57 research outputs found
Seasonal variation of phytoplankton in My Thanh River, Mekong delta, Vietnam
- Publication venue
- Publication date
- 01/01/2023
- Field of study
A study on the seasonal variation of phytoplankton composition was conducted at the upper, middle, and lower parts of the My Thanh River, which supplies an important source of water for aquaculture. Qualitative and quantitative samples of phytoplankton were collected monthly at both high and low tide. The results showed that a total of 171 phytoplankton (algae) species were recorded, belonging to 59 genera and 5 phyla. Diatoms were the most abundant group with the highest species number, followed by green algae. The other phyla possessed a lower number of species. The species composition was more diverse in the rainy season and at high tide at most of the sampling sites. The mean density of algae varied from 30,900-43,521 ind.L^-1^. The density of diatoms was higher in the middle and lower parts. At the same time, euglenoids displayed the highest density in the upper part, showing a difference in the dominant algae group under the influence of salinity. Salinity was found to be significantly positively correlated (p<0.01) with diatoms, whereas it was negatively correlated (p<0.05) with blue-green algae and euglenoids. The algae composition was quite diverse, with the H' index ranging from 2.0-3.3, showing the water quality was slightly to moderately polluted
An Outbreak of Severe Infections with Community-Acquired MRSA Carrying the Panton-Valentine Leukocidin Following Vaccination
- Author
- AA Witney
- Adwoa Bentsi-Enchill
- BA Diep
- BA Diep
- Bach Van Cam
- BE Gonzalez
- BW Frazee
- CE Edmiston Jr
- Constance Schultsz
- EJ Feil
- ES Pan
- F Vandenesch
- FC Tenover
- G Lina
- GJ Moran
- H Sax
- Huynh Tan Son
- J Kluytmans
- J Rutishauser
- JA Lindsay
- James Campbell
- James Simmerman
- Jeremy Farrar
- Jodi Lindsay
- Joshua Cockfield
- K Boubaker
- Le Dieu Linh
- Le Hoang Son
- Le Quoc Thinh
- Le Thanh Hai
- Le Truong Giang
- Le Van Phung
- Le Van Tuan
- LG Miller
- LY Hsu
- Matthew Baylis
- MC Enright
- Megan Counahan
- MM Dinges
- Ngo Thi Hoa
- Nguyen Dac Tho
- Nguyen The Dung
- Nguyen Thi Kim Tien
- Nguyen Thi Minh Phuong
- Nguyen Tran Chinh
- Nguyen Van Vinh Chau
- P Chongtrakool
- PA Simon
- Phan Van Nghiem
- Richard Brown
- S Bassetti
- S Boyle-Vavra
- S Bratu
- S Jarraud
- SK Fridkin
- SV Kazakova
- T Baba
- Tang Chi Thuong
- TL Bannerman
- To Song Diep
- Tran Tinh Hien
- W Zhou
- XW Huijsdens
- XX Ma
- Y Gillet
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2007
- Field of study
Background: Infections with community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) are emerging
worldwide. We investigated an outbreak of severe CA-MRSA infections in children following out-patient vaccination.
Methods and Findings: We carried out a field investigation after adverse events following immunization (AEFI) were reported. We reviewed the clinical data from all cases. S. aureus recovered from skin infections and from nasal and throat swabs were analyzed by pulse-field gel electrophoresis, multi locus sequence typing, PCR and microarray. In May 2006, nine children presented with AEFI, ranging from fatal toxic shock syndrome, necrotizing soft tissue infection, purulent abscesses, to fever
with rash. All had received a vaccination injection in different health centres in one District of Ho Chi Minh City. Eight children had been vaccinated by the same health care worker (HCW). Deficiencies in vaccine quality, storage practices, or preparation and delivery were not found. Infection control practices were insufficient. CA-MRSA was cultured in four children and from nasal and throat swabs from the HCW. Strains from children and HCW were indistinguishable. All carried the Panton-Valentine leukocidine (PVL), the staphylococcal enterotoxin B gene, the gene complex for staphylococcal-cassette-chromosome mec type V, and were sequence type 59. Strain HCM3A is epidemiologically unrelated to a strain of ST59 prevalent in the USA, althoughthey belong to the same lineage.
