9 research outputs found
On-farm evaluation of integrated nutrient and pest management in Cicer arietinum L.
- Publication venue
- Update Publishing House
- Publication date
- 01/05/2012
- Field of study
Chickpea (Cicer arietinum L.) is the world’s third most important pulse crop. In chickpea, wilt caused by Fusarium oxysporum f. sp. ciceri is one of the major production constraints. On-farm demonstration on use of Trichoderma viride, PSB and Rhizobium was conducted during rabi (Nov-Jan) 2006 in Machanapally village, Ranga Reddy district, AP, India. At harvest, data on wilt incidence yield and related parameters were recorded. In T1, where seeds were treated with PSB+Rhizobium+T. viride followed by soil application of T. viride+PSB+Rhizobium after 30 DAS (mixed with 200 kg of FYM), wilt incidence was 4.5% and yield was 0.995 t.ha-1. In T2, where carbendazim was applied as seed treatment followed by the soil application of recommended doses of NPK, wilt incidence was 8.3% with a yield of 1.2 t.ha-1. In T3, where seeds were treated as in T1 and NPK was applied to soil as in T2, wilt incidence was 3.3% and crop yield was 1.13 t. ha-1. Highest plant dry mass (25.5 g.plant-1) and number of effective nodules (6.3 plant-1) were recorded in T3. To conclude, integrated nutrient and disease management is an ideal approach for chickpea cultivation
The global burden of cancer attributable to risk factors, 2010-19: a systematic analysis for the Global Burden of Disease Study 2019
- Author
- Aali A
- Ab Khan M
- Abbas Q
- Abbasi B
- Abbasi-Kangevari M
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- Abbastabar H
- Abd-Elsalam S
- Abdelmasseh M
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- Abdoli G
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- Abolhassani H
- Absalan A
- Abtew YD
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- Publication venue
- Publication date
- 20/08/2022
- Field of study
Combination of searches for heavy spin-1 resonances using 139 fb−1 of proton-proton collision data at s = 13 TeV with the ATLAS detector
- Author
- Aad G
- Aakvaag E
- Abbott B
- Abeling K
- Abicht NJ
- Abidi SH
- Aboelela M
- Aboulhorma A
- Abramowicz H
- Abreu H
- Abulaiti Y
- Acharya BS
- Ackermann A
- Adam Bourdarios C
- Adamczyk L
- Addepalli SV
- Addison MJ
- Adelman J
- Adiguzel A
- Adye T
- Affolder AA
- Afik Y
- Agaras MN
- Agarwala J
- Aggarwal A
- Agheorghiesei C
- Ahmad A
- Ahmadov F
- Ahmed WS
- Ahuja S
- Ai X
- Aielli G
- Aikot A
- Ait Tamlihat M
- Aitbenchikh B
- Aizenberg I
- Akbiyik M
- Akimov AV
- Akiyama D
- Akolkar NN
- Aktas S
- Al Khoury K
- Alberghi GL
- Albert J
- Albicocco P
- Albouy GL
- Alderweireldt S
- Alegria ZL
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexopoulos T
- Alfonsi F
- Algren M
- Alhroob M
- Ali B
- Ali HMJ
- Ali S
- Alibocus SW
- Aliev M
- Alimonti G
- Alkakhi W
- Allaire C
- Allbrooke BMM
- Allen JF
- Allendes Flores CA
- Allport PP
- Aloisio A
- Alonso F
- Alpigiani C
- Alvarez Estevez M
- Alvarez Fernandez A
- Alves Cardoso M
- Alviggi MG
- Aly M
- Amaral Coutinho Y
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- Zhao Y
- Zhao Z
- Zhao Z
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- Zimine NI
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- Ziolkowski M
- Zoccoli A
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- Zorbas TG
- Zormpa O
- Zou W
- Zwalinski L
- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- Springer Nature
- Publication date
- 19/04/2024
- Field of study
A combination of searches for new heavy spin-1 resonances decaying into different pairings of W, Z, or Higgs bosons, as well as directly into leptons or quarks, is presented. The data sample used corresponds to 139 fb−1 of proton-proton collisions at
= 13 TeV collected during 2015–2018 with the ATLAS detector at the CERN Large Hadron Collider. Analyses selecting quark pairs (qq, bb,
