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Journal ArticleDOI

Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010

Rafael Lozano1, Mohsen Naghavi1, Kyle J Foreman2, Stephen S Lim1  +192 moreInstitutions (95)
15 Dec 2012-The Lancet (Elsevier)-Vol. 380, Iss: 9859, pp 2095-2128
TL;DR: The Global Burden of Diseases, Injuries, and Risk Factors Study 2010 aimed to estimate annual deaths for the world and 21 regions between 1980 and 2010 for 235 causes, with uncertainty intervals (UIs), separately by age and sex, using the Cause of Death Ensemble model.
About: This article is published in The Lancet.The article was published on 2012-12-15 and is currently open access. It has received 11809 citations till now. The article focuses on the topics: Mortality rate & Years of potential life lost.

Summary (6 min read)

Introduction

  • Cause-specific mortality is arguably one of the most fundamental metrics of population health.
  • For the remaining deaths which are not medically certified, many different data sources and diagnostic approaches must be used from surveillance systems, demographic research sites, surveys, censuses, disease registries, and police records to construct a consolidated picture of causes of death in various populations.
  • These efforts often include very specific steps undertaken for different data sources and are frequently poorly documented.
  • GBD revisions for 1999, 2000, 2001, 2002, 2004, and 2008 have used these compositional models to allocate deaths according to three broad cause groups: communicable, maternal, neonatal, and nutritional causes; noncommunicable diseases; and injuries.
  • 38 Given the profusion of statistical modeling options, an important innovation has been the reporting of out-of-sample predictive validity to document the performance of complex models.

Data and methods

  • Some general aspects of the analytical framework such as the creation of the 21 GBD regions and the full hierarchical cause list including the mapping of the International Classification of Diseases and Injuries (ICD) to the GBD cause list are reported elsewhere.
  • While results are reported in this paper at the regional level for 1990 and 2010, the cause of death analysis has been undertaken at the country level for 187 countries from 1980 to 2010.
  • Using longer time series improves the performance of many types of estimation models; data prior to 1980, however, are much sparser for developing countries so the authors have restricted the analysis to 1980-2010.

Database development

  • Over the five year duration of the GBD 2010 study, the authors have sought to identify all published and unpublished data sources relevant to estimating causes of death for 187 countries from 1980 to 2010.
  • Web Table 1a provides a summary of the siteyears of data identified by broad type of data system and, similarly, Web Table 1b illustrates the number of site-years by GBD region.
  • Of the GBD regions, subSaharan Africa Central has the most limited evidence base with data on only 27 causes from at least one country.
  • In addition, there is country to country variation in the detail used to report causes of death included in national reporting lists, namely the basic tabulation list for ICD9, the ICD10 tabulation list, three digit and four digit detail, and special reporting lists.
  • Verbal autopsy data collected through sample registration systems, demographic surveillance systems, or surveys Verbal autopsy (VA) is a means for ascertaining the cause of death of individuals and the cause-specific mortality fractions in populations with incomplete vital registration systems.

Population-based cancer registries

  • Population-based cancer registries provide an important source of data on incidence of cancers in various countries.
  • The authors identified 2,715 site-years of cancer registry data across 93 countries.
  • The log of the MI ratio has been estimated as a function of national income per capita with random effects for country, year, and age.
  • The estimated mortality to incidence ratios have been used to map cancer registry data on incidence to expected deaths which have been incorporated into the database.
  • MI ratios by country, age, and sex are available on request.

Police reports

  • In most countries, police and crime reports are an important source of information for some types of injuries, notably road injuries and inter-personal violence.
  • The police reports used in this analysis were collected from published studies, national agencies, and institutional surveys such as the United Nations Crime Trends survey and the WHO Global Status Report on Road Safety Survey.30,41.
  • The authors identified 32 site-years of burial and mortuary data in 11 countries from ministries of health, published reports, and mortuaries themselves.
  • The authors also identified 52 surveys/censuses covering injury mortality across 65 survey/census years.
  • Surveillance data on the number of maternal deaths, or the maternal mortality ratio multiplied by births, were converted into cause fractions by dividing by the total number of deaths estimated in the reproductive age groups.