Conclusions. We describe an outbreak of infections with CA-MRSA in children, transmitted by an asymptomatic colonized HCW during immunization injection. Consistent adherence to injection practice guidelines is needed to prevent CA-MRSA transmission in both in- and outpatient settings
The XXL survey: first results and future
- Author
- Adami C
- Alis S
- Altieri B
- Ascaso B
- Baran N
- Barnes D
- Benoist C
- Birkinshaw M
- Bongiorno A
- Bremer M
- Brun AL
- Butler A
- Cappi A
- Caretta C
- Ceja MER
- Chiappetti L
- Ciliegi P
- Clerc N
- Corasaniti PS
- Coupon J
- Delhaize J
- Delvecchio I
- Democles J
- Desai S
- Devriendt J
- Donahue M
- Dubois Y
- Durret F
- Eckert D
- Elyiv A
- Ettori S
- Evrard A
- Faccioli L
- Farahi A
- Ferrari C
- Fevre J-PL
- Forman W
- Fotopoulou S
- Franca FL
- Gastaldello F
- Georgantopoulos I
- Giles P
- Guglielmo V
- Horellou C
- Huynh M
- Iovino A
- Ithana M
- Jarvis M
- Jerlin N
- Johnston-Hollitt M
- Jones C
- Kalfountzou E
- Kay S
- Kilbinger M
- Koulouridis E
- Lavoie S
- Lidman C
- Lieu M
- Mantz A
- Marulli F
- Maughan B
- Maurogordato S
- McCarthy IG
- McGee S
- Melin J-B
- Melnyk O
- Miyazaki S
- Moscardini L
- Muzzin A
- Novak M
- Okabe N
- Pacaud F
- Paltani S
- Petris MD
- Piconcelli E
- Pierre M
- Plionis M
- Poggianti B
- Pomarede D
- Pompei E
- Ponman T
- Ranalli P
- Rapetti D
- Raychaudhury S
- Reiprich T
- Rettura A
- Ricci F
- Ricci M
- Ridl J
- Risaliti G
- Rottgering H
- Sadibekova T
- Sahlén M
- Sauvageot J-L
- Schimd C
- Sereno M
- Smith GP
- Smolcic V
- Snowden S
- Surdej J
- Takizawa M
- Thomas P
- Truong N
- Tsirou M
- Umetsu K
- Valageas P
- Valotti A
- Valtchanov I
- Veropalumbo A
- Vignali C
- Willis J
- Publication venue
- 'Wiley'
- Publication date
- 01/01/2017
- Field of study
The XXL survey currently covers two 25 sq. deg. patches with XMM observations of ~10ks. We summarise the scientific results associated with the first release of the XXL data set, that occurred mid 2016. We review several arguments for increasing the survey depth to 40 ks during the next decade of XMM operations. X-ray (z1 cluster density. It will eventually constitute a reference study and an ideal calibration field for the upcoming eROSITA and Euclid missions
African-specific improvement of a polygenic hazard score for age at diagnosis of prostate cancer
- Author
- Aldrich M.
- Andreassen O.A.
- Bensen J.T.
- Blanchet P.
- Blot W.J.
- Brureau L.
- Bush W.S.
- Cancel-Tassin G.
- Crawford D.C.
- Cullen J.C.
- Cussenot O.
- Dale A.M.
- Drake B.F.
- Eeles R.A.
- Fan C.C.
- Fontham E.T.H.
- Fowke J.
- Goodman P.J.
- Hu J.J.
- Huynh-Le M.-P.
- John E.M.
- Karunamuni R.A.
- Kibel A.S.
- Kote-Jarai Z.
- Leach R.J.
- Lin H.-Y.
- Lophatananon A.
- Menegaux F.
- Mills I.G.
- Mohler J.L.
- Muir K.
- Multigner L.
- Parent M.-É.
- Park J.Y.
- Petrovics G.
- Romana M.
- Sanderson M.
- Seibert T.M.
- Srivastava S.
- Tangen C.M.
- Taylor J.A.
- The PRACTICAL Consortium
- Thompson I.M., Jr.
- Thompson W.
- Truong T.
- UKGPCS Collaborators
- Zheng W.
- Publication venue
- John Wiley and Sons Inc
- Publication date
- 01/01/2021
- Field of study
Polygenic hazard score (PHS) models are associated with age at diagnosis of prostate cancer. Our model developed in Europeans (PHS46) showed reduced performance in men with African genetic ancestry. We used a cross-validated search to identify single nucleotide polymorphisms (SNPs) that might improve performance in this population. Anonymized genotypic data were obtained from the PRACTICAL consortium for 6253 men with African genetic ancestry. Ten iterations of a 10-fold cross-validation search were conducted to select SNPs that would be included in the final PHS46+African model. The coefficients of PHS46+African were estimated in a Cox proportional hazards framework using age at diagnosis as the dependent variable and PHS46, and selected SNPs as predictors. The performance of PHS46 and PHS46+African was compared using the same cross-validated approach. Three SNPs (rs76229939, rs74421890 and rs5013678) were selected for inclusion in PHS46+African. All three SNPs are located on chromosome 8q24. PHS46+African showed substantial improvements in all performance metrics measured, including a 75% increase in the relative hazard of those in the upper 20% compared to the bottom 20% (2.47-4.34) and a 20% reduction in the relative hazard of those in the bottom 20% compared to the middle 40% (0.65-0.53). In conclusion, we identified three SNPs that substantially improved the association of PHS46 with age at diagnosis of prostate cancer in men with African genetic ancestry to levels comparable to Europeans
Use of anticoagulants and antiplatelet agents in stable outpatients with coronary artery disease and atrial fibrillation. International CLARIFY registry
- Author
- A. L. R. Ng
- Abardia Oliva F. J.
- Abdel Malak S.
- Abdel Wahab H.
- Abdul Kareem B. B.
- Abdul Manap H.
- Abdul Rahim A. A.
- Abdulkader F.
- Abdulla A. H. K.
- AbdulWahab M. Z.
- Abduvalieva V.
- Abele S.
- Aboyans V.
- Abreu P. E.
- Adam-Blanpain M.
- Adamaszek K.
- Adamczyk-Kot D.
- Adamkiewicz-Piejko A.
- Adda M.
- Aftab A.
- Agrawal A.
- Aguiar C.
- Ahuad Guerrero A.
- Ahuja R.
- Ai F.
- Aimouch N.