, and tb) or third-generation leptons (τν and ττ) are included in this kind of combination for the first time. A simplified model predicting a spin-1 heavy vector-boson triplet is used. Cross-section limits are set at the 95% confidence level and are compared with predictions for the benchmark model. These limits are also expressed in terms of constraints on couplings of the heavy vector-boson triplet to quarks, leptons, and the Higgs boson. The complementarity of the various analyses increases the sensitivity to new physics, and the resulting constraints are stronger than those from any individual analysis considered. The data exclude a heavy vector-boson triplet with mass below 5.8 TeV in a weakly coupled scenario, below 4.4 TeV in a strongly coupled scenario, and up to 1.5 TeV in the case of production via vector-boson fusion
Global mortality associated with 33 bacterial pathogens in 2019: a systematic analysis for the Global Burden of Disease Study 2019
- Author
- Aali A
- Abate SM
- Abbasi-Kangevari M
- Abbasi-Kangevari Z
- Abd-Elsalam S
- Abdulkader RS
- Abebe G
- Abedi A
- Abhari AP
- Abidi H
- Aboagye RG
- Absalan A
- Acuna JM
- Adane TD
- Addo IY
- Adegboye OA
- Adnan M
- Adnani QES
- Afzal MS
- Afzal S
- Aghdam ZB
- Aguilar GR
- Ahinkorah BO
- Ahmad A
- Ahmad AR
- Ahmad R
- Ahmad S
- Ahmad S
- Ahmadi S
- Ahmed A
- Ahmed H
- Ahmed JQ
- Ajami M
- Aji B
- Akbarzadeh-Khiavi M
- Akunna CJ
- Al Hamad H
- Al-Aly Z
- Alahdab F
- Aldeyab MA
- Aleman A
- Alhalaiqa FAN
- Alhassan RK
- Ali BA
- Ali HA
- Ali L
- Ali SS
- Alimohamadi Y
- Alipour V
- Alizadeh A
- Aljunid SM
- Allel K
- Almustanyir S
- Ameyaw EK
- Amit AML
- Anandavelane N
- Ancuceanu R
- Andrei CL
- Andrei T
- Anggraini D
- Ansar A
- Anyasodor AE
- Arabloo J
- Aravkin AY
- Areda D
- Aripov T
- Artamonov AA
- Arulappan J
- Aruleba RT
- Asaduzzaman M
- Ashraf T
- Athari SS
- Atlaw D
- Attia S
- Ausloos M
- Avval AH
- Awoke T
- Ayana TM
- Azadnajafabad S
- Badar M
- Badiye AD
- Baghcheghi N
- Bagherieh S
- Baig AA
- Bain LE
- Bali AO
- Banerjee I
- Barac A
- Bardhan M
- Barone-Adesi F
- Barqawi HJ
- Barrow A
- Baskaran P
- Basu S
- Batiha A-MM
- Bedi N
- Belete MA
- Belgaumi UI
- Bender RG
- Bhandari B
- Bhandari D
- Bhardwaj P
- Bhaskar S
- Bhattacharyya K
- Bhattarai S
- Bin Zaman S
- Bitaraf S
- Buonsenso D
- Butt ZA
- Cai J
- Calina D
- Camargos P
- Camera LA
- Cardenas R
- Cevik M
- Chadwick J
- Charan J
- Chaurasia A
- Ching PR
- Choudhari SG
- Chowdhury EK
- Chowdhury FR
- Chu D-T
- Chukwu IS
- Dadras O
- Dagnaw FT
- Dai X
- Darshan BB
- Das Gupta R
- Das S
- Dastiridou A
- De Sa ACMGN
- De Sa ATN
- Debela SA
- Demisse FW
- Demissie S
- Dereje D
- Derese M
- Desai HD
- Dessalegn FN
- Dessalegni SAA
- Desye B
- Dhaduk K
- Dhimal M
- Dhingra S
- Diao N
- Diaz D
- Djalalinia S
- Dodangeh M
- Dolecek C
- Dongarwar D
- Dora BT
- Dorostkar F
- Dos Santos FLC
- Dsouza HL
- Dubljanin E
- Dunachie SJ
- Durojaiye OC
- Edinur HA
- Ejigu HB
- Ekholuenetale M
- Ekundayo TC
- El-Abid H
- Elhadi M
- Elmonem MA
- Emami A
- Enyew DB
- Erkhembayar R
- Eshrati B
- Etaee F
- Fagbamigbe AF
- Falahi S
- Fallahzadeh A
- Faraon EJA
- Fatehizadeh A
- Fekadu G
- Fernandes JC
- Ferrari A
- Fetensa G
- Filip I
- Fischer F
- Foroutan M
- Gaal PA
- Gadanya MA
- Gaidhane AM
- Ganesan B
- Gebrehiwot M
- Ghanbari R
- Ghashghaee A
- Gholamrezanezhad A
- Gholizadeh A
- Golechha M
- Goleij P
- Golinelli D
- Goodridge A
- Gray AP
- Gunawardane DA
- Guo Y
- Gupta S
- Gupta VB
- Gupta VK
- Guta A
- Habibzadeh P
- Halwani R
- Han C
- Hanif A
- Hannan MA
- Harapan H
- Hassan S
- Hassankhani H
- Hay S
- Hayat K
- Hayoon AG
- Heibati B
- Heidari G
- Heidari M
- Heidari-Soureshjani R
- Herteliu C
- Heyi DZ
- Hezam K
- Hoogar P
- Horita N
- Hossain MM
- Hosseinzadeh M
- Hostiuc M
- Hostiuc S
- Hoveidamanesh S
- Huang J
- Hussain S
- Hussein NR
- Ibitoye SE
- Ikuta KS
- Il Shin J
- Ilesanmi OS
- Ilic IM
- Ilic MD
- Imam MT
- Immurana M
- Inbaraj LR
- Iradukunda A
- Isfahani HM
- Ismail NE
- Iwu CCD
- Iwu CJ
- Jabbari SHY
- Jafari AA
- Jakovljevic M
- Jamshidi E
- Javaheri T
- Javanmardi F
- Javidnia J
- Jayapal SK
- Jayarajah U
- Jebai R
- Jha RP
- Joo T
- Joseph N
- Joukar F
- Jozwiak JJ
- Kacimi SEO
- Kadashetti V
- Kafil HS
- Kalankesh LR
- Kalhor R
- Kamal VK
- Kandel H
- Kandel SN
- Kapoor N
- Karkhah S
- Kashani HRK
- Kassa BG
- Kassebaum NJ
- Katoto PD
- Keykhaei M
- Khajuria H
- Khan A
- Khan IA
- Khan M
- Khan MAB
- Khan MN
- Khaneghah AM
- Khatatbeh MM
- Khater MM
- Khubchandani J