Health facility data

  • The authors chose to only incorporate deaths due to injury from this source because of known bias.
  • In settings where a data source does not capture all deaths in a population, the cause composition of deaths captured may be different than those that are not.
  • At the global level, the number of deaths estimated in 2010 for ARI and diarrhea for example differ by 0·9% and 1·2%, respectively, between models that include all data and those that exclude data where under-five death registration is below 70% complete.
  • Garbage codes are causes of death that should not be identified as underlying causes of death but have been entered as the underlying cause of death on death certificates.
  • For the GBD 2010, the authors have identified causes that should not be assigned as underlying cause of death at a much more detailed level.

Cause of Death Ensemble modeling (CODEm)

  • For all major causes of death except for HIV/AIDS and measles, the authors have used cause of death ensemble modeling – 133 causes in the cause list and three other special aggregates.
  • In addition, four families of statistical models are developed using covariates: mixed effects linear models of the log of the death rate, mixed effects linear models of the logit of the cause fraction, spatial-temporal Gaussian process regression (ST-GPR) models of the log of the death rate, and ST-GPR of the logit of the cause fraction.
  • 3) Based on out-of-sample predictive validity, the best performing model or ensemble is selected.
  • Web Table 6 summarizes the performance of the CODEm models developed for 133 causes in the cause list for which the authors exclusively use CODEm and three special aggregates in the GBD 2010.
  • In all cases the out-of-sample performance is worse (larger RMSE) than the in-sample performance.

Negative binomial models

  • For 13 causes, the number of deaths observed in the database is too low to generate stable estimates of out-of-sample predictive validity.
  • For these causes, the authors developed negative binomial models using plausible covariates.
  • These causes are identified in Web Table 5.
  • For these negative binomial models, standard model building practice was followed where plausible covariates were included in the model development and reverse stepwise procedures followed for covariate inclusion.
  • Uncertainty distributions were estimated using both uncertainty in the regression betas for the covariates and from the gamma distribution of the negative binomial.

Fixed proportion models

  • In 28 cases where death is a rare event, the authors have first modeled the parent cause in the GBD hierarchy using CODEm and then allocated deaths to specific causes using a fixed proportion.
  • Proportions have been computed using all available data in the database and are fixed over time, but, depending on data density, allowed to vary by region, age, or sex.
  • Finally, cellulitis, decubitus ulcer, other skin and subcutaneous diseases, abscess, impetigo, and other bacterial skin diseases all varied by age and sex.
  • The meta-regression have generated region-age-sex estimates with uncertainty of etiological fractions for diarrhea, LRI, meningitis, chronic kidney disease, maternal conditions, cirrhosis.
  • In the cases of cirrhosis, liver cancer, maternal conditions, and chronic kidney disease, the studies or datasets on etiology identify primary cause as assessed clinically; for diarrhea, LRI, and meningitis, etiology is based on laboratory findings.

Natural History Models

  • For a few selected causes, there is evidence that cause of death data systems do not capture sufficient information for one of two reasons.
  • Second, there are reasons to believe that there is systematic misclassification of deaths in cause of death data sources, particularly for congenital syphilis,54,55 whooping cough,56 measles,57 and HIV/AIDS.58.
  • In the case of HIV/AIDS, a hybrid approach has been used.
  • For 36 countries, with complete and high quality vital registration systems, the authors have used CODEm, in consultation with UNAIDS.
  • For the remaining countries, the authors have used the estimates with uncertainty by age and sex provided directly by UNAIDS based on their 2012 revision.

Mortality Shock Regressions

  • To estimate deaths directly due to natural disasters or collective violence, the authors use a different approach.
  • Details of this approach are outlined in Murray et al.59.
  • To develop the covariate on battle deaths during collective violence, the authors used data from the Armed Conflict Database from the International Institute for Strategic Studies (1997-2011), the Uppsala Conflict Data Program(UCDP)/PRIO Armed Conflict Dataset (1946-present), and available data from complete VR systems.
  • The relationships between under-five mortality and adult mortality and the disaster and collective violence covariates are estimated using 43 empirical observations for disasters and 206 empirical observations for collective violence (only years with over 1 per 10,000 crude death rate from shocks are kept in this analysis).
  • The relationship is estimated for excess mortality from these data sources by first subtracting from observed mortality rates the expected death rates in shock years using the methods outlined in Murray et al.59.

