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Christopher J L Murray

· Institute for Health Metrics and Evaluation

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Christopher J L Murray is a registered researcher in their academic field.

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6 research works linked to this profile

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Cardiac Imaging and Diagnostics, Cardiac, Anesthesia and Surgical Outcomes, Pulmonary Hypertension Research and Treatments · 2023 · Journal of the American College of Cardiology

Global Burden of Cardiovascular Diseases and Risks, 1990-2022

George A. Mensah, Valentı́n Fuster, Christopher J L Murray, Gregory A. Roth, Yohannes Abate, Mohammadreza Abbasian, Foad Abd-Allah, Ashkan Abdollahi, Mohammad Abdollahı, Deldar Morad Abdulah, Auwal Abdullahi, Ayele Mamo Abebe, Aidin Abedi, Armita Abedi, Olugbenga Olusola Abiodun, Hiwa Abubaker Ali, Eman Abu‐Gharbieh, Niveen M. E. Abu-Rmeileh, Salahdein Aburuz, Abdelrahman Ibrahim Abushouk, Ahmed Abu‐Zaid, Tigist Demssew Adane, Nicola J. Adderley, Oladimeji Adebayo, Bashir Aden, Temitayo Esther Adeyeoluwa, Olorunsola Adeyomoye, Qorinah Estiningtyas Sakilah Adnani, Fatemeh Afrashteh, Shadi Afyouni, Saira Afzal, Pradyumna Agasthi, Antonella Agodi, Constanza Elizabeth Aguilera Arriagada, Williams Agyemang‐Duah, Bright Opoku Ahinkorah, Aqeel Ahmad, Danish Ahmad, Firdos Ahmad, Muayyad Ahmad, Ayman Ahmed, Haroon Ahmed, Muktar Beshir Ahmed, Syed Anees Ahmed, Marjan Ajami, Karolina Akinosoglou, Moein Ala, Tareq Mohammed Ali AL-Ahdal, Samer O Alalalmeh, Ziyad Al‐Aly, Nazmul Alam, Rasmieh Al‐Amer, Alaa Alashi, Mohammed ALBashtawy, Mohammad T AlBataineh, Haileselasie Berhane Alema, Sharifullah Alemi, Megbaru Alemu, Adel Al‐Gheethi, Khalid F. AlHabib, Fadwa Alhalaiqa, Mohammed Usman Ali, Rafat Ali, Syed Shujait Ali, Gianfranco Alicandro, Reyhaneh Alikhani, Syed Mohamed Aljunid, François Alla, Wael Almahmeed, Sabah Al-Marwani, Jordi Alonso, Rajaa Al‐Raddadi, Farrukh Jawad Alvi, Nelson Alvis‐Guzmán, Nelson J Alvis-Zakzuk, Hassan Alwafi, Hany Aly, Prince M. Amegbor, Tarek Tawfik Amin, Alireza Amindarolzarbi, Mostafa Amini‐Rarani, Sohrab Amiri, Enrico Ammirati, Tanu Anand, Robert Ancuceanu, Deanna Anderlini, Abhishek Anil, Golnoosh Ansari, P.E. Anyanwu, Anayochukwu Edward Anyasodor, Geminn Louis Carace Apostol, Jalal Arabloo, Mosab Arafat, Aleksandr Y. Aravkin, Olatunde Aremu, Benedetta Armocida, Johan Ärnlöv, Oluwaseyi Olalekan Arowosegbe, Anton A Artamonov

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Parkinson's Disease Mechanisms and Treatments, Voice and Speech Disorders, Cerebral Palsy and Movement Disorders · 2018 · The Lancet Neurology

Global, regional, and national burden of Parkinson's disease, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016

