Table 1 presents exposure distributions in cases and controls, matched ORs, 95% CIs and p-values. For polio vaccination, 16 instances of vaccination were identified among cases, but none among controls; a lower 95% confidence limit for the OR by exact likelihood methods, using the PROC LOGISTIC module in SAS version 9.1 (SAS Institute, North Carolina), was not estimable. The excess risk of GBS in the two months following Campylobacter infection, independent of GP clinic, sex, age and season, was 38-fold (OR = 38.4, 95% CI: 4.3–343.5); for EBV, the excess risk was 20-fold. Confidence intervals are wide, reflecting the small number of these infections identified. Influenza-like illness carried an 18-fold increase in GBS risk (OR = 18.6, 95% CI: 7.5–46.4); for IID and ARI, the excess risks were seven- and five-fold respectively. Influenza vaccination appeared protective (OR = 0.16, 95% CI: 0.02–1.25), although this result was not significant at the 0.05 level of precision.
Among GBS patients with influenza-like illness, there were a total of 256 GP consultations for any condition in the 12 months following GBS diagnosis, compared with 145 in the 12 months prior to GBS. The difference in the median number of presentations between these two time periods was highly significant (post-GBS median = 16, interquartile range (IQR): 10–26; pre-GBS median = 10, IQR: 4–11, Wilcoxon signed-rank z = 3.13, p = 0.0017). No such difference was found for GBS cases with preceding polio vaccination.
Corrected Campylobacter estimates
With a fixed under-ascertainment probability of 0.058, the corrected OR was 44.8. The corrected estimate allowing for clinic-level matching and ascertainment variability yielded an OR distribution with median 58.7 and central 95% range 36.9–105.2 (figure 3). One fifth of GBS cases were attributable to Campylobacter (PAF = 20.1%).
We have found strong, positive associations between infection with Campylobacter, EBV and ILI and GBS risk. Specifically, individuals with Campylobacter enteritis are 38 times more likely to be diagnosed with GBS in the subsequent two months, and our correction for under-ascertainment of Campylobacter infection suggests that the excess risk could be 60-fold. Approximately 20% of GBS cases are attributable to Campylobacter infection.
Our results also provide evidence for an 18-fold increased risk of GBS in the two months following ILI. Such a strong, quantitative association with ILI has not previously been reported. Given the high incidence of influenza during epidemic seasons, the burden of GBS attributable to this organism could be substantial. We found some evidence of significant excess use of primary care services in the 12 months following GBS diagnosis among patients with preceding ILI, with a median of six excess consultations compared with the 12 month period preceding GBS diangosis. However, this does not take into account the nature of the consultations and may not reliably reflect the extent of excess healthcare use, since many GBS cases may receive follow-up care at hospital outpatient departments, and these consultations will not appear on their primary care records. It should be noted that our estimate of the excess risk of GBS following ILI will be influenced both by under-ascertainment of true influenza and inclusion of false-positive influenza, as most cases are not virologically confirmed. In both these situations, the OR will, on average, be under-estimated; the true OR could be higher than that observed. As influenza incidence varies greatly both within and between years, the PAF for this organism will vary over time. The lower ORs for IID and ARI are not surprising, as most of these infections will be caused by pathogens unrelated with GBS.
Unlike previous reports, we found evidence suggesting a protective effect of influenza vaccination on GBS risk. This finding is biologically plausible–influenza vaccination provides some protection against influenza infection and, hence, associated complications. It is, however, also possible that the protective effect of influenza vaccination is a result of individuals suffering a recent acute infection being less likely to be offered vaccine. As there were no individuals who both suffereed ILI and received vaccine within the exposure period, we were unable to investigate this possibility. Historical cohort studies of primary care data comparing GBS risk among vaccinees and non-vaccinees would be better suited to address this. The apparent protective effect of vaccine found here is not inconsistent with an absolute increase in GBS risk following influenza vaccination, but indicates that this is much smaller than the risk associated with influenza infection. The balance between GBS risk and protection from vaccine will reflect the frequency of influenza in a given season. The exact vaccine formulation could also influence risk. An association with polio vaccination was also apparent, although it should be noted that while most such vaccinations take place among young children, the majority of GBS cases occur in older individuals. It is thus unlikely that polio vaccination accounts for a substantial proportion of GBS cases in the UK. Historical cohort studies, as described above for influenza vaccination, could yield further insight into the association between GBS and polio vaccination, and could in addition investigate the effect of vaccine dosage.
