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Global Burden of Disease 2010 Study: A personal reflection Stuart Spencer* The Lancet, 32 Jamestown Road, London NW1 7BY, UK *Email: [email protected]

http://dx.doi.org/ 10.5339/gcsp.2013.15 Submitted: 20 May 2013 Accepted: 17 June 2013 q 2013 Spencer, licensee Bloomsbury Qatar Foundation Journals. This is an open access article distributed under the terms of the Creative Commons Attribution license CC BY 3.0, which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited.

The Global Burden of Disease (GBD) 2010 project is a massive effort to systematically describe the epidemiology of a wide array of major diseases, injuries and risk factors. It collates millions of observations and has involved collaboration of nearly 500 scientists from 50 countries. Just to give some idea of the size of the endeavour, the analysis has included 800 million deaths. It has taken 5 years to come to the point where The Lancet was able to publish the headline results,1 – 7 but the database is so incredibly rich that there are likely to be hundreds of subsequent papers using this data source. One can anticipate papers on each risk factor (or groups of risk factors – such as dietary risk factors); each disease or specialty; each region; each country, and then local papers on disease outcomes within each country or region. This paper gives some indication of the richness of the data and how these can be used. Of course, like anything else, GBD 2010 is not perfect. It would be totally unrealistic to expect such a huge project to fulfill every requirement for absolute scientific rigour. But it has now come to a stage of sufficient maturity that people are able to see not just the importance of these data, but also they can identify weaknesses in the data collection in some geographic and medical areas. Efforts to address the deficiencies have already been initiated and we can look forward to even more reliable estimates in the future. We should remember, however, that this analysis provides estimates rather than definitive numbers; and it’s about relative contributions to medical problems. Does it really matter if the estimates of cardiovascular deaths globally, for example, are out by a million – the uncertainty interval on the estimate2? And does it matter if these errors result in ischaemic heart disease being second in the list of causes of death rather than first in the list? What these estimates do tell us is the relative size of the burden: that cardiovascular disease accounts for vastly more deaths worldwide than, for example, infectious disease. So what sort of things can we learn from GBD 2010? Cardiovascular diseases account for 30% of all deaths worldwide. Ischaemic heart disease (13.3%) and strokes (11.1%) are at the top of the list of causes of death. In the heatmap (Figure 1) in only one region is cardiovascular diseases not in the top 10 causes of death. This suggests that cardiovascular disease, across the world, is where investment in research, policy and treatment might be most effectively employed. Compared with ischaemic heart disease, topics which in the past were considered to be extremely important and warranting huge research budgets apparently contribute relatively little to global deaths: malaria (2.2%), tuberculosis (2.3%), HIV (2.8%).2 A similar pattern is seen for disability adjusted life years (DALYs), where ischaemic heart disease is responsible for twice the number of DALYs as tuberculosis (Figure 2). Overall, non-communicable diseases (NCDs) such as ischaemic heart disease, cerebrovascular disease and respiratory disorders, are responsible for 65.5% of deaths, and much more disability, than the traditional infectious diseases. This might be a positive benefit from research into infectious diseases (vaccines and disease control) through initiatives like the Gates Foundation. The battle against these diseases is still far from won, however. The GBD 2010 studies show not only the causes of disease, but which age groups are affected. Figure 3 shows global deaths by age group. After the susceptible neonatal period, the number of deaths is low and increases slowly through until about 55. It might come as no surprise that death is

Cite this article as: Spencer S. Global Burden of Disease 2010 Study: A personal reflection, Global Cardiology Science and Practice 2013:15 http://dx.doi.org/10.5339/gcsp.2013.15

Central Asia

Andean Latin America

North Africa and Middle East

Caribbean

South Asia

Oceania

Southern sub-Saharan Africa

Eastern sub-Saharan Africa

Central sub-Saharan Africa

Western sub-Saharan Africa

3 4 14 1 38 13 9 18 2 5 10 8 20 41 16 11 19 6 45 30

7 3 10 2 20 1 5 14 6 4 17 18 22 9 12 39 40 13 36 16

10 5 23 2 52 1 4 9 15 6 3 16 20 25 8 35 38 28 44 31

8 7 17 3 41 5 2 12 19 6 1 18 30 23 9 37 45 29 51 28

12 7 24 2 54 3 4 8 16 11 1 15 48 30 10 21 42 26 57 34

1–10

Tropical Latin America

1 4 2 3 25 15 5 9 10 6 42 11 8 17 7 52 31 20 46 29

East Asia

2 3 10 4 7 8 12 13 5 20 54 16 24 6 19 26 28 14 17 18

Eastern Europe

1 2 11 3 12 40 16 4 5 32 59 8 27 7 10 19 17 13 21 6

Southern Latin America

2 3 9 1 19 12 17 4 7 13 97 6 26 14 10 22 8 5 25 15

Central Europe

1 2 5 3 8 26 28 6 11 12 114 4 10 9 14 21 13 16 25 17

High-income North America

2 1 7 3 9 14 13 6 5 4 22 8 18 11 17 12 28 10 20 15

Australasia

2 1 1 1 1 1 1 2 1 1 1 2 2 2 2 2 2 1 2 2 8 4 4 5 5 4 5 3 6 8 3 6 8 7 9 3 11 8 3 6 4 3 3 3 3 5 3 4 11 14 77 60 69 39 60 32 4 30 14 11 48 47 71 45 80 58 49 75 30 16 18 24 15 13 15 12 10 7 7 9 15 9 7 6 10 6 24 11 5 3 31 67 80 80 43 49 18 26 38 31 117 120 117 120 119 120 119 116 107 109 11 12 20 11 8 10 8 14 9 7 9 18 14 16 11 16 6 12 20 19 14 11 26 14 4 9 17 9 8 10 70 61 48 42 54 28 53 36 18 15 7 20 31 25 20 27 34 5 26 21 5 17 23 34 12 15 9 6 16 12 10 14 11 9 18 11 26 17 10 5 6 7 6 8 6 8 7 13 15 22 13 8 12 10 7 7 48 16 13 17

Western Europe

Southeast Asia

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20

Central Latin America

Ischaemic heart disease Stroke Chronic obstructive pulmonary disease Lower respiratory infections Lung cancer HIV/AIDS Diarrhoeal diseases Road injury Diabetes Tuberculosis Malaria Cirrhosis Self-harm Hypertensive heart disease Preterm birth complications Liver cancer Stomach cancer Chronic kidney disease Colorectal cancer Other cardiovascular and circulatory diseases

High-income Asia Pacific

Global

Page 2 of 12 Spencer. Global Cardiology Science and Practice 2013:15

11–20

21–30

31–50

51–90

≥91

Figure 1. Heatmap of the top 20 causes of death by GDB region in 2010. Redrawn from www.healthmetrics andevaluation.org/gbd/visualizations.