BACKGROUND: Neurological disorders are now the leading source of disability globally, and ageing is increasing the burden of neurodegenerative disorders, including Parkinson's disease. We aimed to determine the global burden of Parkinson's disease between 1990 and 2016 to identify trends and to enable appropriate public health, medical, and scientific responses. METHODS: Through a systematic analysis of epidemiological studies, we estimated global, regional, and country-specific prevalence and years of life lived with disability for Parkinson's disease from 1990 to 2016. We estimated the proportion of mild, moderate, and severe Parkinson's disease on the basis of studies that used the Hoehn and Yahr scale and assigned disability weights to each level. We jointly modelled prevalence and excess mortality risk in a natural history model to derive estimates of deaths due to Parkinson's disease. Death counts were multiplied by values from the Global Burden of Disease study's standard life expectancy to compute years of life lost. Disability-adjusted life-years (DALYs) were computed as the sum of years lived with disability and years of life lost. We also analysed results based on the Socio-demographic Index, a compound measure of income per capita, education, and fertility. FINDINGS: In 2016, 6·1 million (95% uncertainty interval [UI] 5·0-7·3) individuals had Parkinson's disease globally, compared with 2·5 million (2·0-3·0) in 1990. This increase was not solely due to increasing numbers of older people, because age-standardised prevalence rates increased by 21·7% (95% UI 18·1-25·3) over the same period (compared with an increase of 74·3%, 95% UI 69·2-79·6, for crude prevalence rates). Parkinson's disease caused 3·2 million (95% UI 2·6-4·0) DALYs and 211 296 deaths (95% UI 167 771-265 160) in 2016. The male-to-female ratios of age-standardised prevalence rates were similar in 2016 (1·40, 95% UI 1·36-1·43) and 1990 (1·37, 1·34-1·40). From 1990 to 2016, age-standardised prevalence, DALY rates, and death rates increased for all global burden of disease regions except for southern Latin America, eastern Europe, and Oceania. In addition, age-standardised DALY rates generally increased across the Socio-demographic Index. INTERPRETATION: Over the past generation, the global burden of Parkinson's disease has more than doubled as a result of increasing numbers of older people, with potential contributions from longer disease duration and environmental factors. Demographic and potentially other factors are poised to increase the future burden of Parkinson's disease substantially. FUNDING: Bill & Melinda Gates Foundation.

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Liver Disease Diagnosis and Treatment, Hepatitis B Virus Studies, Hepatocellular Carcinoma Treatment and Prognosis · 2017 · JAMA Oncology

The Burden of Primary Liver Cancer and Underlying Etiologies From 1990 to 2015 at the Global, Regional, and National Level

Importance Liver cancer is among the leading causes of cancer deaths globally. The most common causes for liver cancer include hepatitis B virus (HBV) and hepatitis C virus (HCV) infection and alcohol use. Objective To report results of the Global Burden of Disease (GBD) 2015 study on primary liver cancer incidence, mortality, and disability-adjusted life-years (DALYs) for 195 countries or territories from 1990 to 2015, and present global, regional, and national estimates on the burden of liver cancer attributable to HBV, HCV, alcohol, and an “other” group that encompasses residual causes. Design, Settings, and Participants Mortality was estimated using vital registration and cancer registry data in an ensemble modeling approach. Single-cause mortality estimates were adjusted for all-cause mortality. Incidence was derived from mortality estimates and the mortality-to-incidence ratio. Through a systematic literature review, data on the proportions of liver cancer due to HBV, HCV, alcohol, and other causes were identified. Years of life lost were calculated by multiplying each death by a standard life expectancy. Prevalence was estimated using mortality-to-incidence ratio as surrogate for survival. Total prevalence was divided into 4 sequelae that were multiplied by disability weights to derive years lived with disability (YLDs). DALYs were the sum of years of life lost and YLDs. Main Outcomes and Measures Liver cancer mortality, incidence, YLDs, years of life lost, DALYs by etiology, age, sex, country, and year. Results There were 854 000 incident cases of liver cancer and 810 000 deaths globally in 2015, contributing to 20 578 000 DALYs. Cases of incident liver cancer increased by 75% between 1990 and 2015, of which 47% can be explained by changing population age structures, 35% by population growth, and −8% to changing age-specific incidence rates. The male-to-female ratio for age-standardized liver cancer mortality was 2.8. Globally, HBV accounted for 265 000 liver cancer deaths (33%), alcohol for 245 000 (30%), HCV for 167 000 (21%), and other causes for 133 000 (16%) deaths, with substantial variation between countries in the underlying etiologies. Conclusions and Relevance Liver cancer is among the leading causes of cancer deaths in many countries. Causes of liver cancer differ widely among populations. Our results show that most cases of liver cancer can be prevented through vaccination, antiviral treatment, safe blood transfusion and injection practices, as well as interventions to reduce excessive alcohol use. In line with the Sustainable Development Goals, the identification and elimination of risk factors for liver cancer will be required to achieve a sustained reduction in liver cancer burden. The GBD study can be used to guide these prevention efforts.

