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Potential risk factors associated with human encephalitis: application of canonical correlation analysis
- Jemila S Hamid^{1, 2, 3}Email author,
- Christopher Meaney^{4},
- Natasha S Crowcroft^{3, 5},
- Julia Granerod^{6},
- Joseph Beyene^{1, 2, 3}Email author and
- the UK Health Protection Agency Aetiology of Encephalitis Study Group
https://doi.org/10.1186/1471-2288-11-120
© Hamid et al; licensee BioMed Central Ltd. 2011
Received: 20 November 2010
Accepted: 22 August 2011
Published: 22 August 2011
Abstract
Background
Infection of the CNS is considered to be the major cause of encephalitis and more than 100 different pathogens have been recognized as causative agents. Despite being identified worldwide as an important public health concern, studies on encephalitis are very few and often focus on particular types (with respect to causative agents) of encephalitis (e.g. West Nile, Japanese, etc.). Moreover, a number of other infectious and non-infectious conditions present with similar symptoms, and distinguishing encephalitis from other disguising conditions continues to a challenging task.
Methods
We used canonical correlation analysis (CCA) to assess associations between set of exposure variable and set of symptom and diagnostic variables in human encephalitis. Data consists of 208 confirmed cases of encephalitis from a prospective multicenter study conducted in the United Kingdom. We used a covariance matrix based on Gini's measure of similarity and used permutation based approaches to test significance of canonical variates.
Results
Results show that weak pair-wise correlation exists between the risk factor (exposure and demographic) and symptom/laboratory variables. However, the first canonical variate from CCA revealed strong multivariate correlation (ρ = 0.71, se = 0.03, p = 0.013) between the two sets. We found a moderate correlation (ρ = 0.54, se = 0.02) between the variables in the second canonical variate, however, the value is not statistically significant (p = 0.68). Our results also show that a very small amount of the variation in the symptom sets is explained by the exposure variables. This indicates that host factors, rather than environmental factors might be important towards understanding the etiology of encephalitis and facilitate early diagnosis and treatment of encephalitis patients.
Conclusions
There is no standard laboratory diagnostic strategy for investigation of encephalitis and even experienced physicians are often uncertain about the cause, appropriate therapy and prognosis of encephalitis. Exploration of human encephalitis data using advanced multivariate statistical modelling approaches that can capture the inherent complexity in the data is, therefore, crucial in understanding the causes of human encephalitis. Moreover, application of multivariate exploratory techniques will generate clinically important hypotheses and offer useful insight into the number and nature of variables worthy of further consideration in a confirmatory statistical analysis.
Keywords
Background
Encephalitis is a complex clinical syndrome of the central nervous system (CNS) associated with fatal outcome or severe permanent damage including cognitive and behavioral impairment and epileptic seizures [1–5]. It is often acute, although symptoms may progress rapidly, causing severe debilitation to patients including otherwise healthy children [2, 3]. Lewis and Glaser define encephalitis as an acute CNS dysfunction with radiographic or laboratory evidence of brain inflammation [2]. There is no standard laboratory diagnostic strategy for investigation of encephalitis and even experienced physicians often are uncertain about the cause, appropriate therapy and prognosis [1–3, 6].
Despite being identified worldwide as an important public health concern, retrospective studies on encephalitis are very few and studies often focus on particular types (often with respect to causative agents) of encephalitis (West Nile, Japanese, etc.). However, there are relatively more studies in the pediatric population [2, 3, 7, 8]. Moreover, current knowledge about encephalitis is limited to descriptive statistics. As a result, a comprehensive understanding of human encephalitis, as generated through high quality evidence-based studies and statistical analyses is limited and much of the current knowledge base lacks generalizability [2, 9–11].
Encephalitis is characterized by fever, headache and altered level of consciousness together with seizures and focal neurological findings in some cases [1, 3, 11]. Using data from the same prospective study presented in this paper, our group previously identified fever, personality and behavioural change, headache and lethargy, as the main characteristics of human encephalitis [10, 11]. It was also shown that diagnostic variables such as abnormal brain scan and cerebrospinal fluid measurements are also indicators of encephalitis. Seizures, focal neurological deficits, stiff neck, urinary symptoms, respiratory symptoms and gastro-intestinal symptoms have also been previously shown to be associated with encephalitis [1, 2, 11]. Fowler et al., in retrospective study of paediatric encephalitis, found that fever and encephalopathy were the main disease characteristics in a Swedish sample [3].