increasingly more likely after 55 years of age, but the rate of changes in life expectancy with age are intriguing. Figure 4 shows the decline in deaths by age. The age-specific decline in deaths is reported by Wang et al. (Figure 4)1. It is a little confusing since a higher point on the graph actually reflects better outcomes. Mortality has decreased less among young adults (especially young males) than in other age groups. This might be because this age group have a naturally low rate of death, but it might also reflect the fact that young adult men are primarily those who are at increased risk of death as combatants in war; this age group is also the most likely to engage in risky behaviours – and to die as a result of traffic accidents.2 Even so, every age group now shows a higher life expectancy than the 1970 estimates. It is encouraging to see there have been huge strides in reducing infant mortality: deaths among the 1–4 year age group have dropped by 70%. In 1970, deaths in those younger than 5 years accounted for 38% of deaths worldwide; by 2010 this was down to 13%. Whether or not it is causal, it seems that the Millennium Development Goals regarding infant mortality are well on the way to being successfully met. The job is not complete since deaths in the first 4 years of life are still greater than any other age group except over 80s (Figure 3) but now might be a time to begin planning for the next focus of priorities. Over the past 20 years global population life expectancy has increased in almost all countries. GBD 2010 also presents the changes in deaths by geographic region.1 Much more detailed analysis can be found at www.healthmetricsandevaluation.org/gbd/visualizations. All regions of the world have seen an increase in life expectancy since 1990 as demonstrated in Figure 5 where all points are below the line. Life expectancy is longest in high-income countries, and shortest in Africa. But Africa has made massive strides. In Western Europe life expectancy has increased by 8 years (from about 68 years to 76 years), but in North Africa and the Middle East, for example, life expectancy has more than doubled from 22 years in 1970 to 52 years in 2010. An extra 30 years of life. Life expectancy in this region is, however, still relatively short. In general, the causes of death in 2010 are similar to causes of death in 1990.2 Lozano et al.2 clearly show (Figure 6) that cardiovascular diseases becomes an increasingly important cause of death with ageing, and cancer remains a big killer of adults, but there have been some notable changes. Amongst females, deaths due to maternal disorders have reduced. By contrast deaths from HIV/AIDS and

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8 Diseases and injuries Risk factors

High blood pressure

7 Smoking* 6

Alcohol use

IHD

5 DALYs (%)

LRI Diet low in fruit Cerebrovascular disease

HAP 4

Low back pain Malaria

High BMI FPG

Diarrhoea HIV COPD Road injury

PM2·5 Amb Inactivity† Preterm birth Underweight Salt complications Diet low in nuts and seeds Tuberculosis Diabetes

3

2

Lung cancer 1

0 0

2

4

6

8

10 Deaths (%)

12

14

16

18

20

Figure 2. Comparison of the ten leading diseases and injuries (blue) and the ten leading risk factors (red) based on percentage of global deaths and percentage of DAYLs. Reprinted from Murray et al 11 by kind permission of the authors and The Lancet.

tuberculosis have risen due to a rise in deaths from HIV/AIDS. It is also interesting to see that transport deaths are much more prevalent in men than women. Figure 7 provides an alternative way of looking at the relative changes in causes of death between 1990 and 2010. HIV deaths have increased massively, but causes of fetal/ neonatal death (preterm complications, neonatal sepsis, neonatal encephalopathy) have been radically reduced. What is striking is that with the exception of HIV/AIDS, the ranking of deaths due to infections have decreased substantially. By contrast non-communicable diseases have become more important causes of death. The lines between the ranking tell the story of relative importance, but one needs to look beyond the lines to get a better idea of change. Although malaria has declined in relative Late neonatal Early neonatal

Postneonatal 1−4 years 5−9 years 10−14 years 15−19 years 20−24 years 25−29 years 30−34 years

≥80 years

35−39 years 40−44 years

75−79 years

45−49 years 50−54 years 70−74 years

55−59 years 60−64 years

65−69 years

Figure 3. Global deaths by age groups in 2010. Reprinted from Wang et al.1 with kind permission of the authors and The Lancet.

Page 4 of 12 Spencer. Global Cardiology Science and Practice 2013:15

80 Male mortality

70

Female mortality

Decline (%)

60 50 40 30 20 10

≥8 0

65 −6 9 70 −7 4 75 –7 9

< 1−1 4 5− 9 10 −1 4 15 −1 9 20 −2 4 25 −2 9 30 −3 4 35 −3 9 40 −4 4 45 −4 9 50 −5 4 55 −5 9 60 −6 4

0

Age group (years)

Figure 4. Decline in age-specific mortality between 1970 and 2010. Reprinted from Wang et al.1 with kind permission of the authors and The Lancet.

importance from 9th to 11th, this masks a 21% increase in absolute numbers of deaths as shown in the right hand column. Overall, however, the picture of change generally reflects absolute changes. Ischaemic heart disease and stroke remain the two biggest causes of death. Of non-communicable diseases, only stomach cancer, rheumatic heart disease and congenital anomalies have declined in importance. Perhaps emphasis on research and policy should now start to focus more on non-communicable diseases. The GBD database is a massive resource and the papers published in December 2012 are headline summaries. It can be expected that there will be many future papers looking at specific diseases and regions. One can expect at least one detailed paper on cardiovascular disease, but the headline data provide some interesting insights, such as the years living with disability due to heart failure around the world.5 These data might be of interest to physicians and health policy-makers in specific regions and can be useful to prioritise policy in particular regions. It can be seen in Figure 8 that the effect of iodine 85 80 75 70

High-income Western Europe North America Australasia

Mean age at death in 1970 (years)

65

Central Europe 60

Eastern Europe

High-income Asia Pacific

55 Southern Latin America

50 45

Central Asia

40

Caribbean

35

East Asia

Southern sub-Saharan Africa Southeast Asia

Oceania

30

Tropical Latin America

Central Latin America

25

Central subSaharan Africa

20

South Asia Andean Latin America Eastern sub-Saharan Africa North Africa and Middle East

Western sub-Saharan Africa 15 15

20

25

30

35

40

45

50

55

60

65

70

75

80

85

Mean age at death in 2010 (years)

Figure 5. Comparison of the mean age of death in 1970 and 2010 in different regions of the world. Reprinted from Wang et al.1 with kind permission of the authors and The Lancet.