Combining Results for Individual Causes of Death to Generate Final Estimates

  • Given that the authors develop single cause models, it is imperative as a final step to ensure that individual cause estimates sum to the all-cause mortality estimate for each age-sex-country-year group.
  • The authors use a simple algorithm called CoDCorrect; at the level of each draw from the posterior distribution of each cause, they proportionately rescale each cause such that the sum of the cause-specific estimates equals the number of deaths from all causes generated from the demographic analysis.47.
  • The authors have chosen levels for each cause based on consideration of the amount and quality of available data.
  • Because there are substantially more data on all cardiovascular causes from verbal autopsy studies than for specific cardiovascular causes, the authors have designated “all cardiovascular” as a level 1 cause for CoDCorrect.

Ranking lists

  • For the presentation of leading causes of death, the level at which one ranks causes is subject to debate.
  • Given the GBD cause list tree structure, multiple options are possible such as all cancers versus sitespecific cancers.
  • The authors have opted to produce tables of rankings using the level of disaggregation that seems most relevant for public health decision-making.
  • The reference standard has been constructed using the lowest observed death rate in each age group across countries with a population greater than five million (see Murray et al39 for details).
  • Because the all-cause mortality analysis is undertaken, however, for more detailed age-groups up to age 110, the authors are able to take into account the mean age of death over 80 in each country-year-sex group in computing YLLs.

Epidemiological Factors

  • To help understand the drivers of change in the numbers of deaths by cause or region, the authors have decomposed change from 1990 to 2010 into growth in total population, change in population age- and sex-structure, and change in age- and sex-specific rates.
  • The difference between 2010 deaths and the population growth and aging scenario is the difference in death numbers due to epidemiological change in age- and sex-specific death rates.
  • Each of these three differences is also presented as a percent change with reference to the 1990 observed death number.
  • Further details on the data and methods used for specific causes of death is available on request.

Global Causes of Death

  • The GBD cause list divides causes into three broad groups.
  • With declining age-specific death rates from all three groups of causes, including noncommunicable diseases, the global shift towards noncommunicable diseases and injuries as leading causes of death is being driven by population growth and aging, and not by increases in age-sex-cause specific death rates.
  • Among communicable diseases, notably lower respiratory infections (194 thousand), diarrhea (77 thousand) and meningitis (46 thousand) account for the remaining neonatal deaths.
  • A number of causes have much larger uncertainty intervals than adjacent causes in the rank list.
  • At both time periods, there is substantial variation across regions in the relative importance of different causes, with communicable diseases and related causes being much more important in parts of sub-Saharan Africa and parts of Asia than in North Africa, and vascular diseases and cancer predominating in most other regions.

Discussion

  • The GBD 2010 is the most comprehensive and systematic analysis of causes of death undertaken to date.
  • The global health community can now draw on annual estimates of mortality, by age and sex, for 21 regions of the world, for each year from 1980 to 2010, for 235 separate causes, each with 95% uncertainty intervals to aid interpretation.
  • An innovative dimension of the GBD 2010 has been the addition of estimates of deaths due to different diarrhea and lower respiratory infection (LRI) pathogens.
  • First, cause of death data even in settings with medical certification may not always accurately capture the underlying cause of death.

Author Contributions

  • CJLM, ADL, and RL prepared the first draft.
  • RL, MN, KF, SL, KS, ADL, and CJLM finalized the draft based on comments from other authors and reviewer feedback.
  • ADL and CJLM conceived of the study and provided overall guidance.
  • All other authors developed cause-specific models, reviewed results, provided guidance on the selection of key covariates, and reviewed the manuscript.

