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Record W2559863651 · doi:10.1186/s13223-016-0164-7

AllerGen’s 8th research conference

2016· article· en· W2559863651 on OpenAlexafffundvenueabout
Marie‐Claire Arrieta, Andrea Arevalos, Leah T. Stiemsma, Marta E. Chico, Carlos Sandoval, Minglian Jin, Jens Walter, Philip J. Cooper, B. Brett Finlay, Émilie Bernatchez, Matthew J. Gold, Anick Langlois, Pascale Blais‐Lecours, Caroline Duchaine, David Marsolais, Kelly M. McNagny, Marie‐Renée Blanchet, Jordan Brubacher, Bimal Chhetri, Kelly Sabaliauskas, Kate Bassil, Jeff Kwong, Frances Coates, Tim K. Takaro, Angela Chow, Gregory E. Miller, Edith Chen, Piush J. Mandhane, Stuart E. Turvey, Susan J. Elliott, Allan B. Becker, Padmaja Subbarao, Malcolm R. Sears, Anita L. Kozyrskyj, Zihang Lu, Susan Balkovec, Krzysztof Kowalik, Per Gustafsson, Félix Ratjen, Rachel D. Edgar, Nicole R. Bush, Julie L. MacIssac, Thomas Boyce, Michael S. Kobor, Melanie Emmerson, Bingqing Shen, Theo J. Moraes, Sofianne Gabrielli, Ann E. Clarke, Harley Eisman, Judy Morris, Lawrence Joseph, Sebastien LaVieille, Moshe Ben‐Shoshan, Sumaiya A. Islam, Christof Brückmann, Vanessa Nieratschker, Kyla C. Jamieson, David Proud, Cynthia Kanagaratham, Pierre Camateros, František Kopřiva, Jennifer Henri, Marián Hajdúch, Danuta Radzioch, Liane J. Kang, Petya Koleva, Catherine J. Field, Tedd Konya, James A. Scott, Theodore Konya, Meghan B. Azad, Jeff Brook, David S. Guttman, Manjeet Kumari, Sarah L. Bridgman, Mon Hnin Tun, Rupasri Mandal, David S. Wishart, Amy Huei‐Yi Lee, Jeff Xia, Erin E. Gill, Bob Hancock, Danay Maestre, Darren Sutherland, Jeremy A. Hirota, Olga M. Pena, Meaghan J. Jones, Julia L. MacIsaac, William H. Dow, Luis Rosero‐Bixby, David H. Rehkopf, Takeshi Morimoto, Steven G. Smith, John-Paul Oliveria, Suzanne Beaudin, Abbey Schlatman, Karen Howie, Caitlin Obminski, Graeme Nusca, Roma Sehmi, Gail M. Gauvreau, Paul M. O’Byrne, Michelle L. North, Cheng Peng, Marco Sánchez-Guerra, Hyang‐Min Byun, Anne K. Ellis, Andrea Baccarelli, Joseph O. Okeme, Suman Dhal, Aman Saini, Miriam L. Diamond, Christopher J. Olesovsky, Brittany Salter, Paige Lacy, Michael J. O’Sullivan, Chan Y. Park, Jeffrey J. Fredberg, Anne‐Marie Lauzon, James G. Martin, Min Hyung Ryu, Neeloffer Mookherjee, Elinor Simons, Diana L. Lefebvre, David Dai, Amrit Singh, Casey P. Shannon, Young Woong Kim, Chen Xi Yang, J. Mark FitzGerald, Louis‐Philippe Boulet, Scott J. Tebbutt, Gurpreet K. Singhera, S. JasemineYang, Delbert R. Dorscheid, Hasantha Sinnock, Susan Goruk, Hamid Tavakoli, Larry D. Lynd, Mohsen Sadatsafavi, Mark W. Tenn, Jenny Thiele, Daniel E. Adams, Lisa M. Steacy, Bahar Torabi, Sarah De Schryver, Duncan Lejtenyi, Ingrid Baerg, Edmond S. Chan, Bruce Mazer, Maxwell Tran, Wei Dai, Wendy Lou, Radha Chari, Edward M. Conway, Helen Neighbour, Mark Larché