Page 5 of 12 Spencer. Global Cardiology Science and Practice 2013:15

A 100

B

80

Deaths (%)

60

40

20

0 C 100

D

War and disaster Intentional injuries Unintentional injuries Transport injuries Other non-communicable diseases Musculoskeletal disorders Diabetes, urogenital, blood, and endocrine Mental and behavioural disorders Neurological disorders Digestive diseases Cirrhosis Chronic respiratory diseases Cardiovascular and circulatory diseases Cancer Other communicable diseases Nutritional deficiencies Neonatal disorders Maternal disorders Neglected tropical diseases and malaria Diarrhoea, lower respiratory infections, and other common infectious diseases HIV/AIDS and tuberculosis

80

Deaths (%)

60

40

20

0– 7 6d 28 –27 ay –3 d s 6 ay 1– 4 da s 4 y 5 ye s 10 –9 ars – y 15 14 ears – ye 20 19 ars – y 25 24 ears – y 30 29 ears – y 35 34 ears – ye 40 39 ars – ye 45 44 ars –4 ye 50 9 y ars – e 55 54 ars – ye 60 59 y ars – e 65 64 ars – y 70 69 ears – ye 75 74 ars –7 yea 9 r ≥8 yea s 0 rs ye ar s

0– 7 6d 28 –27 ay –3 d s 6 ay 1– 4 da s 4 y 5– yea s 10 9 rs –1 ye 15 4 ars – ye 20 19 ars – y 25 24 ears – y 30 29 ears – y 35 34 ears – ye 40 39 ars – ye 45 44 ars – ye 50 49 y ars – e 55 54 ars – ye 60 59 y ars – e 65 64 ars – y 70 69 ears – ye 75 74 ars –7 yea 9 r ≥8 yea s 0 rs ye ar s

0

Figure 6. Global causes of deaths (%) for males (A and C) and females (B and D) in 1990 (A and B) and 2010 (C and D). Reprinted from Lozano et al.2 with kind permission of the authors and The Lancet.

deficiency is largely confined to the North Africa and Middle East. Perhaps this might stimulate more investment in iodised salt in North Africa and Middle East countries. It is also apparent that endocarditis is more prevalent in Oceania than elsewhere, and this might inform funding for endocarditis research in that region. The headline analysis also provides insights into subspecialty causes of deaths.2 A global picture of causes of cardiovascular deaths is in Table 1. The number of cardiovascular deaths has increased 31% from 12 million to 16 million deaths between 1990 and 2010,2 but of course this needs to be considered in the context of an increase in the global population. In that perspective, the 25% reduction in the number of deaths due to rheumatic heart disease is notable. The absolute numbers of deaths due to most other cardiovascular conditions have increased, but so has the mean age of the population. Diseases such as atrial fibrillation which are more prevalent in the elderly, are therefore expected to be more common as the population ages. For most of the cardiovascular diseases in Table 1 age-standardised mortality rate has decreased, but atrial fibrillation shows an 89% age-standardised increase. The other condition with an increased age-standardised mortality is peripheral vascular disease. This probably reflects the increase in diabetes associated with changing life styles and increased age. GBD 2010 doesn’t only report deaths. It also reports the burden of disease in terms of years lived with disabilities,5 disability adjusted life years6 and risk factors for disease and injury.7 The years of life lost (YLL) analysis shows a slightly different pattern. Ischaemic heart disease and stroke are still near the top of the list,2 but Figure 9 reflects the effect of disease early in life on total years lost. Serious diseases of infancy and childhood achieve a greater prominence when analysed by YLL. In this analysis

Page 6 of 12 Spencer. Global Cardiology Science and Practice 2013:15

1990 Mean rank (95% UI)

Disorder

2010 Disorder

Mean rank (95% UI)

% change (95% UI)

1·0 (1 to 2)

1 Ischaemic heart disease

1 Ischaemic heart disease

1·0 (1 to 1)

35 (29 to 39)

2·0 (1 to 2)

2 Stroke

2 Stroke

2·0 (2 to 2)

26 (14 to 32)

3·0 (3 to 4)

3 Lower respiratory infections

3 COPD

3·4 (3 to 4)

–7 (–12 to 0)

4·0 (3 to 4)

4 COPD

4 Lower respiratory infections

3·6 (3 to 4)

–18 (–24 to –11)

5·0 (5 to 5)

5 Diarrhoea

5 Lung cancer

5·8 (5 to 10)

6·1 (6 to 7)

6 Tuberculosis

6 HIV/AIDS

6·4 (5 to 8)

396 (323 to 465)

48 (24 to 61) –42 (–49 to –35)

7·3 (7 to 9)

7 Preterm birth complications

7 Diarrhoea

6·7 (5 to 9)

8·6 (7 to 12)

8 Lung cancer

8 Road injury

8·4 (5 to 11)

9·4 (7 to 13)

9 Malaria

9 Diabetes

9·0 (7 to 11)

93 (68 to 102) –18 (–35 to –3)

47 (18 to 86)

10·4 (8 to 14)

10 Road injury

10 Tuberculosis

10·1 (8 to 13)

10·8 (8 to 14)

11 Protein–energy malnutrition

11 Malaria

10·3 (6 to 13)

21 (–9 to 56)

12·8 (11 to 16)

12 Cirrhosis

12 Cirrhosis

11·8 (10 to 14)

33 (25 to 41)

13·2 (9 to 18)

13 Stomach cancer

13 Self-harm

14·1 (11 to 20)

32 (8 to 49)

15·6 (12 to 20)

14 Self-harm

14 Hypertensive heart disease

14·2 (12 to 18)

48 (39 to 56)

15·8 (13 to 19)

15 Diabetes

15 Preterm birth complications

14·4 (12 to 18)

16·1 (12 to 20)

16 Congenital anomalies

16 Liver cancer

16·9 (14 to 20)

16·9 (13 to 20)

17 Neonatal encephalopathy*

17 Stomach cancer

17·0 (13 to 22)

–2 (–10 to 5)

18·3 (14 to 22)

18 Hypertensive heart disease

18 Chronic kidney disease

17·4 (15 to 21)

82 (65 to 95)

21·1 (6 to 44)

19 Measles

19 Colorectal cancer

18·5 (15 to 21)

46 (36 to 63)

21·1 (12 to 36)

20 Neonatal sepsis

20 Other cardiovascular and circulatory

19·7 (18 to 21)

21·3 (19 to 26)

21 Colorectal cancer

21 Protein–energy malnutrition

21·5 (19 to 25)

21·6 (18 to 26)

22 Meningitis

22 Falls

23·3 (21 to 29)

56 (20 to 84)

23·2 (21 to 26)

23 Other cardiovascular and circulatory

23 Congenital anomalies

24·4 (21 to 29)

–22 (–40 to –3)

23·7 (20 to 28)

24 Liver cancer

24 Neonatal encephalopathy*

24·4 (21 to 30)

–20 (–33 to –2)

23·8 (20 to 27)

25 Rheumatic heart disease

25 Neonatal sepsis

25·1 (15 to 35)