Figures and Tables

  • Decomposition analysis of the change of global death numbers by broad cause groups from 1990 to 2010 into total population growth, population aging and changes in age-,sex-and cause-specific death rates.
  • Percentage of global deaths for females and males in 1990 and 2010 by cause and age.
  • The colors represent the various level one causes; blue is for non-communicable diseases, red is for communicable, maternal, neonatal and nutritional conditions, and green is for injuries.
  • The dashed lines signify descending order in rank, while the solid lines signify ascending order in rank.
  • Some cause abbreviations used in the figure are lower respiratory infections (“LRI”); ischemic heart disease (“IHD”); chronic obstructive pulmonary disorder (“COPD”); protein energy malnutrition (“PEM”); tuberculosis (“TB”); neonatal encephalopathy (“N Enceph”); neonatal sepsis (“N Sepsis”); road injuries (“Road Inj”); cancer (“CA”); and chronic kidney disease (“CKD”).

70 Bates M, O’Grady J, Mudenda V, Shibemba A, Zumla A. New global estimates of malaria deaths.

  • Global Enterics Mutli-Center Study (GEMS): University of Maryland School of Medicine.
  • Differences in the etiology of communityacquired pneumonia according to site of care: A population-based study.
  • Respiratory syncytial virus infection in elderly and high-risk adults.
  • Lancet 2011; 377: 1438–47. 92 Beaglehole R, Yach D. Globalisation and the prevention and control of non-communicable disease: the neglected chronic diseases of adults.
  • Population Health Metrics Research Consortium gold standard verbal autopsy validation study: design, implementation, and development of analysis datasets.

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TL;DR: In this paper, a review of self management interventions in COPD is presented, showing that self-management interventions help patients with chronic obstructive pulmonary disease (COPD) acquire and practise the skills they need to carry out disease-specific medical regimens, guide changes in health behaviour and provide emotional support to enable patients to control their disease.
Abstract: Background Self management interventions help patients with chronic obstructive pulmonary disease (COPD) acquire and practise the skills they need to carry out disease-specific medical regimens, guide changes in health behaviour and provide emotional support to enable patients to control their disease. Since the first update of this review in 2007, several studies have been published. The results of the second update are reported here. Objectives 1. To evaluate whether self management interventions in COPD lead to improved health outcomes. 2. To evaluate whether self management interventions in COPD lead to reduced healthcare utilisation. Search methods We searched the Cochrane Airways Group Specialised Register of trials (current to August 2011). Selection criteria Controlled trials (randomised and non-randomised) published after 1994, assessing the efficacy of self management interventions for individuals with COPD, were included. Interventions with fewer than two contact moments between study participants and healthcare providers were excluded. Data collection and analysis Two review authors independently assessed trial quality and extracted data. Investigators were contacted to ask for additional information. When appropriate, study results were pooled using a random-effects model. The primary outcomes of the review were health-related quality of life (HRQoL) and number of hospital admissions. Main results Twenty-nine studies were included. Twenty-three studies on 3189 participants compared self management versus usual care; six studies on 499 participants compared different components of self management on a head-to-head basis. Although we included non-randomised controlled clinical trials as well as RCTs in this review, we restricted the primary analysis to RCTs only and reported these trials in the abstract. In the 23 studies with a usual care control group, follow-up time ranged from two to 24 months. The content of the interventions was diverse. A statistically relevant effect of self management on HRQoL was found (St George's Respiratory Questionnaire (SGRQ) total score, mean difference (MD) -3.51, 95% confidence interval (CI) -5.37 to -1.65, 10 studies, 1413 participants, moderate-quality evidence). Self management also led to a lower probability of respiratory-related hospitalisations (odds ratio (OR) 0.57, 95% CI 0.43 to 0.75, nine studies, 1749 participants, moderate-quality evidence) and all cause hospitalisations (OR 0.60; 95% CI 0.40 to 0.89, 6 studies, 1365 participants, moderate-quality evidence). Over one year of follow-up, eight (95% CI 5 to 14) participants with a high baseline risk of respiratory-related hospital admission needed to be treated to prevent one participant with at least one hospital admission, and 20 (95% CI 15 to 35) participants with a low baseline risk of hospitalisation needed to be treated to prevent one participant with at least one respiratory-related hospital admission. No statistically significant effect of self management on mortality (OR 0.79, 95% CI 0.58 to 1.07, 8 studies, 2134 participants, very low-quality evidence) was detected. Also, dyspnoea measured by the (modified) Medical Research Council Scale ((m)MRC) was reduced in individuals who participated in self management (MD -0.83, 95% CI -1.36 to -0.30, 3 studies, 119 participants, low-quality evidence). The difference in exercise capacity as measured by the six-minute walking test was not statistically significant (MD 33.69 m, 95% CI -9.12 to 76.50, 6 studies, 570 participants, very low-quality evidence). Subgroup analyses depending on the use of an exercise programme as part of the intervention revealed no statistically significant differences between studies with and without exercise programmes in our primary outcomes of HRQoL and respiratory-related hospital admissions. We were unable to pool head-to-head trials because of heterogeneity among interventions and controls; thus results are presented narratively within the review. Authors' conclusions Self management interventions in patients with COPD are associated with improved health-related quality of life as measured by the SGRQ, a reduction in respiratory-related and all cause hospital admissions, and improvement in dyspnoea as measured by the (m)MRC. No statistically significant differences were found in other outcome parameters. However, heterogeneity among interventions, study populations, follow-up time and outcome measures makes it difficult to formulate clear recommendations regarding the most effective form and content of self management in COPD.

