9 research outputs found
Approaches in biotechnological applications of natural polymers
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- Publication venue
- 'American Institute of Mathematical Sciences (AIMS)'
- Publication date
- 01/01/2016
- Field of study
Natural polymers, such as gums and mucilage, are biocompatible, cheap, easily available and non-toxic materials of native origin. These polymers are increasingly preferred over synthetic materials for industrial applications due to their intrinsic properties, as well as they are considered alternative sources of raw materials since they present characteristics of sustainability, biodegradability and biosafety. As definition, gums and mucilages are polysaccharides or complex carbohydrates consisting of one or more monosaccharides or their derivatives linked in bewildering variety of linkages and structures. Natural gums are considered polysaccharides naturally occurring in varieties of plant seeds and exudates, tree or shrub exudates, seaweed extracts, fungi, bacteria, and animal sources. Water-soluble gums, also known as hydrocolloids, are considered exudates and are pathological products; therefore, they do not form a part of cell wall. On the other hand, mucilages are part of cell and physiological products. It is important to highlight that gums represent the largest amounts of polymer materials derived from plants. Gums have enormously large and broad applications in both food and non-food industries, being commonly used as thickening, binding, emulsifying, suspending, stabilizing agents and matrices for drug release in pharmaceutical and cosmetic industries. In the food industry, their gelling properties and the ability to mold edible films and coatings are extensively studied. The use of gums depends on the intrinsic properties that they provide, often at costs below those of synthetic polymers. For upgrading the value of gums, they are being processed into various forms, including the most recent nanomaterials, for various biotechnological applications. Thus, the main natural polymers including galactomannans, cellulose, chitin, agar, carrageenan, alginate, cashew gum, pectin and starch, in addition to the current researches about them are reviewed in this article.. }To the Conselho Nacional de Desenvolvimento Cientfíico e Tecnológico (CNPq) for fellowships (LCBBC and MGCC) and the Coordenação de Aperfeiçoamento de Pessoal de Nvíel Superior (CAPES) (PBSA). This study was supported by the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UID/BIO/04469/2013 unit, the Project RECI/BBB-EBI/0179/2012 (FCOMP-01-0124-FEDER-027462) and COMPETE 2020 (POCI-01-0145-FEDER-006684) (JAT)
Biological effects of extracts obtained from Stryphnodendron adstringens on Herpetomonas samuelpessoai
- Author
- Audi EA
- Benedito Prado Dias Filho
- Celso Vataru Nakamura
- Cleyton Eduardo Mendes de Toledo
- Endo EH
- Fabíola Barbieri Holetz
- Felfili JM
- Galvão AB
- Herzog-Soares JDA
- Holetz FB
- José Andrés Morgado-Díaz
- João Carlos Palazzo de Mello
- Lima JCS
- Mello JCP
- Mello JCP
- Morgado-Díaz JA
- Panizza S
- Rebecca MA
- Roitman C
- Roitman I
- Santos CAM
- Santos CS
- Santos CS
- Scalbert A
- Teixeira ML
- Thompson RS
- Toledo CEM
- Tânia Ueda-Nakamura
- Publication venue
- Instituto Oswaldo Cruz, Ministério da Saúde
- Publication date
- 01/07/2005
- Field of study