Encephalitis is a rare disease, with annual incidence ranging between 3.5-7.4 cases per 100,000 persons worldwide [1, 2, 12]. It affects people of all ages; however, the condition is more common in children, the elderly and persons with a weakened immune system (e.g. HIV/AIDS patients and patients undergoing cancer treatment). Encephalitis is known to affect both sexes; however, most studies have indicated a slightly higher incidence rate in males [1, 13–15]. The epidemiology of encephalitis is difficult to summarize since few population based studies exist, many causal pathogens are capable of inducing encephalitis-like symptoms and most cases go unreported to health authorities. Consequently, many details about its epidemiology have yet to be explained [1, 2, 10].
To date, infection of the CNS is considered to be the major cause of encephalitis and more than 100 different pathogens have been recognized as causative agents [1, 10]. However, an estimated 32-85% of cases have unknown disease etiology [1, 16–20]. For instance, about 85% of the 189 cases in a study conducted in Minnesota, USA are of unknown cause [20]. In a California based study, about 65% of the 334 cases are of unknown etiology [18]. In a study conducted in the UK, about 60% of 700 cases are of unknown etiology [16]. Among the known causes, Herpes Simplex Virus (HSV) has been recognized as the most common etiology [1, 10, 20]. Viruses, bacteria, fungi as well as parasites can cause encephalitis [1–3]. Rarely, encephalitis can also be triggered by brain injury, brain tumor, drug reactions and lead poisoning. The main infectious causes of encephalitis are listed in a review paper by Granerod and Crowcroft [1].
In many parts of the world, viral infections of the central nervous system are often spread via vector-borne infection, such as mosquito bites and tick bites; however, animal-to-human interactions also can facilitate disease spread (e.g. raccoon feces, cat scratches, animal bites) and human-to-human transmission is also possible. Bacteria causing encephalitis can also spread through animal contact and water exposure. Possible risk factors associated with encephalitis and disease pathologies are provided in Lewis and Glaser [2].
A number of other infectious and non-infectious conditions present with similar symptoms and hence a challenge lies in distinguishing encephalitis from other disguising conditions [1, 2, 6]. Exploration of human encephalitis data using advanced multivariable statistical modelling approaches that can capture the inherent complexity in the data is, therefore, crucial for elucidating the causes of human encephalitis. Moreover, application of multivariate exploratory techniques will generate clinically important and better focused hypotheses that would benefit encephalitis researchers in reducing the number of variables to be considered for further confirmatory statistical analysis. This will ultimately lead towards better evidence-based clinical practices, including: diagnosis, prognosis discovery and development of novel therapeutic options.
In this paper, we use canonical correlation analysis (CCA) to explore the relationship between a set of exposure variables that are potential risk factors and a set of symptom and diagnostic variables in encephalitis. The symptom and diagnostic variables considered in this paper include variables that are previously identified as main indicators of encephalitis as well as those with a potential to be associated with the disease. Our data consist mostly of binary variables (presence or absence of a particular attribute) and as a result, the usual correlation matrix which is particularly designed for continuous measurements is not appropriate. We therefore propose to use a correlation matrix based on Gini's idea of variance or likeability for categorical variables.
Methods
Study population and data description
List of the two sets of variables: One set consisting of 13 exposure and 2 demographic variables, and a second set consisting of 18 symptoms, clinical and 6 diagnostic variables
Exposure and Demographic Variables | Symptom/clinical and Diagnostic Variables |
---|---|
Animal contact | Lethargy |
Tick bite | Personality/behavioral changes |
Mosquito bite | Seizure |
Insect bite | Stiff neck |
Immunization | Headache |
Recent infection | Irritability |
Travel abroad | Fever |
Travel within UK | Focal neurological findings |
Raw fish | Coma |
Untreated water | Neurological signs |
Head trauma | Gastrointestinal symptoms |
Sick person contact | Respiratory symptoms |
Water Exposure | Confusion |
Age | Photophobia |
Gender | Rash |
Urinary symptoms | |
Duration of illness | |
Length of Hospital Stay | |
Abnormal white blood cell count (WCC) | |
Abnormal magnetic resonance imaging (MRI) | |
Abnormal computed tomography (CT) | |
Abnormal electroencephalography (EEG) | |
Abnormal glucose | |
Abnormal protein |
Methods
We used canonical correlation analysis (CCA) to investigate the relationship between the set of exposure and demographic variables (X) and the set of symptom, clinical and diagnostic variables (Y) in human encephalitis.