- Kim H
- Kim MS
- Kimokoti RW
- Kissoon N
- Kochhar S
- Kompani F
- Kosen S
- Kostova NM
- Koul PA
- Krishan K
- Krishnamoorthy V
- Kulkarni V
- Kumar N
- Kurmi OP
- Kuttikkattu A
- Kyu HH
- Lal DK
- Lam J
- Landires I
- Lasrado S
- Laxminarayana SLK
- Lee S-W
- Lenzi J
- Lewycka S
- Li S
- Lim SS
- Liu W
- Lodha R
- Loftus MJ
- Lohiya A
- Lopez FK
- Lorenzovici L
- Lotfi M
- Mahesh PA
- Mahmoodpoor A
- Mahmoud MA
- Mahmoudi R
- Majeed A
- Majidpoor J
- Makki A
- Mamo GA
- Manla Y
- Martorell M
- Matei CN
- McManigal B
- Mehrotra R
- Melese A
- Mendoza-Cano O
- Menezes RG
- Mentis A-FA
- Merin LJ
- Mestrovic T
- Micha G
- Michalek IM
- Mir SA
- Mirghafourvand M
- Mirmoeeni S
- Mirrakhimov EM
- Mirza-Aghazadeh-Attari M
- Misganaw A
- Misganaw AS
- Misra S
- Mohammadi E
- Mohammadi M
- Mohammadian-Hafshejani A
- Mohammed S
- Mohan S
- Mohseni M
- Mokdad AH
- Momtazmanesh S
- Monasta L
- Moore CE
- Moradi M
- Morrison SD
- Motaghinejad M
- Mousavi-Aghdas SA
- Mubarik S
- Mulita F
- Mulu GBB
- Munro SB
- Murray CJL
- Muthupandian S
- Naghavi M
- Nair TS
- Naqvi AA
- Narang H
- Nasab EM
- Natto ZS
- Naveed M
- Nayak BP
- Naz S
- Negoi I
- Nejadghaderi SA
- Ngwa CH
- Niazi RK
- Noroozi N
- Nour MG
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- Nutor JJ
- Nzoputam CI
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- Oancea B
- Obaidur RM
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- Okekunle AP
- Okonji OC
- Olagunju AT
- Olusanya BO
- Omer E
- Otstavnov N
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- Padubidri JR
- Pakshir K
- Palicz T
- Pana A
- Pardhan S
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- Parekh U
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- Pathak A
- Paudel R
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- Pawar S
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- Pensato U
- Pepito VCF
- Pereira M
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- Perico N
- Petcu I-R
- Piracha ZZ
- Podder I
- Pokhrel N
- Poluru R
- Postma MJ
- Pourtaheri N
- Prashant A
- Qattea I
- Quintanilla BPA
- Rabiee M
- Rabiee N
- Radfar A
- Raeghi S
- Rafiei S
- Raghav PR
- Rahbarnia L
- Rahimi-Movaghar V
- Rahman M
- Rahman MA
- Rahmani AM
- Rahmanian V
- Ram P
- Ranjha MMAN
- Rao SJ
- Rashid TA
- Rashidi M-M
- Rasul A
- Ratan ZA
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- Rawassizadeh R
- Razeghinia MS
- Redwan EMM
- Regasa MT
- Remuzzi G
- Reta MA
- Rezaei N
- Rezapour A
- Riad A
- Ripon RK
- Rudd KE
- Saddik B
- Sadeghian S
- Saeed U
- Safaei M
- Safary A
- Safi SZ
- Sahebazzamani M
- Sahebkar A
- Sahoo H
- Salahi S
- Salahi S
- Salari H
- Salehi S
- Samy AM
- Sanadgol N
- Sankararaman S
- Sanmarchi F
- Sarabi MM
- Sartorius B
- Sathian B
- Sawhney M
- Saya GK
- Senthilkumaran S
- Seylani A
- Shah PA
- Shaikh MA
- Shaker E
- Shakhmardanov MZ
- Sharara F
- Sharew MM
- Sharifi-Razavi A
- Sharma P
- Sheikhi RA
- Sheikhy A
- Shetty PH
- Shigematsu M
- Shirzad-Aski H
- Shivakumar KM
- Shobeiri P
- Shorofi SA
- Shrestha S
- Sibhat MM
- Sidemo NB
- Sikder MK
- Silva LMLR
- Singh JA
- Singh P
- Singh S
- Siraj MS
- Siwal SS
- Skryabin VY
- Skryabina AA
- Socea B
- Solomon DD
- Song Y
- Sreeramareddy CT
- Suleman M
- Sultana S
- Swetschinski LR
- Szocska M
- Tabatabaeizadeh S-A
- Tabish M
- Tahbaz SV
- Taheri M
- Taki E
- Tan K-K
- Tandukar S
- Tat NY
- Tat VY
- Tefera BN
- Tefera YM
- Temesgen G
- Temsah M-H
- Tharwat S
- Thiyagarajan A
- Tleyjeh II
- Toroudi HP
- Troeger CE
- Umapathi KK
- Upadhyay E
- Valdez PR
- Van den Eynde J
- Van Doorn HR
- Vaziri S
- Verras G-I
- Viswanathan H
- Vo B
- Waris A
- Wassie GT
- Weaver ND
- Wickramasinghe ND
- Wool EE
- Yaghoubi S
- Yahya GATY
- Yigit A
- Yigit V
- Yon DK
- Yonemoto N
- Zahir M
- Zaman BA
- Zangiabadian M
- Zare I
- Zastrozhin MS
- Zhang Z-J
- Zheng P
- Zhong C
- Zoladl M
- Zumla A
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2022
- Field of study
