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The Global, Regional, and National Burden of Cirrhosis by Cause in 195 Countries and Territories, 1990–2017: A Systematic Analysis for the Global Burden of Disease Study 2017 Publisher Pubmed



Sepanlou SG1, 9 ; Safiri S14, 15 ; Bisignano C23 ; Ikuta KS23, 25 ; Merat S1 ; Saberifiroozi M2 ; Poustchi H1 ; Tsoi D23 ; Colombara DV23 ; Abdoli A26 ; Adedoyin RA27 ; Afarideh M6 ; Agrawal S28, 29 ; Ahmad S30, 31 Show All Authors
Authors
  1. Sepanlou SG1, 9
  2. Safiri S14, 15
  3. Bisignano C23
  4. Ikuta KS23, 25
  5. Merat S1
  6. Saberifiroozi M2
  7. Poustchi H1
  8. Tsoi D23
  9. Colombara DV23
  10. Abdoli A26
  11. Adedoyin RA27
  12. Afarideh M6
  13. Agrawal S28, 29
  14. Ahmad S30, 31
  15. Ahmadian E21, 33
  16. Ahmadpour E17, 19
  17. Akinyemiju T34, 35
  18. Akunna CJ36, 38
  19. Alipour V39, 41
  20. Almasihashiani A46
  21. Almulhim AM47
  22. Alraddadi RM49
  23. Alvisguzman N50, 51
  24. Anber NH52, 53
  25. Angus C54, 122
  26. Anoushiravani A1
  27. Arabloo J42
  28. Araya EM55
  29. Asmelash D58
  30. Ataeinia B8, 145
  31. Ataro Z60
  32. Atout MMW61
  33. Ausloos F62
  34. Awasthi A28
  35. Badawi A63, 64
  36. Banach M65, 66
  37. Ramirez DFB67, 68
  38. Bhagavathula AS69, 70
  39. Bhala N71, 72
  40. Bhattacharyya K73, 74
  41. Biondi A75
  42. Bolla SR76
  43. Boloor A80
  44. Borzi AM75
  45. Butt ZA81, 82
  46. Alberto Camera LLA83, 84
  47. Camposnonato IR87
  48. Carvalho F89, 138
  49. Chu DT91
  50. Chung SC92, 93
  51. Cortesi PA95
  52. Costa VM90
  53. Cowie BC96, 98
  54. Daryani A102
  55. De Courten B104, 105
  56. Demoz GT106, 109
  57. Desai R110
  58. Dharmaratne SD23, 111
  59. Djalalinia S112
  60. Do HT113
  61. Dorostkar F40
  62. Drake TM114
  63. Dubey M115
  64. Duncan BB116
  65. Effiong A117
  66. Eftekhari A18, 119
  67. Elsharkawy A120
  68. Etemadi A11, 121
  69. Farahmand M10
  70. Farzadfar F9
  71. Fernandes E88
  72. Filip I122, 124
  73. Fischer F125
  74. Gebremedhin KBB108
  75. Geta B127
  76. Gilani SA128, 129
  77. Gill PS130
  78. Gutierrez RA131
  79. Haile MT132
  80. Hajmirzaian A5, 136
  81. Hamid SS138
  82. Hasankhani M22
  83. Hasanzadeh A4, 118
  84. Hashemian M139
  85. Hassen HY140, 142
  86. Hay SI23, 24
  87. Hayat K143, 144
  88. Heidari B6
  89. Henok A140
  90. Hoang CL145
  91. Hostiuc M146, 149
  92. Hostiuc S147, 150
  93. Hsieh VCR151
  94. Igumbor EU152, 153
  95. Ilesanmi OS154
  96. Irvani SSN137
  97. Balalami NJ155
  98. James SL23
  99. Jeemon P156
  100. Jha RP157
  101. Jonas JB158, 160
  102. Jozwiak JJ161
  103. Kabir A43
  104. Kasaeian A7, 45
  105. Kassaye HG55
  106. Kefale AT141
  107. Khalilov R32
  108. Khan MA163, 164
  109. Khan EA165
  110. Khater A166
  111. Kim YJ167
  112. Koyanagi A168, 170
  113. Vecchia CL171
  114. Lim LL172, 173
  115. Lopez AD99
  116. Lorkowski S174, 175
  117. Lotufo PA176
  118. Lozano R23, 24
  119. Magdy Abd El Razek M177
  120. Mai HT113
  121. Manafi N44, 178
  122. Manafi A179
  123. Mansournia MA3
  124. Mantovani LG95, 180
  125. Mazzaglia G94
  126. Mehta D130, 181
  127. Mendoza W182
  128. Menezes RG48
  129. Mengesha MM59
  130. Meretoja TJ184, 185
  131. Mestrovic T186, 187
  132. Miazgowski B188, 189
  133. Miller TR190, 191
  134. Mirrakhimov EM192, 193
  135. Mithra P77
  136. Moazen B159, 194
  137. Moghadaszadeh M16, 20
  138. Mohammadianhafshejani A195
  139. Mohammed S159, 196
  140. Mokdad AH23, 24
  141. Monterozamora PA86, 197
  142. Moradi G198, 199
  143. Naimzada MD200, 201
  144. Nayak V78
  145. Negoi I148, 202
  146. Nguyen TH145
  147. Oforiasenso R103, 203
  148. Oh IH204
  149. Olagunju TO205
  150. Padubidri JR79
  151. Pakshir K13
  152. Pana A206, 207
  153. Pathak M208
  154. Pourshams A1
  155. Rabiee N209
  156. Radfar A123, 210
  157. Rafiei A100, 101
  158. Ramezanzadeh K134
  159. Rana SMM211, 212
  160. Rawaf S213, 215
  161. Rawaf DL214, 216
  162. Roever L217
  163. Room R218, 219
  164. Roshandel G1, 220
  165. Safari S135
  166. Samy AM222
  167. Sanabria J223, 224
  168. Sartorius B24, 225
  169. Schmidt MI116
  170. Senthilkumaran S226
  171. Shaikh MA229
  172. Sharif M227, 228
  173. Sharifi A221
  174. Shigematsu M230
  175. Singh JA162, 231
  176. Soheili A233, 234
  177. Suleria HAR97
  178. Teklehaimanot BF56
  179. Tesfay BE56
  180. Vacante M75
  181. Vahedianazimi A235
  182. Valdez PR85, 236
  183. Vasankari TJ237
  184. Vu GT145
  185. Waheed Y238
  186. Weldegwergs KG239
  187. Werdecker A243, 244
  188. Westerman R242
  189. Wondafrash DZ107, 240
  190. Wondmieneh AB109, 126
  191. Yeshitila YG245
  192. Yonemoto N246
  193. Yu C12, 247
  194. Zaidi Z232
  195. Zarghi A133
  196. Zelbersagi S37, 169
  197. Zewdie KA241
  198. Zhang ZJ57
  199. Zhao XJ183
  200. Naghavi M23, 24
  201. Malekzadeh R1, 12