Our study has certain limitations. Individuals consulting general practice are symptomatic. Evidence suggests that, at least for Campylobacter, GBS may arise following asymptomatic infection ; we could not address this in our study. Other than age and sex, GPRD data contain little information on potential confounders, such as geographic location and socioeconomic status; we addressed this by matching on GP clinic. Due to under-ascertainment of infections, our estimates are likely to be biased towards the null. For Campylobacter enteritis, for which a reliable estimate of community incidence exists, we corrected for this by accounting for the magnitude and variability of ascertainment at clinic level, the factor most likely to influence ascertainment. Some residual bias might remain through ascertainment differences by sex and/or age. Although such residual bias could affect the magnitude of bias in the OR, it is unlikely to affect its direction unless ascertainment is differential (dependent on case status) in one or more age/sex strata. We think this highly unlikely, as in our study infection was determined before GBS. Our correction additionally assumes that clinic-level variation in Campylobacter incidence is entirely due to ascertainment differences rather than differences in true incidence. These two factors cannot be disentangled without knowledge of the variation in true Campylobacter incidence across clinics. Given the low ascertainment in all GP clinics, we believe this assumption is reasonable.
Our analysis has several advantages over previous GBS risk factor studies. Firstly, we used a representative sample of cases and controls from the UK population; our results are more generalizable than those of studies conducted in hospital settings. Secondly, although our study suffered from under-ascertainment of infections, this was non-differential. By contrast, exposure misclassification in studies using serology to determine prior Campylobacter infection cannot be expected to be non-differential. Evidence suggests that following Campylobacter infection, antibody levels remain elevated for several months and even years –. The temporal association between Campylobacter and GBS means that seropositivity in GBS cases is more likely to indicate true recent infection, while in controls it could signify recent infection, past infection, or immunity. Such studies thus overestimate the incidence of recent infection in controls relative to cases, yielding ORs substantially below those observed in our study.
Our findings indicate the value of primary care data for studying rare complications of infectious diseases. Although ascertainment of infections can be low, figure 2 clearly demonstrates that such systems are sensitive for detecting temporal associations between infection and sequelae. We recommend more widespread use of such systems for surveillance purposes. The data are routinely available, considerably cheaper than the operating costs for a dedicated surveillance system, and particularly advantageous for rare conditions. There are also considerable advantages for observational studies; cases are effectively nested within a cohort, minimizing the risk of selection, recall and diagnostic biases, common problems in conventional case-control studies.
Using this strategy, we have detected two novel findings: an increased risk of GBS following ILI and a possible protective effect of influenza vaccination. Clinicians should consider recent history of influenza as a possible triggering factor in GBS cases. Our findings also suggest that influenza vaccination may provide additional, indirect effects through protection against complications of influenza infection. Further studies to determine the incidence of GBS following both vaccination against and infection with influenza are warranted.
The authors thank Dr Sara Thomas, Dr Bianca de Stavola and Craig Higgins for helpful discussions on the analysis.
Conceived and designed the experiments: LR CT SO IP AI AH. Analyzed the data: CT. Wrote the paper: LR CT SO.