Background Reducing the burden of death due to infection is an urgent global public health priority. Previous studies have estimated the number of deaths associated with drug-resistant infections and sepsis and found that infections remain a leading cause of death globally. Understanding the global burden of common bacterial pathogens (both susceptible and resistant to antimicrobials) is essential to identify the greatest threats to public health. To our knowledge, this is the first study to present global comprehensive estimates of deaths associated with 33 bacterial pathogens across 11 major infectious syndromes. Methods We estimated deaths associated with 33 bacterial genera or species across 11 infectious syndromes in 2019 using methods from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019, in addition to a subset of the input data described in the Global Burden of Antimicrobial Resistance 2019 study. This study included 343 million individual records or isolates covering 11 361 study-location-years. We used three modelling steps to estimate the number of deaths associated with each pathogen: deaths in which infection had a role, the fraction of deaths due to infection that are attributable to a given infectious syndrome, and the fraction of deaths due to an infectious syndrome that are attributable to a given pathogen. Estimates were produced for all ages and for males and females across 204 countries and territories in 2019. 95% uncertainty intervals (UIs) were calculated for final estimates of deaths and infections associated with the 33 bacterial pathogens following standard GBD methods by taking the 2·5th and 97·5th percentiles across 1000 posterior draws for each quantity of interest. Findings From an estimated 13·7 million (95% UI 10·9–17·1) infection-related deaths in 2019, there were 7·7 million deaths (5·7–10·2) associated with the 33 bacterial pathogens (both resistant and susceptible to antimicrobials) across the 11 infectious syndromes estimated in this study. We estimated deaths associated with the 33 bacterial pathogens to comprise 13·6% (10·2–18·1) of all global deaths and 56·2% (52·1–60·1) of all sepsis-related deaths in 2019. Five leading pathogens—Staphylococcus aureus, Escherichia coli, Streptococcus pneumoniae, Klebsiella pneumoniae, and Pseudomonas aeruginosa—were responsible for 54·9% (52·9–56·9) of deaths among the investigated bacteria. The deadliest infectious syndromes and pathogens varied by location and age. The age-standardised mortality rate associated with these bacterial pathogens was highest in the sub-Saharan Africa super-region, with 230 deaths (185–285) per 100 000 population, and lowest in the high-income super-region, with 52·2 deaths (37·4–71·5) per 100 000 population. S aureus was the leading bacterial cause of death in 135 countries and was also associated with the most deaths in individuals older than 15 years, globally. Among children younger than 5 years, S pneumoniae was the pathogen associated with the most deaths. In 2019, more than 6 million deaths occurred as a result of three bacterial infectious syndromes, with lower respiratory infections and bloodstream infections each causing more than 2 million deaths and peritoneal and intra-abdominal infections causing more than 1 million deaths. Interpretation The 33 bacterial pathogens that we investigated in this study are a substantial source of health loss globally, with considerable variation in their distribution across infectious syndromes and locations. Compared with GBD Level 3 underlying causes of death, deaths associated with these bacteria would rank as the second leading cause of death globally in 2019; hence, they should be considered an urgent priority for intervention within the global health community. Strategies to address the burden of bacterial infections include infection prevention, optimised use of antibiotics, improved capacity for microbiological analysis, vaccine development, and improved and more pervasive use of available vaccines. These estimates can be used to help set priorities for vaccine need, demand, and development
Age-sex differences in the global burden of lower respiratory infections and risk factors, 1990-2019: results from the Global Burden of Disease Study 2019
- Author
- Abate SM
- Abdelmasseh M
- Abdoli A
- Abdoli G
- Abedi A
- Abedi V
- Abegaz TM
- Abidi H
- Aboagye RG
- Abolhassani H
- Abtew YD
- Abu-Gharbieh E
- Abu-Zaid A
- Adamu K