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Blood Pressure and Hypertension Studies, Sodium Intake and Health, Cardiovascular Health and Risk Factors · 2017 · JAMA

Global Burden of Hypertension and Systolic Blood Pressure of at Least 110 to 115 mm Hg, 1990-2015

Importance: Elevated systolic blood (SBP) pressure is a leading global health risk. Quantifying the levels of SBP is important to guide prevention policies and interventions. Objective: To estimate the association between SBP of at least 110 to 115 mm Hg and SBP of 140 mm Hg or higher and the burden of different causes of death and disability by age and sex for 195 countries and territories, 1990-2015. Design: A comparative risk assessment of health loss related to SBP. Estimated distribution of SBP was based on 844 studies from 154 countries (published 1980-2015) of 8.69 million participants. Spatiotemporal Gaussian process regression was used to generate estimates of mean SBP and adjusted variance for each age, sex, country, and year. Diseases with sufficient evidence for a causal relationship with high SBP (eg, ischemic heart disease, ischemic stroke, and hemorrhagic stroke) were included in the primary analysis. Main Outcomes and Measures: Mean SBP level, cause-specific deaths, and health burden related to SBP (≥110-115 mm Hg and also ≥140 mm Hg) by age, sex, country, and year. Results: Between 1990-2015, the rate of SBP of at least 110 to 115 mm Hg increased from 73 119 (95% uncertainty interval [UI], 67 949-78 241) to 81 373 (95% UI, 76 814-85 770) per 100 000, and SBP of 140 mm Hg or higher increased from 17 307 (95% UI, 17 117-17 492) to 20 526 (95% UI, 20 283-20 746) per 100 000. The estimated annual death rate per 100 000 associated with SBP of at least 110 to 115 mm Hg increased from 135.6 (95% UI, 122.4-148.1) to 145.2 (95% UI 130.3-159.9) and the rate for SBP of 140 mm Hg or higher increased from 97.9 (95% UI, 87.5-108.1) to 106.3 (95% UI, 94.6-118.1). For loss of DALYs associated with systolic blood pressure of 140 mm Hg or higher, the loss increased from 95.9 million (95% uncertainty interval [UI], 87.0-104.9 million) to 143.0 million (95% UI, 130.2-157.0 million) [corrected], and for SBP of 140 mm Hg or higher, the loss increased from 5.2 million (95% UI, 4.6-5.7 million) to 7.8 million (95% UI, 7.0-8.7 million). The largest numbers of SBP-related deaths were caused by ischemic heart disease (4.9 million [95% UI, 4.0-5.7 million]; 54.5%), hemorrhagic stroke (2.0 million [95% UI, 1.6-2.3 million]; 58.3%), and ischemic stroke (1.5 million [95% UI, 1.2-1.8 million]; 50.0%). In 2015, China, India, Russia, Indonesia, and the United States accounted for more than half of the global DALYs related to SBP of at least 110 to 115 mm Hg. Conclusions and Relevance: In international surveys, although there is uncertainty in some estimates, the rate of elevated SBP (≥110-115 and ≥140 mm Hg) increased substantially between 1990 and 2015, and DALYs and deaths associated with elevated SBP also increased. Projections based on this sample suggest that in 2015, an estimated 3.5 billion adults had SBP of at least 110 to 115 mm Hg and 874 million adults had SBP of 140 mm Hg or higher.

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Health disparities and outcomes, Insurance, Mortality, Demography, Risk Management, Health Systems, Economic Evaluations, Quality of Life · 2015 · The Lancet

Global, regional, and national disability-adjusted life years (DALYs) for 306 diseases and injuries and healthy life expectancy (HALE) for 188 countries, 1990–2013: quantifying the epidemiological transition