We report the effect of Stryphnodendron adstringens on the trypanosomatid Herpetomonas samuelpessoai. The parasites were grown at 28ºC in a chemically defined medium containing crude extract and fractions at concentrations from 100 to 5000 µg/ml obtained from S. adstringens. Concentrations of 500, 1000, 2500, and 5000 µg/ml both crude extract and semi-purified fraction progressively inhibited the protozoans' growth. At a concentration of 100 µg/ml, crude extract or a semi-purified (F3) fraction did not affect the growth of the protozoans. The F3-9 - F3-12 sub-fractions, at a concentration of 1000 µg/ml, also showed increased inhibitory activity on H. samuelpessoai. The IC50 of the crude extract and the F3 fraction were 538 and 634 µg/ml, respectively. Ultrastructural and enzymatic alterations in the trypanosomatids were also evaluated. H. samuelpessoai cultivated in the presence of IC50 crude extract showed considerable ultrastructural alterations, such as marked mitochondrial swelling with a large number of cristae and evident Golgi complex vesiculation, as observed by transmission electron microscopy. Cells exposed to 538 µg/ml of crude extract at 28ºC for 72 h, showed decreased activity of the enzyme succinate cytochrome c reductase, a typical mitochondrion marker, as compared to untreated cell
Cell fractionation of parasitic protozoa: a review
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- Aman RA
- Aman RA
- Amos WB
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- Benchimol M
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- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
Addition of α-O-GlcNAc to threonine residues define the post-translational modification of mucin-like molecules in Trypanosoma cruzi
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- AA Serrano
- AR Todeschini
- AR Todeschini
- B Zingales
- C Jones
- C Slawson
- CA Buscaglia
- Christopher Jones
- CM West
- F Guhl
- F Vandekerckhove
- F Wang
- FS Machado
- IC Almeida
- JA Morgado-Díaz
- JD Ramírez
- JM Noia Di
- JO Previato
- JO Previato
- JO Previato
- JO Previato
- Jose Osvaldo Previato
- KG Hagen Ten
- L Mendonça-Previato
- L Mendonça-Previato
- L Mendonça-Previato
- Lucia Mendonça-Previato
- Luciana Penha
- MA Miles
- MC Fernandes
- ML Chiribao
- MM Camargo
- N Heise
- N Yoshida
- N Yoshida
- N Yoshida
- NA Salazar
- NE Zachara
- OA Agrellos
- P Scudder
- PJ Cullen
- R Agustí
- RA Mortara
- RC Ruiz
- RC Ruiz
- RS Haltiwanger
- S Schenkman
- S Schenkman
- S Schenkman
- S Tomlinson
- SJ North
- Tatiana Cortes Garcez
- VL Pereira-Chioccola
- Z Brener
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Plant Epigenetic Mechanisms in Response to Biotic Stress
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- A Berr
- A Bilichak
- A Boyko
- A Dutta
- A Eamens
- A Jeyaraj
- A Koch
- A Koornneef
- A López
- A López Sánchez
- A Mengel
- A Molnar
- A Slaughter
- A Verkest
- A Weiberg
- A Wibowo
- A Yu
- A Zemach
- A-V Gendrel
- AA Agrawal
- AA Agrawal
- AA Agrawal
- AF Ross
- AI Badeaux
- AJ Bannister
- AJ Bewick
- AR Krol van der
- B Ding
- B Ding
- B Li
- B Wang
- B Zou
- B Zou
- BT Hofmeister
- C Castillo-González
- C De-La-Peña
- C Grativol
- C Hipper
- C Li
- C Napoli
- C Tateda
- C Wang
- C Zhang
- C Zhou
- C-G Duan
- CC Nunes
- CE Niederhuth
- CH Waddington
- CMJ Pieterse
- CP terHorst
- D Coleman-Derr
- D Gonsalves
- D Latrasse
- D Li
- D Nowara
- D Qiu
- D Shen
- D Worrall
- DA Cambiagno
- DA Roberts
- DB Collinge
- DF Klessig
- DH Chitwood
- DR Walters
- E Heard
- E Hollwey
- E Luna
- E Luna
- E Luna
- E Quintana-Rodriguez
- E Ramirez-Parra
- E Rodríguez-Negrete
- EJ Richards
- F Borges
- F Johannes
- F Li
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- F Turck
- FG Malinovsky
- G Jagadeeswaran
- G Kungulovski
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- GP Martelli
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- IA Vos
- IL Kothari
- J Dekker
- J Gallego-Bartolomé
- J Glazebrook
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- J Reinders
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- M Boccara
- M Hauben
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- M Jaskiewicz
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- M Pigllucci
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- MW Aktar
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- S Lee
- S Lu
- S Nuthikattu
- S Paudel
- S Rasmann