494 citations

Journal ArticleDOI
01 Nov 2013-Thorax
TL;DR: A range of lifestyle factors and underlying medical conditions are associated with an increased risk of CAP in European adults, and the presence of comorbid conditions including chronic respiratory and cardiovascular diseases, cerebrovascular disease, Parkinson's disease, epilepsy, dementia, dysphagia, HIV or chronic renal or liver disease all increased the risk.
Abstract: Background Community-acquired pneumonia (CAP) causes considerable morbidity and mortality in adults, particularly in the elderly. Methods Structured searches of PubMed were conducted to identify up-to-date information on the incidence of CAP in adults in Europe, as well as data on lifestyle and medical risk factors for CAP. Results The overall annual incidence of CAP in adults ranged between 1.07 to 1.2 per 1000 person-years and 1.54 to 1.7 per 1000 population and increased with age (14 per 1000 person-years in adults aged ≥65 years). Incidence was also higher in men than in women and in patients with chronic respiratory disease or HIV infection. Lifestyle factors associated with an increased risk of CAP included smoking, alcohol abuse, being underweight, having regular contact with children and poor dental hygiene. The presence of comorbid conditions, including chronic respiratory and cardiovascular diseases, cerebrovascular disease, Parkinson’s disease, epilepsy, dementia, dysphagia, HIV or chronic renal or liver disease all increased the risk of CAP by twofold to fourfold. Conclusion A range of lifestyle factors and underlying medical conditions are associated with an increased risk of CAP in European adults. Understanding of the types of individual at greatest risk of CAP can help to ensure that interventions to reduce the risk of infection and burden of disease are targeted appropriately.

494 citations

Journal ArticleDOI
TL;DR: This article provides an update for 2015 on the burden of cardiovascular disease (CVD), with a particular focus on coronary heart disease (CHD) and stroke, across the countries of Europe, and uses the 2013 European Standard Population to calculate age-standardized death rates (ASDRs).
Abstract: This article provides an update for 2015 on the burden of cardiovascular disease (CVD), with a particular focus on coronary heart disease (CHD) and stroke, across the countries of Europe. Cardiovascular disease is still the most common cause of death within Europe, causing almost two times as many deaths as cancer across the continent. Although there is clear evidence, where data are available, that mortality from CHD and stroke has decreased substantially over the last 5-10 years, there are still large inequalities found between European countries, in both current rates of death and the rate at which these decreases have occurred. Similarly, rates of treatment, particularly surgical intervention, differ widely between those countries for which data are available, indicating a range of inequalities between them. This is also the first time in the series that we use the 2013 European Standard Population (ESP) to calculate age-standardized death rates (ASDRs). This new standard results in ASDRs around two times as large as the 1976 ESP for CVD conditions such as CHD but changes little the relative rankings of countries according to ASDR.