- Aiyegbayo O.
- Ajani A.
- Akbar M.
- Aksyutina N.
- Al Dhanki M.
- Al Ghool S.
- Al Kandari F.
- Al Lawati A.
- Al Mahmeed W.
- Al Radaideh G.
- Al Rashdan I.
- Al Sousi A.
- Al Suwaidi J.
- Al Tamimi F.
- Al Wahshi Y.
- Al Yazeedi J.
- Al Zaibag M.
- Al-Baker H.
- Al-Faleh H.
- Al-Hersi A.
- Al-Khalidi B.
- Al-Shamiri M.
- Al-Zaibag M.
- Alam A.
- Alanazy M.
- Alanbaei M.
- Albero Martinez V.
- Alberto Ramirez Reyes H.
- Albuquerque A.
- Alcaravela J.
- Alcocer Gamba M.
- Alegret Colomer J. M.
- Alegria Ezquerra E.
- Alekseenko V.
- Alekseeva T.
- Alexanderson E.
- Alexopoulos I.
- Alford K.
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- Allcock A.
- Almeida Fernandez C. A.
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- Altmann U.
- Alvarenga Recalde N.
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- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2015
- Field of study
Lawson Criterion for Ignition Exceeded in an Inertial Fusion Experiment
- Author
- Abu-Shawareb H
- Acree R
- Adams J
- Adams P
- Addis B
- Aden R
- Adrian P
- Afeyan B
- Aggleton M
- Aghaian L
- Aguirre A
- Aikens D
- Akre J
- Albert F
- Albrecht M
- Albright B
- Albritton J
- Alcala J
- Alday C
- Alessi D
- Alexander N
- Alfonso J
- Alfonso N
- Alger E
- Ali S
- Ali Z
- Alley W
- Amala P
- Amendt P
- Amick P
- Ammula S
- Amorin C
- Ampleford D
- Anderson R
- Anklam T
- Antipa N
- Appelbe B
- Aracne-Ruddle C
- Araya E
- Arend M
- Arnold P
- Arnold T
- Asay J
- Atherton L
- Atkinson D
- Atkinson R
- Auerbach J
- Austin B
- Auyang L
- Awwal A
- Ayers J
- Ayers S
- Ayers T
- Azevedo S
- Bachmann B
- Back C
- Bae J
- Bailey D
- Bailey J
- Baisden T
- Baker K
- Baldis H
- Barber D
- Barberis M
- Barker D
- Barnes A
- Barnes C
- Barrios M
- Barty C
- Bass I
- Batha S
- Baxamusa S
- Bazan G
- Beagle J
- Beale R
- Beck B
- Beck J
- Bedzyk M
- Beeler R
- Behrendt W
- Belk L
- Bell P
- Belyaev M
- Benage J
- Benedetti L
- Benedict L
- Bennett G
- Berger R
- Bernat T
- Bernstein L
- Berry B
- Bertolini L
- Berzak Hopkins L
- Besenbruch G
- Betcher J
- Bettenhausen R
- Betti R
- Bezzerides B
- Bhandarkar S
- Bickel R
- Biener J
- Biesiada T
- Bigelow K
- Bigelow-Granillo J
- Bigman V
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- Publication venue
- Publication date
- 01/01/2022
- Field of study
Lawson criterion for ignition exceeded in an inertial fusion experiment
- Author
- Abu-Shawareb H
- Acree R
- Adams J
- Adams P
- Addis B
- Aden R
- Adrian P
- Afeyan BB
- Aggleton M
- Aghaian L
- Aguirre A
- Aikens D
- Akre J
- Albert F
- Albrecht M
- Albright BJ
- Albritton J
- Alcala J
- Alday C
- Alessi DA
- Alexander N
- Alfonso J
- Alfonso N
- Alger E
- Ali SJ
- Ali ZA
- Alley WE
- Amala P
- Amendt PA
- Amick P
- Ammula S
- Amorin C
- Ampleford DJ
- Anderson RW
- Anklam T
- Antipa N
- Appelbe B
- Aracne-Ruddle C
- Araya E
- Arend M
- Arnold P
- Arnold T
- Asay J
- Atherton LJ
- Atkinson D
- Atkinson R
- Auerbach JM
- Austin B
- Auyang L
- Awwal AS
- Ayers J
- Ayers S
- Ayers T
- Azevedo S
- Bachmann B
- Back CA
- Bae J
- Bailey DS
- Bailey J
- Baisden T
- Baker KL
- Baldis H
- Barber D
- Barberis M
- Barker D
- Barnes A
- Barnes CW
- Barrios MA
- Barty C
- Bass I
- Batha SH
- Baxamusa SH
- Bazan G
- Beagle JK
- Beale R
- Beck BR
- Beck JB
- Bedzyk M
- Beeler RG
- Beeler RG
- Behrendt W
- Belk L
- Bell P
- Belyaev M
- Benage JF
- Benedetti LR
- Benedict LX
- Bennett G
- Berger R
- Bernat T
- Bernstein LA
- Berry B
- Bertolini L
- Berzak Hopkins L
- Besenbruch G
- Betcher J
- Bettenhausen R
- Betti R
- Bezzerides B
- Bhandarkar SD
- Bickel R
- Biener J
- Biesiada T
- Bigelow K
- Bigelow-Granillo J
- Bigman V
- Bionta RM
- Birge NW
- Bitter M
- Black AC
- Bleile R
- Bleuel DL
- Bliss E
- Bliss E
- Blue B
- Boehly T
- Boehm K
- Boley CD
- Bonanno R
- Bond EJ
- Bond T
- Bonino MJ
- Borden M
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- Zylstra AB
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 06/07/2022
- Field of study
