Figures
Abstract
Methods
Suspected Creutzfeldt-Jakob disease (CJD) cases that were reported under CJD surveillance were diagnosed and subtyped using the diagnostic criteria issued by the WHO. The general information concerning the patient, their clinical, MRI and EEG data, and the results of CSF 14-3-3 and PRNP sequencing were carefully collected from the database of the national CJD surveillance program and analyzed using the SPSS 11.5 statistical software program.
Results
Since 2006, 69 patients were diagnosed with genetic prion diseases and as having 15 different mutations. The median age of the 69 patients at disease onset was 53.5 years, varying from 19 to 80 years. The majority of patients displaying clinical symptoms were in the 50–59 years of age. FFI, T188K gCJD and E200K were the three most common subtypes. The disease appeared in the family histories of 43.48% of the patients. The clinical manifestations varied considerably among the various diseases. Patients who carried mutations in the N-terminus displayed a younger age of onset, were CSF 14-3-3 negative, had a family history of the condition, and experienced a longer duration of the condition. The clinical courses of T188K were significantly shorter than those of FFI and E200K gCJD, while the symptoms in the FFI group appeared at a younger age and for a longer duration. Moreover, the time intervals between the initial neurologist visit to the final diagnosis were similar among patients with FFI, T188K gCJD, E200K gCJD and other diseases.
Citation: Shi Q, Zhou W, Chen C, Zhang B-Y, Xiao K, Zhang X-C, et al. (2015) The Features of Genetic Prion Diseases Based on Chinese Surveillance Program. PLoS ONE 10(10): e0139552. https://doi.org/10.1371/journal.pone.0139552
Editor: Ina Maja Vorberg, Deutsches Zentrum für Neurodegenerative Erkrankungen e.V., GERMANY
Received: May 28, 2015; Accepted: September 14, 2015; Published: October 21, 2015
Copyright: © 2015 Shi 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
Data Availability: All relevant data are within the paper and its Supporting Information files
Funding: This work was supported by Chinese National Natural Science Foundation Grants (81301429,81572048), China Mega-Project for Infectious Disease (2012ZX10004215) and SKLID Development Grant (2012SKLID102, 2015 SKLID503).
Competing interests: The authors have declared that no competing interests exist.
Introduction
Human prion diseases are a group of rare, fatal and transmissible neurodegenerative diseases. They are etiologically classified as sporadic, inherited or acquired and include Creutzfeldt-Jakob disease (CJD), Kuru, Gerstmann—Sträussler—Scheinker syndrome (GSS) and fatal familial insomnia (FFI) [1]. CJD has an incidence of 1 or 2 cases per million per year and manifests as rapidly progressive dementia, cerebellar ataxia, myoclonus and behavioral changes. Generally, approximately 85% of all CJD cases are sporadic, 10–15% of the cases are inherited and less than 1% of the cases are infectious [2]. Prion diseases are characterized by an accumulation of an abnormally folded isoform (PrPSc) of the host encoded cellular prion protein (PrPC) [3]. In humans, the PrP protein is encoded by the PRNP gene, which is located on chromosome 20. Currently, more than 55 dominant mutations in the PRNP gene that are directly associated with human genetic prion diseases have been described [4]. In neurology, human genetic prion diseases include genetic CJD (gCJD), GSS and FFI.
The clinical manifestations and neuropathological abnormalities of human genetic prion diseases may not only differ considerably from those of sporadic CJD (sCJD) but also vary largely among themselves depending on the various genotypes [5]. In addition to the routine diagnostic elements that are utilized for CJD, the definitive diagnosis of the human genetic prion disease requires genetic evidence of a mutation in PRNP. Since 2006, China has conducted a CJD surveillance program that focuses primarily on 12 provinces. As part of this CJD surveillance, all reported suspected cases in the China National Surveillance Program for CJD have undergone PRNP sequencing. Through Sept 2014, 69 different genetic prion diseases have been identified and diagnosed using the fixed genetic data, thereby covering 15 different diseases.
In this study, we present and compare the demographic, epidemiological, clinical and laboratory data of these 69 patients. The majority of patients who display clinical symptoms are 50–59 years or 40–49 years of age. FFI, T188K and E200K gCJD were the most frequently identified genetic prion diseases in China. The time intervals between disease onset and the first neurologist visit and the end of the disease among the different genetic prion diseases, and particularly of FFI, T188K and E200K gCJD, were analyzed. The time interval between the neurologist visit and the final diagnosis and the factors that potentially influence this interval, including the disease subtype, surveillance year, age at onset and permanent residence of the patients, were also evaluated.