488 citations

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TL;DR: The authors summarize the molecular concepts of progression, discuss the potential reasons for clinical trial failure and propose new concepts of drug development, which might lead to clinical implementation of emerging targeted agents.
Abstract: Mortality owing to liver cancer has increased in the past 20 years, and the latest estimates indicate that the global health burden of this disease will continue to grow. Most patients with hepatocellular carcinoma (HCC) are still diagnosed at intermediate or advanced disease stages, where curative approaches are often not feasible. Among the treatment options available, the molecular targeted agent sorafenib is able to significantly increase overall survival in these patients. Thereafter, up to seven large, randomized phase III clinical trials investigating other molecular therapies in the first-line and second-line settings have failed to improve on the results observed with this agent. Potential reasons for this include intertumour heterogeneity, issues with trial design and a lack of predictive biomarkers of response. During the past 5 years, substantial advances in our knowledge of the human genome have provided a comprehensive picture of commonly mutated genes in patients with HCC. This knowledge has not yet influenced clinical decision-making or current clinical practice guidelines. In this Review the authors summarize the molecular concepts of progression, discuss the potential reasons for clinical trial failure and propose new concepts of drug development, which might lead to clinical implementation of emerging targeted agents.

487 citations

Journal ArticleDOI
Hmwe H Kyu1, Christine Pinho1, Joseph Wagner1, Jonathan C Brown1  +199 moreInstitutions (118)
TL;DR: Understanding the levels and trends of the leading causes of death and disability among children and adolescents is critical to guide investment and inform policies and give guidance to policy makers in countries where more attention is needed.
Abstract: Importance The literature focuses on mortality among children younger than 5 years. Comparable information on nonfatal health outcomes among these children and the fatal and nonfatal burden of diseases and injuries among older children and adolescents is scarce. Objective To determine levels and trends in the fatal and nonfatal burden of diseases and injuries among younger children (aged Evidence Review Data from vital registration, verbal autopsy studies, maternal and child death surveillance, and other sources covering 14 244 site-years (ie, years of cause of death data by geography) from 1980 through 2013 were used to estimate cause-specific mortality. Data from 35 620 epidemiological sources were used to estimate the prevalence of the diseases and sequelae in the GBD 2013 study. Cause-specific mortality for most causes was estimated using the Cause of Death Ensemble Model strategy. For some infectious diseases (eg, HIV infection/AIDS, measles, hepatitis B) where the disease process is complex or the cause of death data were insufficient or unavailable, we used natural history models. For most nonfatal health outcomes, DisMod-MR 2.0, a Bayesian metaregression tool, was used to meta-analyze the epidemiological data to generate prevalence estimates. Findings Of the 7.7 (95% uncertainty interval [UI], 7.4-8.1) million deaths among children and adolescents globally in 2013, 6.28 million occurred among younger children, 0.48 million among older children, and 0.97 million among adolescents. In 2013, the leading causes of death were lower respiratory tract infections among younger children (905 059 deaths; 95% UI, 810 304-998 125), diarrheal diseases among older children (38 325 deaths; 95% UI, 30 365-47 678), and road injuries among adolescents (115 186 deaths; 95% UI, 105 185-124 870). Iron deficiency anemia was the leading cause of years lived with disability among children and adolescents, affecting 619 (95% UI, 618-621) million in 2013. Large between-country variations exist in mortality from leading causes among children and adolescents. Countries with rapid declines in all-cause mortality between 1990 and 2013 also experienced large declines in most leading causes of death, whereas countries with the slowest declines had stagnant or increasing trends in the leading causes of death. In 2013, Nigeria had a 12% global share of deaths from lower respiratory tract infections and a 38% global share of deaths from malaria. India had 33% of the world’s deaths from neonatal encephalopathy. Half of the world’s diarrheal deaths among children and adolescents occurred in just 5 countries: India, Democratic Republic of the Congo, Pakistan, Nigeria, and Ethiopia. Conclusions and Relevance Understanding the levels and trends of the leading causes of death and disability among children and adolescents is critical to guide investment and inform policies. Monitoring these trends over time is also key to understanding where interventions are having an impact. Proven interventions exist to prevent or treat the leading causes of unnecessary death and disability among children and adolescents. The findings presented here show that these are underused and give guidance to policy makers in countries where more attention is needed.

