Dichotomy between postprandial glucose and lipid profiles in adults with cystic fibrosis: A pilot study  I. Hammana, L. Coderre, S. Potvin, M. Costa,

Slides:



Advertisements
Similar presentations
Use of the insulin pump in treat cystic fibrosis related diabetes Dana S. Hardin, Julie Rice, Mark Rice, Randall Rosenblatt Journal of Cystic Fibrosis.
Advertisements

The relationship of angiographically defined coronary artery disease with insulin sensitivity and secretion in subjects with different glucose tolerance 
Comparing age of cystic fibrosis diagnosis and treatment initiation after newborn screening with two common strategies  Don B. Sanders, Huichuan J. Lai,
Cheryl Cameron, Mark W. Lodes, William M. Gershan 
The prevalence of “risky behaviour” in adults with cystic fibrosis
Reduced levels of active GLP-1 in patients with cystic fibrosis with and without diabetes mellitus  Magnus Hillman, Leif Eriksson, Lena Mared, Karin Helgesson,
Oxidative stress and cystic fibrosis-related diabetes: A pilot study in children  Thierry Ntimbane, Preetha Krishnamoorthy, Céline Huot, Laurent Legault,
Development, validation, and implementation of a questionnaire assessing disease knowledge and understanding in adult cystic fibrosis patients  Karen.
HbA1c as a screening tool for cystic fibrosis related diabetes
R. Roberts, L. Speight, J. Lee, L. George, R. I. Ketchell, D. Lau, J
Abaigeal D. Jackson, Christopher H. Goss  Journal of Cystic Fibrosis 
How does heart rate recovery after sub-maximal exercise correlate with maximal exercise testing in children with CF?  Sarah P. Cohen, David M. Orenstein 
Katarine Egressy, Michaelene Jansen, Keith C. Meyer 
Megan R. Nelson, Craig R. Adamski, Audrey Tluczek 
Urinary incontinence in 9���16��year olds with cystic fibrosis compared to other respiratory conditions and a normal group  W.J. Browne, C.J. Wood, M.
Measures of body habitus are associated with lung function in adults with cystic fibrosis: A population-based study  Doug L. Forrester, Alan J. Knox,
Laura Viviani, Baroukh M. Assael, Eitan Kerem 
Cirrhosis and other liver disease in cystic fibrosis
Katelyn Krivchenia, Don Hayes, Joseph D. Tobias, Dmitry Tumin 
John Widger, Sarath Ranganathan, Philip J. Robinson 
Characterization of patients with cystic fibrosis presenting an indeterminate glucose tolerance (INDET)  Adèle Coriati, Sophie Ziai, Mirna Azar, Yves.
Update on cystic fibrosis-related diabetes
Long-term azitromycin treatment of cystic fibrosis patients with chronic Pseudomonas aeruginosa infection; an observational cohort study  Christine Rønne.
Anju Anand, Elizabeth Tullis, Anne Stephenson, Preyanka Abhyankar 
D. Stevens, P.J. Oades, N. Armstrong, C.A. Williams 
Claire J. Tipping, Rebecca L. Scholes, Narelle S. Cox 
Cystic fibrosis mortality trend in Italy from 1970 to 2011
Disposition index identifies defective beta-cell function in cystic fibrosis subjects with normal glucose tolerance  L. Merjaneh, Q. He, Q. Long, L.S.
Vitamin A and lung function in CF
A.H. Gifford  Journal of Cystic Fibrosis 
M. Wouthuyzen-Bakker, F.A.J.A. Bodewes, H.J. Verkade 
Demographics of glucose metabolism in cystic fibrosis
Effectiveness of inhaled tobramycin in eradicating Pseudomonas aeruginosa in children with cystic fibrosis  Sanja Stanojevic, Valerie Waters, Joseph L.
Cystic fibrosis related diabetes in an extremely young patient
Agreement of bioelectric impedance analysis and dual-energy X-ray absorptiometry for body composition evaluation in adults with cystic fibrosis  S. Ziai,
Antonia V. Bennett, Donald L. Patrick, James F. Lymp, Todd C
Characterisation of mutations and genotype–phenotype correlation in cystic fibrosis: Experience from India  Shivaram S. Shastri, Madhulika Kabra, Sushil.
Sophia L. Markantonis, Anna Katelari, Eleni Pappa, Stavros Doudounakis 
E. Tschiedel, H. Grasemann, F. Ratjen  Journal of Cystic Fibrosis 
Colon Cancer in Cystic Fibrosis patients: Is this a growing problem?
Sally H. Pattison, Geraint B. Rogers, Martin Crockard, J
Marie-Angela Schnyder, Christian Benden, Christoph Schmid 
Cytokine gene polymorphisms and severity of CF lung disease
Nasal polyposis in lung transplant recipients with cystic fibrosis
Hypertriglyceridemia is associated with insulin levels in adult cystic fibrosis patients  Marie-Claire Ishimo, Linda Belson, Sophie Ziai, Emile Levy, Yves.
Novel concepts in evaluating antimicrobial therapy for bacterial lung infections in patients with cystic fibrosis  Geraint B. Rogers, Lucas R. Hoffman,
Nutritional decline in cystic fibrosis related diabetes: The effect of intensive nutritional intervention  H. White, K. Pollard, C. Etherington, I. Clifton,
Gender differences in treatment adherence among youth with cystic fibrosis: Development of a new questionnaire  Joän M. Patterson, Melanie Wall, Jerica.
Higher risk of hospitalization among females with cystic fibrosis
Trends in pathogens colonising the respiratory tract of adult patients with cystic fibrosis, 1985–2005  F.A. Millar, N.J. Simmonds, M.E. Hodson  Journal.
A new method of sweat testing: the CF Quantum®sweat test
Diabetes mellitus and survival in cystic fibrosis patients after lung transplantation  Markus Hofer, Christoph Schmid, Christian Benden, Rudolf Speich,
Comparing age of cystic fibrosis diagnosis and treatment initiation after newborn screening with two common strategies  Don B. Sanders, Huichuan J. Lai,
H. White, A.M. Morton, S.P. Conway, D.G. Peckham 
J.E. Spahr, R.B. Love, M. Francois, K. Radford, K.C. Meyer 
Variation of glucose tolerance in adult patients with cystic fibrosis: What is the potential contribution of insulin sensitivity?  Valérie Boudreau, Adèle.
D.F. Waterhouse, A.M. McLaughlin, C.G. Gallagher 
The role of respiratory viruses in adult patients with cystic fibrosis receiving intravenous antibiotics for a pulmonary exacerbation  C. Etherington,
CFTR modulators and pregnancy: Our work has only just begun
‘Peeling paint’ dermatitis as a presenting sign of cystic fibrosis
Beta-lactam allergy in adults with cystic fibrosis
Cheryl Cameron, Mark W. Lodes, William M. Gershan 
Patients with cystic fibrosis and normoglycemia exhibit diabetic glucose tolerance during pulmonary exacerbation  Noa Nezer M. Sc, David Shoseyov, Eitan.
Lutz Goldbeck, Sven Zerrer, Tim G. Schmitz  Journal of Cystic Fibrosis 
Khin M. Gyi, Margaret E. Hodson, Magdi Y. Yacoub 
David Adeboyeku, Sandra Scott, Margaret E. Hodson 
Increasing resistance of the Liverpool Epidemic Strain (LES) of Pseudomonas aeruginosa (Psa) to antibiotics in cystic fibrosis (CF)—A cause for concern? 
Elisabeth P. Dellon, Margaret W. Leigh, James R. Yankaskas, Terry L
Absence of a gender gap in survival
H. White, A.M. Morton, D.G. Peckham, S.P. Conway 
Presentation transcript:

