| Literature DB >> 28011977 |
Tao Zhang1, Fei Yin1, Ting Zhou1, Xing-Yu Zhang2, Xiao-Song Li3.
Abstract
The surveillance of infectious diseases is of great importance for disease control and prevention, and more attention should be paid to the Class B notifiable diseases in China. Meanwhile, according to the International Monetary Fund (IMF), the annual growth of Chinese gross domestic product (GDP) would decelerate below 7% after many years of soaring. Under such circumstances, this study aimed to answer what will happen to the incidence rates of infectious diseases in China if Chinese GDP growth remained below 7% in the next five years. Firstly, time plots and cross-correlation matrices were presented to illustrate the characteristics of data. Then, the multivariate time series (MTS) models were proposed to explore the dynamic relationship between incidence rates and GDP. Three kinds of MTS models, i.e., vector auto-regressive (VAR) model for original series, VAR model for differenced series and error-correction model (ECM), were considered in this study. The rank of error-correction term was taken as an indicator for model selection. Finally, our results suggested that four kinds of infectious diseases (epidemic hemorrhagic fever, pertussis, scarlet fever and syphilis) might need attention in China because their incidence rates have increased since the year 2010.Entities:
Mesh:
Year: 2016 PMID: 28011977 PMCID: PMC5515987 DOI: 10.1038/s41598-016-0020-5
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379
Figure 1The process of modelling.
Class B infectious diseases.
| Disease | Whether included in this study | Reasons for exclusion | Type of multivariate time series analysis model* |
|---|---|---|---|
| AIDS | No | Too short period | — |
| Virus hepatitis | Yes | — | ECM |
| Poliomyelitis | No | Too low rate | — |
| Severe acute respiratory syndromes | No | Treated as Class A notifiable diseases | — |
| Human avian influenza | No | Treated as Class A notifiable diseases | — |
| Measles | No | Outlier** | — |
| Epidemic hemorrhagic fever | Yes | — | VAR for original series |
| Rabies | Yes | — | VAR for original series |
| Epidemic encephalitis B | Yes | — | VAR for original series |
| Dengue | No | Too short period | — |
| Anthrax | No | Treated as Class A notifiable diseases | — |
| Bacterial and amebic dysentery | Yes | — | VAR for original series |
| Tuberculosis | No | Too short period | — |
| Typhoid fever | Yes | — | ECM |
| Pertussis | Yes | — | VAR for original series |
| Diphtheria | No | Too low rate | — |
| Epidemic cerebrospinal meningitis | No | Too low rate | — |
| Infantum tetanus | No | Too low rate | — |
| Scarlet fever | Yes | — | ECM |
| Brucellosis | No | Endemic disease | — |
| Gonorrhoea | Yes | — | VAR for original series |
| Syphilis | Yes | — | VAR for differenced series |
| Leptospirosis | No | Too low rate | — |
| Schistosomiasis | No | Endemic disease | — |
| Malaria | Yes | — | VAR for differenced series |
| Influenza A(H1N1)/H7N9 avian influenza*** | No | Task adjustment | — |
*Three types of multivariate time series analysis models were used in this study, that is, the VAR for original series, VAR for differenced series and the ECM, see more information in the rest of paper. **The incidence rate of measles was zero in 2003, but was far great than zero in 2002 and 2004. This study did not find reasonable explanation for this outlier, so measles was not included for analysis. ***According to regulation of government, influenza A (H1N1) has been adjusted from Class B to Class C notifiable disease since 2014, while H7N9 avian influenza was included as Class B since 2013 (http://www.nhfpc.gov.cn/jkj/s3577/201311/f6ee56b5508a4295a8d552ca5f0f5edd.shtml).
Figure 2(a) The time plot of the standardised scarlet fever incidence and GDP; (b) The time plot of the standardised syphilis incidence and GDP.
Figure 3(a) The fitting plot for epidemic hemorrhagic fever; (b) The fitting plot for syphilis; (c) The fitting plot for typhoid fever.
