TY - JOUR
T1 - Global burden and strength of evidence for 88 risk factors in 204 countries and 811 subnational locations, 1990–2021
T2 - a systematic analysis for the Global Burden of Disease Study 2021
AU - GBD 2021 Risk Factors Collaborators
AU - Brauer, Michael
AU - Roth, Gregory A.
AU - Aravkin, Aleksandr Y.
AU - Zheng, Peng
AU - Abate, Kalkidan Hassen
AU - Abate, Yohannes Habtegiorgis
AU - Abbafati, Cristiana
AU - Abbasgholizadeh, Rouzbeh
AU - Abbasi, Madineh Akram
AU - Abbasian, Mohammadreza
AU - Abbasifard, Mitra
AU - Abbasi-Kangevari, Mohsen
AU - Abd ElHafeez, Samar
AU - Abd-Elsalam, Sherief
AU - Abdi, Parsa
AU - Abdollahi, Mohammad
AU - Abdoun, Meriem
AU - Abdulah, Deldar Morad
AU - Abdullahi, Auwal
AU - Abebe, Mesfin
AU - Abedi, Aidin
AU - Abedi, Armita
AU - Abegaz, Tadesse M.
AU - Zuñiga, Roberto Ariel Abeldaño
AU - Abiodun, Olumide
AU - Abiso, Temesgen Lera
AU - Aboagye, Richard Gyan
AU - Abolhassani, Hassan
AU - Abouzid, Mohamed
AU - Aboye, Girma Beressa
AU - Abreu, Lucas Guimarães
AU - Abualruz, Hasan
AU - Abubakar, Bilyaminu
AU - Abu-Gharbieh, Eman
AU - Abukhadijah, Hana Jihad Jihad
AU - Aburuz, Salahdein
AU - Abu-Zaid, Ahmed
AU - Adane, Mesafint Molla
AU - Addo, Isaac Yeboah
AU - Addolorato, Giovanni
AU - Adedoyin, Rufus Adesoji
AU - Adekanmbi, Victor
AU - Aden, Bashir
AU - Adetunji, Juliana Bunmi
AU - Adeyeoluwa, Temitayo Esther
AU - Adha, Rishan
AU - Adibi, Amin
AU - Adnani, Qorinah Estiningtyas Sakilah
AU - Adzigbli, Leticia Akua
AU - Afolabi, Aanuoluwapo Adeyimika
AU - Afolabi, Rotimi Felix
AU - Afshin, Ashkan
AU - Afyouni, Shadi
AU - Afzal, Muhammad Sohail
AU - Afzal, Saira
AU - Agampodi, Suneth Buddhika
AU - Agbozo, Faith
AU - Aghamiri, Shahin
AU - Agodi, Antonella
AU - Agrawal, Anurag
AU - Agyemang-Duah, Williams
AU - Ahinkorah, Bright Opoku
AU - Ahmad, Aqeel
AU - Ahmad, Danish
AU - Ahmad, Firdos
AU - Ahmad, Noah
AU - Ahmad, Shahzaib
AU - Ahmad, Tauseef
AU - Ahmed, Ali
AU - Ahmed, Anisuddin
AU - Ahmed, Ayman
AU - Ahmed, Luai A.
AU - Ahmed, Muktar Beshir
AU - Ahmed, Safoora
AU - Ahmed, Syed Anees
AU - Ajami, Marjan
AU - Akalu, Gizachew Taddesse
AU - Akara, Essona Matatom
AU - Akbarialiabad, Hossein
AU - Akhlaghi, Shiva
AU - Akinosoglou, Karolina
AU - Akinyemiju, Tomi
AU - Akkaif, Mohammed Ahmed
AU - Akkala, Sreelatha
AU - Akombi-Inyang, Blessing
AU - Al Awaidy, Salah
AU - Al Hasan, Syed Mahfuz
AU - Alahdab, Fares
AU - AL-Ahdal, Tareq Mohammed Ali
AU - Alalalmeh, Samer O.
AU - Alalwan, Tariq A.
AU - Al-Aly, Ziyad
AU - Alam, Khurshid
AU - Alam, Nazmul
AU - Alanezi, Fahad Mashhour
AU - Alanzi, Turki M.