- Addo IY
- Adegboye OA
- Adnan M
- Adnani QES
- Afzal MS
- Afzal S
- Ahinkorah BO
- Ahmad A
- Ahmad AR
- Ahmad S
- Ahmadi A
- Ahmadi S
- Ahmed H
- Ahmed JQ
- Akbarzadeh-Khiavi M
- Al Hamad H
- Al-Jumaily A
- Al-Raddadi RM
- Al-Rifai RHH
- Albano L
- Albertson SB
- Aldeyab MA
- Alemu BM
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- Publication venue
- Publication date
- 01/01/2022
- Field of study
Background The global burden of lower respiratory infections (LRIs) and corresponding risk factors in children older than 5 years and adults has not been studied as comprehensively as it has been in children younger than 5 years. We assessed the burden and trends of LRIs and risk factors across a groups by sex, for 204 countries and territories.Methods In this analysis of data for the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019, we used dinician-diagnosed pneumonia or bronchiolitis as our case definition for LRIs. We included International Classification of Diseases 9th edition codes 079.6, 466-469, 470.0, 480-482.8, 483.0-483.9, 484.1-484.2, 484.6-484.7, and 487-489 and International Classification of Diseases 10th edition codes A48.1, A70, B97.4 B97.6, 109-115.8, J16 J16.9, J20-121.9, J91.0, P23.0 P23.4, and U04 U04.9. We used the Cause of Death Ensemble modelling strategy to analyse 23109 site-years of vital r *stration data, 825 site-years of sample vital registration data, 1766 site-years of verbal autopsy data, and 681 site-years of mortality surveillance data. We used DisMod-MR 2.1, a Bayesian metaregression tool, to analyse age sex-specific incidence and prevalence data identified via systematic reviews of the literature, population-based survey data, and daims and inpatient data. Additio y, we estimated age sex-specific LRI mortality that is attributable to the independent effects of 14 risk factors.Findings Globally, in 2019, we estimated that there were 257 million (95% uncertainty interval [UI] 240-275) LRI incident episodes in males and 232 million (217-248) in females. In the same year, LRIs accounted for 1.30 million (95% UI 1.18-1.42) male deaths and 1.20 million (1.07-1.33) female deaths. Age-standardised incidence and mortality rates were 1.17 times (95% UI 1.16-1.18) and 1.31 times (95% UI 1.23-1.41) greater in males than in fe es in 2019. Between 1990 and 2019, LRI incidence and mortality rates declined at different rates across age groups and an increase in LRI episodes and deaths was estimated among all adult age groups, with males aged 70 years and older having the highest increase in LRI episodes (126.0% [95% UI 121.4-131.1]) and deaths (100.0% [83.4-115.9]). During the same period, LRI episodes and deaths in children younger than 15 years were estimated to have decreased, and the greatest dedine was observed for LRI deaths in males younger than 5 years (-70.7% [-77.2 to 61.8]). The leading risk factors for LRI mortality varied across age groups and sex. More than half of global LRI deaths in children younger than 5 years were attributable to child wasting (population attributable fraction [PAF] 53.0% [95% UI 37.7-61.8] in males and 56.4% [40.7-65.1] in females), and more than a quarter of LRI deaths among those aged 5-14 years were attributable to household air pollution (PAF 26.0% [95% UI 16.6-35.5] for males and PAF 25.8% [16.3-35.4] for females). PAFs of male LRI deaths attributed to smoking were 20.4% (95% UI 15.4-25.2) in those aged 15-49 years, 305% (24.1-36. 9) in those aged 50-69 years, and 21.9% (16. 8-27. 3) in those aged 70 years and older. PAFs of female LRI deaths attributed to household air pollution were 21.1% (95% UI 14.5-27.9) in those aged 15-49 years and 18 " 2% (12.5-24.5) in those aged 50-69 years. For females aged 70 years and older, the leading risk factor, ambient particulate matter, was responsible for 11-7% (95% UI 8.2-15.8) of LRI deaths.Interpretation The patterns and progress in reducing the burden of LRIs and key risk factors for mortality varied across age groups and sexes. The progress seen in children you - than 5 years was dearly a result of targeted interventions, such as vaccination and reduction of exposure to risk factors. Similar interventions for other age groups could contribute to the achievement of multiple Sustainable Development Goals targets, induding promoting wellbeing at all ages and reducing health inequalities. Interventions, including addressing risk factors such as child wasting, smoking, ambient particulate matter pollution, and household air pollution, would prevent deaths and reduce health disparities.Copyright 2022 The Author(s). Published by Elsevier Ltd