- 1. Hughes RA, Rees JH (1997) Clinical and epidemiologic features of Guillain-Barre syndrome. J Infect Dis 176 Suppl 2: S92–98.RA HughesJH Rees1997Clinical and epidemiologic features of Guillain-Barre syndrome.J Infect Dis176 Suppl 2S9298
- 2. Rees JH, Soudain SE, Gregson NA, Hughes RA (1995) Campylobacter jejuni infection and Guillain-Barre syndrome. N Engl J Med 333: 1374–1379.JH ReesSE SoudainNA GregsonRA Hughes1995Campylobacter jejuni infection and Guillain-Barre syndrome.N Engl J Med33313741379
- 3. Mishu B, Ilyas AA, Koski CL, Vriesendorp F, Cook SD, et al. (1993) Serologic evidence of previous Campylobacter jejuni infection in patients with the Guillain-Barre syndrome. Ann Intern Med 118: 947–953.B. MishuAA IlyasCL KoskiF. VriesendorpSD Cook1993Serologic evidence of previous Campylobacter jejuni infection in patients with the Guillain-Barre syndrome.Ann Intern Med118947953
- 4. Enders U, Karch H, Toyka KV, Michels M, Zielasek J, et al. (1993) The spectrum of immune responses to Campylobacter jejuni and glycoconjugates in Guillain-Barre syndrome and in other neuroimmunological disorders. Ann Neurol 34: 136–144.U. EndersH. KarchKV ToykaM. MichelsJ. Zielasek1993The spectrum of immune responses to Campylobacter jejuni and glycoconjugates in Guillain-Barre syndrome and in other neuroimmunological disorders.Ann Neurol34136144
- 5. Hao Q, Saida T, Kuroki S, Nishimura M, Nukina M, et al. (1998) Antibodies to gangliosides and galactocerebroside in patients with Guillain-Barre syndrome with preceding Campylobacter jejuni and other identified infections. J Neuroimmunol 81: 116–126.Q. HaoT. SaidaS. KurokiM. NishimuraM. Nukina1998Antibodies to gangliosides and galactocerebroside in patients with Guillain-Barre syndrome with preceding Campylobacter jejuni and other identified infections.J Neuroimmunol81116126
- 6. Guarino M, Casmiro M, D'Alessandro R (1998) Campylobacter jejuni infection and Guillain-Barre syndrome: a case-control study. Emilia-Romagna Study Group on Clinical and Epidemiological problems in neurology. Neuroepidemiol 17: 296–302.M. GuarinoM. CasmiroR. D'Alessandro1998Campylobacter jejuni infection and Guillain-Barre syndrome: a case-control study. Emilia-Romagna Study Group on Clinical and Epidemiological problems in neurology.Neuroepidemiol17296302
- 7. Ho TW, Mishu B, Li CY, Gao CY, Cornblath DR, et al. (1995) Guillain-Barre syndrome in northern China. Relationship to Campylobacter jejuni infection and anti-glycolipid antibodies. Brain 118(Pt 3): 597–605.TW HoB. MishuCY LiCY GaoDR Cornblath1995Guillain-Barre syndrome in northern China. Relationship to Campylobacter jejuni infection and anti-glycolipid antibodies.Brain118Pt 3597605
- 8. Jacobs BC, Rothbarth PH, van der Meche FG, Herbrink P, Schmitz PI, et al. (1998) The spectrum of antecedent infections in Guillain-Barre syndrome: a case-control study. Neurology 51: 1110–1115.BC JacobsPH RothbarthFG van der MecheP. HerbrinkPI Schmitz1998The spectrum of antecedent infections in Guillain-Barre syndrome: a case-control study.Neurology5111101115
- 9. Kaldor J, Speed BR (1984) Guillain-Barre syndrome and Campylobacter jejuni: a serological study. BMJ (Clin Res Ed) 288: 1867–1870.J. KaldorBR Speed1984Guillain-Barre syndrome and Campylobacter jejuni: a serological study.BMJ (Clin Res Ed)28818671870