AU - Albakri, Almaza
AU - AlBataineh, Mohammad T.
AU - Aldhaleei, Wafa A.
AU - Aldridge, Robert W.
AU - Alemayohu, Mulubirhan Assefa
AU - Alemu, Yihun Mulugeta
AU - Al-Fatly, Bassam
AU - Al-Gheethi, Adel Ali Saeed
AU - Al-Habbal, Khairat
AU - Alhabib, Khalid F.
AU - Alhassan, Robert Kaba
AU - Ali, Abid
AU - Ali, Amjad
AU - Ali, Beriwan Abdulqadir
AU - Ali, Iman
AU - Ali, Liaqat
AU - Ali, Mohammed Usman
AU - Ali, Rafat
AU - Ali, Syed Shujait Shujait
AU - Ali, Waad
AU - Alicandro, Gianfranco
AU - Alif, Sheikh Mohammad
AU - Aljunid, Syed Mohamed
AU - Alla, François
AU - Al-Marwani, Sabah
AU - Al-Mekhlafi, Hesham M.
AU - Almustanyir, Sami
AU - Alomari, Mahmoud A.
AU - Alonso, Jordi
AU - Alqahtani, Jaber S.
AU - Alqutaibi, Ahmed Yaseen
AU - Al-Raddadi, Rajaa M.
AU - Alrawashdeh, Ahmad
AU - Al-Rifai, Rami Hani
AU - Alrousan, Sahel Majed
AU - Al-Sabah, Salman Khalifah
AU - Alshahrani, Najim Z.
AU - Altaany, Zaid
AU - Altaf, Awais
AU - Al-Tawfiq, Jaffar A.
AU - Altirkawi, Khalid A.
AU - Aluh, Deborah Oyine
AU - Alvis-Guzman, Nelson
AU - Alvis-Zakzuk, Nelson J.
AU - Alwafi, Hassan
AU - Al-Wardat, Mohammad Sami
AU - Al-Worafi, Yaser Mohammed
AU - Aly, Hany
AU - Aly, Safwat
AU - Alzoubi, Karem H.
AU - Al-Zyoud, Walid
AU - Amaechi, Uchenna Anderson
AU - Mohammadi, Masous Aman
AU - Amani, Reza
AU - Amiri, Sohrab
AU - Amirzade-Iranaq, Mohammad Hosein
AU - Ammirati, Enrico
AU - Amu, Hubert
AU - Amugsi, Dickson A.
AU - Amusa, Ganiyu Adeniyi
AU - Ancuceanu, Robert
AU - Anderlini, Deanna
AU - Anderson, Jason A.
AU - Andrade, Pedro Prata
AU - Andrei, Catalina Liliana
AU - Andrei, Tudorel
AU - Anenberg, Susan C.
AU - Angappan, Dhanalakshmi
AU - Angus, Colin
AU - Anil, Abhishek
AU - Anil, Sneha
AU - Anjum, Afifa
AU - Anoushiravani, Amir
AU - Antonazzo, Ippazio Cosimo
AU - Antony, Catherine M.
AU - Antriyandarti, Ernoiz
AU - Anuoluwa, Boluwatife Stephen
AU - Anvari, Davood
AU - Anvari, Saeid
AU - Anwar, Saleha
AU - Anwar, Sumadi Lukman
AU - Anwer, Razique
AU - Anyabolo, Ekenedilichukwu Emmanuel
AU - Anyasodor, Anayochukwu Edward
AU - Apostol, Geminn Louis Carace
AU - Arabloo, Jalal
AU - Bahri, Razman Arabzadeh
AU - Arafat, Mosab
AU - Areda, Demelash
AU - Aregawi, Brhane Berhe
AU - Aremu, Abdulfatai
AU - Armocida, Benedetta
AU - Arndt, Michael Benjamin
AU - Ärnlöv, Johan
AU - Arooj, Mahwish
AU - Artamonov, Anton A.
AU - Artanti, Kurnia Dwi
AU - Aruleba, Idowu Thomas
AU - Arumugam, Ashokan
AU - Asbeutah, Akram M.