- S Ro
- S Takuno
- S-K Han
- S-K Han
- S-M Choi
- SJ Cokus
- SL Berger
- SP Pandey
- SW Wilkinson
- T Blevins
- T Coursey
- T Csorba
- T Hewezi
- T Kawakatsu
- T Kouzarides
- T Li
- T Mak
- T Tsuchiya
- T-N Le
- TS Furey
- U Conrath
- U Conrath
- U Ellendorff
- V Ayyappan
- V Latzel
- V Pavet
- V Ruiz-Ferrer
- V Singh
- V Singh
- VI Shattuck
- VM Weake
- W Chen
- W Zhang
- W Zhao
- X Fang
- X He
- X Li
- X Yang
- X-F He
- Y Cohen
- Y Ding
- Y Hou
- Y Li
- Y Li
- Y Zhang
- Y-Y Zhang
- Z Liang
- Z Yang
- Z Yin
- ÁL Pérez-Quintero
- Publication venue
- Springer International Publishing
- Publication date
- 28/05/2019
- Field of study
The environment changes faster than the ability of genetic recombination to generate natural genetic diversity. In this context, epigenetic regulation of gene expression has the potential to provide organisms with an alternative mechanism for phenotypic variation by controlling the extent of plasticity that can be achieved in response to environmental changes. There is now substantial evidence suggesting roles for epigenetic regulation of several different aspects of the plant response to biotic stress. At the basic level of gene expression, posttranscriptional gene silencing mediated by small RNAs and chromatin remodelling controlling transcriptional gene silencing are essential for the induced resistance responses activated during pest and pathogen attack. Beyond this, there is also evidence that histone modifications and DNA methylation are associated with immune memory, or defence priming, such as systemic acquired resistance (SAR). In addition, recent evidence indicates that epigenetic modifications can also generate longer-term defence priming responses that can be inherited across generations. In this chapter, we will discuss the roles of epigenetics in these different modes of biotic stress resistance, and suggest ways in which we may in the future be able to exploit epigenetic systems for crop protection
Clinical manifestations of intermediate allele carriers in Huntington disease
- Author
- 't Hart Ep
- Aanonsen No
- Aaserud O
- Acera Gil Ma
- Akhtar S
- Allain P
- Almagro Ca
- Almeida M
- Alonso Frech F
- Andrew A
- Andrews T
- Anjum U
- Anna Bryl Ja
- Antczak J
- Antequera Torres Mm
- Arbelo Jm
- Arkuszewski M
- Armstrong R
- Arques Pn
- Arran N
- Azulay Jp
- Baake V
- Baake V
- Babiloni B
- Bachmeier M
- Bachoud Lévi Ac
- Bachoud Lévi Ac
- Badei F
- Banaszkiewicz K
- Bandmann O
- Barbera Ma
- Barnett L
- Barral Vm
- Barth K
- Barth K
- Bartoli C
- Bas J
- Bascuñana M
- Bechtel N
- Beckmann H
- Bek J
- Bentivoglio Ar
- Berglund P
- Bertini E
- Bertrand M
- Bethwaite P
- Betz S
- Biunno I
- Bjørgo K
- Boczarska Jedynak M
- Boelmans K
- Bohlen S
- Bojakowska Jaremek K
- Bojarsky Jk
- Bonelli Rm
- Borgerød N
- Bos R
- Bos R
- Bosca M
- Boudali L
- Bourdet C
- Boćwińska D
- Bradbury A
- Brockie P
- Brown S
- Brugada Carmen Peiró Vilaplana Fc
- Bruno S
- Buck A
- Burguera Ja
- Burgunder Jm
- Burgunder Jm
- Busquets N
- Busse M
- Butcher C
- Bárcenas Ah
- Błaszczyk M
- Calado A
- Caldentey Jg
- Caldentey Jg
- Caldentey Jg
- Callaghan J
- Callaghan J
- Callaghan J
- Calopa M
- Calvas F
- Calzado N
- Campolongo A
- Cannella M
- Capodarca S
- Carruesco Gt
- Cass G
- Catena Jl
- Chabot C
- Charpentier S
- Cheriet S
- Chu E
- Ciach Wysocka E
- Ciesielska A
- Classen Sj
- Clayton C
- Clenaghan C
- Cléret L
- Coarelli G
- Codella V
- Coebergh J
- Coelho M
- Come A
- Connemann J
- Constantinescu R
- Cormio C
- Corrales Kb
- Cortegana Ep
- Cosgrove J
- Couette M
- Coulthard E
- Craufurd D
- Crooks J
- Cubillo Pt
- Cubillo Pt
- Cubo E
- Curtis A
- D'Alessio B
- Davidson L
- Davison J
- De Gregorio F
- De Michele G
- De Nicola A
- de Souza J
- de Tommaso M
- Debruxelles S
- Dec M
- Dedichá Nr
- Delfini M
- Dellomonaco Ar
- Descals Am
- Di Maio L
- Di Renzo M
- Diago Eb
- Dias M
- Diercks G
- Difruscolo O
- Dipple H