Materials and Methods
Ethics Statement
The use of patient information stored in the China CJD Surveillance System has been approved by the Research Ethics Committee of the National Institute for Viral Disease Control and Prevention of the China CDC. The written informed content of each suspected case was obtained either through a family member or a relative of the patient, according to the requirement of CJD surveillance.
Constitution of the national CJD surveillance system
Chinese national CJD surveillance formally began in 2006 under the leadership of the China CDC. It consisted of 12 provincial CDCs and 15 hospitals, which are located in Beijing, Shanghai, Tianjin, Chongqing, Jilin, Shaanxi, Hubei, Guangdong, Guizhou, Anhui, Henan and Xinjiang [6]. These sentinel hospitals are large university hospitals that employ experienced neurologists. The surveillance program was approved by the Ethical Review Committee of the China CDC. Using surveillance documents, the clinical data and specimens of the suspected patients were collected by a clinician from the hospitals. Meanwhile, the staff of the provincial CDCs collected epidemiological data. The collected data and samples were transferred to the national reference laboratory for human prion disease in China CDC, for laboratory tests and a final diagnosis [7].
Case definition
The suspected CJD cases that were reported from CJD surveillance were diagnosed and subtyped using the diagnostic criteria of the China CDC, which was designed using the diagnostic criteria for CJD from the WHO [8]. Since 2010, the addition of a high signal in the caudate/putamen using an MRI brain scan, according to the renewed version of diagnostic requirements that was issued by the WHO [9]. The clinical and epidemiological data of the suspected patients were collected using designed questionnaires. The clinical data included the general information of the patient, main clinical manifestations, the major symptom and results of clinical examinations (e.g., MRI, EEG and routine CSF biochemistry). The epidemiological data included the location of residence, family history, anamnesis (e.g., surgical or neurosurgical history, organ transplantation, blood donation and transfusion, use of extracts of pituitary or other blood products), and profession. The laboratory tests, including a neuropathological assay, immunohistochemistry (IHC) analysis of PrPSc in brain tissues, Western blots for PrPSc in brain tissues and for 14-3-3 in the CSF, and PRNP PCR and sequencing were performed using established protocols, as previously described [10,11]. The final diagnosis was made by an expert board of neurologists, neuropathologists, epidemiologists and laboratory staff.
Study population and data collection
All 69 patients with a diagnosed genetic human prion disease, including gCJD, FFI and GSS, reported via the China CJD surveillance program between Jan 2006 and Sept 2014 were enrolled in this study. The general information concerning the patient, their clinical data, MRI and EEG data, and the results of CSF 14-3-3 and PRNP sequencing were carefully collected from the database of the national CJD surveillance program and analyzed using SPSS 11.5 statistical software program. The geographical distribution of the patients was calculated using the provinces in which they permanently lived. EEG abnormalities were recorded only in the event that periodic sharp wave complexes (PSWC) were observed. MRI abnormalities were recorded in the event of a high signal in the caudate/putamen. The interval between the onset of the disease and the first neurologist visit was calculated according to the appearance of neurological or mental symptoms during the first hospital visit with neurologists. The interval between disease onset and diagnosis was calculated using a method described by the CJD surveillance center.
Laboratory tests
Blood, CSF and brain tissue of suspected patients were collected by the sentinel hospital. All samples were transported to the national reference laboratory for human prion disease in CCDC. Peripheral blood leukocytes were used for sequencing analysis of PRNP and of polymorphisms of codon 129 using an automatic genetic analyzer (ABI3130XL). CSF samples were obtained by a routine lumbar puncture and analyzed using a Western blot to detect protein 14-3-3. Brain tissue samples were obtained during an autopsy or biopsy and analyzed using neuropathologic assays and for the detection of PrPSc using immunohistochemistry and/or Western blot. The standard operation procedure (SOP) of each test has been documented in the CJD surveillance program, which has been previously described [6,7].
Results
The constitutions and distributions of Chinese genetic prion diseases
Between Jan 2006 and Sept 2014, a total of 1670 suspected genetic prion disease cases were reported to the CJD surveillance system of China. Among these, 721 sCJD cases were diagnosed, including two definitive, 538 probable and 181 possible cases. Of these, 69 cases with various genetic prion diseases were identified and diagnosed. Five of these cases underwent brain autopsies upon death for neuropathological examination. The blood samples of all suspected CJD cases were collected and PRNP sequencing assays were performed. Among the 69 cases of genetic prion diseases, 15 different types of human genetic prion diseases were identified, including D178N FFI (27 cases), T188K gCJD (16 cases), E200K gCJD (9 cases, 13%), P102L GSS (3 cases), G114V gCJD (2 cases), E196A gCJD (2 cases), R208H gCJD (2 cases), R148H gCJD (1 case), V180I gCJD (1 case), T183A gCJD (1 case), E196K gCJD (1 case), E200A gCJD (1 case), V203I gCJD (1 case), as well as gCJD with 1-extra-octarepeat (1 OR) insertion (1 case) and 7-extra-octarepeat (7 ORs) insertion (1 case). Three types of these diseases, FFI (39%), T188K gCJD (23%) and E200K gCJD (13%), were predominant.