Source: The Lancet Gastroenterology and Hepatology Published:2020


Abstract

Background: Cirrhosis and other chronic liver diseases (collectively referred to as cirrhosis in this paper) are a major cause of morbidity and mortality globally, although the burden and underlying causes differ across locations and demographic groups. We report on results from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2017 on the burden of cirrhosis and its trends since 1990, by cause, sex, and age, for 195 countries and territories. Methods: We used data from vital registrations, vital registration samples, and verbal autopsies to estimate mortality. We modelled prevalence of total, compensated, and decompensated cirrhosis on the basis of hospital and claims data. Disability-adjusted life-years (DALYs) were calculated as the sum of years of life lost due to premature death and years lived with disability. Estimates are presented as numbers and age-standardised or age-specific rates per 100 000 population, with 95% uncertainty intervals (UIs). All estimates are presented for five causes of cirrhosis: hepatitis B, hepatitis C, alcohol-related liver disease, non-alcoholic steatohepatitis (NASH), and other causes. We compared mortality, prevalence, and DALY estimates with those expected according to the Socio-demographic Index (SDI) as a proxy for the development status of regions and countries. Findings: In 2017, cirrhosis caused more than 1·32 million (95% UI 1·27–1·45) deaths (440 000 [416 000–518 000; 33·3%] in females and 883 000 [838 000–967 000; 66·7%] in males) globally, compared with less than 899 000 (829 000–948 000) deaths in 1990. Deaths due to cirrhosis constituted 2·4% (2·3–2·6) of total deaths globally in 2017 compared with 1·9% (1·8–2·0) in 1990. Despite an increase in the number of deaths, the age-standardised death rate decreased from 21·0 (19·2–22·3) per 100 000 population in 1990 to 16·5 (15·8–18·1) per 100 000 population in 2017. Sub-Saharan Africa had the highest age-standardised death rate among GBD super-regions for all years of the study period (32·2 [25·8–38·6] deaths per 100 000 population in 2017), and the high-income super-region had the lowest (10·1 [9·8–10·5] deaths per 100 000 population in 2017). The age-standardised death rate decreased or remained constant from 1990 to 2017 in all GBD regions except eastern Europe and central Asia, where the age-standardised death rate increased, primarily due to increases in alcohol-related liver disease prevalence. At the national level, the age-standardised death rate of cirrhosis was lowest in Singapore in 2017 (3·7 [3·3–4·0] per 100 000 in 2017) and highest in Egypt in all years since 1990 (103·3 [64·4–133·4] per 100 000 in 2017). There were 10·6 million (10·3–10·9) prevalent cases of decompensated cirrhosis and 112 million (107–119) prevalent cases of compensated cirrhosis globally in 2017. There was a significant increase in age-standardised prevalence rate of decompensated cirrhosis between 1990 and 2017. Cirrhosis caused by NASH had a steady age-standardised death rate throughout the study period, whereas the other four causes showed declines in age-standardised death rate. The age-standardised prevalence of compensated and decompensated cirrhosis due to NASH increased more than for any other cause of cirrhosis (by 33·2% for compensated cirrhosis and 54·8% for decompensated cirrhosis) over the study period. From 1990 to 2017, the number of prevalent cases more than doubled for compensated cirrhosis due to NASH and more than tripled for decompensated cirrhosis due to NASH. In 2017, age-standardised death and DALY rates were lower among countries and territories with higher SDI. Interpretation: Cirrhosis imposes a substantial health burden on many countries and this burden has increased at the global level since 1990, partly due to population growth and ageing. Although the age-standardised death and DALY rates of cirrhosis decreased from 1990 to 2017, numbers of deaths and DALYs and the proportion of all global deaths due to cirrhosis increased. Despite the availability of effective interventions for the prevention and treatment of hepatitis B and C, they were still the main causes of cirrhosis burden worldwide, particularly in low-income countries. The impact of hepatitis B and C is expected to be attenuated and overtaken by that of NASH in the near future. Cost-effective interventions are required to continue the prevention and treatment of viral hepatitis, and to achieve early diagnosis and prevention of cirrhosis due to alcohol-related liver disease and NASH. Funding: Bill & Melinda Gates Foundation. © 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
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