- Dixon K
- Doherty K
- Donovan Jo
- Dose M
- Downie L
- Dramstad E
- Dressler D
- Duché C
- Dumas Em
- Dunnett S
- Dunnett Sb
- Dziadkiewicz A
- Ecker D
- Ecker D
- Eddy C
- Edwards R
- Eklund P
- Elifani F
- Ellrichmann G
- Esposito C
- Eusebio A
- Fairtlough H
- Fannemel M
- Feliz Cf
- Fenollar Mdel M
- Fernandez de Bobadilla R
- Fernandez Jdel V
- Fernandez Cm
- Ferraldeschi M
- Ferreira Jj
- Ferreira Jj
- Ferrer Pq
- FIGORILLI MICHELA
- Fillingham K
- Finisterra Am
- Finisterra Am
- Fluchere F
- Focseneanu C
- Fortunato F
- Foster J
- Foustanos I
- Frades B
- Francis F
- Franco G
- Frech Fa
- Fredlund G
- Frich J
- Frontali M
- Frost J
- Fullam R
- Fullam R
- Fullam R
- Fuller K
- Fullerton N
- Gallantree D
- Ganos C
- García de Yébenes J
- García Moreno Jm
- García Ramos García R
- García A
- Garde Mb
- Garreau C
- Gaston I
- Gayde Stephan S
- Geitner C
- Genoves C
- Gethin L
- Ghelli E
- Ghenam A
- Gill P
- Gilling M
- Ginestroni A
- Goerendt I
- Gogol A
- Gohier B
- Goizet C
- Golding C
- Gomez Esteban Jc
- González A
- González S
- Gorospe A
- Gorzkowska A
- Gorzolla H
- Gowers L
- Grabska N
- Grosjean H
- Guedes Lc
- Guedes Lc
- Guia Db
- Guisasola Lm
- Gundersen H
- Guérid Ma
- Göpfert N
- Gørvell P
- Haggag K
- Haider S
- Hallam C
- Hamer S
- Handley Oj
- Handley Oj
- Hare M
- Harrison D
- Hayward B
- Heiberg A
- Heiberg A
- Heinicke W
- Held C
- Held C
- Hensman D
- Hermoso Fd
- Hernanz Lc
- Herrera Cd
- Herrmann L
- Hidding U
- Hiivola H
- Hjermind L
- Hobson E
- Hoffmann R
- Hofstetter N
- Holmes K
- Horta Barba A
- Howard L
- Hughes M
- Hunt S
- Huson S
- Hvalstedt C
- Hypponen H
- Hölzner E
- Høsterey Ugander U
- Illmann T
- Jachinska K
- Jack R
- Jacobs M
- Jacobsen O
- Jacopini G
- Jameau L
- Jamieson S
- Jamrozik Z
- Janik P
- Januário C
- Jasińska Myga B
- Johannessen Ch
- Johns N
- Johnson L
- Jones L
- Jones M
- Jones U
- José García Ruíz P
- José Sainz Artiga M
- Júlio F
- Kaczmarczyk A
- Kaelin A
- Kaminska A
- Kaminski B
- Kampstra A
- Kazoka M
- Kesse A
- Khalil H
- Klebe S
- Klimberg A
- Koivisto Sp
- Koivisto Sp
- Komati S
- Konkel A
- Koppers K
- Kosinski Cm
- Kramer B
- Kraus A
- Krawczyk M
- Krishnamoorthy A
- Krysa W
- Kubowicz E
- Kwiecinski H
- Kłodowska Duda G
- Lafoucrière D
- Lahiri N
- Lahiri N
- Lamanna C
- Landwehrmeyer B
- Landwehrmeyer Gb
- Lange H
- Large S
- Larsen Iu
- Laurà M
- Lemoine L
- Levey J
- Lewerenz J
- Lewerenz J
- Lewis M
- Leypold C
- Lezius F
- Lindquist S
- Longthorpe M
- Lopera Mr
- Lovo F
- Lozano Ps
- Lucena Cm
- López Del Val J
- López Sendón Moreno Jl
- López E
- López Rg
- Malec Litwinowicz M
- Malo de Molina R
- Manzanares S
- Marcinkowski J
- Marie Bost Db
- Mariscal N
- Marit de Weert A
- Markova I
- Marquard R
- Marquine L
- MARROSU FRANCESCO
- Martikainen K
- Martin Vp
- Martinez Horta S
- Martinez Horta S
- Martinez Jaurrieta Md
- Martinez Lm
- Martino T
- Martín I
- Martínez Descals A
- Martínez Nr
- Massarelli M
- Mata Mp
- Matheson K
- Mazzante I
- Mcdonnell S
- Mcentagart M
- Mckenzie S
- Mechi C
- Mendes T
- Merino Bt
- Mestre T
- Mestre T
- Middleton J
- Miedzybrodzka Z
- Milkereit E
- Minet C
- Minschke R
- Minster S
- Minster S
- Mohammed Z
- Monza D
- Moreau Lv
- Moreno Pg
- Morgado G
- Morgado J
- Morgan K
- Mundler L
- Muroni A
- Murphy H
- Musacchio T
- Musgrave H
- Muñoz Jm
- Mühlbäck A
- Münchau A
- Mütze L
- Narożańska E
- Neleborn Lingefjärd L
- Nemeth Ah
- Nepper S
- Nevitt L
- Nielsen J
- Nielsen Je
- Niess A
- Noad R
- Novak M
- Nowak M
- Nowak M
- Nöth K
- O'Donovan K
- O'Donovan K
- Oehmen M
- Olivier A
- Opala G
- Orth M
- Orth M
- Oughton E
- Owen M
- Padieu H
- Paganini M
- Pagonabarraga J
- Palmer A
- Pardo Sa
- Pariente J
- Parkinson A
- Partington Jones L
- Pastor Bv
- Patel A
- Paterski L
- Patino Df
- Patton M
- Peacy C
- Peluso S
- Peppa N
- Peppa N
- Perea Fn
- Perez Jp
- Periañez Jm
- Peterson M
- Petrollini M
- Peña Jc
- Phillips M.