The global burden of cancer attributable to risk factors, 2010-19: a systematic analysis for the Global Burden of Disease Study 2019
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- Publication venue
- 'Elsevier BV'
- Publication date
- 01/08/2022
- Field of study
Background Understanding the magnitude of cancer burden attributable to potentially modifiable risk factors is crucial for development of effective prevention and mitigation strategies. We analysed results from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019 to inform cancer control planning efforts globally. Methods The GBD 2019 comparative risk assessment framework was used to estimate cancer burden attributable to behavioural, environmental and occupational, and metabolic risk factors. A total of 82 risk–outcome pairs were included on the basis of the World Cancer Research Fund criteria. Estimated cancer deaths and disability-adjusted life-years (DALYs) in 2019 and change in these measures between 2010 and 2019 are presented. Findings Globally, in 2019, the risk factors included in this analysis accounted for 4·45 million (95% uncertainty interval 4·01–4·94) deaths and 105 million (95·0–116) DALYs for both sexes combined, representing 44·4% (41·3–48·4) of all cancer deaths and 42·0% (39·1–45·6) of all DALYs. There were 2·88 million (2·60–3·18) risk-attributable cancer deaths in males (50·6% [47·8–54·1] of all male cancer deaths) and 1·58 million (1·36–1·84) risk-attributable cancer deaths in females (36·3% [32·5–41·3] of all female cancer deaths). The leading risk factors at the most detailed level globally for risk-attributable cancer deaths and DALYs in 2019 for both sexes combined were smoking, followed by alcohol use and high BMI. Risk-attributable cancer burden varied by world region and Socio-demographic Index (SDI), with smoking, unsafe sex, and alcohol use being the three leading risk factors for risk-attributable cancer DALYs in low SDI locations in 2019, whereas DALYs in high SDI locations mirrored the top three global risk factor rankings. From 2010 to 2019, global risk-attributable cancer deaths increased by 20·4% (12·6–28·4) and DALYs by 16·8% (8·8–25·0), with the greatest percentage increase in metabolic risks (34·7% [27·9–42·8] and 33·3% [25·8–42·0]). Interpretation The leading risk factors contributing to global cancer burden in 2019 were behavioural, whereas metabolic risk factors saw the largest increases between 2010 and 2019. Reducing exposure to these modifiable risk factors would decrease cancer mortality and DALY rates worldwide, and policies should be tailored appropriately to local cancer risk factor burden. Funding Bill & Melinda Gates Foundation
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- Yacoob S
- Yamaguchi Y
- Yamashita E
- Yamauchi H
- Yamazaki T
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- Yao W-M
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- Yeh Y
- Yeletskikh I
- Yeo BK
- Yexley MR
- Yin P
- Yorita K
- Younas S
- Young C
- Young CJS
- Yu C
- Yu Y
- Yuan M
- Yuan R
- Yue L
- Zaazoua M
- Zabinski B
- Zaid E
- Zak ZK
- Zakareishvili T
- Zakharchuk N
- Zambito S
- Zamora Saa JA
- Zang J
- Zanzi D
- Zaplatilek O
- Zeitnitz C
- Zeng H
- Zeng JC
- Zenger DT
- Zenin O
- Zenz S
- Zerradi S
- Zerwas D
- Zhai M
- Zhang DF
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- Zhang X
- Zhang X
- Zhang Y
- Zhang Y
- Zhang Y
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- Zhang Z
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- Zhao T
- Zhao Y
- Zhao Z
- Zhao Z
- Zhemchugov A
- Zheng J
- Zheng K
- Zheng X
- Zheng Z
- Zhong D
- Zhou B
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- Zhou N
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- Zimine NI
