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2018, Journal of Parkinson's disease
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4 pages
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Recent epidemiological observations have drawn attention to the rapid rise in the burden caused by Parkinson's disease over the past years, emphasizing that Parkinson's disease is a matter of serious concern for our future generations. A recent report by Public Health England corroborates this message, by providing new insight on trends in deaths associated with neurological diseases in England between 2001 to 2014. The report indicates that mortality associated with Parkinson's disease and related disorders increased substantially between 2001 and 2014. This trend is partially explained by increased longevity in the population. However, it is possible that changes in exposure to risk factors, recent improvements in multidisciplinary care (leading to prolonged survival), and improved diagnostic awareness or improved registration also influenced the observed trend. Furthermore, patients with Parkinson's disease and related disorders were found to die at an advanced ag...
European Journal of Neurology, 2009
Background: This paper describes changes in ParkinsonÕs disease (PD) mortality in England and Wales between 1993 and 2006 using all information on death certificates. Methods: Information on deaths was obtained from the Office for National Statistics. Mortality rates for any mention of PD on death certificates were directly age-standardized using the European standard population. Average yearly changes in mortality rates were estimated using linear regression. The underlying cause of death on death certificates where PD was mentioned was examined by sex and calendar period. Results: Male PD age-standardized mortality rates for any mention of PD decreased from 15.0 to 11.7 per 100 000 between 1993 and 2006. Female PD mortality rates fell from 6.3 to 4.9 per 100 000. Decreases were greater for older age-groups. The proportion of deaths with PD recorded as the underlying cause increased by 50% in 2001 following implementation of the 10th revision of the International Classification of Diseases (ICD). Conclusion: ParkinsonÕs disease mortality rates in England and Wales are decreasing, especially for men and for older age-groups. Because of data limitations we are unable to ascertain whether the decrease of PD recorded on death certificates is because of a reduction in PD incidence, or to improved survival for PD patients resulting from advancements in PD treatments or to improvements in general medical care. The dramatic increase in PD as the underlying cause of death following ICD revision in 2001 demonstrates the dangers of using underlying cause of death to investigate mortality trends without being aware of the potential for artifacts.
American journal of epidemiology, 2016
We investigated trends in the incidence of parkinsonism and Parkinson disease (PD) by comparing data from the first 2 subcohorts of the Rotterdam Study, a prospective, population-based cohort study (first subcohort: baseline 1990 with 10 years of follow-up; second subcohort, baseline 2000 with 10 years of follow-up). From the baseline years, we observed differences in the second subcohort that were associated with a lower risk of PD for some but not all baseline risk factors. Participants in both subcohorts were followed for a maximum of 10 years and monitored for the onset of parkinsonism, the onset of dementia, or death, until January 1, 2011. We used Poisson regression models to compare the incidences of parkinsonism, both overall and by cause (PD and secondary causes), and competitive events (incident dementia and death) as well as the mortality of parkinsonism patients in the 2 subcohorts. In the 1990 subcohort, there were 182 cases of parkinsonism (84 of which were PD) during ...
npj Parkinson's Disease, 2022
Parkinson’s disease (PD) has the fastest rising prevalence of all neurodegenerative diseases worldwide. However, it is unclear whether its incidence has increased after accounting for age and changes in diagnostic patterns in the same population. We conducted a cohort study in individuals aged ≥50 years within a large UK primary care database between January 2006 and December 2016. To account for possible changes in diagnostic patterns, we calculated the incidence of PD using four case definitions with different stringency derived from the combination of PD diagnosis, symptoms, and treatment. Using the broadest case definition, the incidence rate (IR) per 100,000 person years at risk (PYAR) was 149 (95% CI 143.3–155.4) in 2006 and 144 (95% CI 136.9–150.7) in 2016. In conclusion, the incidence of PD in the UK remained stable between 2006 and 2016, when accounting for age and diagnostic patterns, suggesting no major change in underlying risk factors for PD during this time period in t...