Christopher J L Murray, Ryan M Barber, Kyle J Foreman, Ayşe Abbasoğlu Özgören, Foad Abd-Allah, Semaw Ferede Abera, Victor Aboyans, Jerry Abraham, Ibrahim Abubakar, Laith J. Abu‐Raddad, Niveen M. E. Abu-Rmeileh, Tom Achoki, Ilana N. Ackerman, Zanfina Ademi, Arsène Kouablan Adou, José Carmelo Adsuar, Ashkan Afshin, Emilie Agardh, Sayed Saidul Alam, Deena Alasfoor, Mohammed I Albittar, Miguel Alegretti, Zewdie Aderaw Alemu, Rafael Alfonso‐Cristancho, Samia Alhabib, Raghib Ali, François Alla, Peter Allebeck, Mohammad A. AlMazroa, Ubai Alsharif, Elena Álvarez, Nelson Alvis‐Guzmán, Azmeraw T. Amare, Emmanuel A Ameh, Heresh Amini, Walid Ammar, H Ross Anderson, Benjamin O. Anderson, Carl Abelardo T. Antonio, Palwasha Anwari, Johan Ärnlöv, Valentina Arsić‐Arsenijević, Al Artaman, Rana J Asghar, Reza Assadi, Lydia S Atkins, Marco Antonio Navarrete Ávila, Baffour Awuah, Victoria F Bachman, Alaa Badawi, Maria C Bahit, Kalpana Balakrishnan, Amitava Banerjee, Suzanne Barker‐Collo, Sı́món Barquera, Lars Barregård, Lope H. Barrero, Arindam Basu, Sanjay Basu, Mohammed Basulaiman, Justin Beardsley, Neeraj Bedi, Ettore Beghi, Tolesa Bekele, Michelle L. Bell, Corina Benjet, Derrick Bennett, Isabela M. Benseñor, Habib Benzian, Eduardo Bernabé, Amelia Bertozzi-Villa, Tariku J. Beyene, Neeraj Bhala, Ashish Bhalla, Zulfiqar A Bhutta, Kelly Bienhoff, Boris Bikbov, Stan Biryukov, Jed D Blore, Christopher D. Blosser, Fiona Blyth, Megan A Bohensky, Ian Bolliger, Berrak Bora Başara, Natan M. Bornstein, Dipan Bose, Soufiane Boufous, Rupert Bourne, Lindsay N. Boyers, Michael Brainin, Carol Brayne, Alexandra Bražinová, Nicholas J. K. Breitborde, Hermann Brenner, Adam Briggs, Peter Brooks, Jonathan C. Brown, Traolach Brugha, Rachelle Buchbinder, Geoffrey Buckle

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Health disparities and outcomes, Cerebral Palsy and Movement Disorders, Injury Epidemiology and Prevention · 2012 · The Lancet

Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010

Christopher J L Murray, Theo Vos, Rafael Lozano, Mohsen Naghavi, Abraham D Flaxman, Catherine Michaud, Majid Ezzati, Kenji Shibuya, Joshua A. Salomon, Safa Abdalla, Victor Aboyans, Jerry Abraham, Ilana N. Ackerman, Rakesh Aggarwal, Stephanie Y Ahn, Mohammed K. Ali, Mohammad A. AlMazroa, Miriam Alvarado, H Ross Anderson, Laurie Anderson, Kathryn Andrews, Charles Atkinson, Larry M. Baddour, Adil N Bahalim, Suzanne Barker‐Collo, Lope H. Barrero, David Bartels, Marı́a-Gloria Basáñez, Amanda Baxter, Michelle L. Bell, Emelia J. Benjamin, Derrick Bennett, Eduardo Bernabé, Kavi Bhalla, Bishal Bhandari, Boris Bikbov, Aref Bin Abdulhak, Gretchen L. Birbeck, James A Black, Hannah Blencowe, Jed D Blore, Fiona Blyth, Ian Bolliger, Audrey Bonaventure, Soufiane Boufous, Rupert Bourne, Michel Boussinesq, Tasanee Braithwaite, Carol Brayne, Lisa Bridgett, Simon Brooker, Peter Brooks, Traolach Brugha, Claire Bryan-Hancock, Chiara Bucello, Rachelle Buchbinder, Geoffrey Buckle, Christine M. Budke, Michael Burch, Peter Burney, Roy Burstein, Bianca Calabria, Benjamin Campbell, Charles E. Canter, Hélène Carabin, Jonathan R. Carapetis, Loreto Carmona, Claudia Cella, Fiona Charlson, Honglei Chen, Andrew Tai-Ann Cheng, David Chou, Sumeet S. Chugh, Luc E. Coffeng, Steven D Colan, Samantha Colquhoun, K. Ellicott Colson, John R. Condon, Myles Connor, Leslie T. Cooper, Matthew Corriere, Monica Cortinovis, Karen Courville de Vaccaro, William Couser, Benjamin C Cowie, Michael H Criqui, Marita Cross, Kaustubh Dabhadkar, Manu Dahiya, Nabila Dahodwala, James Damsere-Derry, Goodarz Danaei, Adrian Davis, Diego De Leo, Louisa Degenhardt, Robert P. Dellavalle, Allyne Delossantos, Julie O. Denenberg, Sarah Derrett, Don C. Des Jarlais