Canonical Correlation Analysis (CCA)
where, the Eigen-values λ, which sometimes are denoted by r^{2}, represent the squared canonical correlations. The set of Eigen-vectors ( a , b ) corresponding to the leading eigenvalue are solutions to equation (1). The first canonical covariate is therefore the one which explains most of the relationship. CCA has been successfully applied in medical and epidemiological research [26, 27]
Covariance/Correlation matrix for categorical data
Since data in this study consist mostly of binary variables (presence or absence of a particular attribute), the usual correlation matrix, which is particularly designed for continuous measurements would not be an appropriate choice. Covariance or correlation matrices for categorical data have been previously considered by many and several formulations have been proposed to assess the strength of association between two categorical variables. Here we use the covariance/correlation matrix proposed by Okada et al. [29, 30]. Their approach is a generalization of Gini's definition of variance or likeability for categorical data, which is also known as Gini's index [28–33].
Simplified formulas for two special cases (binary and trinomial variables), using 2 × 2 and 3 × 3 contingency tables, can be found in Okada et al. [30, 33]. We implemented the above variance-covariance/correlation formula in the R statistical software and used it in our CCA analysis. Pairwise available data were used when missing values occur.
Statistical analysis is performed using the Canonical Correlation Analysis (CCA) and Significance Tests for Canonical Correlation Analysis (CCP) libraries in the R software package [34–36]. Parametric multivariate tests are not appropriate since our data consists of binary variables and hence violates the multivariate normality assumption. We, therefore, used a non-parametric permutation approach and calculated standard errors and p-values based on 10,000 permutations.
Results and Discussion
Descriptive statistics for data on the 208 confirmed encephalitis patients
Variables | Present | Absent | Missing |
---|---|---|---|
Exposure Variables and Demographic | |||
Sex (male) | 113 (54.3%) | 95 (45.7%) | 0 (0%) |
Age (≤ 10) | 55 (26.4%) | 146 (70.2%) | 7 (3.4%) |
Animal Contact | 101 (48.6%) | 95 (45.7%) | 12 (5.8%) |
Tick Bite | 7 (3.4%) | 188(90.4%) | 13 (6.3%) |
Mosquito Bite | 13 (6.3%) | 182 (87.5%) | 13 (6.3%) |
Insect Bite | 14(6.7%) | 179 (86.1%) | 15 (7.2%) |
Immunization | 14 (6.7%) | 182 (87.5%) | 12 (5.8%) |
Recent Infection | 78 (37.5%) | 113 (54.3%) | 17 (8.2%) |
Travel Abroad | 27 (13%) | 174 (83.7%) | 7 (3.4%) |
Travel UK | 31 (14.9%) | 164 (78.8%) | 13 (6.3%) |
Raw Fish | 7 (3.4%) | 184(88.5%) | 17 (8.2%) |
Untreated Water | 6 (2.9%) | 185 (88.9%) | 17 (8.2%) |
Water Exposure | 38 (12.3%) | 157 (75.5%) | 13 (6.3%) |
Head Trauma | 23 (11.1%) | 173 (83.2%) | 12 (5.8%) |
Sick Person Contact | 54 (26%) | 136(65.4%) | 18 (8.7%) |
Symptom and Diagnostic Variables | |||
Abnormal CT | 51(24.5%) | 123 (59.1%) | 34 (16.3%) |
Abnormal MRI | 102 (49%) | 69 (33.2%) | 37 (17.8%) |
Abnormal EEG | 100 (48.1%) | 20 (9.6%) | 88(42.3%) |
Abnormal Glucose | 46(22.1%) | 84 (40.4%) | 78 (37.5%) |
Abnormal Protein | 124 (59.6%) | 71 (34.1%) | 13 (6.3%) |
Abnormal WCC | 160 (76.9%) | 42 (20.2%) | 6 (2.9%) |
Lethargy | 116 (55.8%) | 92(44.2%) | 0 (0%) |
Irritability | 77(37%) | 131 (63%) | 0 (0%) |