JAMA Neurology, 2016
To the Editor We read with interest the article by Savica et al, 1 who described an increase in the incidence rate of parkinsonism in the Rochester Epidemiology Project between 1976 and 2005. This finding contradicts our recently reported observation that the incidence rate of parkinsonism was lower in a subcohort of the Rotterdam Study that was followed up between 2000 and 2011 compared with a subcohort that was followed up between 1990 and 2000. 2 Similarly, a UK primary care study previously reported a significant decline in Parkinson disease (PD) incidence rates between 1999 and 2009. 3 Savica et al 1 hypothesized that the changes observed in the Rochester Epidemiology Project could be attributed to a decrease in the prevalence of smoking in the second half of the 20th century, but they were unable to test this hypothesis in their cohort. Within the Rotterdam Study, we assessed smoking habits at baseline of both subcohorts (1990 and 2000). As expected, we observed that the ageand sex-adjusted prevalence of current smoking was lower across all ages (55-106 years) in the subcohort that started in 2000. 2 During follow-up, incident parkinsonism was diagnosed in 182 of 6752 persons in the subcohort that started in 1990, and in 28 of 2440 persons in the subcohort that started in 2000. The age-and sex-adjusted incidence rate (IR) of parkinsonism for smokers was similar in both subcohorts (IR, 0.63; 95% CI,0.43-0.91 in the 1990 subcohort; IR, 0.61; 95% CI, 0.27-1.44 in the 2000 subcohort). The age-and sex-adjusted incidence rate ratio (IRR) for parkinsonism of persons in the 2000 subcohort vs the 1990 subcohort was 0.55 (95% CI, 0.36-0.81). After additional adjustment for smoking status, the IRR remained virtually unchanged (IRR, 0.57; 95% CI, 0.37-0.84). Unfortunately, the small number of PD cases in the 2000 subcohort prevented PD-specific analyses on the effect of smoking. We conclude that it is unlikely that the decline in smoking prevalence drove a change in the incidence of parkinsonism in the Rotterdam Study. The discrepant findings of the study by Savica et al 1 compared with previous studies, including the Rotterdam Study, highlight the lack of insight on causality of risk factors for parkinsonism and PD. For smoking in particular, causality of its inverse association with the risk for parkinsonism and PD remains highly contentious, 4 and the inference that the increase in parkinsonism incidence in the Rochester Epidemiology Project can be attributed to a decline in smoking may shift focus from other putative etiological factors. To better understand factors that drive differential trends in the incidence of parkinsonism across populations, there is an urgent need for cross-cohort collaboration, similar to recently initiated efforts for dementia. 5
Age and Ageing, 2013
Background: Parkinson's disease is a common disorder among older people. Accurate epidemiological information is essential to identify possible aetiological factors, plan health services and set priorities for medical research. Objective: to determine the incidence of idiopathic Parkinson's disease in a defined geographical area in the NorthEast of England. Methods: using a prospective, longitudinal design, we sought to identify every new case of Parkinson's disease arising in the Newcastle and Gateshead area in the NorthEast of England. The base population comprised 488 576 individuals and multiple sources of case ascertainment were employed. All the patients with newly diagnosed idiopathic Parkinson's disease or parkinsonism between 1 June 2009 and 31 May 2011 were invited to participate. Patients were examined by a specialist and followed longitudinally to permit diagnostic review. Results: we identified 257 potential cases, of whom 181 had suspected idiopathic Parkinson's disease. After a follow-up period of 18 months, 155 patients retained a clinical diagnosis of probable Parkinson's disease. The mean age at diagnosis was 72.4 ± 10 years. The crude incidence of PD in Newcastle and Gateshead was 15.9 per 100 000 persons per year (95% CI: 13.4-18.4). Age-standardised to the European population the incidence of Parkinson's disease was 12.0 per 100 000 (95% CI: 10.1-14.0). We found a higher crude incidence among men 17.7 per 100 000 (95% CI: 14.0-21.4) than women 14.0 per 100 000 (95% CI: 10.7-17.4). Conclusion: in this prospective longitudinal study, the incidence rate of Parkinson's disease in NorthEast England is similar to that of other modern European and American studies.
Neurology
ObjectiveTo examine mortality and associated risk factors, including possible effects of mild cognitive impairment, imaging, and CSF abnormalities, in a community-based population with incident parkinsonism and Parkinson disease.MethodsOne hundred eighty-two patients with new-onset, idiopathic parkinsonism were diagnosed from January 2004 through April 2009, in a catchment area of 142,000 inhabitants in Sweden. Patients were comprehensively investigated according to a multimodal research protocol and followed prospectively for up to 13.5 years. A total of 109 patients died. Mortality rates in the general Swedish population were used to calculate standardized mortality ratio and expected survival, and Cox proportional hazard models were used to investigate independent predictors of mortality.ResultsThe standardized mortality ratio for all patients was 1.84 (95% confidence interval 1.50–2.22, p < 0.001). Patients with atypical parkinsonism (multiple system atrophy or progressive su...
Acta Neurologica Scandinavica, 2009
After the introduction of L-dopa the mortality rate in Parkinson&#39;s disease (PD) patients has changed, but is still higher than in the background population. Mortality, age at death and cause of death in a group of PD patients compared with the background population were studied. The diagnosis on the death certificate were registered. The material consisted of 458 patients who in a period 1.4.1973-31.10.1991 were registered as having PD. Death in the period amounted to 253 patients. Median age of death was 77.29 years for men and 79.11 years for women. In the background population the median age at death was 80.69 years for men and 84.37 years for women. The SMR for men was 1.92 and for women 2.47. Infections, in particular lung infections, and heart diseases were the most common causes of death. Seventy percent of the death certificates had PD as a diagnosis. It is likely that several factors can influence the changed mortality of PD: more effective treatment, changing diagnostic practice, and inter-disease competition.