AU - Asgary, Saeed
AU - Asgedom, Akeza Awealom
AU - Ashbaugh, Charlie
AU - Ashemo, Mubarek Yesse
AU - Ashraf, Tahira
AU - Askarinejad, Amir
AU - Assmus, Michael
AU - Astell-Burt, Thomas
AU - Athar, Mohammad
AU - Athari, Seyyed Shamsadin
AU - Atorkey, Prince
AU - Atreya, Alok
AU - Aujayeb, Avinash
AU - Ausloos, Marcel
AU - Avila-Burgos, Leticia
AU - Awoke, Andargie Abate
AU - Quintanilla, Beatriz Paulina Ayala
AU - Ayatollahi, Haleh
AU - Portugal, Carlos Ayestas
AU - Ayuso-Mateos, Jose L.
AU - Azadnajafabad, Sina
AU - Azevedo, Rui M.S.
AU - Azhar, Gulrez Shah
AU - Azizi, Hosein
AU - Azzam, Ahmed Y.
AU - Backhaus, Insa Linnea
AU - Badar, Muhammad
AU - Badiye, Ashish D.
AU - Bagga, Arvind
AU - Baghdadi, Soroush
AU - Bagheri, Nasser
AU - Bagherieh, Sara
AU - Taghanaki, Pegah Bahrami
AU - Bai, Ruhai
AU - Baig, Atif Amin
AU - Baker, Jennifer L.
AU - Bakkannavar, Shankar M.
AU - Balasubramanian, Madhan
AU - Baltatu, Ovidiu Constantin
AU - Bam, Kiran
AU - Bandyopadhyay, Soham
AU - Banik, Biswajit
AU - Banik, Palash Chandra
AU - Banke-Thomas, Aduragbemi
AU - Bansal, Hansi
AU - Barchitta, Martina
AU - Bardhan, Mainak
AU - Bardideh, Erfan
AU - Barker-Collo, Suzanne Lyn
AU - Bärnighausen, Till Winfried
AU - Hoque, Mohammad Enamul
AU - Sahebkar, Amirhossein
AU - Takahashi, Ken
AU - Ward, Paul
N1 - Publisher Copyright:
© 2024 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
PY - 2024/5/18
Y1 - 2024/5/18
N2 - Background: Understanding the health consequences associated with exposure to risk factors is necessary to inform public health policy and practice. To systematically quantify the contributions of risk factor exposures to specific health outcomes, the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2021 aims to provide comprehensive estimates of exposure levels, relative health risks, and attributable burden of disease for 88 risk factors in 204 countries and territories and 811 subnational locations, from 1990 to 2021. Methods: The GBD 2021 risk factor analysis used data from 54 561 total distinct sources to produce epidemiological estimates for 88 risk factors and their associated health outcomes for a total of 631 risk–outcome pairs. Pairs were included on the basis of data-driven determination of a risk–outcome association. Age-sex-location-year-specific estimates were generated at global, regional, and national levels. Our approach followed the comparative risk assessment framework predicated on a causal web of hierarchically organised, potentially combinative, modifiable risks. Relative risks (RRs) of a given outcome occurring as a function of risk factor exposure were estimated separately for each risk–outcome pair, and summary exposure values (SEVs), representing risk-weighted exposure prevalence, and theoretical minimum risk exposure levels (TMRELs) were estimated for each risk factor. These estimates were used to calculate the population attributable fraction (PAF; ie, the proportional change in health risk that would occur if exposure to a risk factor were reduced to the TMREL). The product of PAFs and disease burden associated with a given outcome, measured in disability-adjusted life-years (DALYs), yielded measures of attributable burden (ie, the proportion of total disease burden attributable to a particular risk factor or combination of risk factors). Adjustments for mediation were applied to account for relationships involving risk factors that act indirectly on outcomes via intermediate risks. Attributable burden estimates were stratified by Socio-demographic Index (SDI) quintile and presented as counts, age-standardised rates, and rankings. To complement estimates of RR and attributable burden, newly developed burden of proof risk function (BPRF) methods were applied to yield supplementary, conservative interpretations of risk–outcome associations based on the consistency of underlying evidence, accounting for unexplained heterogeneity between input data from different studies. Estimates reported represent the mean value across 500 draws from the estimate's distribution, with 95% uncertainty intervals (UIs) calculated as the 2·5th and 97·5th percentile values across the draws. Findings: Among the specific risk factors analysed for this study, particulate matter air pollution was the leading contributor to the global disease burden in 2021, contributing 8·0% (95% UI 6·7–9·4) of total DALYs, followed by high systolic blood pressure (SBP; 7·8% [6·4–9·2]), smoking (5·7% [4·7–6·8]), low birthweight and short gestation (5·6% [4·8–6·3]), and high fasting plasma glucose (FPG; 5·4% [4·8–6·0]). For