–3 (–25 to 27)

27 Chronic kidney disease

29 Meningitis

30 Falls

33 Rheumatic heart disease

35 HIV/AIDS

62 Measles

Communicable, maternal, neonatal, and nutritional disorders Non-communicable diseases Injuries

–28 (–39 to –17) 63 (49 to 78)

46 (40 to 55) –32 (–42 to –21)

Ascending order in rank Descending order in rank

Figure 7. Top 25 causes of death in 1990 and 2010. Reprinted from Lozano et al.2 with kind permission of the authors and The Lancet.

infectious diseases are more important causes of YLL but they have all (except HIV) also decreased in number – presumably as a result of the success of immunisation programmes. There remain too many people in the world who are hungry. It is encouraging that deaths due to malnutrition have fallen by 32%, but it still ranks as 21st in the list. And there is also a decline in ranking by YLL but, because malnutrition in childhood has long term effects, it remains as the 15th commonest 100

80

YLD (%)

60

40

20

Thalassaemias Rheumatic heart disease Pneumoconiosis Other haemoglobinopathies and haemolytic anaemias Other endocrine, nutritional, blood, or immune disorders Other cardiovascular and circulatory diseases Ischaemic heart disease Iron-deficiency anaemia Iodine deficiency Interstitial lung disease and pulmonary sarcoidosis Hypertensive heart disease G6PD deficiency Endocarditis Congenital heart anomalies Chronic obstructive pulmonary disease Chagas disease Cardiomyopathy and myocarditis

Hi

gh

-in

co m

e

A W sia Hi es gh te Pac -in rn ific co Eu m e Au rop No st e rth rala So ut Ce Am sia he nt rn ra eric La l Eu a tin ro Ea Am pe st e r eric Tr n op Eu a ica ro Ce l L Ea pe nt at st A ra in l L Am sia at in e So Am rica ut he eric No An rth de C ast a e a Af n nt Asia ric La ra a a tin l A nd Am sia M er id ic dl a e Ca Eas So rib t ut he So b e a ut n Ea r n s h st u b As er - S O n ah ce ia Ce s nt ub ar an i W ral -Sa an e s su h A a te b ar fric r n -S a n a su ah Af b- ara ric Sa n a ha Af ra ric n Af a ric a

0

Figure 8. Years lived with disability from heart failure by cause and region in 2010. Reprinted from Vos et al.5 with kind permission of the authors and The Lancet.

Cardiovascular and circulatory diseases Rheumatic heart disease Ischaemic heart disease Cerebrovascular disease Ischaemic stroke Non-ischaemic stroke Hypertensive heart disease Cardiomyopathy and myocarditis Atrial fibrillation and flutter Aortic aneurysm Peripheral vascular disease Endocarditis Other cardiovascular diseases

11 903.7 462.6 5211.8 4660.4 2241.1 2419.4 590.7 286.8 34.4 131.9 18.6 35.8 470.6

(11 329.4 –12 589.3) (431.5–517.7) (5014.5 –5643.9) (4436.1 –5154.9) (2088.0 –2494.9) (2050.9 –2827.9) (481.0– 740.6) (250.5 –316.8) (27.9–43.1) (94.6 –173.3) (12.2–28.7) (30.0 –44.4) (446.3 –489.9)

1990

2010

15 616.1 (14 542.2 –16 315.1) 345.1 (305.8 –374.3) 7029.3 (6577.2 –7431.1) 5874.2 (5304.7 –6280.1) 2835.4 (2657.0 –3262.8) 3038.8 (2643.4 –3496.9) 873.2 (715.5 –1074.1) 403.9 (361.5 –450.4) 114.7 (92.7–144.7) 191.7 (140.3 –249.2) 49.8 (32.9–74.8) 48.3 (39.3–55.4) 685.9 (664.0 –705.3)

All ages deaths (thousands)

31.2% 225.4% 34.9% 26.0% 26.5% 25.6% 47.8% 40.8% 233.9% 45.3% 167.0% 34.8% 45.7%

D%

298.1 11.1 131.3 105.7 57.6 59.7 14.9 6.7 0.9 3.3 0.5 0.8 11.5

(283.9– 314.9) (10.3 –12.4) (126.4–142.2) (98.8 –111.9) (53.7 –64.0) (50.6–69.7) (12.1–18.6) (5.9–7.4) (0.7 –1.1) (2.4 –4.3) (0.3 –0.7) (0.7 –1.0) (11.0–11.9)

1990

234.8 (218.7 –245.2) 5.2 (4.6 –5.6) 105.7 (98.8 –111.9) 88.4 (79.8 –94.4) 42.3 (39.6 –48.7) 46.1 (40.1 –53.1) 13.1 (10.8 –16.2) 6.1 (5.4 –6.8) 1.7 (1.4 –2.1) 2.9 (2.1 –3.8) 0.7 (0.5 –1.1) 0.7 (0.6 –0.8) 10.3 (9.9 –10.5)

2010

Age-standardised death rates (per 100 000)

Table 1. Causes of deaths and age-standardised death rates, with 95% uncertainty interval, from cardiovascular and circulatory diseases in 1990 and 2010.

2 21.2 253.1 219.5 224.6 226.6 222.7 211.5 29.8 89.6 2 12.7 53.3 28.0 210.9

D%

Page 7 of 12 Spencer. Global Cardiology Science and Practice 2013:15

Page 8 of 12 Spencer. Global Cardiology Science and Practice 2013:15

1990 Mean rank (95% UI)

Disorder

2010 Disorder

Mean rank (95% UI)

% change (95% UI)

1·0 (1 to 2)

1 Lower respiratory infections

1 Ischaemic heart disease

1·1 (1 to 2)

2·0 (2 to 2)

2 Diarrhoea

2 Lower respiratory infections

1·9 (1 to 3)

3·3 (3 to 5)

3 Preterm birth complications

3 Stroke

3·1 (3 to 4)

177 (2 to 24)

4·0 (3 to 5)

4 Ischaemic heart disease

4 Diarrhoea

4·8 (4 to 7)

–54 (–60 to –47)

5·1 (4 to 6)

5 Stroke

5 Malaria

5·5 (3 to 8)

19 (–11 to 63)

6·9 (6 to 11)

6 Malaria

6 HIV/AIDS

5·6 (4 to 7)

372 (302 to 439) –28 (–39 to –17)

28 (20 to 33) –45 (–49 to –40)

8·3 (6 to 11)

7 COPD

7 Preterm birth complications

6·3 (4 to 8)

8·8 (6 to 12)

8 Protein–energy malnutrition

8 Road injury

7·9 (5 to 9)

9·7 (7 to 12)

9 Tuberculosis

9 COPD

9·8 (9 to 12)

–19 (–24 to –12)