For more than half a century, researchers around the world have been engaged in attempts to achieve fusion ignition as a proof of principle of various fusion concepts. Following the Lawson criterion, an ignited plasma is one where the fusion heating power is high enough to overcome all the physical processes that cool the fusion plasma, creating a positive thermodynamic feedback loop with rapidly increasing temperature. In inertially confined fusion, ignition is a state where the fusion plasma can begin "burn propagation" into surrounding cold fuel, enabling the possibility of high energy gain. While "scientific breakeven" (i.e., unity target gain) has not yet been achieved (here target gain is 0.72, 1.37 MJ of fusion for 1.92 MJ of laser energy), this Letter reports the first controlled fusion experiment, using laser indirect drive, on the National Ignition Facility to produce capsule gain (here 5.8) and reach ignition by nine different formulations of the Lawson criterion
Global, regional, and national comparative risk assessment of 84 behavioural, environmental and occupational, and metabolic risks or clusters of risks for 195 countries and territories, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017
- Author
- Abate Degu
- Abate Degu
- Abate Kalkidan Hassell
- Abate Kalkidan Hassell
- Abbafati Cristiana
- Abbafati Cristiana
- Abbasi Nooshin
- Abbasi Nooshin
- Abbastabar Hedayat
- Abbastabar Hedayat
- Abd-Allah Foad
- Abd-Allah Foad
- Abdela Jemal
- Abdela Jemal
- Abdelalim Ahmed
- Abdelalim Ahmed
- Abdollahpour Ibrahim
- Abdollahpour Ibrahim
- Abdulkader Rizwan Suliankatchi
- Abdulkader Rizwan Suliankatchi
- Abebe Molla
- Abebe Molla
- Abebe Zegeye
- Abebe Zegeye
- Abera Semaw F.
- Abera Semaw F.
- Abil Olifan Zewdie
- Abil Olifan Zewdie
- Abraha Haftom Niguse
- Abraha Haftom Niguse
- Abrham Aklilu Roba
- Abrham Aklilu Roba
- Abu-Raddad Laith Jamal
- Abu-Raddad Laith Jamal
- Abu-Rmeileh Niveen M. E.
- Abu-Rmeileh Niveen M. E.
- Accrombessi Manfred Mario Kokou
- Accrombessi Manfred Mario Kokou
- Acharya Dilaram
- Acharya Dilaram
- Acharya Pawan
- Acharya Pawan
- Adamu Abdu A.
- Adamu Abdu A.
- Adane Akikw Awoke
- Adane Akikw Awoke
- Adebayo Oladimeji M.
- Adebayo Oladimeji M.
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- Ahmadi Mehdi
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- Ahmed Muktar Beshir
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- Khan Gulfaraz
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- Skirbekk Vegard
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- Tavakkoli Mohammad
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- Taveira Nuno
- Tehrani-Banihashemi Arash
- Tehrani-Banihashemi Arash
- Tekalign Tigist Gashaw
- Tekalign Tigist Gashaw
- Tekelemedhin Shishay Wandey
- Tekelemedhin Shishay Wandey
- Tekle Merhawi Gebremedhin
- Tekle Merhawi Gebremedhin
- Temesgen Habtamu
- Temesgen Habtamu
- Temsah Mohamad-Rani
- Temsah Mohamad-Rani
- Temsah Omar
- Temsah Omar
- Terkawi Abdullah Sulieman
- Terkawi Abdullah Sulieman
- Tessema Belay
- Tessema Belay
- Teweldemedhin Mebrahtu
- Teweldemedhin Mebrahtu
- Thankappan Kavumpurathu Raman
- Thankappan Kavumpurathu Raman
- Theis Andrew
- Theis Andrew
- Thirunavukkarasu Sathish
- Thirunavukkarasu Sathish
- Thomas Hannah J.
- Thomas Hannah J.
- Thomas Matthew Lloyd
- Thomas Matthew Lloyd
- Thomas Nihal
- Thomas Nihal
- Thou Maigeng
- Thou Maigeng
- Thurston George D.
- Thurston George D.
- Tilahun Binyam
- Tilahun Binyam
- Tillmana Taavi
- Tillmana Taavi
- To Quyen G.
- To Quyen G.
- Tobollik Myriarn
- Tobollik Myriarn
- Tonelli Marcello
- Tonelli Marcello
- Topor-Madry Roman
- Topor-Madry Roman
- Torre Anna E.
- Torre Anna E.
- Tortajada-Girbes Miguel
- Tortajada-Girbes Miguel
- Touvier Mathilde
- Touvier Mathilde
- Tovani-Palone Marcos Roberto
- Tovani-Palone Marcos Roberto
- Towbin Jeffrey A.
- Towbin Jeffrey A.
- Tran Bach Xuan
- Tran Bach Xuan
- Tran Khanh Baca
- Tran Khanh Baca
- Truelsen Thomas Clement
- Truelsen Thomas Clement
- Tsadik Afewerki Gebremeskel
- Tsadik Afewerki Gebremeskel
- Tuzcu E. Murat
- Tuzcu E. Murat
- Tymeson Hayley D.