The number of diagnosed cases of genetic prion diseases per year are shown in Fig 1A. More cases have been identified since 2010, which is concomitant with the increase in reported suspected CJD cases since 2010. Upon calculating the portion of all CJD cases that were genetic prion diseases, we identified that the rate of genetic prion diseases varied from 6.25% to 12.33%, with the average rate being 9.0 ± 1.77%. FFI cases were identified in every surveillance year, with the exception of 2007. To understand the geographical distribution of Chinese patients with genetic prion diseases, the case numbers were sub-counted based upon their permanent residences in the provinces. The patients were observed to have lived in 18 different provinces. Among these provinces, the three with the highest density of cases included Henan (20 cases), Anhui (6 cases) and Beijing (6 cases) (Fig 1B). A previous epidemiological survey verified that, in addition to the two FFI cases (an uncle and a niece) [12,13,14] and the two G114V gCJD cases (an aunt and niece) [15,16], no further genetic relationships could be identified.
A. Surveillance year distribution. The rates of genetic prion diseases among all diagnosed human prion diseases are shown by a blue triangle and a dotted line. B. Geographic distribution. The residences of the patients are given by province.
The demographic and clinical features of Chinese genetic prion diseases
Among the 69 cases, 68 patients were Han-Chinese and one was Miao-Chinese. All patients were Met/Met homozygotes at codon 129 in the PRNP gene. The gender ratio of male/female was 1/1.09 (33/36). The occupations and education levels of the patients varied largely, with no disease relationship. The median age of onset among the 69 patients was 53.5 years of age and varied between 19 and 80 years of age. Among the patients, the average age of onset for 7-ORs, P102L, G114V, D178N, T183A and R208H was below the median onset age of onset of patients with a genetic prion disease. The average age of onset for the remaining types of disease are shown in Fig 2A. An age-group analysis revealed that the majority of the patients were between 50–59 (24; 34.78%), 40–49 (16; 23.19%) and 60–69 (10; 14.49%) years of age (Fig 2B). Disease-age distributions are illustrated in Fig 2C. Among patients who carried mutations in the N-terminal segments, such as insertions of extra octarepeats, those in the P102L and G114V groups demonstrated an earlier clinical manifestation than did the other groups. For example, the patient with a 7-extra-octarepeat insertion presented clinical signs of the disease much earlier than did the case with a 1-extra-octarepeat insertion. The age of onset in the D178N FFI cases was distributed widely, with no FFI case being identified above 70 years of age. Conversely, the age of onset of the T188K and E200K gCJD cases was older, with no case being identified before 40 years of age. In addition, other gCJD cases with mutations in the C-terminal region, such as V180I, E196A, E196K, E200A and V203I, demonstrated clinical manifestations at older ages.
A. Distribution of the age of onset based upon the types of disease. The median onset age of all 69 patients is indicated by a dotted line. The median onset age of each disease is illustrated with a short, red bar. B. Distribution of the age of onset based upon decade of life. C. Distribution of the age of onset based upon the disease type and decade of life.
The clinical symptoms and signs of the Chinese genetic prion diseases varied considerably. Based upon the major neurological symptoms of sporadic CJD, including dementia, myoclonus, visual or cerebella disturbance, pyramidal or extrapyramidal dysfunction, akinetic mutism, the presence and/or rate of various genetic prion diseases are summarized in Table 1. Approximately 70% of FFI patients were recorded as having dementia during the clinical course of their diseases and approximately half of them presented with myoclonus, visual or cerebella disturbance, and pyramidal or extrapyramidal dysfunction. Only a small portion (11.11%) of FFI patients was recorded as having akinetic mutism at the late stage of the disease. Insomnia and hypersomnia were the most common symptoms in approximately 70% of FFI cases. Along with the progression of the disease, sleep disturbances appeared in all FFI cases and persisted through the entirety of the clinical course. Some of the progressive sympathetic symptoms, including excessive sweating, salivation, minor evening pyrexia and weight loss, were noticed in most cases [12, 13]. Three of the FFI cases underwent brain autopsies and demonstrated marked astrogliosis in the thalamus and neuron loss in various brain regions [14]. T188K gCJD is the second most common form of gCJD in China. Rapidly progressive dementia and mental symptoms appeared in most of the cases at the time of disease onset and cerebellar disorders and walking instability were also described among the initial symptoms. With the development of disease, dementia, visual or cerebella disturbance and pyramidal or extrapyramidal dysfunction appeared in over 80% of the cases. Myoclonus and akinetic mutism appeared in over half of the cases. E200K gCJD cases were more abundant than sCJD, in which dementia and additional neurological symptoms were commonly observed.