35 (8 to 69)

10 Neonatal encephalopathy*

10 Neonatal encephalopathy*

10·8 (9 to 14)

–20 (–33 to –2)

11·2 (7 to 14)

11 Congenital anomalies

11 Tuberculosis

11·2 (9 to 14)

–22 (–39 to –8)

12·2 (3 to 25)

12 Measles

12 Neonatal sepsis

11·3 (7 to 17)

–3 (–25 to 27)

12·4 (6 to 18)

13 Neonatal sepsis

13 Self-harm

13·4 (11 to 18)

24 (–1 to 42)

9·8 (6 to 13)

12·7 (9 to 14)

14 Road injury

14 Congenital anomalies

13·6 (11 to 17)

–30 (–46 to –11)

14·7 (13 to 16)

15 Meningitis

15 Protein–energy malnutrition

15·5 (12 to 19)

–44 (–53 to –34)

16·5 (14 to 20)

16 Self-harm

16 Lung cancer

15·6 (12 to 19)

36 (18 to 47)

16·9 (15 to 20)

17 Drowning

17 Cirrhosis

16·5 (14 to 19)

27 (19 to 36)

18·8 (17 to 22)

18 Cirrhosis

18 Meningitis

18·3 (16 to 20)

19·3 (16 to 23)

19 Lung cancer

19 Diabetes

18·7 (17 to 21)

70 (54 to 78)

21·0 (15 to 29)

20 Tetanus

20 Interpersonal violence

19·9 (16 to 22)

31 (19 to 48)

21·3 (19 to 25)

21 Maternal

21 Drowning

22·1 (20 to 25)

–31 (–40 to –6)

23·2 (20 to 31)

22 Interpersonal violence

22 Liver cancer

22·4 (20 to 25)

45 (32 to 68)

23·5 (19 to 29)

23 Stomach cancer

23 Fire

24·4 (21 to 32)

10 (–18 to 48)

25·4 (21 to 30)

24 HIV/AIDS

24 Chronic kidney disease

24·5 (22 to 28)

51 (38 to 64)

25·7 (18 to 37)

25 Syphilis

25 Stomach cancer

26·1 (21 to 32)

–11 (–18 to –4)

26 Fire

28 Maternal

27 Diabetes

37 Syphilis

30 Liver cancer

38 Measles

32 Chronic kidney disease

52 Tetanus

Communicable, maternal, neonatal, and nutritional disorders Non-communicable diseases Injuries

–23 (–34 to –13)

Ascending order in rank Descending order in rank

Figure 9. The top 25 causes of years of life lost in 1990 and 2010. Reprinted from Lozano et al.2 with kind permission of the authors and The Lancet.

cause of years lost (Figure 9). The decrease in malnutrition probably reflects major advances in agriculture as well as medicine. Although less headline-grabbing than deaths, DALYs are particularly important to inform government health policies. The causes of DALYs by regions6 are interesting as a reflection of events (both natural and man-made). It is well known that there has been an explosion of HIV in Southern subSaharan Africa and this is clearly demonstrated in Figure 10. The effect of the Haitian earthquake is also reflected in the war and disaster statistics in the Caribbean region. And in good news, the DALYs due to diarrhoea and respiratory infections have declined substantially in central and southern America and in south east and central Asia. The data presented here are regional estimates, but national estimates (available at www.healthmetricsandevaluation.org/gbd/country-profiles/) can help governments decide which diseases should be their priority for treatment and prevention. In terms of reducing incidence of disease, the risk factors data provides information that needs careful consideration that can have an impact on government decisions. Some of the risk factors for disease are not a surprise: smoking causes cancer; high glucose is associated with diabetes. The change in relative importance of risk factors between 1990 and 2010 can be found in the paper by Lim et al.7 Risk factors are especially important for the predicting the future global burden of diseases. Identifying the most important risk factors to reduce DALYs can help decide on health policy strategies. For example, is money best spent on anti-smoking campaigns, on promoting exercise, or reducing pollution? Figure 11 shows the analysis for 2010 and this can be a starting point for policy changes that will influence future health outcomes. A careful look at Figure 11 provides some interesting insights into how policies to address health issues might sometimes promote solutions which might not necessarily be those that will have the biggest effect on health. The analysis in Figure 11 provides an example of where perhaps these analyses might influence future priorities. It is no surprise that tobacco is a prominent cause of DALYs, and around the world Governments are working to reduce tobacco consumption. It might be less obvious that household air pollution is so important. These data might stimulate promotion of cleaner

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0

War and disaster Intentional injuries Unintentional injuries Transport injuries Other non-communicable diseases Musculoskeletal disorders Diabetes, urogenital, blood, and endocrine Mental and behavioural disorders Neurological disorders Digestive diseases Cirrhosis Chronic respiratory diseases Cardiovascular and circulatory diseases Cancer Other communicable diseases Nutritional deficiencies Neonatal disorders Maternal disorders Neglected tropical diseases and malaria Diarrhoea, lower respiratory infections, and other common infectious diseases HIV/AIDS and tuberculosis

Figure 10. Disability adjusted life years (%) by cause and region in 1990 (A) and 2010 (B). Reprinted from Murray et al.6 with kind permission of the authors and The Lancet.

household fuels. However, there are some anomalies. High blood pressure is identified as the major burden of DALYs. To counteract this there are moves to reduce salt intake, but this might not be the most effective way to promote health since a diet high in sodium is way down the list of risk factors. That discrepancy supports the fact that, despite association studies linking salt intake and hypertension, direct evidence that high salt intake increases blood pressure in non-hypertensive people is very weak. Perhaps focusing health campaigns on other factors would be more beneficial. Much further up the list of important risk factors is a diet low in fruit. It is known that fruit is beneficial in avoiding major killers like heart disease and cancer,8 but this gets little positive action from governments. At the very least, the risk factors identified in GBD 2010 should encourage a critical scientific re-evaluation of the hard evidence underpinning policies on risk factors. It might be fashionable (and easy) to blame the fast food industry for obesity or the soft drinks industry for diabetes, but it seems that increasing fruit intake would be a more important initiative for improving health. This paper indicates some of the ways in which the Global Burden of Disease 2010 study can be of interest and value, but it merely scratches the surface. The main analyses of GBD 2010 are

High blood pressure Tobacco smoking, including second-hand smoke Household air pollution from solid fuels Diet low in fruits Alcohol use High body-mass index High fasting plasma glucose Childhood underweight Ambient particulate matter pollution Physical inactivity and low physical activity Diet high in sodium Diet low in nuts and seeds Iron deficiency Suboptimal breastfeeding High total cholesterol Diet low in whole grains Diet low in vegetables Diet low in seafood omega-3 fatty acids Drug use Occupational risk factors for injuries –0·5 0

Cancer Cardiovascular and circulatory diseases Chronic respiratory diseases Cirrhosis Digestive diseases Neurological disorders Mental and behavioural disorders Diabetes, urogenital, blood, and endocrine Musculoskeletal disorders Other non-communicable diseases 2

4 Disability-adjusted life-years (%)

6

HIV/AIDS and tuberculosis Diarrhoea, lower respiratory infections, and other common infectious diseases Neglected tropical diseases and malaria Maternal disorders Neonatal disorders Nutritional deficiencies Other communicable diseases Transport injuries Unintentional injuries Intentional injuries War and disaster 8

Figure 11. Top 20 risk factors for disease in 2010 expressed as disability-adjusted life-years. Redrawn from Lim et al.7 with permission of the authors and The Lancet.