PB Change | 133 (63.9%) | 75 (36.1%) | 0 (0%) |
Seizure | 105(50.5%) | 103(49.5%) | 0 (0%) |
Stiff Neck | 46 (22.1%) | 162(77.9%) | 0 (0%) |
Headache | 125 (60.1%) | 83(39.9%) | 0 (0%) |
Fever | 162 (77.9%) | 46(22.1%) | 0 (0%) |
Focal-Neurological | 76 (36.5%) | 132(63.5%) | 0 (0%) |
Coma | 8 (3.8%) | 200(96.2%) | 0 (0%) |
Neurological | 63 (30.3%) | 145 (69.7%) | 0 (0%) |
GI Symptoms | 103(49.5%) | 105(50.5%) | 0 (0%) |
Respiratory | 42 (20.2%) | 166 (79.8%) | 0 (0%) |
Confusion | 74(35.6%) | 134(64.4%) | 0 (0%) |
Rash | 25 (12%) | 183 (88%) | 0 (0%) |
Photophobia | 16 (7.7%) | 192 (92.3%) | 0 (0%) |
Urinary | 21(10.1%) | 187 (89.9%) | 0 (0%) |
Hospital Stay (≤ 50 days) | 145(69.7%) | 60(28.8%) | 3(1.4%) |
Duration of illness (≤ 100 days) | 167(80.3%) | 31(14.9%) | 10(4.8%) |
The results in Table 2 show that men are at a slightly higher (54%, n = 113) risk of encephalitis than women (46%, n = 95). This is in agreement with previous findings [13–15]. Most of the encephalitis patients are children and young adults (median age = 30, IQR = 45) where a large proportion of the patients are children of age ≤ 10 (26%, n = 55) indicating that young children are at higher risk of developing encephalitis. The age distribution is quite uniform after age 10 where approximately equal proportions of patients (9.6%, n = 20) are observed in 10 years age intervals. We, therefore, used 10 as a cutoff point when dichotomizing age for the CCA analysis.
Our results show that the majority of encephalitis patients (69.7%, n = 145) had been hospitalized for ≤ 50 days (median = 27; IQR: 43) and duration of illness is less than 100 days (median = 37, IQR = 46.25) for large proportion (80%, n = 167) of the patients. Consequently, we used 50 days and 100 days as cutoffs when dichotomizing hospital stay and duration of illness for CCA analysis, respectively.
On the other hand, symptom and diagnostic variables have relatively larger event rates (Figure 2) where variables with the smallest rates are coma and photophobia which were observed on only 3.8% (n = 8) and 7.7% (n = 16) of the patients, respectively. Fever and abnormal white blood cell count (abnormal WCC)are indicated as the two main characteristics of encephalitis where 77.9% and 76.9% of the patients had fever and abnormal WCC, respectively (Figure 2, Table 2). The results also show that personality and behavioral change, headache, lethargy and abnormal protein are the next most frequently occurring characteristics of encephalitis. Some missingness are observed in the exposure variables (Figure 2); however, a significant amount of missing data are observed in diagnostic variables where measurements from EEG and Glucose were missing for 42.3% (n = 88) and 37.5% (n = 78) of the patients, respectively (Table 2 Figure 2). Consequently, abnormal EEG, although previously shown to be one of the main indicators of encephalitis, is observed on only half of the patients (48.1%). Nevertheless, among patients with available EEG measurements (n = 120), 83.3% (n = 100) of them have abnormal EEG which is in agreement with previous findings. This is mainly because the diagnostic decision tree often leads clinicians to carry out an EEG in patients with a high likelihood of it being abnormal. One of the triggers is seizures, for example. So patients with EEGs are a particular clinical cluster of their own.