A disease-related family history of each patient was carefully collected by the local clinical neurologists and the staff of the CJD surveillance center. Analysis of these histories indicated that 43.48% of patients (30 of 69) had family members in their parents' or grandparents' generations who exhibited similar neurological disorders or manifestations, including the case with 7-ORs insertion, one (out of three) P102L case, two G114V cases, the R148H case, 16 (out of 27) FFI cases, the T183A case, six (out of 16) T188K cases, one (out of 9) E200K case and one (out of two) R208H case (Table 2). The case with a 1-OR insertion, the V180I case, two E196A cases, the E196K case, the E200A case and the V203I case did not record this family relationship (Table 2). The number of patients with a family history of the condition is similar with the rate of incidence in Europe [17]. This study assumes that patients with mutations in the N-terminal segment might be more likely to have family problems. When compared with the data of the T188K (37.50%) and E200K (11.11%) groups, more FFI cases (59.26%) exhibited this disease-related family history. Additionally, we asked all families with disease-related family histories to perform PRNP gene assays for their family members. Family members from 23 families agreed to donate blood samples. As shown in Table 2, the same mutations within the PRNP gene that were observed in the indexed patients were also identified in at least one family member of all tested families.
The clinical examinations and laboratory tests for Chinese genetic prion diseases
Out of 69 patients, only five cases had postmortem brain tissue collected: the case with 7-ORs insertion [17], three FFI cases [12,13,14] and one G114V gCJD case [15,16,18], whose neuropathological changes and the presence of PrPSc were previously described. Sixty-five (94.2%), 61 (90.41%) and 55 (79.71%) cases underwent CSF 14-3-3 tests, MRI recordings and EEG examinations, respectively. All 69 cases underwent at least one of these three examinations. The results of CSF 14-3-3 tests as well as of MRI and EEG examinations of these 69 cases are summarized in Table 3 In the assay of CSF 14-3-3, all tested cases with point-mutations (i.e., P102L, G114V, R148H) at the N-terminal segment as well as a majority of the FFI cases (62.96%) were negative. Meanwhile, those with mutations at the C-terminus (E196A, E200K, E200A, V203I and R208H) as well as most of the T188K gCJD cases (68.75%) were positive. sCJD-associated abnormalities in the MRI recordings were much more frequently observed in the T188K (68.75%) and E200K (77.78%) groups but were very rare in the FFI cases (1/27; 3.7%). In these genetic prion diseases, MRI abnormalities were seen in the patients with 7-ORs, one tested P102L case, the V180I case, two E196K cases and the E200A case. PSWCs in EEG were detected in 66.67% of E200K cases, but only in 12.50% of T188K cases. As expected, none of the tested FFI cases showed PSWCs in EEG examinations. EEG abnormalities were also recorded in the patients with 7-ORs, two tested P102L cases, the V180I case, the E196A case and the V203I case.
Intervals between disease onset and neurologist visit, diagnosis and disease outcome in Chinese patients with genetic prion diseases
To understand disease progression and persistence, the time intervals between disease onset and the first neurologist visit, the final diagnosis and the death of the patient were individually assessed and the data are listed in Table 4. Among the 69 patients, 40 cases had definitive death times, 15 cases resulted in a loss of contact after diagnosis or during follow-up, and the remaining 14 patients were still alive by the end of Sept 2014. Although the median times of the intervals from onset to neurologist visit, to final diagnosis and to death of the 69 patients were 92, 153 and 252 days, respectively, the actual interval times differed considerably across various diseases and across individuals with the same diseases. The patients with an extra octarepeat insertion demonstrated longer intervals for diagnosis and a longer clinical course, despite having lost contact with the patient whose disease included an insertion more than 3 years after onset. The cases with the point-mutations in the region of the N-terminus (P102L, G114V and R148H) appeared to require more time for diagnosis and enjoyed a longer survival time than those with the mutations in the C-terminus; however, the number of cases in the diseases types are limited.