Page 10 of 12 Spencer. Global Cardiology Science and Practice 2013:15

published in The Lancet1 – 7 and regional, country and specialty specific analysis are likely to follow. Many more GBD 2010 analyses are available at www.healthmetricsandevaluation.org/ gbd/visualizations. In conclusion, GBD 2010 can be important in framing health policies and objectives both globally and in specific countries. The first country specific analysis from the GDB team was an assessment of the UK.9 The UK government was represented at the launch of the GBD 2010 presentation in London in 2012 and recognised the findings should inform policy. In March 2013 the Department of Health in the UK published a call to action.10 It would be surprising if other governments did not follow this lead, and more country-specific analyses are expected. In depth analysis of the data will also help refine attitudes to risk factors and influence research priorities in specific regions and countries. As NCDs are the major cause of death and disability perhaps it is time to reconsider the priorities for research and policy initiatives away from the current HIV, tuberculosis and malaria programmes. And now might be the time to start considering whether more emphasis might be placed on death and disease in adults now infant mortality has been so substantially reduced. Analysis by medical specialty will also shape research priorities and research programmes in specific regions. Finally, the GBD 2010 has highlighted weaknesses in data collection in some geographic and specialty areas and moves have already begun to improve the databases to make future assessments more rigorous. Conflicts of interest SS is a full time editor at The Lancet but has no other relations with any aspect of the Global Burden of Disease Study, and no financial interests.

Acknowledgement My thanks to Prof CJL Murray and The Lancet for permission to re-use figures from the GBD 2010 papers. I am especially grateful to A Roots for redrawing the figures. REFERENCES [1] Wang H, Dwyer-Lindgren L, Lofgren KT, Rajaratnam JK, Marcus JR, Levin-Rector A, Levitz C, Lopez AD, Murray CJL. Agespecific and sex-specific mortality in 187 countries, 1970–2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2012;380:2071–2094. [2] Lozano R, Naghavi M, Foreman K, Lim S, Shibuya K, Aboyans V, Abraham J, Adair T, Aggarwal R, Ahn SY, Alvarado M, Anderson HR, Anderson LM, Andrews KG, Atkinson C, Baddour LM, Barker-Collo S, Bartels DH, Bell ML, Benjamin EJ, Bennett D, Bhalla K, Bikbov B, Bin Abdulhak A, Birbeck G, Blyth F, Bolliger I, Boufous S, Bucello C, Burch M, Burney P, Carapetis J, Chen H, Chou D, Chugh SS, Coffeng LE, Colan SD, Colquhoun S, Colson KE, Condon J, Connor MD, Cooper LT, Corriere M, Cortinovis M, de Vaccaro KC, Couser W, Cowie BC, Criqui MH, Cross M, Dabhadkar KC, Dahodwala N, DeLeo D, Degenhardt L, Delossantos A, Denenberg J, Des Jarlais DC, Dharmaratne SD, Dorsey ER, Driscoll T, Duber H, Ebel B, Erwin PJ, Espindola P, Ezzati M, Feigin V, Flaxman AD, Forouzanfar MH, Fowkes FGR, Franklin R, Fransen M, Freeman MK, Gabriel SE, Gakidou E, Gaspari F, Gillum RF, Gonzalez-Medina D, Halasa YA, Haring D, Harrison JE, Havmoeller R, Hay RJ, Hoen B, Hotez PJ, Hoy D, Jacobsen KH, James SL, Jasrasaria R, Jayaraman S, Johns N, Karthikeyan G, Kassebaum N, Keren A, Khoo J-P, Knowlton LM, Kobusingye O, Koranteng A, Krishnamurthi R, Lipnick M, Lipshultz SE, Ohno SL, Mabweijano J, MacIntyre MF, Mallinger L, March L, Marks GB, Marks R, Matsumori A, Matzopoulos R, Mayosi BM, McAnulty JH, McDermott MM, McGrath J, Mensah GA, Merriman TR, Michaud C, Miller M, Miller TR, Mock C, Mocumbi AO, Mokdad AA, Moran A, Mulholland K, Nair MN, Naldi L, Venkat Narayan KM, Nasseri K, Norman P, O’Donnell M, Omer SB, Ortblad K, Osborne R, Ozgediz D, Pahari B, Pandian JD, Rivero AP, Padilla RP, PerezRuiz F, Perico N, Phillips D, Pierce K, Pope CA III, Porrini E, Pourmalek F, Raju M, Ranganathan D, Rehm JT, Rein DB, Remuzzi G, Rivara FP, Roberts T, De Leo`n FR, Rosenfeld LC, Rushton L, Sacco RL, Salomon JA, Sampson U, Sanman E, Schwebel DC, Segui-Gomez M, Shepard DS, Singh D, Singleton J, Sliwa K, Smith E, Steer A, Taylor JA, Thomas B, Tleyjeh IM, Towbin JA, Truelsen T, Undurraga EA, Venketasubramanian N, Vijayakumar L, Vos T, Wagner GR, Wang M, Wang W, Watt K, Weinstock MA, Weintraub R, Wilkinson JD, Woolf AD, Wulf S, Yeh P-H, Yip P, Zabetian A, Zheng Z-J, Lopez AD, Murray CJL. Global and regional mortality from 253 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2012;380:2095–2128. [3] Salomon JA, Vos T, Hogan DR, Gagnon M, Naghavi M, Mokdad A, Begum N, Shah R, Karyana M, Kosen S, Farje MR, Moncada G, Dutta A, Sazawal S, Dyer A, Seiler J, Aboyans V, Baker L, Baxter A, Benjamin EJ, Bhalla K, Bin Abdulhak A, Blyth F, Bourne R, Braithwaite T, Brooks P, Brugha TS, Bryan-Hancock C, Buchbinder R, Burney P, Calabria B, Chen H, Chugh SS, Cooley R, Criqui MH, Cross M, Dabhadkar KC, Dahodwala N, Davis A, Degenhardt L, Dı´az-Torne´ C, Dorsey ER, Driscoll T, Edmond K, Elbaz A, Ezzati M, Feigin V, Ferri CP, Flaxman AD, Flood L, Fransen M, Fuse K, Gabbe BJ, Gillum RF, Haagsma J, Harrison JE, Havmoeller R, Hay RJ, Hel-Baqui A, Hoek HW, Hoffman H, Hogeland E, Hoy D, Jarvis D, Karthikeyan G, Knowlton LM, Lathlean T, Leasher JL, Lim SS, Lipshultz SE, Lopez AD, Lozano R, Lyons R, Malekzadeh R, Marcenes W, March L, Margolis DJ, McGill N, McGrath J, Mensah GA, Meyer AC, Michaud C, Moran A, Mori R, Murdoch ME, Naldi L, Newton CR, Norman R, Omer SB, Osborne R, Pearce N, Perez-Ruiz F, Perico N, Pesudovs K, Phillips D, Pourmalek F, Prince M, Rehm JT, Remuzzi G, Richardson K, Room R, Saha S, Sampson U, Sanchez-Riera L, Segui-Gomez M, Shahraz S, Shibuya K, Singh D, Sliwa K, Smith E, Soerjomataram I, Steiner T, Stolk WA, Stovner LJ, Sudfeld C, Taylor HR, Tleyjeh IM, van der Werf MJ, Watson WL, Weatherall DJ, Weintraub R, Weisskopf MG, Whiteford H, Wilkinson JD,