- 10. Koga M, Yuki N, Takahashi M, Saito K, Hirata K (1998) Close association of IgA anti-ganglioside antibodies with antecedent Campylobacter jejuni infection in Guillain-Barre and Fisher's syndromes. J Neuroimmunol 81: 138–143.M. KogaN. YukiM. TakahashiK. SaitoK. Hirata1998Close association of IgA anti-ganglioside antibodies with antecedent Campylobacter jejuni infection in Guillain-Barre and Fisher's syndromes.J Neuroimmunol81138143
- 11. Kuroki S, Saida T, Nukina M, Haruta T, Yoshioka M, et al. (1993) Campylobacter jejuni strains from patients with Guillain-Barre syndrome belong mostly to Penner serogroup 19 and contain beta-N-acetylglucosamine residues. Ann Neurol 33: 243–247.S. KurokiT. SaidaM. NukinaT. HarutaM. Yoshioka1993Campylobacter jejuni strains from patients with Guillain-Barre syndrome belong mostly to Penner serogroup 19 and contain beta-N-acetylglucosamine residues.Ann Neurol33243247
- 12. McCarthy N, Giesecke J (2001) Incidence of Guillain-Barré Syndrome following infection with Campylobacter jejuni. Am J Epidemiol 153: 610–614.N. McCarthyJ. Giesecke2001Incidence of Guillain-Barré Syndrome following infection with Campylobacter jejuni.Am J Epidemiol153610614
- 13. Tam CC, Rodrigues LC, O'Brien SJ (2003) Guillain-Barre syndrome associated with Campylobacter jejuni infection in England, 2000–2001. Clin Infect Dis 37: 307–310.CC TamLC RodriguesSJ O'Brien2003Guillain-Barre syndrome associated with Campylobacter jejuni infection in England, 2000–2001.Clin Infect Dis37307310
- 14. Tam CC, Rodrigues LC, Petersen I, Islam A, Hayward A, et al. (2006) Incidence of Guillain-Barré syndrome following Campylobacter infection in the General Practice Research Database. J Infect Dis 194: 95–97.CC TamLC RodriguesI. PetersenA. IslamA. Hayward2006Incidence of Guillain-Barré syndrome following Campylobacter infection in the General Practice Research Database.J Infect Dis1949597
- 15. Winer JB, Hughes RA, Anderson MJ, Jones DM, Kangro H, et al. (1988) A prospective study of acute idiopathic neuropathy. II. Antecedent events. J Neurol Neurosurg Psychiatry 51: 613–618.JB WinerRA HughesMJ AndersonDM JonesH. Kangro1988A prospective study of acute idiopathic neuropathy. II. Antecedent events.J Neurol Neurosurg Psychiatry51613618
- 16. Ju YY, Womersley H, Pritchard J, Gray I, Hughes RA, et al. (2004) Haemophilus influenzae as a possible cause of Guillain-Barre syndrome. J Neuroimmunol 149: 160–166.YY JuH. WomersleyJ. PritchardI. GrayRA Hughes2004Haemophilus influenzae as a possible cause of Guillain-Barre syndrome.J Neuroimmunol149160166
- 17. Susuki K, Odaka M, Mori M, Hirata K, Yuki N (2004) Acute motor axonal neuropathy after Mycoplasma infection: Evidence of molecular mimicry. Neurology 62: 949–956.K. SusukiM. OdakaM. MoriK. HirataN. Yuki2004Acute motor axonal neuropathy after Mycoplasma infection: Evidence of molecular mimicry.Neurology62949956
- 18. Ang CW, Tio-Gillen AP, Groen J, Herbrink P, Jacobs BC, et al. (2002) Cross-reactive anti-galactocerebroside antibodies and Mycoplasma pneumoniae infections in Guillain-Barre syndrome. J Neuroimmunol 130: 179–183.CW AngAP Tio-GillenJ. GroenP. HerbrinkBC Jacobs2002Cross-reactive anti-galactocerebroside antibodies and Mycoplasma pneumoniae infections in Guillain-Barre syndrome.J Neuroimmunol130179183