Bibliographic record

VenueAllergy Asthma and Clinical Immunology · 2016
Typearticle
Languageen
FieldMedicine
TopicAsthma and respiratory diseases
Canadian institutionsCanadian Respiratory Research NetworkEnvironment and Climate Change CanadaOccupational Cancer Research CentreSt. Paul's HospitalHospital for Sick ChildrenMcMaster UniversityChildren's Hospital Research Institute of ManitobaUniversity of WaterlooCanadian Nuclear LaboratoriesThe Scarborough HospitalPublic Health OntarioUniversity of TorontoMcGill UniversityHôpital du Sacré-Cœur de MontréalMcGill University Health CentreInstitute for Clinical Evaluative SciencesSimon Fraser UniversityUniversity of CalgaryCentre for Advancing Health OutcomesPrincess Margaret Cancer CentreKingston General HospitalQueen's UniversityHealth CanadaToronto Public HealthUniversity of ManitobaThe Metabolomics Innovation CentreInstitut universitaire de cardiologie et de pneumologie de QuébecBC Children's HospitalPrevention of Organ FailureUniversité LavalUniversity of AlbertaChild and Family Research InstituteCanada's Michael Smith Genome Sciences CentreUniversity of British Columbia
FundersCanadian Institutes of Health ResearchUniversity of California, San FranciscoNational Institute of Mental HealthBerkeley Population Center, University of California BerkeleyHospital for Sick ChildrenUniversity of TorontoUniversity of AlbertaNational Institute on Minority Health and Health DisparitiesVancouver Coastal Health Research InstituteBritish Columbia Lung AssociationInstitute for Clinical Evaluative SciencesNatural Sciences and Engineering Research Council of CanadaUniversity of California BerkeleyFondation Brain CanadaManitoba Medical Service FoundationFonds de Recherche du Québec - SantéMitacsHealth CanadaReseau canadien de recherche respiratoireAstraZeneca CanadaUniversity of ManitobaAstraZeneca
KeywordsAllergenMedicineImmunologyAllergy

Abstract

fetched live from OpenAlex

Background: Asthma is the most prevalent chronic disease among children and affects 235 million people worldwide [1].Although the incidence of asthma in South America is among the highest worldwide, underlying causes and disease phenotypes are poorly defined and may differ to developed countries.Recent evidence in mice [2] and human [3] has identified a 'critical window' early in life where the effects of gut microbial changes (dysbiosis) are most influential in immune development and experimental asthma.Given the differences in gut microbiota between North and South American populations, we aimed to validate our previous work in a microbially-different human population.Methods: We compared the gut microbiota of 97 infants from the coastal community Las Esmeraldas, Ecuador at 3 months of age by 16S sequencing (V4 region) Illumina MiSeq.Subjects were grouped into atopic-wheezers (n = 27) and controls (n = 70) based on a skin prick test and wheezing history at 1 year of age.An exact logistic regression model was developed to evaluate the risk associated with the AW group according to specific clinical and epidemiological metadata.Metagenomes were predicted from 16S rRNA OTU data using PIC-RUSt, and categorized by function using KEGG Orthology.The concentration of fecal short chain fatty acids (SCFA) was determined by gas chromatography.Results: Atopy and wheezing at 1 year of age was significantly associated with asthma diagnosis at 5 years (OR 17.8), birth by C-section (OR 3.1), potable water at home (OR 2.7) and in utero exposure to antibiotics (OR 2.9).This phenotype was also significantly associated with eosinophil concentration at 2 and 5 years (p < 0.05), number of episodes of respiratory infections (p < 0.01), maternal load with Trichuris trichiura during pregnancy (p < 0.05), and inversely associated with the number of diarrheal episodes by 1 year of age (p < 0.05).Similar to what we had previously found in Canadian babies, atopic-wheezing Ecuadorian babies also exhibit gut microbial dysbiosis at 3 months of age.However, the microbial alterations were different and more pronounced in Ecuadorian babies.Predicted metagenomic analysis showed significant differences in genes involved in carbohydrate and taurine metabolism.Fecal acetate was significantly reduced in atopic wheezers.Ongoing experiments will determine if differences in eukaryome are also associated with asthma risk in this population. Conclusions:This study further supports the importance of the microbiota during the first 100 days of life, although the characteristics of the microbial dysbiosis and epidemiological associations depend on geographical location.Reduced fecal acetate as a common feature in both populations suggests that different microbial alterations may have similar metabolic outcomes.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.003
metaresearch head score (Gemma)0.004
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesInsufficient payload (model declined to judge)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: Not applicable
GenreCandidate signal: Other · Consensus signal: Other
Teacher disagreement score0.391
Threshold uncertainty score0.869

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0030.004
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0020.001
Science and technology studies0.0010.001
Scholarly communication0.0060.002
Open science0.0020.003
Research integrity0.0030.003
Insufficient payload (model declined to judge)0.3910.240

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.083
GPT teacher head0.407
Teacher spread0.324 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

Study designNot applicable
Domainnot available
GenreOther

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2016
Admission routes4
Has abstractyes

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