- Piacentini S
- Piedad J
- Pierre M
- PIRAS VALERIA
- Powell K
- Pradella S
- Price K
- Prieto Mp
- Probst D
- Prouzet J
- Prundean A
- Pueyo Am
- Päivärinta M
- Quarrell O
- Rae D
- Rakowicz M
- Raman A
- Ramirez Il
- Ramos Arroyo M
- Ramos Arroyo Ma
- Raseta R
- Read J
- Redondo L
- Reetz K
- Regeur L
- Reilmann R
- Retterstøl L
- Ribacoba R
- Riballo Av
- Ribas Gg
- Ribaï P
- Richter P
- Rickards H
- Rinaldi C
- Rindal B
- Ristori G
- Robert Mf
- Robertson N
- Robowski P
- Roca A
- Roca E
- Rogers D
- Rogers D
- Rohm S
- Rola R
- Rolland S
- Romano S
- Romero Lemos Md
- Romero I
- Romero Sg
- Romoli Am
- Roos Ra
- Roos Ra
- Rosa Mm
- Rosby O
- Rose S
- Rosser A
- Rosser E
- Rothery J
- Rowett L
- Rudzińska M
- Rudzińska M
- Ruiz Idiago Jm
- Rummel J
- Rumpf S
- Russo Cv
- Ryglewicz D
- Røren N
- Saft C
- Salgueiro A
- Salvador C
- Salvatore E
- Samara H
- Sass C
- Sass C
- Savage L
- Schepers S
- Scherer Gagou C
- Schiefer J
- Schlangen C
- Schmalfeld J
- Schneider A
- Schoonderbeek A
- Schrader C
- Schwenk D
- Schüpbach M
- Sciruicchio V
- Sebaiti M
- Sebastián Ar
- Sebastián Ar
- Seliverstov Y
- Semedo C
- Sempołowicz J
- Seris A
- Serpino C
- Sienkiewicz Jarosz H
- Sieradzan K
- Sikiric A
- Simonelli M
- Simpson Sa
- Singh B
- Sitek E
- Siuda G
- Slawek J
- Snowden J
- Solberg O
- Sollom A
- Soltan W
- Soltysiak B
- Sorbi S
- Sorrentino P
- Spampinato U
- Squitieri F
- Stebler Y
- Stenwak A
- Stockholm J
- Stompel D
- Stopford C
- Stubbe L
- Stępniak I
- Summers F
- Sułek A
- Szczudlik A
- Szczygieł E
- Szinwelski M
- Sánchez V
- Süssmuth S
- Tabrizi S
- Tabrizi Sj
- Tacik P
- Tartari Díaz Zorita Jp
- Taylor C
- Taylor C
- Taylor R
- Thiriez C
- Thomas G
- Thompson J
- Tidswell K
- Timewell E
- Timings L
- Toscano J
- Townhill J
- Townhill J
- Trautmann S
- Trender Gerhard I
- Tucci T
- Tuuha K
- Udaeta B
- Uhrova T
- Ure A
- VACCA MELISA IRIS SABINA
- Valadas A
- Valentine R
- van den Bogaard Sj
- van Hout Ms
- Van Paemel D
- van Vugt Jp
- van Walsem M
- van Walsem Mr
- Vandenberghe W
- Vangsted Hansen C
- Vaquie V
- Vaughn V
- Ventura Mf
- Verellen Dumoulin C
- Verellen Dumoulin C
- Verhoeven M
- Verny C
- Verstraelen N
- Vervoitte L
- Vezza M
- Vieira da Silva W
- Viladrich Cm
- Villa C
- Villanueva C
- Villanueva Má
- Vinther Jensen T
- Wahlström J
- Wahlström J
- Warner T
- Wasielewska A
- Weber N
- Wehus R
- Werner Cj
- Westmoreland L
- Weydt P
- Wild E
- Wild S
- Williams J
- Witjes Ané Mn
- Witkowski G
- Witkowski G
- Wiśniewski B
- Wood J
- Wright A
- Wright A
- Wright J
- Wójcik M
- Yardumian P
- Yates S
- Youssov K
- Yudina E
- Zaremba J
- Zaremba J
- Zaugg Sw
- Zdzienicka E
- Zea Sevilla Ma
- Zielonka D
- Zielonka D
- Zielonka E
- Zinzi P
- Zinzi P
- Ziora Jakutowicz K
- Zittel S
- Šašinková P
- Publication venue
- 'Ovid Technologies (Wolters Kluwer Health)'
- Publication date
- 01/01/2016
- Field of study
Objective: There is controversy about the clinical consequences of intermediate alleles (IAs) in Huntington disease (HD). The main objective of this study was to establish the clinical manifestations of IA carriers for a prospective, international, European HD registry. Methods: We assessed a cohort of participants at risk with <36 CAG repeats of the huntingtin (HTT) gene. Outcome measures were the Unified Huntington's Disease Rating Scale (UHDRS) motor, cognitive, and behavior domains, Total Functional Capacity (TFC), and quality of life (Short Form-36 [SF-36]). This cohort was subdivided into IA carriers (27-35 CAG) and controls (<27 CAG) and younger vs older participants. IA carriers and controls were compared for sociodemographic, environmental, and outcome measures. We used regression analysis to estimate the association of age and CAG repeats on the UHDRS scores. Results: Of 12,190 participants, 657 (5.38%) with <36 CAG repeats were identified: 76 IA carriers (11.56%) and 581 controls (88.44%). After correcting for multiple comparisons, at baseline, we found no significant differences between IA carriers and controls for total UHDRS motor, SF-36, behavioral, cognitive, or TFC scores. However, older participants with IAs had higher chorea scores compared to controls (p 0.001). Linear regression analysis showed that aging was the most contributing factor to increased UHDRS motor scores (p 0.002). On the other hand, 1-year follow-up data analysis showed IA carriers had greater cognitive decline compared to controls (p 0.002). Conclusions: Although aging worsened the UHDRS scores independently of the genetic status, IAs might confer a late-onset abnormal motor and cognitive phenotype. These results might have important implications for genetic counseling. ClinicalTrials.gov identifier: NCT01590589