Furthermore, the differences in the time intervals between onset and neurologist visit, final diagnosis and death among the FFI, T188K and E200K gCJD groups that possessed sufficient cases for statistical analysis were individually analyzed. When compared with those of the T188K and E200K gCJD groups, the patients of FFI presented a wider range of time in the intervals between disease onset and neurologist visit, final diagnosis and death (S1 Fig). Significantly longer intervals between onset and neurologist visit and final diagnosis of FFI cases (P<0.05) might indicate a relatively slow progression and indistinguishable clinical manifestation at the early stage. The time interval between disease onset to death of the FFI cases was significantly longer than that of the T188K cases (P<0.01) but comparable with the time interval in the E200K case. The cases in the T188K gCJD group demonstrated similar intervals between onset and neurologist visit and final diagnosis as, but shorter intervals from onset to death (P<0.05) than, the E200K cases. This may indicate a more rapid progression and shorter survival time of T188K gCJD.
To assess the potential differences in the difficulty of diagnosis and relevant influence factors among various genetic prion diseases, the time between neurologist visit and the final diagnosis of each patient was analyzed. The interval times varied largely from one week to more than two years, with a median of 45 days. Because of the limited number of cases in the many subtypes of prion diseases, the patients were grouped as FFI, T188K, E200K and others. The FFI and T188K groups demonstrated slightly long and short median interval times, but without significant differences among these four groups. These patients were further grouped based on the year of diagnosis, the age at onset, and the location of residency. This allowed for us to screen for factors that influence the interval times. No significant differences were observed among the groups based on the surveillance year between 2006 and 2014, the age at which patients presented clinical manifestations, or the location of residency (S2 Fig).
Discussion
Between 2006 and Sept 2014, 69 cases of 15 different genetic prion diseases were diagnosed genetically and/or pathologically via the China National Surveillance Program for CJD. This is the first and largest systematic report concerning genetic prion diseases in China. Except one Miao-Chinese, all cases included Han-Chinese patients. In China, there are 56 nationalities. Han nationality is the majority of the population and accounts for 90.56% of the population. Miao nationality is the fourth largest of the national minorities and whose members reside mostly in the Southwestern provinces of China. The total population of Miao-Chinese is approximately 9 million. Similar to the Han-Chinese [7], the polymorphisms of codon 129 of all cases of genetic prion diseases are the Met/Met homozygote. FFI, T188K and E200K gCJD are the most frequently identified genetic prion diseases, which account for approximately 75% of all cases. Three cases with the P102L mutation and that are associated with GSS have been detected in the past eight years and no other GSS-associated mutation has been observed. The remaining cases are rare PRNP mutations, which account for one to two percent of gCJD cases. In agreement with the idea that genetic CJD accounts for 5–15% of all CJD cases, Chinese genetic prion diseases account for 6–12% (median 8.7%) of all diagnosed CJD cases each surveillance year. More than 56% of cases do not have clear disease family histories. The age at disease onset of the patients with genetic prion diseases is approximately 10 years younger than that of sCJD cases [7]. These data highlight that the pattern of Chinese genetic prion diseases possesses common features of genetic prion diseases worldwide [19,20,21,22,23,24], though subtle differences remain across disease sub-types.
The geographical distribution of the cases of genetic prion diseases seems to be dispersed across mainland China; however, 20 cases are from one province (Henan) and consists of six different diseases, including 13 FFI cases. Analysis of these 20 cases did not identify any genetic relationship among families, except in two FFI cases, which originated from one family. The Henan province is the most populous province in China, containing approximately 100 million residents. The CJD surveillance in the Henan province is also the most active, with more reported suspected CJD cases each year. This may partially account for this geographical pattern; however, the total number of genetic prion diseases and the involved provinces from the northern part of China (bounded by the Yangtze river) are extensive when compared to the southern part of China. Whether such disease distribution features are linked to the large migrations of the Han Chinese in the past requires further analysis.
The clear predominance of FFI (39%), T188K (23%) and E200K (13%) cases in Chinese genetic prion diseases may illustrate a unique pattern that differs from not only Caucasian but also North-east Asian (e.g., Japanese and Korean) disease trends [4,25,26]. The literature indicates that E200K is the most common mutation in many European countries [22,27], while FFI and various GSS mutations are also frequently observed [19,28,29,30]. In some special regions, such as the Italo-Greek villages of the southeast Calabria region in Italy [31], the Slovakian [32] and the Libyan Jews in Israel [33], the distributions of the E200K mutation, either in patients or in the health carriers, are extremely elevated. E200K gCJD is also the most common genetic prion disease in Argentina, which accounts for 15.6% of all reported human prion diseases between 1997 and 2008 [22]. In Japan, the most common mutation in PRNP is V180I (41.2%). Other frequent mutations include P102L (18.1%), E200K (17.1%) and M232R (15.3%) [34]. In Korea, the V180I, E200K, P102L, V203I, and M232R mutations have each been reported in more than two clinical cases [4]. When compared with Japanese and Korean cases, the prevalence of the E200K mutation in Chinese genetic prion diseases appears similar. Yet, the number of FFI and T188K gCJD cases are markedly more increased while P105L, V180I and V232R gCJD cases are rare or even undetected.