- 19. Bertrand A, Janbon F, Clot J, Milane J, Bosc E (1971) [Guillain-Barre polyradiculoneuritis and influenza virus]. Presse Med 79: 2328.A. BertrandF. JanbonJ. ClotJ. MilaneE. Bosc1971[Guillain-Barre polyradiculoneuritis and influenza virus].Presse Med792328
- 20. Kruger H, Franke M (1974) [Postinfluenzal, chronic Guillain-Barre syndrome with oligoclonic gammopathy and generalized amyloidosis]. Psychiatr Neurol Med Psychol (Leipz) 26: 513–526.H. KrugerM. Franke1974[Postinfluenzal, chronic Guillain-Barre syndrome with oligoclonic gammopathy and generalized amyloidosis].Psychiatr Neurol Med Psychol (Leipz)26513526
- 21. Migita M, Matsumoto T, Fujino O, Takaishi Y, Yuki N, et al. (2001) Two cases of influenza with impaired ocular movement. Eur J Paediatr Neurol 5: 83–85.M. MigitaT. MatsumotoO. FujinoY. TakaishiN. Yuki2001Two cases of influenza with impaired ocular movement.Eur J Paediatr Neurol58385
- 22. Novak M (1975) [Guillain-Barre syndrome as a sequela of influenza]. Cesk Neurol Neurochir 38: 314–316.M. Novak1975[Guillain-Barre syndrome as a sequela of influenza].Cesk Neurol Neurochir38314316
- 23. Wells CE, James WR, Evans AD (1959) Guillain-Barre syndrome and virus of influenza A (Asian strain); report of two fatal cases during the 1957 epidemic in Wales. AMA Arch Neurol Psychiatry 81: 699–705.CE WellsWR JamesAD Evans1959Guillain-Barre syndrome and virus of influenza A (Asian strain); report of two fatal cases during the 1957 epidemic in Wales.AMA Arch Neurol Psychiatry81699705
- 24. Tam CC, O'Brien SJ, Rodrigues LC (2006) Influenza, Campylobacter and Mycoplasma Infections, and Hospital Admissions for Guillain-Barré Syndrome, England. Emerg Infect Dis 12: 1881–1887.CC TamSJ O'BrienLC Rodrigues2006Influenza, Campylobacter and Mycoplasma Infections, and Hospital Admissions for Guillain-Barré Syndrome, England.Emerg Infect Dis1218811887
- 25. Safranek TJ, Lawrence DN, Kurland LT, Culver DH, Wiederholt WC, et al. (1991) Reassessment of the association between Guillain-Barre syndrome and receipt of swine influenza vaccine in 1976–1977: results of a two-state study. Expert Neurology Group. Am J Epidemiol 133: 940–951.TJ SafranekDN LawrenceLT KurlandDH CulverWC Wiederholt1991Reassessment of the association between Guillain-Barre syndrome and receipt of swine influenza vaccine in 1976–1977: results of a two-state study. Expert Neurology Group.Am J Epidemiol133940951
- 26. Kinnunen E, Junttila O, Haukka J, Hovi T (1998) Nationwide oral poliovirus vaccination campaign and the incidence of Guillain-Barre Syndrome. Am J Epidemiol 147: 69–73.E. KinnunenO. JunttilaJ. HaukkaT. Hovi1998Nationwide oral poliovirus vaccination campaign and the incidence of Guillain-Barre Syndrome.Am J Epidemiol1476973
- 27. Bogliun G, Beghi E (2004) Incidence and clinical features of acute inflammatory polyradiculoneuropathy in Lombardy, Italy, 1996. Acta Neurol Scand 110: 100–106.G. BogliunE. Beghi2004Incidence and clinical features of acute inflammatory polyradiculoneuropathy in Lombardy, Italy, 1996.Acta Neurol Scand110100106
- 28. Hughes RA, Charlton J, Latinovic R, Gulliford MC (2006) No association between immunization and Guillain-Barre syndrome in the United Kingdom, 1992 to 2000. Arch Intern Med 166: 1301–1304.RA HughesJ. CharltonR. LatinovicMC Gulliford2006No association between immunization and Guillain-Barre syndrome in the United Kingdom, 1992 to 2000.Arch Intern Med16613011304