Clinical and genetic characteristics of late-onset Huntington's disease
- Author
- Aanonsen No
- Aaserud O
- Abbruzzese G
- Acera Gil Ma
- Ackermann O
- Adarmes A
- Agarwal V
- Agosti C
- Akhtar S
- Alaerts N
- Alarcón Md
- Albanese A
- Allain P
- Almagro Ca
- Almeida M
- Alonso-Frech F
- Alusi S
- Anderson M
- Andersson C
- Andrade C
- Andrew A
- Andrews T
- Andrews T
- Andrich J
- Anheim M
- Anjum U
- Anna Bryl Ja
- Annic A
- Antczak J
- Antequera Torres Mm
- Antonova V
- Arbelo Jm
- Arkuszewski M
- Armstrong R
- Armstrong R
- Arntsen V
- Arques Pn
- Arran N
- Azulay Jp
- Baake V
- Babiloni B
- Bachmeier M
- Bachoud-Lévi Ac
- Bachoud-Lévi Ac
- Badei F
- Bailey W
- Banaszkiewicz K
- Bandettini di Poggio M
- Bandmann O
- Barbera Ma
- Barker Ra
- Barlati S
- Barral Vm
- Barrero F
- Barrett W
- Barth K
- Barth K
- Barthélémy R
- Bartoli C
- Barun N
- Bas J
- Bascuñana M
- Becanovic K
- Bechtel N
- Beckmann H
- Bek J
- Bellonet M
- Benaich S
- Benaminov S
- Benito Dm
- Bentivoglio Ar
- Bentivoglio Ar
- Berglund M
- Berglund M
- Berglund P
- Bergmann U
- Bernal-Escudero M
- Bernard T
- Bertini E
- Bethwaite P
- Betz S
- Beuth M
- Bezdíček O
- Bijlsma Emilia K
- Bioux S
- Biunno I
- Björnsson E
- Bjørgo K
- Bjørnevoll I
- Bled D
- Bliaux E
- Blin S
- Blinkenberg Eø
- Blondeau L
- Boczarska-Jedynak M
- Boelmans K
- Bohlen S
- Boissé Mf
- Bojakowska-Jaremek K
- Bojarsky Jk
- Bonelli Rm
- Bonelli Rm
- Bonelli Rm
- Bonneau D
- Boogaerts A
- Boogaerts A
- Borgerød N
- Bos R
- Bos R
- Bosca M
- Bosredon C
- Bost M
- Boster S
- Boudali L
- Bove F
- Boćwińska D
- Bradbury A
- Braunwarth Em
- Brice A
- Brockie P
- Bronzova J
- Brown P
- Brugada Fc
- Brugger F
- Bruno S
- Bruun A
- Buchanan L
- Buck A
- Buongiorno Mt
- Buratti L
- Burguera Ja
- Burgunder Jm
- Burgunder Jm
- Burgunder Jm
- Burn J
- Burrows L
- Busquets N
- Busse M
- Butcher C
- Bárcenas Ah
- Böringer R
- Bürk K
- Błaszczyk M
- Cabaret M
- Calado A
- Calandra-Buonaura G
- Caldentey Jg
- Caldentey Jg
- Caldentey Jg
- Callaghan J
- Callaghan J
- Callaghan J
- Calmeyn G
- Calopa M
- Calvas F
- Calzado N
- Campolongo A
- Cannella M
- Capellari S
- Capetian P
- Capodarca S
- Cardoso H
- Carette As
- Carrillo F
- Carrière N
- Carruesco Gt
- Casado Rv
- Cass G
- Castagliuolo S
- Castaldo A
- Catalli C
- Catena Jl
- Cavaco S
- Cação G
- Charles P
- Charpentier S
- Chen S
- Cheriet S
- Chiara P
- Chu C
- Chu E
- Chu E
- Ciach-Wysocka E
- Ciesielska A
- Classen Sj
- Clayton C
- Clenaghan C
- Cleret de Langavant L
- Coarelli G
- Codella V
- Coebergh J
- Coelho M
- Coleman C
- Come A
- Compostella S
- Connemann J
- Constant E
- Constantinescu R
- Cormio C
- Corrales Kb
- Cortelli P
- Cosgrove J
- Costa A
- Costa C
- Coulthard E
- Couttier J
- Craufurd D
- Craven J
- Craven J
- Crooks J
- Cubillo Pt
- Cubillo Pt
- Cubo E
- Curtis A
- D'Alessio B
- Damásio J
- Davidson L
- Davies R
- Davison J
- De Bruycker C
- de Die-Smulders Christine Em
- De Gregorio F
- De Michele G
- De Nicola A
- de Raedt S
- de Souza Keylock J
- de Tommaso M
- Debilly B
- Debruxelles S
- Dec M
- Decorte E
- Dedichá Nr
- Defebvre L
- Deith C
- Dekker M
- Delabaere H
- Delaigue C
- Delfini M
- Delliaux M
- Delval A
- Delvaux I
- Demonet Jf
- Depelchin A
- Derost P
- Descals Am
- Destee A
- Dewulf-Pasz N
- Di Bella D
- Di Donato S
- Di Giacopo R
- Di Maio L
- Di Maria E
- Di Renzo M
- Diago Eb
- Dias M
- Diercks G
- Difruscolo O
- Dipple H
- Dixon K
- Dixon K
- Diéguez E
- Doherty K
- Dondaine T
- Donovan Jo
- Dose M
- Dougherty A
- Downie L
- Dramstad E
- Dressler D
- Duché C
- Duffell A
- Dugauquier F
- Duits A
- Dujardin K
- Dumas Em
- Dunnett S
- Dunnett Sb
- Duport S
- Dupuis M
- Durif F
- Durr A
- Dziadkiewicz A