- Tymeson Hayley D.
- Tyrovolas Stefanos
- Tyrovolas Stefanos
- Ukwaja Kingsley N.
- Ukwaja Kingsley N.
- Ullah Irfan
- Ullah Irfan
- Updike Rachel L.
- Updike Rachel L.
- Usman Muhammad Shariq
- Usman Muhammad Shariq
- Uthman Olalekan A.
- Uthman Olalekan A.
- Vaduganathan Mutblab
- Vaduganathan Mutblab
- Vaezi Afsane
- Vaezi Afsane
- Valdez Pascual R.
- Valdez Pascual R.
- Van Donkelaar Aaron
- Van Donkelaar Aaron
- Varavikova Elena
- Varavikova Elena
- Varughese Santosh
- Varughese Santosh
- Vasankari Tommi Juhani
- Vasankari Tommi Juhani
- Vbsoughi Kia
- Vbsoughi Kia
- Venkateswaran Vidhya
- Venkateswaran Vidhya
- Venketasubramanian Narayanaswamy
- Venketasubramanian Narayanaswamy
- Villafaina Santos
- Villafaina Santos
- Violante Francesco S.
- Violante Francesco S.
- Vladimirov Sergey Konstantinovitch
- Vladimirov Sergey Konstantinovitch
- Vlassov Vasily
- Vlassov Vasily
- Vollset Stein Emil
- Vollset Stein Emil
- Vos Theo
- Vos Theo
- Vu Giang Thu
- Vu Giang Thu
- Vujcic Isidora S.
- Vujcic Isidora S.
- Wagnew Fasil Shiferaw
- Wagnew Fasil Shiferaw
- Waheed Yasir
- Waheed Yasir
- Waller Stephen G.
- Waller Stephen G.
- Walson Judd L.
- Walson Judd L.
- Wang Yafeng
- Wang Yafeng
- Wang Yanping
- Wang Yanping
- Wang Yuan-Pang
- Wang Yuan-Pang
- Weiderpass Elisabete
- Weiderpass Elisabete
- Weiknah Adhena Ayaliew
- Weiknah Adhena Ayaliew
- Weintraub Robert G.
- Weintraub Robert G.
- Weldegebreal Fitsum
- Weldegebreal Fitsum
- Werdecker Andrea
- Werdecker Andrea
- West J. Jason
- West J. Jason
- Westerman Ronny
- Westerman Ronny
- Whiteford Harvey A.
- Whiteford Harvey A.
- Widecka Justyna
- Widecka Justyna
- Wijeratne Tissa
- Wijeratne Tissa
- Winkler Andrea Sylvia
- Winkler Andrea Sylvia
- Wiyeh Alison B.
- Wiyeh Alison B.
- Wiysonge Charles Shey
- Wiysonge Charles Shey
- Wolfe Charles D. A.
- Wolfe Charles D. A.
- Wong Tien Yin
- Wong Tien Yin
- Wu Shoaling
- Wu Shoaling
- Xavier Denis
- Xavier Denis
- Xu Gelin
- Xu Gelin
- Yadgir Simon
- Yadgir Simon
- Yadollahpour Ali
- Yadollahpour Ali
- Yamada Tomohide
- Yamada Tomohide
- Yan Lijing L.
- Yan Lijing L.
- Yano Yuichiro
- Yano Yuichiro
- Yaseri Mehdi
- Yaseri Mehdi
- Yasin Jemal Yasin
- Yasin Jemal Yasin
- Yeshanely Alex
- Yeshanely Alex
- Yimer Ebrahim M.
- Yimer Ebrahim M.
- Yip Paul
- Yip Paul
- Yisma Engida
- Yisma Engida
- Yonemoto Naohiro
- Yonemoto Naohiro
- Yoon Seok-Jun
- Yoon Seok-Jun
- Yotebieng Marcel
- Yotebieng Marcel
- Younis Mustafa Z.
- Younis Mustafa Z.
- Yousefifard Mahmoud
- Yousefifard Mahmoud
- Yu Chuanhua
- Yu Chuanhua
- Zaidi Zoubida
- Zaidi Zoubida
- Zamani Mohammad
- Zamani Mohammad
- Zavala-Arciniega Luis
- Zavala-Arciniega Luis
- Zhang Anthony Lin
- Zhang Anthony Lin
- Zhang Hao
- Zhang Hao
- Zhang Kai
- Zhang Kai
- Zimsen Stephanie M.
- Zimsen Stephanie M.
- Zodpey Sanjay
- Zodpey Sanjay
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2018
- Field of study
Background
The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2017 comparative risk assessment (CRA) is a comprehensive approach to risk factor quantification that offers a useful tool for synthesising evidence on risks and risk–outcome associations. With each annual GBD study, we update the GBD CRA to incorporate improved methods, new risks and risk–outcome pairs, and new data on risk exposure levels and risk–outcome associations.