The clinical signs and clinical examinations among those 15 genetic prion diseases widely vary. As expected, the number of Chinese FFI cases displays a distinct pattern among the gCJD cases, with fewer clinical manifestations being described for sCJD. PSWCs in EEG are not detected in all FFI cases and MRI abnormalities have been observed in only one FFI case. CSF 14-3-3 is positive in approximately a third of FFI cases. Conversely, considerably greater portions of patients with T188K and E200K demonstrate abnormalities in these three examinations, thereby indicating again the significance of CSF-14-3-3, MRI and EEG in some types of gCJD.
Despite the limited patient numbers for many subtypes of gCJD in this study, we noticed some unique patterns regarding different locations of the disease-associated mutations. The diseases that are associated with mutations in the N-terminus (i.e., before aa 183) of the PrP protein are associated with an earlier age of onset of the disease symptoms, are negative in CSF-14-3-3, are frequently associated with a family history and have longer time intervals between diagnosis of the disease and completion of its clinical course. Conversely, the patients with mutations in the C-terminus of the PrP have relatively high ratios of CSF-14-3-3 positivity and short intervals for disease recognition and clinical course. Meanwhile, the age of onset is older, and fewer patients demonstrate a family history of the disease. The relevant molecular mechanisms remain unclear. Two Chinese patients with extra octarepeat insertions in this study appear to have longer disease durations. For example, disease duration is more than four years in the cases with 7-Ors [10]. Other reported cases with extra octarepeat insertions also present long durations, being 16 years in one case [35,36,37]. Unfortunately, the case with 1-OR insertion went without contact after eight months following diagnosis. The known duration of this case is already 43 months at the last follow-up.
T188K gCJD is the second most common genetic prion disease in the Han Chinese population, which has been described only in three German and one Austrian previously [38,39]. Surprisingly, the T188K mutation has not reported in Japanese and Korean patients in the literature so far, which reflects the diversity in genetics among the East Asian races. The onset ages of T188K gCJD cases are older than those of FFI case, but similar to the E200K case. Although the time intervals between disease onset to neurologist visit and to final diagnosis are comparable between the cases of T188K and E200K, the clinical courses of T188K patients are markedly shorter. The durations of the other four T188K gCJD Caucasian cases, whose genotypes of codon 129 are Met/Val heterozygote, are also relatively short (ranging from 5 to 13 months) [38]. Meanwhile, an older age at onset, a high ratio of MRI abnormality, fewer cases with a family history of the disease and a short survival time may constitute the features of T188K gCJD. Like the characteristics of FFI in many other studies, Chinese FFI cases also demonstrate relatively long clinical durations. The time until diagnosis of FFI cases is also longer than in T188K and E200K gCJD, which may indicate a relatively slow progression and a more atypical clinical appearance at early stages.
We have also analyzed the time intervals between the initial neurologist visit and the final diagnosis and the factors that possibly influence this interval in the 69 patients. Because all suspected CJD cases that are reported to the CJD Surveillance Center include PRNP sequencing assays, the time interval from neurologist visit to final diagnosis fairly reflects the recognition times by neurologists. Although the individual interval of the patient varies considerably, with the average and median times being 71.1 and 45 days, respectively, there is no large difference among the patients in the FFI, T188K, E200K and other mutation groups. Other factors, such as the surveillance year, age at onset and place of residence of the patients (which may represent the economic status of the patient) are also unrelated to disease recognition time. Further analysis revealed that the patients with longer intervals between the initial neurologist visit and final diagnosis usually have had multiple hospital transfers between small clinics and large polyclinics. In another study, we proposed that the diagnosed CJD patients from the Beijing region have fewer hospital transfers and a shorter time interval between disease onset and the final diagnosis than do those outside of the Beijing region [40], which implies that clinician knowledge of prions and prion diseases is essential for shortening the diagnostic time for CJD.
Supporting Information
S1 Fig. Comparison of the intervals between onset and neurologist visit.
A. Final diagnosis. B. Death of the patients of FFI, T188K and E200K gCJD. The P values are indicated above.
https://doi.org/10.1371/journal.pone.0139552.s001
(TIF)
S2 Fig. Analysis of the intervals from neurologist visit to final diagnosis based on the different diseases.