- Ecker D
- Ecker D
- Eddy C
- Edwards M
- Edwards R
- Eklund P
- Ekwall C
- El-Nimr G
- Elifani F
- Ellrichmann G
- Esmaeilzadeh M
- Esposito C
- Esposito F
- Eusebio A
- Evans C
- Ewenczyk C
- Fairtlough H
- Fannemel M
- Fasano A
- Feliz C
- Fenollar Mdm
- Fernandes J
- Fernandez de Bobadilla R
- Fernandez Cm
- Ferraldeschi M
- Ferrandes G
- Ferreira Jj
- Ferreira Jj
- Ferrer Pq
- Figorilli M
- Figuerola Bj
- Fillingham K
- Finisterra Am
- Fisher K
- Flamez A
- Fletcher A
- Fluchere F
- Formerly Rödig Vb
- Fortuna L
- Fortunato F
- Foster J
- Foustanos I
- Foy K
- Frades B
- Fraisse S
- Francis F
- Francisque H
- Franco G
- Fredlund G
- Freire-Patino D
- Frich J
- Frich Jc
- Frontali M
- Frontali M
- Frost J
- Fullam R
- Fullam R
- Fullam R
- Fuller K
- Fullerton N
- Gago M
- Gallantree D
- Gallassi R
- Gallentree D
- Ganos C
- Ganos C
- Garcia-Amigot F
- García de Yébenes J
- García Moreno Jm
- García Ruíz Pj
- García A
- García-Ramos García R
- Garde Mb
- Garrett C
- Gaston I
- Gayde-Stephan S
- Geitner C
- Gelderblom H
- Gellera C
- Genitrini S
- Genoves C
- Germain V
- Gerrans E
- Gerrtiz Nee Di Pietro A
- Gethin L
- Ghelli E
- Gill P
- Gillardin Af
- Gilling M
- Ginestroni A
- Girard C
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- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2019
- Field of study
Background: The frequency of late-onset Huntington's disease (>59 years) is assumed to be low and the clinical course milder. However, previous literature on late-onset disease is scarce and inconclusive. Objective: Our aim is to study clinical characteristics of late-onset compared to common-onset HD patients in a large cohort of HD patients from the Registry database. Methods: Participants with late- and common-onset (30\u201350 years)were compared for first clinical symptoms, disease progression, CAG repeat size and family history. Participants with a missing CAG repeat size, a repeat size of 6435 or a UHDRS motor score of 645 were excluded. Results: Of 6007 eligible participants, 687 had late-onset (11.4%) and 3216 (53.5%) common-onset HD. Late-onset (n = 577) had significantly more gait and balance problems as first symptom compared to common-onset (n = 2408) (P <.001). Overall motor and cognitive performance (P <.001) were worse, however only disease motor progression was slower (coefficient, 120.58; SE 0.16; P <.001) compared to the common-onset group. Repeat size was significantly lower in the late-onset (n = 40.8; SD 1.6) compared to common-onset (n = 44.4; SD 2.8) (P <.001). Fewer late-onset patients (n = 451) had a positive family history compared to common-onset (n = 2940) (P <.001). Conclusions: Late-onset patients present more frequently with gait and balance problems as first symptom, and disease progression is not milder compared to common-onset HD patients apart from motor progression. The family history is likely to be negative, which might make diagnosing HD more difficult in this population. However, the balance and gait problems might be helpful in diagnosing HD in elderly patients
Safety of hospital discharge before return of bowel function after elective colorectal surgery
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- Publication venue
- 'Wiley'
- Publication date
- 01/04/2020
- Field of study
© 2020 BJS Society Ltd Published by John Wiley & Sons LtdBackground: Ileus is common after colorectal surgery and is associated with an increased risk of postoperative complications. Identifying features of normal bowel recovery and the appropriateness for hospital discharge is challenging. This study explored the safety of hospital discharge before the return of bowel function. Methods: A prospective, multicentre cohort study was undertaken across an international collaborative network. Adult patients undergoing elective colorectal resection between January and April 2018 were included. The main outcome of interest was readmission to hospital within 30 days of surgery. The impact of discharge timing according to the return of bowel function was explored using multivariable regression analysis. Other outcomes were postoperative complications within 30 days of surgery, measured using