The goodness-of-fit results of MTS and ARIMA model for each disease.
| Disease |
| MSPE of MTS model | MSPE of ARIMA model |
|---|---|---|---|
| Bacterial and amebic dysentery | 0.2687 | 0.012967 | 0.0543 |
| Epidemic encephalitis B | 0.9867 | 0.038293 | 0.0741 |
| Epidemic hemorrhagic fever | 0.9009 | 0.029741 | 0.0355 |
| Gonorrhoea | 0.9072 | 0.018547 | 0.0403 |
| Malaria | 0.8817 | 0.041325 | 0.0402 |
| Pertussis | 0.6865 | 0.032576 | 0.0439 |
| Rabies | 0.8484 | 0.045806 | 0.0543 |
| Scarlet fever | 0.6995 | 0.041423 | 0.0497 |
| Syphilis | 0.5432 | 0.036579 | 0.0447 |
| Typhoid fever | 0.3546 | 0.020911 | 0.0336 |
| Virus hepatitis | 0.6839 | 0.015540 | 0.0166 |
*The significance level α was set to be 0.05 in advance. The null hypothesis of Ljung-Box test declared that the testing series to be white noise, thus it was reasonable to say the model was good at fitting if such null hypothesis for its corresponding residual series could not be rejected.
The testing results of spatial stratified heterogeneity for each disease.
| Disease |
|
|
| lambda | cutoff point |
|
|---|---|---|---|---|---|---|
| Bacterial and amoebic dysentery | 3.151833 | 2 | 28 | 0.351702 | 3.9048 | >0.05 |
| Epidemic encephalitis B | 0.942817 | 2 | 28 | 0.456857 | 4.0651 | >0.05 |
| Epidemic hemorrhagic fever | 0.142923 | 2 | 28 | 0.054094 | 3.4302 | >0.05 |
| Gonorrhoea | 0.517519 | 2 | 28 | 0.559956 | 4.2188 | >0.05 |
| Malaria | 0.229567 | 2 | 28 | 0.048982 | 3.4217 | >0.05 |
| Pertussis | 3.138548 | 2 | 28 | 0.599739 | 4.2772 | >0.05 |
| Rabies | 2.768148 | 2 | 27 | 0.580805 | 4.2672 | >0.05 |
| Scarlet fever | 2.535921 | 2 | 28 | 0.810873 | 4.5799 | >0.05 |
| Syphilis | 1.584857 | 2 | 20 | 1.73419 | 6.0807 | >0.05 |
| Typhoid fever | 0.461945 | 2 | 20 | 2.97123 | 7.6324 | >0.05 |
| Virus hepatitis | 0.817709 | 2 | 28 | 0.180542 | 3.6358 | >0.05 |
*The significance level α was set to be 0.05 in advance. The F-statistics (column 2) was constructed based on the q-statistics, which followed a non-central F-distribution, with first and second degree of freedom f 1 (column 3) and f 2 (column 4), and noncentrality parameter lambda (column 5). Column 6 listed the 95% cutoff point, and by comparing it with the F statistics, it could be inferred whether P > α or not (column 7).
The change rate for each disease from 1978 to 2020.
| Disease | 1978~1989* | 1990~1999 | 2000~2009 | 2010~2014 | 2015~2020 |
|---|---|---|---|---|---|
| Bacterial and amoebic dysentery | −0.80 | −0.62 | −0.50 | −0.40 | −0.21 |
| Epidemic encephalitis B | −0.70 | −0.80 | −0.69 | −0.68 | −0.53 |
| Epidemic hemorrhagic fever | 1.32 | 0.07 | −0.78 | 0.17 | −0.33 |
| Gonorrhoea** | 495.50 | 1.77 | −0.60 | −0.13 | −0.27 |
| Malaria | −0.96 | −0.77 | −0.48 | −0.60 | −0.51 |
| Pertussis | −0.98 | −0.72 | −0.74 | 0.92 | −0.32 |
| Rabies | 0.88 | −0.91 | 3.25 | −0.53 | −0.87 |
| Scarlet fever | −0.72 | −0.54 | 0.54 | 1.56 | 0.83 |
| Syphilis*** | 1.25 | 27.26 | 2.84 | 0.07 | −0.59 |
| Typhoid fever | −0.30 | −0.60 | −0.69 | −0.03 | −0.33 |
| Virus hepatitis | 0.22 | −0.39 | 0.65 | −0.09 | −0.25 |
*For each column, the change rate = (the incidence of the last year-the incidence of first year)/the incidence of first year. **The first period for gonorrhoea was from 1981 to 1989. ***The first period for syphilis was from 1987 to 1989.