younger demographics (ie, those aged 0–4 years and 5–14 years), risks such as low birthweight and short gestation and unsafe water, sanitation, and handwashing (WaSH) were among the leading risk factors, while for older age groups, metabolic risks such as high SBP, high body-mass index (BMI), high FPG, and high LDL cholesterol had a greater impact. From 2000 to 2021, there was an observable shift in global health challenges, marked by a decline in the number of all-age DALYs broadly attributable to behavioural risks (decrease of 20·7% [13·9–27·7]) and environmental and occupational risks (decrease of 22·0% [15·5–28·8]), coupled with a 49·4% (42·3–56·9) increase in DALYs attributable to metabolic risks, all reflecting ageing populations and changing lifestyles on a global scale. Age-standardised global DALY rates attributable to high BMI and high FPG rose considerably (15·7% [9·9–21·7] for high BMI and 7·9% [3·3–12·9] for high FPG) over this period, with exposure to these risks increasing annually at rates of 1·8% (1·6–1·9) for high BMI and 1·3% (1·1–1·5) for high FPG. By contrast, the global risk-attributable burden and exposure to many other risk factors declined, notably for risks such as child growth failure and unsafe water source, with age-standardised attributable DALYs decreasing by 71·5% (64·4–78·8) for child growth failure and 66·3% (60·2–72·0) for unsafe water source. We separated risk factors into three groups according to trajectory over time: those with a decreasing attributable burden, due largely to declining risk exposure (eg, diet high in trans-fat and household air pollution) but also to proportionally smaller child and youth populations (eg, child and maternal malnutrition); those for which the burden increased moderately in spite of declining risk exposure, due largely to population ageing (eg, smoking); and those for which the burden increased considerably due to both increasing risk exposure and population ageing (eg, ambient particulate matter air pollution, high BMI, high FPG, and high SBP). Interpretation: Substantial progress has been made in reducing the global disease burden attributable to a range of risk factors, particularly those related to maternal and child health, WaSH, and household air pollution. Maintaining efforts to minimise the impact of these risk factors, especially in low SDI locations, is necessary to sustain progress. Successes in moderating the smoking-related burden by reducing risk exposure highlight the need to advance policies that reduce exposure to other leading risk factors such as ambient particulate matter air pollution and high SBP. Troubling increases in high FPG, high BMI, and other risk factors related to obesity and metabolic syndrome indicate an urgent need to identify and implement interventions. Funding: Bill & Melinda Gates Foundation.
AB - Background: Understanding the health consequences associated with exposure to risk factors is necessary to inform public health policy and practice. To systematically quantify the contributions of risk factor exposures to specific health outcomes, the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2021 aims to provide comprehensive estimates of exposure levels, relative health risks, and attributable burden of disease for 88 risk factors in 204 countries and territories and 811 subnational locations, from 1990 to 2021. Methods: The GBD 2021 risk factor analysis used data from 54 561 total distinct sources to produce epidemiological estimates for 88 risk factors and their associated health outcomes for a total of 631 risk–outcome pairs. Pairs were included on the basis of data-driven determination of a risk–outcome association. Age-sex-location-year-specific estimates were generated at global, regional, and national levels. Our approach followed the comparative risk assessment framework predicated on a causal web of hierarchically organised, potentially combinative, modifiable risks. Relative risks (RRs) of a given outcome occurring as a function of risk factor exposure were estimated separately for each risk–outcome pair, and summary exposure values (SEVs), representing risk-weighted exposure prevalence, and theoretical minimum risk exposure levels (TMRELs) were estimated for each risk factor. These estimates were used to calculate the population attributable fraction (PAF; ie, the proportional change in health risk that would occur if exposure to a risk factor were reduced to the TMREL). The product of PAFs and disease burden associated with a given outcome, measured in disability-adjusted