the Clavien–Dindo classification system. Results: A total of 3288 patients were included in the analysis, of whom 301 (9·2 per cent) were discharged before the return of bowel function. The median duration of hospital stay for patients discharged before and after return of bowel function was 5 (i.q.r. 4–7) and 7 (6–8) days respectively (P < 0·001). There were no significant differences in rates of readmission between these groups (6·6 versus 8·0 per cent; P = 0·499), and this remained the case after multivariable adjustment for baseline differences (odds ratio 0·90, 95 per cent c.i. 0·55 to 1·46; P = 0·659). Rates of postoperative complications were also similar in those discharged before versus after return of bowel function (minor: 34·7 versus 39·5 per cent; major 3·3 versus 3·4 per cent; P = 0·110). Conclusion: Discharge before return of bowel function after elective colorectal surgery appears to be safe in appropriately selected patients
Edoxaban versus warfarin in patients with atrial fibrillation
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- Young C
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- Yukhno E
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- Zachar A
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- Zamlynskyy M
- Zamorano JL
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- Zarpentin C
- Zateyshchikov D
- Zateyshchikova A
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- Zhang HQ
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- Zimmermann EB
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- Zubeeva G
- Zyatenkova E
- Åkerberg A
- Östberg S
- Ŝpinar J
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2013
- Field of study
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125374.pdf (publisher's version ) (Open Access)BACKGROUND: Edoxaban is a direct oral factor Xa inhibitor with proven antithrombotic effects. The long-term efficacy and safety of edoxaban as compared with warfarin in patients with atrial fibrillation is not known. METHODS: We conducted a randomized, double-blind, double-dummy trial comparing two once-daily regimens of edoxaban with warfarin in 21,105 patients with moderate-to-high-risk atrial fibrillation (median follow-up, 2.8 years). The primary efficacy end point was stroke or systemic embolism. Each edoxaban regimen was tested for noninferiority to warfarin during the treatment period. The principal safety end point was major bleeding. RESULTS: The annualized rate of the primary end point during treatment was 1.50% with warfarin (median time in the therapeutic range, 68.4%), as compared with 1.18% with high-dose edoxaban (hazard ratio, 0.79; 97.5% confidence interval [CI], 0.63 to 0.99; P<0.001 for noninferiority) and 1.61% with low-dose edoxaban (hazard ratio, 1.07; 97.5% CI, 0.87 to 1.31; P=0.005 for noninferiority). In the intention-to-treat analysis, there was a trend favoring high-dose edoxaban versus warfarin (hazard ratio, 0.87; 97.5% CI, 0.73 to 1.04; P=0.08) and an unfavorable trend with low-dose edoxaban versus warfarin (hazard ratio, 1.13; 97.5% CI, 0.96 to 1.34; P=0.10). The annualized rate of major bleeding was 3.43% with warfarin versus 2.75% with high-dose edoxaban (hazard ratio, 0.80; 95% CI, 0.71 to 0.91; P<0.001) and 1.61% with low-dose edoxaban (hazard ratio, 0.47; 95% CI, 0.41 to 0.55; P<0.001). The corresponding annualized rates of death from cardiovascular causes were 3.17% versus 2.74% (hazard ratio, 0.86; 95% CI, 0.77 to 0.97; P=0.01), and 2.71% (hazard ratio, 0.85; 95% CI, 0.76 to 0.96; P=0.008), and the corresponding rates of the key secondary end point (a composite of stroke, systemic embolism, or death from cardiovascular causes) were 4.43% versus 3.85% (hazard ratio, 0.87; 95% CI, 0.78 to 0.96; P=0.005), and 4.23% (hazard ratio, 0.95; 95% CI, 0.86 to 1.05; P=0.32). CONCLUSIONS: Both once-daily regimens of edoxaban were noninferior to warfarin with respect to the prevention of stroke or systemic embolism and were associated with significantly lower rates of bleeding and death from cardiovascular causes. (Funded by Daiichi Sankyo Pharma Development; ENGAGE AF-TIMI 48 ClinicalTrials.gov number, NCT00781391.)