Methods
We used the CRA framework developed for previous iterations of GBD to estimate levels and trends in exposure, attributable deaths, and attributable disability-adjusted life-years (DALYs), by age group, sex, year, and location for 84 behavioural, environmental and occupational, and metabolic risks or groups of risks from 1990 to 2017. This study included 476 risk–outcome pairs that met the GBD study criteria for convincing or probable evidence of causation. We extracted relative risk and exposure estimates from 46 749 randomised controlled trials, cohort studies, household surveys, census data, satellite data, and other sources. We used statistical models to pool data, adjust for bias, and incorporate covariates. Using the counterfactual scenario of theoretical minimum risk exposure level (TMREL), we estimated the portion of deaths and DALYs that could be attributed to a given risk. We explored the relationship between development and risk exposure by modelling the relationship between the Socio-demographic Index (SDI) and risk-weighted exposure prevalence and estimated expected levels of exposure and risk-attributable burden by SDI. Finally, we explored temporal changes in risk-attributable DALYs by decomposing those changes into six main component drivers of change as follows: (1) population growth; (2) changes in population age structures; (3) changes in exposure to environmental and occupational risks; (4) changes in exposure to behavioural risks; (5) changes in exposure to metabolic risks; and (6) changes due to all other factors, approximated as the risk-deleted death and DALY rates, where the risk-deleted rate is the rate that would be observed had we reduced the exposure levels to the TMREL for all risk factors included in GBD 2017.
Findings
In 2017, 34·1 million (95% uncertainty interval [UI] 33·3–35·0) deaths and 1·21 billion (1·14–1·28) DALYs were attributable to GBD risk factors. Globally, 61·0% (59·6–62·4) of deaths and 48·3% (46·3–50·2) of DALYs were attributed to the GBD 2017 risk factors. When ranked by risk-attributable DALYs, high systolic blood pressure (SBP) was the leading risk factor, accounting for 10·4 million (9·39–11·5) deaths and 218 million (198–237) DALYs, followed by smoking (7·10 million [6·83–7·37] deaths and 182 million [173–193] DALYs), high fasting plasma glucose (6·53 million [5·23–8·23] deaths and 171 million [144–201] DALYs), high body-mass index (BMI; 4·72 million [2·99–6·70] deaths and 148 million [98·6–202] DALYs), and short gestation for birthweight (1·43 million [1·36–1·51] deaths and 139 million [131–147] DALYs). In total, risk-attributable DALYs declined by 4·9% (3·3–6·5) between 2007 and 2017. In the absence of demographic changes (ie, population growth and ageing), changes in risk exposure and risk-deleted DALYs would have led to a 23·5% decline in DALYs during that period. Conversely, in the absence of changes in risk exposure and risk-deleted DALYs, demographic changes would have led to an 18·6% increase in DALYs during that period. The ratios of observed risk exposure levels to exposure levels expected based on SDI (O/E ratios) increased globally for unsafe drinking water and household air pollution between 1990 and 2017. This result suggests that development is occurring more rapidly than are changes in the underlying risk structure in a population. Conversely, nearly universal declines in O/E ratios for smoking and alcohol use indicate that, for a given SDI, exposure to these risks is declining. In 2017, the leading Level 4 risk factor for age-standardised DALY rates was high SBP in four super-regions: central Europe, eastern Europe, and central Asia; north Africa and Middle East; south Asia; and southeast Asia, east Asia, and Oceania. The leading risk factor in the high-income super-region was smoking, in Latin America and Caribbean was high BMI, and in sub-Saharan Africa was unsafe sex. O/E ratios for unsafe sex in sub-Saharan Africa were notably high, and those for alcohol use in north Africa and the Middle East were notably low.
Interpretation
By quantifying levels and trends in exposures to risk factors and the resulting disease burden, this assessment offers insight into where past policy and programme efforts might have been successful and highlights current priorities for public health action. Decreases in behavioural, environmental, and occupational risks have largely offset the effects of population growth and ageing, in relation to trends in absolute burden. Conversely, the combination of increasing metabolic risks and population ageing will probably continue to drive the increasing trends in non-communicable diseases at the global level, which presents both a public health challenge and opportunity. We see considerable spatiotemporal heterogeneity in levels of risk exposure and risk-attributable burden. Although levels of development underlie some of this heterogeneity, O/E ratios show risks for which countries are overperforming or underperforming relative to their level of development. As such, these ratios provide a benchmarking tool to help to focus local decision making. Our findings reinforce the importance of both risk exposure monitoring and epidemiological research to assess causal connections between risks and health outcomes, and they highlight the usefulness of the GBD study in synthesising data to draw comprehensive and robust conclusions that help to inform good policy and strategic health planning
Erratum: Global, regional, and national comparative risk assessment of 84 behavioural, environmental and occupational, and metabolic risks or clusters of risks for 195 countries and territories, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017
- Author
- Abate Degu
- Abate Kalkidan Hassen
- Abbafati Cristiana
- Abbasi Nooshin
- Abbastabar Hedayat
- Abd-Allah Foad
- Abdela Jemal
- Abdelalim Ahmed
- Abdollahpour Ibrahim
- Abdulkader Rizwan Suliankatchi
- Abebe Molla
- Abebe Zegeye
- Abera Semaw Ferede
- Abil Olifan Zewdie
- Abraha Haftom Niguse
- Abu Raddad Laith J
- Abun Rmeileh Niveen M.E
- Accrombessi Manfred Mario Kokou
- Acharya Dilaram
- Acharya Pawan
- Adamu Abdu Abdullahi
- Adane Akilew Awoke
- Adebayo Oladimeji
- Adedoyin Rufus Adesoji
- Adekanmbi Victor T
- Ademi Zanfina
- Adetokunboh Olatunji O
- Adib Mina G
- Admasie Amha
- Adsuar Jose C
- Afanvi Kossivi Agbélénko
- Afarideh Mohsen
- Afshin Ashkan
- Agarwal Gina
- Aggarwal Anju
- Aghayan Sargis A
- Agrawal Anurag
- Agrawal Sutapa
- Ahmadi Moghadam M
- Ahmadi Alireza
- Ahmadieh Hamid
- Ahmed Muktar Beshir
- Aichour Amani Nidhal
- Aichour Ibtihel
- Aichour Miloud Taki Eddine
- Akbari Mohammad Esmaeil
- Akinyemiju Tomi F.