486 citations

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Abstract: Estimates of the worldwide incidence and mortality from 27 cancers in 2008 have been prepared for 182 countries as part of the GLOBOCAN series published by the International Agency for Research on Cancer. In this article, we present the results for 20 world regions, summarizing the global patterns for the eight most common cancers. Overall, an estimated 12.7 million new cancer cases and 7.6 million cancer deaths occur in 2008, with 56% of new cancer cases and 63% of the cancer deaths occurring in the less developed regions of the world. The most commonly diagnosed cancers worldwide are lung (1.61 million, 12.7% of the total), breast (1.38 million, 10.9%) and colorectal cancers (1.23 million, 9.7%). The most common causes of cancer death are lung cancer (1.38 million, 18.2% of the total), stomach cancer (738,000 deaths, 9.7%) and liver cancer (696,000 deaths, 9.2%). Cancer is neither rare anywhere in the world, nor mainly confined to high-resource countries. Striking differences in the patterns of cancer from region to region are observed.

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Related Papers (5)
Frequently Asked Questions (15)
Q1. What have the authors contributed in "Global and regional mortality from 235 causes of death for 20 age- groups in 1990 and 2010: a systematic analysis" ?

In this paper, the authors proposed a method to provide timely and accurate information on causes of death by age and sex. 

Improved estimation of mortality from HIV/AIDS including uncertainty in the future will come both from continued progress in the estimation of the time course of the HIV epidemic by UNAIDS as well as further data on the levels of adult mortality in some key countries such as Nigeria. These are important both for the prioritization of existing treatments, such as rotavirus or pneumococcal vaccines, but also for the development of future technologies. When large multi-center studies such as GEMS publish their results this will be an important addition to the analysis ; future revisions of the GBD should make use of these results as they become available. The authors believe that for causes where the magnitude of these corrections is comparatively large, future research should be targeted to trying to build a better understanding of the strengths and weaknesses of the various data sources, whether epidemiological or demographic. 

Because of known bias in the epidemiological composition of burial and mortuary data, the authors only use information on the fraction of injuries due to specific sub-causes from these sources. 

Much could be learned about causes of death in countries where death certification is poor through the more widespread testing and application of recent advances in verbal autopsy methods which greatly reduce heterogeneity in diagnostic practices across populations where VA is currently used. 

By the post-neonatal period, causes of death are dominated by diarrhea, LRI, and other infectious diseases such as measles, among others. 

Because of the variety of data sources and their associated biases, cause of death assessments are inherently uncertain and subject to vigorous debate. 

The ambition to estimate mortality from 235 causes with uncertainty for 187 countries over time from 1980 to 2010 means that many choices about data sources, quality adjustments to data and modeling strategies had to be made. 

Although the authors report more disaggregated causes, because of considerations related to public health programs, the authors have chosen to include diarrheal diseases, lower respiratory infections, maternal causes, cerebrovascular disease, liver cancer, cirrhosis, drug use, road injury, exposure to mechanical forces, animal contact, homicide, and congenital causes in the ranking list. 

In addition, four families of statistical models are developed using covariates: mixed effects linear models of the log of the death rate, mixed effects linear models of the logit of the cause fraction, spatial-temporal Gaussian process regression (ST-GPR) models of the log of the death rate, and ST-GPR of the logit of the cause fraction. 

60–62The relationships between under-five mortality and adult mortality and the disaster and collective violence covariates are estimated using 43 empirical observations for disasters and 206 empirical observations for collective violence (only years with over 1 per 10,000 crude death rate from shocks are kept in this analysis). 

For 13 causes, the number of deaths observed in the database is too low to generate stable estimates of out-of-sample predictive validity. 

Opportunities for strengthening death registration, cause of death certification, and the more widespread use of verbal autopsy exist. 

The coefficients from these regressions and the disaster and collective violence covariates are used to predict excess deaths from these two causes. 

There are reasons, however, to also be concerned that deaths recorded in systems with low coverage may be biased towards selected causes that are more likely to occur in hospital. 

Although at the draw level the same scalar is applied to all causes, the net effect of CoDCorrect is to change the size of more uncertain causes by more than is done for more certain causes, a desirable property.