A. The surveillance year. B. The age of onset. C. The residence of patients. D. The P values are indicated.
https://doi.org/10.1371/journal.pone.0139552.s002
(TIF)
Author Contributions
Conceived and designed the experiments: QS XPD. Performed the experiments: WZ CC BYZ KX JH. Analyzed the data: XCZ XJS QL LQD JHD WQL PH WJJ JL. Contributed reagents/materials/analysis tools: CC KX. Wrote the paper: QS XPD.
References
- 1. Prusiner SB (1998) Prions. Proc Natl Acad Sci U S A 95: 13363–13383. pmid:9811807
- 2. Prusiner SB (1998) The prion diseases. Brain Pathol 8: 499–513. pmid:9669700
- 3. Safar J, Prusiner SB (1998) Molecular studies of prion diseases. Prog Brain Res 117: 421–434. pmid:9932423
- 4. Jeong BH, Kim YS (2014) Genetic studies in human prion diseases. J Korean Med Sci 29: 623–632. pmid:24851016
- 5. Zerr I, Poser S (2002) Clinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests. APMIS 110: 88–98. pmid:12064260
- 6. Shi Q, Gao C, Zhou W, Zhang BY, Chen JM, Tian C, et al. (2008) Surveillance for Creutzfeldt-Jakob disease in China from 2006 to 2007. BMC Public Health 8: 360. pmid:18928564
- 7. Gao C, Shi Q, Tian C, Chen C, Han J, Zhou W, et al. (2011) The epidemiological, clinical, and laboratory features of sporadic Creutzfeldt-Jakob disease patients in China: surveillance data from 2006 to 2010. PLoS One 6: e24231. pmid:21904617
- 8. Zerr I, Kallenberg K, Summers DM, Romero C, Taratuto A, Heinemann U, et al. (2009) Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Brain 132: 2659–2668. pmid:19773352
- 9. Newey CR, Sarwal A, Wisco D, Alam S, Lederman RJ (2013) Variability in diagnosing Creutzfeldt-Jakob disease using standard and proposed diagnostic criteria. J Neuroimaging 23: 58–63. pmid:23163590
- 10. Wang XF, Guo YJ, Zhang BY, Zhao WQ, Gao JM, Wan YZ, et al. (2007) Creutzfeldt-Jakob disease in a Chinese patient with a novel seven extra-repeat insertion in PRNP. J Neurol Neurosurg Psychiatry 78: 201–203. pmid:17229753
- 11. Zhang J, Chen L, Zhang BY, Han J, Xiao XL, Tian HY, et al. (2004) Comparison study on clinical and neuropathological characteristics of hamsters inoculated with scrapie strain 263K in different challenging pathways. Biomed Environ Sci 17: 65–78. pmid:15202866
- 12. Shi Q, Chen C, Gao C, Tian C, Zhou W, Zhang BY, et al. (2012) Clinical and familial characteristics of ten chinese patients with fatal family insomnia. Biomed Environ Sci 25: 471–475. pmid:23026528
- 13. Shi XH, Han J, Zhang J, Shi Q, Chen JM, Xia SL, et al. (2010) Clinical, histopathological and genetic studies in a family with fatal familial insomnia. Infect Genet Evol 10: 292–297. pmid:20096809
- 14. Xie WL, Shi Q, Xia SL, Zhang BY, Gong HS, Wang SB, et al. (2013) Comparison of the pathologic and pathogenic features in six different regions of postmortem brains of three patients with fatal familial insomnia. Int J Mol Med 31: 81–90. pmid:23175354
- 15. Ye J, Han J, Shi Q, Zhang BY, Wang GR, Tian C, et al. (2008) Human prion disease with a G114V mutation and epidemiological studies in a Chinese family: a case series. J Med Case Rep 2: 331. pmid:18925969
- 16. Shi Q, Zhang BY, Gao C, Han J, Wang GR, Chen C, et al. (2012) The diversities of PrP(Sc) distributions and pathologic changes in various brain regions from a Chinese patient with G114V genetic CJD. Neuropathology 32: 51–59. pmid:21732990
- 17. EUROCJD Group (2001) Genetic epidemiology of Creutzfeldt-Jakob disease in Europe. Rev Neurol. 157:633–637. pmid:11458182
- 18. Shi Q, Xie WL, Zhang B, Chen LN, Xu Y, Wang K, et al. (2013) Brain microglia were activated in sporadic CJD but almost unchanged in fatal familial insomnia and G114V genetic CJD. Virol J 10: 216. pmid:23816234
- 19. Brandel JP, Peckeu L, Haik S (2013) The French surveillance network of Creutzfeldt-Jakob disease. Epidemiological data in France and worldwide. Transfus Clin Biol 20: 395–397. pmid:23587616