CCA produced min (p, q) = 15 canonical variates; p = 15 is the number of variables in the Xset and q = 24 is the number of variables in the Yset. However, only the first canonical variate is statistically significant at α = 0.05 level. We will, therefore, discuss only the first canonical variate in this paper.
The cross-correlation matrix displayed in Figure 3 shows that weak pair-wise correlation exists between the risk factor (exposure and demographic) and outcome (symptom, clinical and diagnostic) variables. However, the first canonical solution/variate from CCA revealed strong multivariate correlation (ρ = 0.71, standard error (se) = 0.03, p-value = 0.013) between the two sets. We found a moderate correlation (ρ = 0.54, se = 0.02) between the variables in the second canonical variate, however, the value is not statistically significant (p-value = 0.68).
Canonical loadings of individual variables in their respective canonical variates for the first canonical solution of the CCA
Canonical Loadings (Structural Coefficients) | |||
---|---|---|---|
Exposure and Demographic Variables | Symptom and Diagnostic Variables | ||
Sex (male) | 0.03 | Abnormal CT | 0.07 |
Age (≤ 10) | 0.94 | Abnormal MRI | 0.08 |
Animal Contact | -0.04 | Abnormal EEG | 0.22 |
Tick Bite | 0.05 | Abnormal Glucose | -0.19 |
Mosquito Bite | 0.11 | Abnormal Protein | -0.39 |
Insect Bite | -0.08 | Abnormal WCC | -0.52 |
Immunization | 0.27 | Lethargy | 0.27 |
Recent Infection | -0.10 | Irritability | 0.28 |
Travel Abroad | -0.06 | PB Change | -0.36 |
Travel UK | -0.13 | Seizure | 0.24 |
Raw Fish | -0.05 | Stiff Neck | -0.12 |
Untreated Water | -0.05 | Headache | -0.51 |
Water Exposure | 0.18 | Fever | -0.03 |
Head Trauma | 0.13 | Focal-Neurological | -0.06 |
Sick Person Contact | 0.47 | Coma | 0.001 |
Neurological | -0.24 | ||
GI Symptoms | 0.08 | ||
Respiratory | 0.13 | ||
Confusion | -0.50 | ||
Rash | 0.11 | ||
Photophobia | -0.18 | ||
Urinary | -0.11 | ||
Hospital Stay (≤ 50 days) | 0.30 | ||
Duration of illness (≤ 100 days) | 0.30 |
Among the symptom and diagnostic variables, abnormal WCC, headache and confusion are the three top ranked variables contributing 27%, 26%, and 25% of the variation in the first canonical variate of the symptom sets, respectively. The other variables with a considerable contribution towards the first canonical variate are abnormal protein, PB change, length of hospital stay and duration of illness, explaining 15%, 12%, 9% and 9% of the variation, respectively. The canonical cross loadings also indicate that symptom variables, provided in Figure 4, explain considerable amount of the variation in the first canonical variate of the exposure sets.
Fever, although present in the majority of the patients (77.9%, Table 2), does not contribute much towards the first canonical variates, explaining only 0.04% and 0.16% of the variation in the symptom and exposure variates, respectively.
We also performed CCA on the 263 patients who met the case definition criteria as presented in the original paper [10]. In general, the pattern observed in the within and between correlations for this data set is similar to those obtained for the 208 confirmed encephalitis cases where weak to moderate correlations exist between the variables. A correlation of ρ = 0.68 (p-value = 0.007) was obtained between sets of variables in the first canonical solution. The second canonical solution resulted in ρ = 0.54 (p-value = 0.19). Overall, the canonical loadings for Xand their rankings are similar to those presented in Table 3 and Figure 4, respectively. Therefore, our analysis based on 263 patients indentified the same sets of exposure variables to be strongly associated with symptom, clinical and diagnostic variables.
Redundancy coefficients indicate that very small amount of the variation in the original symptom variables were explained by the exposure canonical variates. Only 6% of the variation in the symptom variables is explained by the first exposure canonical variate; 5% by the second canonical variate and 4% by the third. This indicates that, the variation in the symptoms might be caused by host factors rather than environmental and exposure factors. The idea that characteristics of the host may be more important than the pathogen is consistent with the observation that for some causes, such as herpes simplex virus (HSV), encephalitis is a rare outcome of a common infection. Another possible hypothesis, that might be drawn from our results, is the possibility that exposure and symptom variables might provide independent information towards understanding the etiology of encephalitis. Further case-control type of analysis based on exposure, symptom and host factors might shed light to better understanding of factors that might help facilitate diagnosis and treatment of encephalitis patients.