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Woolf AD, Zheng ZJ, Murray CJ, Jonas JB. Common values in assessing health outcomes from disease and injury: disability weights measurement study for the Global Burden of Disease Study 2010. Lancet. 2012;380:2129–2143. [4] Salomon JA, Wang H, Freeman MK, Vos T, Flaxman AD, Lopez AD, Murray CJL. Healthy life expectancy for 187 countries, 1990–2010: a systematic analysis for the global burden of disease study 2010. Lancet. 2012;380:2144–2162. [5] Vos T, Flaxman AD, Naghavi M, Lozano R, Michaud C, Ezzati M, Shibuya K, Salomon JA, Abdalla S, Aboyans V, Abraham J, Ackerman I, Aggarwal R, Ahn SY, Ali MK, Alvarado M, Anderson HR, Anderson LM, Andrews KG, Atkinson C, Baddour LM, Bahalim AN, Barker-Collo S, Barrero LH, Bartels DH, Basa´n ˜ez MG, Baxter A, Bell ML, Benjamin EJ, Bennett D, Bernabe´ E, Bhalla K, Bhandari B, Bikbov B, Bin Abdulhak A, Birbeck G, Black JA, Blencowe H, Blore JD, Blyth F, Bolliger I, Bonaventure A, Boufous S, Bourne R, Boussinesq M, Braithwaite T, Brayne C, Bridgett L, Brooker S, Brooks P, Brugha TS, Bryan-Hancock C, Bucello C, Buchbinder R, Buckle G, Budke CM, Burch M, Burney P, Burstein R, Calabria B, Campbell B, Canter CE, Carabin H, Carapetis J, Carmona L, Cella C, Charlson F, Chen H, Cheng AT, Chou D, Chugh SS, Coffeng LE, Colan SD, Colquhoun S, Colson KE, Condon J, Connor MD, Cooper LT, Corriere M, Cortinovis M, de Vaccaro KC, Couser W, Cowie BC, Criqui MH, Cross M, Dabhadkar KC, Dahiya M, Dahodwala N, Damsere-Derry J, Danaei G, Davis A, De Leo D, Degenhardt L, Dellavalle R, Delossantos A, Denenberg J, Derrett S, Des Jarlais DC, Dharmaratne SD, Dherani M, Diaz-Torne C, Dolk H, Dorsey ER, Driscoll T, Duber H, Ebel B, Edmond K, Elbaz A, Ali SE, Erskine H, Erwin PJ, Espindola P, Ewoigbokhan SE, Farzadfar F, Feigin V, Felson DT, Ferrari A, Ferri CP, Fe`vre EM, Finucane MM, Flaxman S, Flood L, Foreman K, Forouzanfar MH, Fowkes FG, Franklin R, Fransen M, Freeman MK, Gabbe BJ, Gabriel SE, Gakidou E, Ganatra HA, Garcia B, Gaspari F, Gillum RF, Gmel G, Gosselin R, Grainger R, Groeger J, Guillemin F, Gunnell D, Gupta R, Haagsma J, Hagan H, Halasa YA, Hall W, Haring D, Haro JM, Harrison JE, Havmoeller R, Hay RJ, Higashi H, Hill C, Hoen B, Hoffman H, Hotez PJ, Hoy D, Huang JJ, Ibeanusi SE, Jacobsen KH, James SL, Jarvis D, Jasrasaria R, Jayaraman S, Johns N, Jonas JB, Karthikeyan G, Kassebaum N, Kawakami N, Keren A, Khoo JP, King CH, Knowlton LM, Kobusingye O, Koranteng A, Krishnamurthi R, Lalloo R, Laslett LL, Lathlean T, Leasher JL, Lee YY, Leigh J, Lim SS, Limb E, Lin JK, Lipnick M, Lipshultz SE, Liu W, Loane M, Ohno SL, Lyons R, Ma J, Mabweijano J, MacIntyre MF, Malekzadeh R, Mallinger L, Manivannan S, Marcenes W, March L, Margolis DJ, Marks GB, Marks R, Matsumori A, Matzopoulos R, Mayosi BM, McAnulty JH, McDermott MM, McGill N, McGrath J, Medina-Mora ME, Meltzer M, Mensah GA, Merriman TR, Meyer AC, Miglioli V, Miller M, Miller TR, Mitchell PB, Mocumbi AO, Moffitt TE, Mokdad AA, Monasta L, Montico M, Moradi-Lakeh M, Moran A, Morawska L, Mori R, Murdoch ME, Mwaniki MK, Naidoo K, Nair MN, Naldi L, Narayan KM, Nelson PK, Nelson RG, Nevitt MC, Newton CR, Nolte S, Norman P, Norman R, O’Donnell M, O’Hanlon S, Olives C, Omer SB, Ortblad K, Osborne R, Ozgediz D, Page A, Pahari B, Pandian JD, Rivero AP, Patten SB, Pearce N, Padilla RP, Perez-Ruiz F, Perico N, Pesudovs K, Phillips D, Phillips MR, Pierce K, Pion S, Polanczyk GV, Polinder S, Pope CA 3rd, Popova S, Porrini E, Pourmalek F, Prince M, Pullan RL, Ramaiah KD, Ranganathan D, Razavi H, Regan M, Rehm JT, Rein DB, Remuzzi G, Richardson K, Rivara FP, Roberts T, Robinson C, De Leo`n FR, Ronfani L, Room R, Rosenfeld LC, Rushton L, Sacco RL, Saha S, Sampson U, Sanchez-Riera L, Sanman E, Schwebel DC, Scott JG, Segui-Gomez M, Shahraz S, Shepard DS, Shin H, Shivakoti R, Singh D, Singh GM, Singh JA, Singleton J, Sleet DA, Sliwa K, Smith E, Smith JL, Stapelberg NJ, Steer A, Steiner T, Stolk WA, Stovner LJ, Sudfeld C, Syed S, Tamburlini G, Tavakkoli M, Taylor HR, Taylor JA, Taylor WJ, Thomas B, Thomson WM, Thurston GD, Tleyjeh IM, Tonelli M, Towbin JA, Truelsen T, Tsilimbaris MK, Ubeda C, Undurraga EA, van der Werf MJ, van Os J, Vavilala MS, Venketasubramanian N, Wang M, Wang W, Watt K, Weatherall DJ, Weinstock MA, Weintraub R, Weisskopf MG, Weissman MM, White RA, Whiteford H, Wiersma ST, Wilkinson JD, Williams HC, Williams SR, Witt E, Wolfe F, Woolf AD, Wulf S, Yeh PH, Zaidi AK, Zheng ZJ, Zonies D, Lopez AD, Murray CJ, Al Mazroa MA, Memish ZA. Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2012;380:2163–2196. [6] Murray CJ, Vos T, Lozano R, Naghavi M, Flaxman AD, Michaud C, Ezzati M, Shibuya K, Salomon JA, Abdalla S, Aboyans V, Abraham J, Ackerman I, Aggarwal R, Ahn SY, Ali MK, Alvarado M, Anderson HR, Anderson LM, Andrews KG, Atkinson C, Baddour LM, Bahalim AN, Barker-Collo S, Barrero LH, Bartels DH, Basa´n ˜ez MG, Baxter A, Bell ML, Benjamin EJ, Bennett D, Bernabe´ E, Bhalla K, Bhandari B, Bikbov B, Bin Abdulhak A, Birbeck G, Black JA, Blencowe H, Blore JD, Blyth F, Bolliger I, Bonaventure A, Boufous S, Bourne R, Boussinesq M, Braithwaite T, Brayne C, Bridgett L, Brooker S, Brooks P, Brugha TS, Bryan-Hancock C, Bucello C, Buchbinder R, Buckle G, Budke CM, Burch M, Burney P, Burstein R, Calabria B, Campbell B, Canter CE, Carabin H, Carapetis J, Carmona L, Cella C, Charlson F, Chen H, Cheng AT, Chou D, Chugh SS, Coffeng LE, Colan SD, Colquhoun S, Colson KE, Condon J, Connor MD, Cooper LT, Corriere M, Cortinovis M, de Vaccaro KC, Couser W, Cowie BC, Criqui MH, Cross M, Dabhadkar KC, Dahiya M, Dahodwala N, Damsere-Derry J, Danaei G, Davis A, De Leo D, Degenhardt L, Dellavalle R, Delossantos A, Denenberg J, Derrett S, Des Jarlais DC, Dharmaratne SD, Dherani M, DiazTorne C, Dolk H, Dorsey ER, Driscoll T, Duber H, Ebel B, Edmond K, Elbaz A, Ali SE, Erskine H, Erwin PJ, Espindola P, Ewoigbokhan SE, Farzadfar F, Feigin V, Felson DT, Ferrari A, Ferri CP, Fe`vre EM, Finucane MM, Flaxman S, Flood L, Foreman K, Forouzanfar MH, Fowkes FG, Fransen M, Freeman MK, Gabbe BJ, Gabriel SE, Gakidou E, Ganatra HA, Garcia B, Gaspari F, Gillum RF, Gmel G, Gonzalez-Medina D, Gosselin R, Grainger R, Grant B, Groeger J, Guillemin F, Gunnell D, Gupta R, Haagsma J, Hagan H, Halasa YA, Hall W, Haring D, Haro JM, Harrison JE, Havmoeller R, Hay RJ, Higashi H, Hill C, Hoen B, Hoffman H, Hotez PJ, Hoy D, Huang JJ, Ibeanusi SE, Jacobsen KH, James SL, Jarvis D, Jasrasaria R, Jayaraman S, Johns N, Jonas JB, Karthikeyan G, Kassebaum N, Kawakami N, Keren A, Khoo JP, King CH, Knowlton LM, Kobusingye O, Koranteng A, Krishnamurthi R, Laden F, Lalloo R, Laslett LL, Lathlean T, Leasher JL, Lee YY, Leigh J, Levinson D, Lim SS, Limb E, Lin JK, Lipnick M, Lipshultz SE, Liu W, Loane M, Ohno SL, Lyons R, Mabweijano J, MacIntyre MF, Malekzadeh R, Mallinger L, Manivannan S, Marcenes W, March L, Margolis DJ, Marks GB, Marks R, Matsumori A, Matzopoulos R, Mayosi BM, McAnulty JH, McDermott MM, McGill N, McGrath J, Medina-Mora ME, Meltzer M, Mensah GA, Merriman TR, Meyer AC, Miglioli V, Miller M, Miller TR, Mitchell PB, Mock C, Mocumbi AO, Moffitt TE, Mokdad AA, Monasta L, Montico M, MoradiLakeh M, Moran A, Morawska L, Mori R, Murdoch ME, Mwaniki MK, Naidoo K, Nair MN, Naldi L, Narayan KM, Nelson PK, Nelson RG, Nevitt MC, Newton CR, Nolte S, Norman P, Norman R, O’Donnell M, O’Hanlon S, Olives C, Omer SB, Ortblad K, Osborne R, Ozgediz D, Page A, Pahari B, Pandian JD, Rivero AP, Patten SB, Pearce N, Padilla RP, Perez-Ruiz F, Perico N, Pesudovs K, Phillips D, Phillips MR, Pierce K, Pion S, Polanczyk GV, Polinder S, Pope CA 3rd, Popova S, Porrini E, Pourmalek F, Prince M, Pullan RL, Ramaiah KD, Ranganathan D, Razavi H, Regan M, Rehm JT, Rein DB, Remuzzi G, Richardson K, Rivara FP, Roberts T, Robinson C, De Leo`n FR, Ronfani L, Room R, Rosenfeld LC, Rushton L, Sacco RL, Saha S, Sampson U, Sanchez-Riera L, Sanman E, Schwebel DC, Scott JG, Segui-Gomez M, Shahraz S, Shepard DS, Shin H,

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[7]

[8] [9]

[10] [11]

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Global Burden of Disease 2010 Study: A personal reflection.

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