life-years (DALYs), yielded measures of attributable burden (ie, the proportion of total disease burden attributable to a particular risk factor or combination of risk factors). Adjustments for mediation were applied to account for relationships involving risk factors that act indirectly on outcomes via intermediate risks. Attributable burden estimates were stratified by Socio-demographic Index (SDI) quintile and presented as counts, age-standardised rates, and rankings. To complement estimates of RR and attributable burden, newly developed burden of proof risk function (BPRF) methods were applied to yield supplementary, conservative interpretations of risk–outcome associations based on the consistency of underlying evidence, accounting for unexplained heterogeneity between input data from different studies. Estimates reported represent the mean value across 500 draws from the estimate's distribution, with 95% uncertainty intervals (UIs) calculated as the 2·5th and 97·5th percentile values across the draws. Findings: Among the specific risk factors analysed for this study, particulate matter air pollution was the leading contributor to the global disease burden in 2021, contributing 8·0% (95% UI 6·7–9·4) of total DALYs, followed by high systolic blood pressure (SBP; 7·8% [6·4–9·2]), smoking (5·7% [4·7–6·8]), low birthweight and short gestation (5·6% [4·8–6·3]), and high fasting plasma glucose (FPG; 5·4% [4·8–6·0]). For younger demographics (ie, those aged 0–4 years and 5–14 years), risks such as low birthweight and short gestation and unsafe water, sanitation, and handwashing (WaSH) were among the leading risk factors, while for older age groups, metabolic risks such as high SBP, high body-mass index (BMI), high FPG, and high LDL cholesterol had a greater impact. From 2000 to 2021, there was an observable shift in global health challenges, marked by a decline in the number of all-age DALYs broadly attributable to behavioural risks (decrease of 20·7% [13·9–27·7]) and environmental and occupational risks (decrease of 22·0% [15·5–28·8]), coupled with a 49·4% (42·3–56·9) increase in DALYs attributable to metabolic risks, all reflecting ageing populations and changing lifestyles on a global scale. Age-standardised global DALY rates attributable to high BMI and high FPG rose considerably (15·7% [9·9–21·7] for high BMI and 7·9% [3·3–12·9] for high FPG) over this period, with exposure to these risks increasing annually at rates of 1·8% (1·6–1·9) for high BMI and 1·3% (1·1–1·5) for high FPG. By contrast, the global risk-attributable burden and exposure to many other risk factors declined, notably for risks such as child growth failure and unsafe water source, with age-standardised attributable DALYs decreasing by 71·5% (64·4–78·8) for child growth failure and 66·3% (60·2–72·0) for unsafe water source. We separated risk factors into three groups according to trajectory over time: those with a decreasing attributable burden, due largely to declining risk exposure (eg, diet high in trans-fat and household air pollution) but also to proportionally smaller child and youth populations (eg, child and maternal malnutrition); those for which the burden increased moderately in spite of declining risk exposure, due largely to population ageing (eg, smoking); and those for which the burden increased considerably due to both increasing risk exposure and population ageing (eg, ambient particulate matter air pollution, high BMI, high FPG, and high SBP). Interpretation: Substantial progress has been made in reducing the global disease burden attributable to a range of risk factors, particularly those related to maternal and child health, WaSH, and household air pollution. Maintaining efforts to minimise the impact of these risk factors, especially in low SDI locations, is necessary to sustain progress. Successes in moderating the smoking-related burden by reducing risk exposure highlight the need to advance policies that reduce exposure to other leading risk factors such as ambient particulate matter air pollution and high SBP. Troubling increases in high FPG, high BMI, and other risk factors related to obesity and metabolic syndrome indicate an urgent need to identify and implement interventions. Funding: Bill & Melinda Gates Foundation.
UR - http://www.scopus.com/inward/record.url?scp=85192940010&partnerID=8YFLogxK
U2 - 10.1016/S0140-6736(24)00933-4
DO - 10.1016/S0140-6736(24)00933-4
M3 - Article
C2 - 38762324
AN - SCOPUS:85192940010
SN - 0140-6736
VL - 403
SP - 2162
EP - 2203
JO - The Lancet
JF - The Lancet
IS - 10440
ER -