- Zinsser J
- Ziolkowski M
- Zoccoli A
- Zoch K
- Zorbas TG
- Zormpa O
- Zou W
- Zwalinski L
- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- Journal of High Energy Physics
- Publication date
- 28/03/2024
- Field of study
Acknowledgements: We thank CERN for the very successful operation of the LHC, as well as the support staff from our institutions without whom ATLAS could not be operated efficiently. We acknowledge the support of ANPCyT, Argentina; YerPhI, Armenia; ARC, Australia; BMWFW and FWF, Austria; ANAS, Azerbaijan; CNPq and FAPESP, Brazil; NSERC, NRC and CFI, Canada; CERN; ANID, Chile; CAS, MOST and NSFC, China; Minciencias, Colombia; MEYS CR, Czech Republic; DNRF and DNSRC, Denmark; IN2P3-CNRS and CEA-DRF/IRFU, France; SRNSFG, Georgia; BMBF, HGF and MPG, Germany; GSRI, Greece; RGC and Hong Kong SAR, China; ISF and Benoziyo Center, Israel; INFN, Italy; MEXT and JSPS, Japan; CNRST, Morocco; NWO, Netherlands; RCN, Norway; MEiN, Poland; FCT, Portugal; MNE/IFA, Romania; MESTD, Serbia; MSSR, Slovakia; ARRS and MIZŠ, Slovenia; DSI/NRF, South Africa; MICINN, Spain; SRC and Wallenberg Foundation, Sweden; SERI, SNSF and Cantons of Bern and Geneva, Switzerland; MOST, Taipei; TENMAK, Türkiye; STFC, United Kingdom; DOE and NSF, United States of America. In addition, individual groups and members have received support from BCKDF, CANARIE, CRC and DRAC, Canada; PRIMUS 21/SCI/017 and UNCE SCI/013, Czech Republic; COST, ERC, ERDF, Horizon 2020, ICSC-NextGenerationEU and Marie Skłodowska-Curie Actions, European Union; Investissements d’Avenir Labex, Investissements d’Avenir Idex and ANR, France; DFG and AvH Foundation, Germany; Herakleitos, Thales and Aristeia programmes co-financed by EU-ESF and the Greek NSRF, Greece; BSF-NSF and MINERVA, Israel; Norwegian Financial Mechanism 2014-2021, Norway; NCN and NAWA, Poland; La Caixa Banking Foundation, CERCA Programme Generalitat de Catalunya and PROMETEO and GenT Programmes Generalitat Valenciana, Spain; Göran Gustafssons Stiftelse, Sweden; The Royal Society and Leverhulme Trust, United Kingdom. The crucial computing support from all WLCG partners is acknowledged gratefully, in particular from CERN, the ATLAS Tier-1 facilities at TRIUMF/SFU (Canada), NDGF (Denmark, Norway, Sweden), CC-IN2P3 (France), KIT/GridKA (Germany), INFN-CNAF (Italy), NL-T1 (Netherlands), PIC (Spain), RAL (U.K.) and BNL (U.S.A.), the Tier-2 facilities worldwide and large non-WLCG resource providers. Major contributors of computing resources are listed in ref. [143].Abstract
A search is conducted for new phenomena in events with a top quark pair and large missing transverse momentum, where the top quark pair is reconstructed in final states with one isolated electron or muon and multiple jets. The search is performed using the Large Hadron Collider proton-proton collision data sample at a centre-of-mass energy of s
s
= 13 TeV recorded by the ATLAS detector that corresponds to an integrated luminosity of 140 fb−1. An analysis based on neural network classifiers is optimised to search for directly produced pairs of supersymmetric partners of the top quark (stop), and to search for spin-0 mediators, produced in association with a pair of top quarks, that decay into dark-matter particles. In the stop search, the analysis is designed to target models in which the mass difference between the stop and the neutralino from the stop decay is close to the top quark mass. This new search is combined with previously published searches in final states with different lepton multiplicities. No significant excess above the Standard Model background is observed, and limits at 95% confidence level are set. Models with neutralinos with masses up to 570 GeV are excluded, while for small neutralino masses models are excluded for stop masses up to 1230 GeV. Scalar (pseudoscalar) dark matter mediator masses as large as 350 (370) GeV are excluded when the coupling strengths of the mediator to Standard Model and dark-matter particles are both set to one. At lower mediator masses, models with production cross-sections as small as 0.15 (0.16) times the nominal predictions are excluded. Results of this search are also used to set constraints on effective four-fermion contact interactions between top quarks and neutrinos.</jats:p