Conclusion
We performed exploratory multivariate analysis using CCA to study associations between two sets of variables in encephalitis patients. One set consists of exposure and demographic variables including variables that are previously indentified in the literature as potential risk factors. The second set includes symptom, clinical and diagnostic variables where some items in the set have been shown to be important clinical characteristics of encephalitis. Although pair-wise cross correlations between the two sets of variables are weak to moderate, CCA revealed strong multivariate correlation between the two sets.
Our analysis provided a set consisting of 3 exposure/demographic variables (age, sick person contact, immunization and water exposure) to be strongly associated with 7 symptom/diagnostic variables (abnormal WCC, headache, confusion, abnormal protein, personality and behavioral change, length of stay and duration of illness) to be strongly associated.
Our analysis also revealed that a very small amount of the variation in the symptom sets is explained by the exposure variables. This indicates that host factors, rather than environmental factors might be important towards understanding the etiology of encephalitis and facilitate early diagnosis and treatment of encephalitis patients.
CCA is exploratory in nature and measures associations rather than causation. However, our analysis indentified exposure variables that might be strongly associated with encephalitis and generated important hypotheses that can be investigated further to indentify risk factors that are predictive of encephalitis. A confirmatory case-control analysis involving encephalitis and non-encephalitis patients is needed to indentify risk factors and important symptom variables that can be used to facilitate diagnosis. CCA results may, however, provide insight into potentially smaller sets of variables worth investigating further. Furthermore, it is important to highlight that exposure variables such as tick bite do not occur frequently in the UK and also do not often lead to encephalitis, and so are difficult to study using conventional methods such as logistic regression analysis. CCA can, therefore, be a useful tool in indentifying risk factors associated with human encephalitis and other rare and complex diseases where regression approaches may not be optimal.
Declarations
Acknowledgements
The UK etiology of encephalitis group consists of Julia Granerod, Helen E Ambrose, Nicholas W S Davies, Jonathan P Clewley, Amanda L Walsh, Dilys Morgan, Richard Cunningham, Mark Zuckerman, Ken J Mutton, Tom Solomon, Katherine N Ward, Michael P T Lunn, Sarosh R Irani, Angela Vincent, David W G Brown, Natasha S Crowcroft, Craig Ford, Emily Rothwell, William Tong, Jean-Pierre Lin, Ming Lim, Javeed Ahmed, David Cubitt, Sarah Benton, Cheryl Hemingway, David Muir, Hermione Lyall, Ed Thompson, Geoff Keir, Viki Worthington, Paul Griffi ths, Susan Bennett, Rachel Kneen, Paul Klapper. The views expressed are those of the authors and not necessarily those of the UK Department of Health
Authors’ Affiliations
References
- Granerod J, Crowcroft N: The epidemiology of acute encephalitis. Neuropsychological Rehabilitation. 2007, 17 (4): 406-428. 10.1080/09602010600989620.View ArticlePubMedGoogle Scholar
- Lewis P, Glaser CA: Encephalitis. Pediatric Reviews. 2005, 26: 353-363. 10.1542/pir.26-10-353.View ArticleGoogle Scholar
- Flower A, Stodberg T, Eriksson M, Wickstrom R: Childhood encephalitis in Sweden: Etiology, clinical presentation and outcome. European Journal of Pediatric Neurology. 2008, 12: 484-490. 10.1016/j.ejpn.2007.12.009.View ArticleGoogle Scholar