Dichotomy between postprandial glucose and lipid profiles in adults with cystic fibrosis: A pilot study  I. Hammana, L. Coderre, S. Potvin, M. Costa, Y. Berthiaume, A. Lavoie, J.-L. Chiasson, E. Levy, R. Rabasa-Lhoret  Journal of Cystic Fibrosis  Volume 8, Issue 2, Pages 128-134 (March 2009) DOI: 10.1016/j.jcf.2008.11.002 Copyright © 2008 European Cystic Fibrosis Society. Terms and Conditions

Fig. 1 Plasma glucose profile in response to a TM (A) and an OGTT (B) in CF patients and controls. CF-normal glucose tolerance (CF-NGT); CF-related diabetes (CFRD). *P<0.05 CFRD vs. Controls; ΔP<0.05 CFRD vs. NGT; ΨP<0.05 NGT vs. Controls. Journal of Cystic Fibrosis 2009 8, 128-134DOI: (10.1016/j.jcf.2008.11.002) Copyright © 2008 European Cystic Fibrosis Society. Terms and Conditions

Fig. 2 Total glucose area under the curve (AUC) of the OGTT and TM. ⁎P<0.005 TM vs OGTT; ΔP<0.0001 NGT vs Controls for TM and OGTT; €P<0.0001 CFRD vs Controls for the TM and OGTT; ¥P<0.0001 CFRD vs NGT for TM and OGTT. Journal of Cystic Fibrosis 2009 8, 128-134DOI: (10.1016/j.jcf.2008.11.002) Copyright © 2008 European Cystic Fibrosis Society. Terms and Conditions

Fig. 3 Insulin profile in response to a TM (A) and an OGTT (B) in CF patients and controls. CF-normal glucose tolerance (CF-NGT); CF-related diabetes (CFRD). Journal of Cystic Fibrosis 2009 8, 128-134DOI: (10.1016/j.jcf.2008.11.002) Copyright © 2008 European Cystic Fibrosis Society. Terms and Conditions

Fig. 4 Triglyceride levels in response to a TM (A) and an OGTT (B) in CF-patients and controls. CF-normal glucose tolerance (CF-NGT); CF-related diabetes (CFRD). *P<0.01 versus basal condition (time 0). Journal of Cystic Fibrosis 2009 8, 128-134DOI: (10.1016/j.jcf.2008.11.002) Copyright © 2008 European Cystic Fibrosis Society. Terms and Conditions

Fig. 5 FFA levels in response to a TM (A) and an OGTT (B) in CF patients and controls. CF-normal glucose tolerance (CF-NGT); CF-related diabetes (CFRD). *P<0.05 versus basal condition (time 0). Journal of Cystic Fibrosis 2009 8, 128-134DOI: (10.1016/j.jcf.2008.11.002) Copyright © 2008 European Cystic Fibrosis Society. Terms and Conditions