Movement …, 2006
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The Lancet. Neurology, 2018
Neurological disorders are now the leading source of disability globally, and ageing is increasing the burden of neurodegenerative disorders, including Parkinson's disease. We aimed to determine the global burden of Parkinson's disease between 1990 and 2016 to identify trends and to enable appropriate public health, medical, and scientific responses. Through a systematic analysis of epidemiological studies, we estimated global, regional, and country-specific prevalence and years of life lived with disability for Parkinson's disease from 1990 to 2016. We estimated the proportion of mild, moderate, and severe Parkinson's disease on the basis of studies that used the Hoehn and Yahr scale and assigned disability weights to each level. We jointly modelled prevalence and excess mortality risk in a natural history model to derive estimates of deaths due to Parkinson's disease. Death counts were multiplied by values from the Global Burden of Disease study's standard ...
2024
Salmos que meditamos y estudiamos o por lo menos leímos con la ayuda de una guía de Gianfranco Ravasi por el año de la oración como preparación al jubileo.
INTRODUCTION
At population level, the burden caused by Parkinson's disease (PD) has recently increased, leading some to label this as a Parkinson "pandemic" [1,2]. * Correspondence to: Bastiaan R. Bloem, MD, PhD, Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, The Netherlands. E-mail: bas.bloem@rad boudumc.nl.
Scrutiny of temporal trends in causes of death can offer useful complementary information in this regard. Here, we draw attention to a recently published report by Public Health England on trends in deaths associated with neurological diseases in England between 2001 to 2014, [3] which contains several interesting observations concerning Parkinson's disease and related disorders (PDRD). (Box 1) We will summarise these findings, and address some implications for future healthcare needs. Specifically, we focus on the frequency, age and place of deaths associated with PDRD, as well as on temporal trends in the frequency of these deaths.
CAUSES OF DEATH IN THE AGEING POPULATION: THE PUBLIC HEALTH ENGLAND REPORT
In the United Kingdom, it has long been a legal requirement to report deaths to the Office of National Statistics, yielding near-complete mortality data on a population-wide scale (https://www.ons.gov.uk/peop lepopulationandcommunity/birthsdeathsandmarriag es/deaths). For each deceased individual, healthcare professionals register a single underlying cause of death, as well as up to 15 contributory conditions on the death certificate. Conditions are coded in line with the International Statistical Classification of Diseases and Related Health Problems.
According to the Public Health England report, [3] 6.590.453 individuals aged 20 years and over died in England between 2001 and 2014. Of these deaths, 366.728 (6%) were associated with at least one neurological condition (listed as the underlying cause or a contributory cause of death). The report also contains data on deaths associated with seven specific groups of neurological conditions: epilepsy; motor neurone disease and spinal muscular atrophy; multiple sclerosis and inflammatory disorders; neuromuscular diseases; traumatic brain and spine injury; tumours of the nervous system; and PDRD. The latter group comprised all disorders characterized by parkinsonism (including atypical parkinsonisms), other extrapyramidal disorders (including chorea), or tic disorder. Of note, dementia (including dementia with Lewy bodies) and stroke were not among the groups of neurological conditions analysed in the above-referenced report, however, they could be recorded as the underlying cause of death on a death certificate.
COMMON CAUSES OF DEATH
The group that was most commonly listed on death certificates between 2001 and 2014 was PDRD; these were mentioned on 31% of deaths associated with a neurological condition as the underlying cause, the contributory cause, or both. PD was the most commonly recorded underlying neurological cause of death (14% of deaths associated with a neurological condition). Remarkably, falls (6%) and pneumonia (3%) were among the 10 most common underlying causes of deaths associated with a neurological condition, while Alzheimer's disease, vascular dementia and unspecified dementia were each recorded on only 1% of death certificates. Falls and pneumonia may have occurred as a complication of parkinsonism or dementia (including dementia with Lewy bodies) in some patients, which implies that the report may have underestimated how often these diseases are the underlying cause of death. Indeed, falls and fall-related injuries are very common in Parkinson patients, and hip fractures in this population are associated with high mortality rates [4,5]. Aspiration pneumonia secondary to dysphagia is also a common cause of death for Parkinson patients [6]. On the other hand, some misclassification of a diagnosis of PD may have occurred, as a previous study showed that almost one in six patients with a diagnosis of PD in the population did not fulfil strict clinical criteria for the disease [7].