- 20. Head MW, Ironside JW (2012) Review: Creutzfeldt-Jakob disease: prion protein type, disease phenotype and agent strain. Neuropathol Appl Neurobiol 38: 296–310. pmid:22394291
- 21. Imran M, Mahmood S (2011) An overview of human prion diseases. Virol J 8: 559. pmid:22196171
- 22. Begue C, Martinetto H, Schultz M, Rojas E, Romero C, D'Giano C, et al. (2011) Creutzfeldt-Jakob disease surveillance in Argentina, 1997–2008. Neuroepidemiology 37: 193–202. pmid:22067221
- 23. Doi Y, Yokoyama T, Sakai M, Nakamura Y (2007) Creutzfeldt-Jakob disease mortality in Japan, 1979–2004: analysis of national death certificate data. J Epidemiol 17: 133–139. pmid:17641449
- 24. Klug GM, Boyd A, Zhao T, Stehmann C, Simpson M, McLean CA, et al. (2013) Surveillance for Creutzfeldt-Jakob disease in Australia: update to December 2012. Commun Dis Intell Q Rep 37: E115–120. pmid:24168084
- 25. Higuma M, Sanjo N, Satoh K, Shiga Y, Sakai K, Nozaki I, et al. (2013) Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases. PLoS One 8: e60003. pmid:23555862
- 26. Windl O, Dempster M, Estibeiro JP, Lathe R, de Silva R, Esmonde T, et al. (1996) Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene. Hum Genet 98: 259–264. pmid:8707291
- 27. Kovacs GG, Seguin J, Quadrio I, Hoftberger R, Kapas I, Streichenberger N, et al. (2011) Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy. Acta Neuropathol 121: 39–57. pmid:20593190
- 28. Kovacs GG, Puopolo M, Ladogana A, Pocchiari M, Budka H, van Duijn C, et al. (2005) Genetic prion disease: the EUROCJD experience. Hum Genet 118: 166–174. pmid:16187142
- 29. Mead S (2006) Prion disease genetics. Eur J Hum Genet 14: 273–281. pmid:16391566
- 30. Heinemann U, Krasnianski A, Meissner B, Varges D, Kallenberg K, Schulz-Schaeffer WJ, et al. (2007) Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillance. Brain 130: 1350–1359. pmid:17472986
- 31. D'Alessandro M, Petraroli R, Ladogana A, Pocchiari M (1998) High incidence of Creutzfeldt-Jakob disease in rural Calabria, Italy. Lancet 352: 1989–1990. pmid:9872257
- 32. Mitrova E, Belay G (2002) Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development. Acta Virol 46: 31–39. pmid:12197632
- 33. Spudich S, Mastrianni JA, Wrensch M, Gabizon R, Meiner Z, Kahana I, et al. (1995) Complete penetrance of Creutzfeldt-Jakob disease in Libyan Jews carrying the E200K mutation in the prion protein gene. Mol Med 1: 607–613. pmid:8529127
- 34. Nozaki I, Hamaguchi T, Sanjo N, Noguchi-Shinohara M, Sakai K, Nakamura Y, et al. (2010) Prospective 10-year surveillance of human prion diseases in Japan. Brain 133: 3043–3057. pmid:20855418
- 35. Goldfarb LG, Brown P, McCombie WR, Goldgaber D, Swergold GD, Wills PR, et al. (1991) Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene. Proc Natl Acad Sci U S A 88: 10926–10930. pmid:1683708
- 36. Cannella M, Martino T, Simonelli M, Ciammola A, Gradini R, Ciarmiello A, et al. (2007) De novo seven extra repeat expanded mutation in the PRNP gene in an Italian patient with early onset dementia. J Neurol Neurosurg Psychiatry 78: 1411–1413. pmid:17682007
- 37. Jansen C, Voet W, Head MW, Parchi P, Yull H, Verrips A, et al. (2011) A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Straussler-Scheinker disease phenotype: comparison with similar cases from the literature. Acta Neuropathol 121: 59–68. pmid:20198483
- 38. Finckh U, Muller-Thomsen T, Mann U, Eggers C, Marksteiner J, Meins W, et al. (2000) High frequency of mutations in four different disease genes in early-onset dementia. Ann N Y Acad Sci 920: 100–106. pmid:11193137
- 39. Roeber S, Grasbon-Frodl EM, Windl O, Krebs B, Xiang W, Vollmert C, et al. (2008) Evidence for a pathogenic role of different mutations at codon 188 of PRNP. PLoS One 3: e2147. pmid:18478114
- 40. Shi Q, Zhang XC, Zhou W, Xiao K, Chen C, Zhang HY, et al. (2015) Analysis of the advantage features of Beijing surveillance network for Creutzfeldt-Jakob disease. Prion. 9:304–14. pmid:26251963