- Akseer Nadia
- Al Aly Ziyad
- Al Eyadhy Ayman A
- Al Mekhlafi H. M
- Alahdab Fares
- Alam Khurshid
- Alam Samiah
- Alam Tahiya
- Alashi Alaa
- Alavian Seyed Moayed
- Alene Kefyalew Addis
- Ali Komal
- Ali Syed Mustafa
- Alijanzadeh Mehran
- Alizadeh Navaei Reza
- Aljunid Syed Mohamed
- Alkerwi Ala'a
- Alla F
- Alsharif Ubai
- Altirkawi Khalid A
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- Amare Azmeraw T
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- Asayesh Hamid
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- Avokpaho Euripide Frinel G.Arthur
- Awasthi Ashish
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- Ayer Rakesh
- Ayuk Tambe Betrand
- Azzopardi Peter S
- Babazadeh Arefeh
- Badali Hamid
- Badawi Alaa
- Balakrishnan Kalpana
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- Beghi Ettore
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- Denova Gutiérrez Edgar
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- Dervenis Nikolaos Alemayehu
- Deshpande Aniruddha
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- Devasahayam Jesudas Christopher
- DeVeber Gabrielle Aline
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- Gebre Abadi Kahsu
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- Gebremichael Teklu Gebrehiwo
- Gelano Tilayie Feto
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- Geramo Yilma Chisha Dea
- Gething Peter William
- Gezae Kebede Embaye
- Ghadimi Reza
- Ghadiri Keyghobad
- Ghasemi Falavarjani Khalil
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- Ghimire Mamata
- Ghosh Rakesh
- Ghoshal Aloke Gopal
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- Gill Paramjit Singh
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- Jeemon Panniyammakal
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- Kesavachandran Chandrasekharan Nair
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- Kissimova Skarbek Katarzyna
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- Levi Miriam
- Lewycka Sonia
- Li Shanshan
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- Liang Juan
- Liang Xiaofeng
- Liao Yu
- Liben Misgan Legesse
- Lim Lee Ling
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- Liu Shiwei
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- Logroscino Giancarlo C
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- Lotufo Paulo Andrade
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- West James Jason
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- Winkler Andrea Sylvia
- Wiyeh Alison Beriliy
- Wiysonge Charles Shey
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- Wu Shouling
- Xavier Denis
- Xu Gelin
- Yadgir Simon
- Yadollahpour Ali
- Yahyazadeh Jabbari Seyed Hossein
- Yamada Tomohide
- Yan Lijing L
- Yano Yuichirou
- Yaseri Mehdi
- Yasin Yasin Jemal
- Yeshaneh Alex
- Yimer Ebrahim M
- Yip Paul S.F
- Yisma Engida
- Yonemoto Naohiro
- Yoon Seokjun
- Yotebieng Marcel
- Younis Mustafa Z.“Mike”
- Yousefifard Mahmoud
- Yu Chuanhua
- Zaidi Zoubida
- Zaman Sojib Bin
- Zamani Mohammad
- Zavala-Arciniega Luis
- Zhang Anthonylin
- Zhang Hao
- Zhang Kai
- Zhou Maigeng
- Zimsen Stephanie R.M
- Zodpey Sanjay P
- Øverland Simon
- Šantrić Milićević Milena M.M
- Šekerija Mario
- Publication venue
- 'Elsevier BV'
- Publication date
- 28/06/2019
- Field of study
Interpretation: By quantifying levels and trends in exposures to risk factors and the resulting disease burden, this assessment offers insight into where past policy and programme efforts might have been successful and highlights current priorities for public health action. Decreases in behavioural, environmental, and occupational risks have largely offset the effects of population growth and ageing, in relation to trends in absolute burden. Conversely, the combination of increasing metabolic risks and population ageing will probably continue to drive the increasing trends in non-communicable diseases at the global level, which presents both a public health challenge and opportunity. We see considerable spatiotemporal heterogeneity in levels of risk exposure and risk-attributable burden. Although levels of development underlie some of this heterogeneity, O/E ratios show risks for which countries are overperforming or underperforming relative to their level of development. As such, these ratios provide a benchmarking tool to help to focus local decision making. Our findings reinforce the importance of both risk exposure monitoring and epidemiological research to assess causal connections between risks and health outcomes, and they highlight the usefulness of the GBD study in synthesising data to draw comprehensive and robust conclusions that help to inform good policy and strategic health planning
Recommended from our members
Global age-sex-specific mortality, life expectancy, and population estimates in 204 countries and territories and 811 subnational locations, 1950–2021, and the impact of the COVID-19 pandemic: a comprehensive demographic analysis for the Global Burden of Disease Study 2021
- Author
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- Publication venue
- Elsevier BV
- Publication date
- 11/03/2024
- Field of study
Background
Estimates of demographic metrics are crucial to assess levels and trends of population health outcomes. The profound impact of the COVID-19 pandemic on populations worldwide has underscored the need for timely estimates to understand this unprecedented event within the context of long-term population health trends. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2021 provides new demographic estimates for 204 countries and territories and 811 additional subnational locations from 1950 to 2021, with a particular emphasis on changes in mortality and life expectancy that occurred during the 2020–21 COVID-19 pandemic period.