- Misra UK, Kalita J: Seizures in encephalitis: Predictors and outcome. Seizure. 2009, 18: 583-587. 10.1016/j.seizure.2009.06.003.View ArticlePubMedGoogle Scholar
- Aygun AD, Kabakus N, Celik I, Turgut M, Yoldas T, Gok U, Guler R: Long-term neurological outcome of acute encephalitis. Journal of Tropical Pediatrics. 2001, 47 (4): 243-247. 10.1093/tropej/47.4.243.View ArticlePubMedGoogle Scholar
- Resznicek JE, Bloch KC: Diagnostic Testing for Encephalitis, Part I. Clinical Microbiology. 2010, 32 (3): 17:23Google Scholar
- Kolski H, Ford-Jones EL, Richardson S, Petric M, Nelson S, Jamieson F, Blaser S, Gold R, Otsubo H, Heurter H, MacGregor D: Eitology of Acute Childhood Encephalitis at the hospital for sick children, Toronto, 1994-1995. Clinical Infectious Diseases. 1998, 26 (2): 398-409. 10.1086/516301.View ArticlePubMedGoogle Scholar
- Koskiniemi M, Korppi M, Mustonen K, Rantala H, Muttilainen Herrgård E, Ukkonen P, Vaheri A, Study Group: Epidemiology of encephalitis in children. A prospective multicenter study. 1997, 156 (7): 541-545.Google Scholar
- Starza-Smith A, Talbot E, Grant C: Encephalitis in Children: A clinical neuropsychology perspective. Neurological Rehabilitation. 2007, 17 (4): 506-527.Google Scholar
- Granerod J, Ambrose HE, Davies NWS, Clewley JP, Walsh A, Morgan D, Cunningham R, Zuckerman M, Mutton K, Solomon T, Ward K, Lunn MPT, Irani SR, Vincent A, Brown DWG, Crowcroft NS, on behalf of the UK HPA Aetiology of Encephalitis Study Group: Causes of encephalitis and differences in their clinical presentations in England: a multicenter, population-based prospective study. Lancet Infectious Diseases. 2010, 10 (12): 835-844. 10.1016/S1473-3099(10)70222-X.View ArticlePubMedGoogle Scholar
- Hamid JS, Meaney C, Crowcroft NS, Granerod J, Beyene J: Cluster analysis for indentifying sub-groups and selecting potential discriminatory variables in human encephalitis. BMC Infectious Diseases. 10: 364-Google Scholar
- Johnson RT: Acute encephalitis. Clinical Infectious Diseases. 1996, 23: 219-226. 10.1093/clinids/23.2.219.View ArticlePubMedGoogle Scholar
- Cizman M, Jazbec J: Aetiology of acute encephalitis in childhood in Slovenia. Pediatric Infectious Diseases Journal. 1993, 12: 903-908. 10.1097/00006454-199311000-00002.View ArticleGoogle Scholar
- Lee T, Tsai C, Yuan C, Wei C, Tsao W, Lee R, Cheih S, Huang I, Chen K: Encephalitis in Taiwan: A prospective hospital-based study. Japanese Journal of Infectious Diseases. 2003, 56: 193-199.PubMedGoogle Scholar
- Studahl M, Bergstrom T, Hagberg L: Acute viral encephalitis in adults: A prospective study. Scandinavian Journal of Infectious Diseases. 1998, 30: 215-220. 10.1080/00365549850160828.View ArticlePubMedGoogle Scholar
- Davison KL, Crowcroft NS, Ramsay ME, Brown DWG, Andrews NJ: Viral encephalitis in England, 1989-1998: What did we miss?. Emerging Infectious Diseases. 2003, 9: 234-240.View ArticlePubMedPubMed CentralGoogle Scholar
- Koskiniemi M, Rantalaiho T, Piiparinen H, von Bonsdorff CH, Fakkila M, Jarvinen A, Koskiniemi S, Kinnunen E, Mannonen L, Muttilainen M, Linnavuory K, Porras J, Puolakkainen M, Raiha K, Salonen E, Ukkonen P, Vaheri A, Valtonen V, The Study Group: Infections of the central nervous system of suspected viral origin: a collaborative study from Finland. Journal of NeuroVirology. 2001, 7: 400-408. 10.1080/135502801753170255.View ArticlePubMedGoogle Scholar
- Glaser CA, Gilliam S, Schnurr D, Forghani B, Honarmand S, Khetsuriani N, Fischer N, Cossen CK, Anderson LJ: In search of encephalitis etiologies-diagnostic challenges in the California encephalitis project, 1998-2000. Clinical Infectious Diseases. 2003, 36 (6): 731-742. 10.1086/367841.View ArticlePubMedGoogle Scholar