Search for new phenomena with top-quark pairs and large missing transverse momentum using 140 fb−1 of pp collision data at s = 13 TeV with the ATLAS detector
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- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- Springer Science and Business Media LLC
- Publication date
- 26/03/2024
- Field of study
Abstract
A search is conducted for new phenomena in events with a top quark pair and large missing transverse momentum, where the top quark pair is reconstructed in final states with one isolated electron or muon and multiple jets. The search is performed using the Large Hadron Collider proton-proton collision data sample at a centre-of-mass energy of s
s
= 13 TeV recorded by the ATLAS detector that corresponds to an integrated luminosity of 140 fb−1. An analysis based on neural network classifiers is optimised to search for directly produced pairs of supersymmetric partners of the top quark (stop), and to search for spin-0 mediators, produced in association with a pair of top quarks, that decay into dark-matter particles. In the stop search, the analysis is designed to target models in which the mass difference between the stop and the neutralino from the stop decay is close to the top quark mass. This new search is combined with previously published searches in final states with different lepton multiplicities. No significant excess above the Standard Model background is observed, and limits at 95% confidence level are set. Models with neutralinos with masses up to 570 GeV are excluded, while for small neutralino masses models are excluded for stop masses up to 1230 GeV. Scalar (pseudoscalar) dark matter mediator masses as large as 350 (370) GeV are excluded when the coupling strengths of the mediator to Standard Model and dark-matter particles are both set to one. At lower mediator masses, models with production cross-sections as small as 0.15 (0.16) times the nominal predictions are excluded. Results of this search are also used to set constraints on effective four-fermion contact interactions between top quarks and neutrinos.</jats:p
Recommended from our members
Combination of searches for heavy spin-1 resonances using 139 fb−1 of proton-proton collision data at s = 13 TeV with the ATLAS detector
- Author
- Aad G
- Aakvaag E
- Abbott B
- Abeling K
- Abicht NJ
- Abidi SH
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- Abramowicz H
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- Zhemchugov A
- Zheng J
- Zheng K
- Zheng X
- Zheng Z
- Zhong D
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- Zimine NI
- Zinsser J
- Ziolkowski M
- Zoccoli A
- Zoch K
- Zorbas TG
- Zormpa O
- Zou W
- Zwalinski L
- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- Journal of High Energy Physics
- Publication date
- 23/04/2024
- Field of study
Abstract
A combination of searches for new heavy spin-1 resonances decaying into different pairings of W, Z, or Higgs bosons, as well as directly into leptons or quarks, is presented. The data sample used corresponds to 139 fb−1 of proton-proton collisions at s
s
= 13 TeV collected during 2015–2018 with the ATLAS detector at the CERN Large Hadron Collider. Analyses selecting quark pairs (qq, bb, tt
t
t
¯
, and tb) or third-generation leptons (τν and ττ) are included in this kind of combination for the first time. A simplified model predicting a spin-1 heavy vector-boson triplet is used. Cross-section limits are set at the 95% confidence level and are compared with predictions for the benchmark model. These limits are also expressed in terms of constraints on couplings of the heavy vector-boson triplet to quarks, leptons, and the Higgs boson. The complementarity of the various analyses increases the sensitivity to new physics, and the resulting constraints are stronger than those from any individual analysis considered. The data exclude a heavy vector-boson triplet with mass below 5.8 TeV in a weakly coupled scenario, below 4.4 TeV in a strongly coupled scenario, and up to 1.5 TeV in the case of production via vector-boson fusion.</jats:p