Methods
22 223 data sources from vital registration, sample registration, surveys, censuses, and other sources were used to estimate mortality, with a subset of these sources used exclusively to estimate excess mortality due to the COVID-19 pandemic. 2026 data sources were used for population estimation. Additional sources were used to estimate migration; the effects of the HIV epidemic; and demographic discontinuities due to conflicts, famines, natural disasters, and pandemics, which are used as inputs for estimating mortality and population. Spatiotemporal Gaussian process regression (ST-GPR) was used to generate under-5 mortality rates, which synthesised 30 763 location-years of vital registration and sample registration data, 1365 surveys and censuses, and 80 other sources. ST-GPR was also used to estimate adult mortality (between ages 15 and 59 years) based on information from 31 642 location-years of vital registration and sample registration data, 355 surveys and censuses, and 24 other sources. Estimates of child and adult mortality rates were then used to generate life tables with a relational model life table system. For countries with large HIV epidemics, life tables were adjusted using independent estimates of HIV-specific mortality generated via an epidemiological analysis of HIV prevalence surveys, antenatal clinic serosurveillance, and other data sources. Excess mortality due to the COVID-19 pandemic in 2020 and 2021 was determined by subtracting observed all-cause mortality (adjusted for late registration and mortality anomalies) from the mortality expected in the absence of the pandemic. Expected mortality was calculated based on historical trends using an ensemble of models. In location-years where all-cause mortality data were unavailable, we estimated excess mortality rates using a regression model with covariates pertaining to the pandemic. Population size was computed using a Bayesian hierarchical cohort component model. Life expectancy was calculated using age-specific mortality rates and standard demographic methods. Uncertainty intervals (UIs) were calculated for every metric using the 25th and 975th ordered values from a 1000-draw posterior distribution.
Findings
Global all-cause mortality followed two distinct patterns over the study period: age-standardised mortality rates declined between 1950 and 2019 (a 62·8% [95% UI 60·5–65·1] decline), and increased during the COVID-19 pandemic period (2020–21; 5·1% [0·9–9·6] increase). In contrast with the overall reverse in mortality trends during the pandemic period, child mortality continued to decline, with 4·66 million (3·98–5·50) global deaths in children younger than 5 years in 2021 compared with 5·21 million (4·50–6·01) in 2019. An estimated 131 million (126–137) people died globally from all causes in 2020 and 2021 combined, of which 15·9 million (14·7–17·2) were due to the COVID-19 pandemic (measured by excess mortality, which includes deaths directly due to SARS-CoV-2 infection and those indirectly due to other social, economic, or behavioural changes associated with the pandemic). Excess mortality rates exceeded 150 deaths per 100 000 population during at least one year of the pandemic in 80 countries and territories, whereas 20 nations had a negative excess mortality rate in 2020 or 2021, indicating that all-cause mortality in these countries was lower during the pandemic than expected based on historical trends. Between 1950 and 2021, global life expectancy at birth increased by 22·7 years (20·8–24·8), from 49·0 years (46·7–51·3) to 71·7 years (70·9–72·5). Global life expectancy at birth declined by 1·6 years (1·0–2·2) between 2019 and 2021, reversing historical trends. An increase in life expectancy was only observed in 32 (15·7%) of 204 countries and territories between 2019 and 2021. The global population reached 7·89 billion (7·67–8·13) people in 2021, by which time 56 of 204 countries and territories had peaked and subsequently populations have declined. The largest proportion of population growth between 2020 and 2021 was in sub-Saharan Africa (39·5% [28·4–52·7]) and south Asia (26·3% [9·0–44·7]). From 2000 to 2021, the ratio of the population aged 65 years and older to the population aged younger than 15 years increased in 188 (92·2%) of 204 nations.
Interpretation
Global adult mortality rates markedly increased during the COVID-19 pandemic in 2020 and 2021, reversing past decreasing trends, while child mortality rates continued to decline, albeit more slowly than in earlier years. Although COVID-19 had a substantial impact on many demographic indicators during the first 2 years of the pandemic, overall global health progress over the 72 years evaluated has been profound, with considerable improvements in mortality and life expectancy. Additionally, we observed a deceleration of global population growth since 2017, despite steady or increasing growth in lower-income countries, combined with a continued global shift of population age structures towards older ages. These demographic changes will likely present future challenges to health systems, economies, and societies. The comprehensive demographic estimates reported here will enable researchers, policy makers, health practitioners, and other key stakeholders to better understand and address the profound changes that have occurred in the global health landscape following the first 2 years of the COVID-19 pandemic, and longer-term trends beyond the pandemic
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