- 29. Walley T, Mantgani A (1997) The UK General Practice Research Database. Lancet 350: 1097–1099.T. WalleyA. Mantgani1997The UK General Practice Research Database.Lancet35010971099
- 30. Lewis JD, Bilker WB, Weinstein RB, Strom BL (2005) The relationship between time since registration and measured incidence rates in the General Practice Research Database. Pharmacoepidemiol Drug Saf 14: 443–451.JD LewisWB BilkerRB WeinsteinBL Strom2005The relationship between time since registration and measured incidence rates in the General Practice Research Database.Pharmacoepidemiol Drug Saf14443451
- 31. Wheeler JG, Sethi D, Cowden JM, Wall PG, Rodrigues LC, et al. (1999) Study of infectious intestinal disease in England: rates in the community, presenting to general practice, and reported to national surveillance. The Infectious Intestinal Disease Study Executive. BMJ 318: 1046–1050.JG WheelerD. SethiJM CowdenPG WallLC Rodrigues1999Study of infectious intestinal disease in England: rates in the community, presenting to general practice, and reported to national surveillance. The Infectious Intestinal Disease Study Executive.BMJ31810461050
- 32. Flegal KM, Brownie C, Haas JD (1986) The effects of exposure misclassification on estimates of relative risk. Am J Epidemiol 123: 736–751.KM FlegalC. BrownieJD Haas1986The effects of exposure misclassification on estimates of relative risk.Am J Epidemiol123736751
- 33. Coughlin SS, Benichou J, Weed DL (1994) Attributable risk estimation in case-control studies. Epidemiol Rev 16: 51–64.SS CoughlinJ. BenichouDL Weed1994Attributable risk estimation in case-control studies.Epidemiol Rev165164
- 34. Kuroki S, Haruta T, Yoshioka M, Kobayashi Y, Nukina M, et al. (1991) Guillain-Barre syndrome associated with Campylobacter infection. Pediatr Infect Dis J 10: 149–151.S. KurokiT. HarutaM. YoshiokaY. KobayashiM. Nukina1991Guillain-Barre syndrome associated with Campylobacter infection.Pediatr Infect Dis J10149151
- 35. Cawthraw SA, Feldman RA, Sayers AR, Newell DG (2002) Long-term antibody responses following human infection with Campylobacter jejuni. Clin Exp Immunol 130: 101–106.SA CawthrawRA FeldmanAR SayersDG Newell2002Long-term antibody responses following human infection with Campylobacter jejuni.Clin Exp Immunol130101106
- 36. Strid MA, Engberg J, Larsen LB, Begtrup K, Molbak K, et al. (2001) Antibody responses to Campylobacter infections determined by an enzyme-linked immunosorbent assay: 2-year follow-up study of 210 patients. Clin Diagn Lab Immunol 8: 314–319.MA StridJ. EngbergLB LarsenK. BegtrupK. Molbak2001Antibody responses to Campylobacter infections determined by an enzyme-linked immunosorbent assay: 2-year follow-up study of 210 patients.Clin Diagn Lab Immunol8314319
- 37. Taylor BV, Williamson J, Luck J, Coleman D, Jones D, et al. (2004) Sensitivity and specificity of serology in determining recent acute Campylobacter infection. Intern Med J 34: 250–258.BV TaylorJ. WilliamsonJ. LuckD. ColemanD. Jones2004Sensitivity and specificity of serology in determining recent acute Campylobacter infection.Intern Med J34250258