Taken together, these data demonstrate that deaths associated with PDRD are common in the population.
AGE AND PLACE OF DEATHS
Deaths associated with PDRD were the only group of neurological conditions for which the mean age at death was higher than the overall mean age at death in the population (82 vs. 78 years, data reported for the 2012-2014 period). PD is not exclusively diagnosed in the very elderly, [8] and the high age at death suggests that PD patients live for long periods of time with this condition. Considering the projected rise in life expectancy globally, more resources will be needed to take care of elderly patients with PD.
Care homes were the most common place of death among patients with PDRD, occurring in 43% of cases. Notably, healthcare professionals working in these institutions frequently lack Parkinson-specific expertise [9]. Perhaps dedicated Parkinson nursing homes or Parkinson-specific training programs could help to reduce some preventable deaths. Aside from care homes, 41% of deaths associated with PDRD were recorded in hospitals, 14% occurred at home, and 2% in other places. By comparison, 23% of all-cause deaths and 18% of deaths associated with neurological conditions occurred at home. These data suggest that, despite recent improvements, [9,10] the end-of-life for PD patients is often unplanned and occurring in hospitals or care homes. Although there are undeniably instances when dying in a hospital is more appropriate than dying at home, most patients indicate a preference for dying at home [10]. Family caregivers also typically indicate their own home as the preferred place of care for their relatives towards the end-of-life [11]. Furthermore, the vast majority of hospital admissions of PD patients are unplanned, resulting from either complications of the disease or its treatments or comorbidities [12,13].
Parkinson-specific training of professionals working in the community might prevent some of these unscheduled admissions. For instance, care delivery by physiotherapists with specific expertise in Parkinson management was associated with fewer hospital admissions due to fractures, other orthopaedic injuries or pneumonia, as compared to regular care by a generically trained therapist [14]. Further gains may be made by introducing intensive case management for community-dwelling Parkinson patients, entailing a personalised, collaborative plan of care, not only for but also with patients and their families. Also, closer collaboration between university clinics and regional community hospitals may improve delivery of optimal patient care, with an emphasis on care delivered close to the patient's home whenever possible, but with seamless access to more remote specialized care whenever needed. Specific areas of collaboration may include peer-to-peer support (e.g., university centres supporting community-based colleagues with less expertise), diagnostics in university clinics for unclear cases, shared education programs for patients and professionals, and improved regional guideline development.
TEMPORAL TRENDS
The number of all-cause deaths per year gradually declined between 2001 and 2006 and remained relatively stable between 2007 and 2014. Compared to 492,205 deaths in 2001, there were 464.556 in 2014, representing a 6% decline. By contrast, the yearly number of deaths associated with a neurological condition increased steadily from 23,051 in 2001 to 31,925 in 2014, representing a 39% increase over this relatively short time period. The number of deaths associated with PDRD increased from 6,963 to 10,067 during the study period, indicating a marked 45% rise. There were even steeper relative rises in mortality associated with neuromuscular diseases (+83%), epilepsy (+70%), and traumatic brain and spine injury (+64%). Ageing of the population did not fully account for the observed rise in mortality associated with a neurological condition, since age-standardised mortality for deaths associated with a neurological condition only increased by 12%. Age-standardised mortality of deaths associated with PDRD rose by 10%.
The increase in mortality associated with PDRD may be reflective of a rise in the incidence, a longer survival after diagnosis, an increased awareness of coding these conditions on death certificates in England, or a combination thereof. Temporal trends in the incidence of parkinsonism, including its most common cause PD, have varied substantially across populations around the world [15][16][17][18]. It is possible that differential temporal changes in exposure to risk factors (e.g., exposure to airborne pollutants, toxins such as pesticides, heavy metals or solvents) have resulted in discrepant trends in the incidence of parkinsonism across populations. Furthermore, we consider the possibility that survival after diagnosis among parkinsonism patients may have increased as a result of improvements in multidisciplinary care during the last decade [14,19,20]. Future studies are warranted to elucidate to what extent such changes may have affected the observations in the Public Health England report.
Interestingly, age-standardised mortality of almost every group of neurological conditions increased throughout the study period. This suggests that an improved awareness of neurological conditions or a more complete registration of contributory causes on death certificates by healthcare professionals over time may have contributed to the observed rise in mortality associated with PDRD. Unfortunately, it is not clear whether the number of contributory conditions listed on death certificates changed during the study period. We also note that some individuals who were diagnosed with dementia but not with PDRD may have had an alpha-synucleinopathy, suggesting that the observed mortality rate associated with PDRD reflects an underestimate of the mortality rate associated with alpha-synucleinopathies. Conversely, it is possible that not all individuals with PDRD had an alpha-synucleinopathy.
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