- Nicolosi A, Hauser WA, Beghi E, Kurland LT: Epidemiology of central nervous system infections in Olmsted County, Minnesota, 1950-1981. Journal of Infectious Diseases. 1986, 154: 399-408. 10.1093/infdis/154.3.399.View ArticlePubMedGoogle Scholar
- Cinque P, Cleator GM, Weber T, Monteyne P, Sindic CJ, van Loon AM: The role of laboratory investigation in the diagnosis and management of patients with suspected herpes simplex encephalitis: A consensus report. Journal of Neurology, Neurosurgery and Psychiatry. 1996, 61: 339-345. 10.1136/jnnp.61.4.339.View ArticlePubMedPubMed CentralGoogle Scholar
- Hotelling H: Relations between 2 sets of variants. Biometrika. 1936, 28: 321-327.View ArticleGoogle Scholar
- Mardia K, Kent J, Bibby J: Multivariate Analysis. 1979, Academic Press, San Francisco, CaliforniaGoogle Scholar
- Cooley W, Lohnes P: Multivariate Data Analysis. 1971, Wiley-Interscience, Hoboken, New JerseyGoogle Scholar
- McGarigal K, Cushman S, Stafford S: Multivariate Statistics for Wildlife and Ecology Research. 2000, Springer-Verlag, New York, New YorkView ArticleGoogle Scholar
- Darlington R, Weinberg S, Walberg H: Canonical variate analysis and related techniques. Review of Educational Research. 1973, 43: 433-446.View ArticleGoogle Scholar
- Razavi A, Gill H, Stal O, Sundquist M, Thorstenson S, Ahlfeldt N: Exploring cancer register data to find risk factors for recurrence of breast cancer-application of Canonical Correlation Analysis. BMC Medical Informatics and Decision Making. 2005, 5: 29-36. 10.1186/1472-6947-5-29.View ArticlePubMedPubMed CentralGoogle Scholar
- Ridderstolpe L, Gill H, Borga M, Rutberg H, Ahlfeldt H: Canonical Correlation Analysis of risk factors and clinical outcomes in cardiac surgery. Journal of Medical Systems. 2005, 29 (4): 357-377. 10.1007/s10916-005-5895-9.View ArticlePubMedGoogle Scholar
- Gini CW: Variability and Mutability, contribution to the study of statistical distributions and relations. Studi Economico-Giuridici della R. Universita de Cagliari. 1912Google Scholar
- Light RJ, Margolin BH: An Analysis of Variance for Categorical Data. J American Statistical Association. 1971, 66: 534-544. 10.2307/2283520. 1971 (Review of Gini (1912) paper)View ArticleGoogle Scholar
- Okada T: A note on covariances for categorical data. Intelligent Data Engineering and Automated Learning-IDEAL 2000 LNCS 1983. Edited by: Leung KS, Chan LW, Meng H. 2000, 150-157.Google Scholar
- Niitsuma H, Okada T: Covariance and PCA for Categorical Variables. Lecture Notes in Computer Science. 2005, 3518: 523-528. 10.1007/11430919_61.View ArticleGoogle Scholar
- Okada T: Sum of Squares Decomposition for Categorical Data. Kwansei Gakuin Studies in Computer Science. 1999, 14: 1-6.Google Scholar
- Okada T: Attribute Selection in Chemical Graph Mining Using Correlations among Linear Fragments. Department of Informatics, Kwansei Gakuin University, 2-1 Gakuen, Sanda-shi, Hyogo, Japan. 2008Google Scholar
- González I, Déjean S, Martin PGP, Baccini A: CCA: An R Package to Extend Canonical Correlation Analysis. Journal of Statistical Software. 2008, 23: 12-View ArticleGoogle Scholar
- Menzel U: CCP: Significance Tests for Canonical Correlation Analysis (CCA), R Package. 2009Google Scholar
- R Development Core Team: R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. 2009, ISBN 3-900051-07-0, [http://www.R-project.org]Google Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2288/11/120/prepub
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