Disposition index identifies defective beta-cell function in cystic fibrosis subjects with normal glucose tolerance  L. Merjaneh, Q. He, Q. Long, L.S.

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

Comparing age of cystic fibrosis diagnosis and treatment initiation after newborn screening with two common strategies  Don B. Sanders, Huichuan J. Lai,
Reduced levels of active GLP-1 in patients with cystic fibrosis with and without diabetes mellitus  Magnus Hillman, Leif Eriksson, Lena Mared, Karin Helgesson,
Sweat conductivity: An accurate diagnostic test for cystic fibrosis?
Zachary M. Sellers, Lori McGlocklin, Andrea Brasch 
R. Roberts, L. Speight, J. Lee, L. George, R. I. Ketchell, D. Lau, J
How does heart rate recovery after sub-maximal exercise correlate with maximal exercise testing in children with CF?  Sarah P. Cohen, David M. Orenstein 
Development of a quantitative immunofluorescence assay for detection of Stenotrophomonas maltophilia antibodies in patients with cystic fibrosis  P. Gonçalves.
Katarine Egressy, Michaelene Jansen, Keith C. Meyer 
Megan R. Nelson, Craig R. Adamski, Audrey Tluczek 
Comparison of two treatment regimens for eradication of Pseudomonas aeruginosa infection in children with cystic fibrosis  M. Proesmans, F. Vermeulen,
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 
A longitudinal analysis of chronic MRSA and Pseudomonas aeruginosa co-infection in cystic fibrosis: A single-center study  Maret L. Maliniak, Arlene A.
Cirrhosis and other liver disease in cystic fibrosis
Katelyn Krivchenia, Don Hayes, Joseph D. Tobias, Dmitry Tumin 
John Widger, Sarath Ranganathan, Philip J. Robinson 
Rate of improvement of CF life expectancy exceeds that of general population— Observational death registration study  Matthew N. Hurley, Tricia M. McKeever,
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
Controlled clinical trials in cystic fibrosis — are we doing better?
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
D.J. Serisier, M.P. Carroll  Journal of Cystic Fibrosis 
Dichotomy between postprandial glucose and lipid profiles in adults with cystic fibrosis: A pilot study  I. Hammana, L. Coderre, S. Potvin, M. Costa,
Vitamin A and lung function in CF
Amyloidosis in cystic fibrosis: A case series
Spontaneous coronary artery dissection associated with coughing
A.H. Gifford  Journal of Cystic Fibrosis 
Demographics of glucose metabolism in cystic fibrosis
Cystic fibrosis related diabetes in an extremely young patient
Inhalation solutions — Which ones may be mixed
Antonia V. Bennett, Donald L. Patrick, James F. Lymp, Todd C
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
Anastasios Lekkas, Khin M. Gyi, Margaret E. Hodson 
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.
Inflammatory and immunological biomarkers are not related to survival in adults with Cystic Fibrosis  K.L. Moffitt, S.L. Martin, A.M. Jones, A.K. Webb,
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.
Alina A. Ionescu, Lisette S. Nixon, Dennis J. Shale 
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.
F. Vermeulen, P. Lebecque, K. De Boeck, T. Leal 
A new method of sweat testing: the CF Quantum®sweat test
V. Thompson, N. Mayer-Hamblett, M. Kloster, D. Bilton, P.A. Flume 
Comparing age of cystic fibrosis diagnosis and treatment initiation after newborn screening with two common strategies  Don B. Sanders, Huichuan J. Lai,
J.E. Spahr, R.B. Love, M. Francois, K. Radford, K.C. Meyer 
James H. Hull, Rachel Garrod, Timothy B. Ho, Ronald K. Knight, John R
Variation of glucose tolerance in adult patients with cystic fibrosis: What is the potential contribution of insulin sensitivity?  Valérie Boudreau, Adèle.
Daniel J. Smith, Gregory J. Anderson, Scott C. Bell, David W. Reid 
Michael W. Konstan, David J. Pasta, Jeffrey S. Wagener, Donald R
C. R. Hansen, T. Pressler, K. G. Nielsen, P. Ø. Jensen, T
D.F. Waterhouse, A.M. McLaughlin, C.G. Gallagher 
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
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
Cystic fibrosis and pregnancy in the modern era: A case control study
Respiratory physicians and clinic coordinators' attitudes to population-based cystic fibrosis carrier screening  Fiona Cunningham, Sharon Lewis, Lisette.
Presentation transcript:

Disposition index identifies defective beta-cell function in cystic fibrosis subjects with normal glucose tolerance  L. Merjaneh, Q. He, Q. Long, L.S. Phillips, A.A. Stecenko  Journal of Cystic Fibrosis  Volume 14, Issue 1, Pages 135-141 (January 2015) DOI: 10.1016/j.jcf.2014.06.004 Copyright © 2014 European Cystic Fibrosis Society. Terms and Conditions

Fig. 1 The computed slopes for ln(Insulin secretion) versus ln(Insulin sensitivity) in the five groups showing that the slope includes −1 for all groups except CFRD. The slope and confidence interval (CI) for each of the groups is as follows. Con-NGT: slope −0.5364 with CI [−1.6383, 0.5655]; Con-prediabetes: slope −0.9698 with CI [−1.4689, −0.4707]; CF-NGT: slope −0.0824 with CI [−1.0339, 0.8690]; CF-prediabetes: slope −0.4622 with CI [−1.2518, 0.3273]; CFRD: slope −21.2791 with CI [−35.0945, −7.4637]. Journal of Cystic Fibrosis 2015 14, 135-141DOI: (10.1016/j.jcf.2014.06.004) Copyright © 2014 European Cystic Fibrosis Society. Terms and Conditions

Fig. 2 The disposition index in controls and CF subjects according to their glucose tolerance category. Journal of Cystic Fibrosis 2015 14, 135-141DOI: (10.1016/j.jcf.2014.06.004) Copyright © 2014 European Cystic Fibrosis Society. Terms and Conditions

Fig. 3 ROC curves for DI and 30-min glucose levels on determination of normal glucose tolerance (a) and determination of diabetes (b). TPR: true-positive rate; FPR: false-positive rate. Journal of Cystic Fibrosis 2015 14, 135-141DOI: (10.1016/j.jcf.2014.06.004) Copyright © 2014 European Cystic Fibrosis Society. Terms and Conditions