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Sökning: id:"swepub:oai:lup.lub.lu.se:c84dd260-b230-45f7-849c-d236d45300dc" > Predictors of deter...

Predictors of deterioration of lung function in cystic fibrosis.

Schaedel, Charlotta (författare)
Lund University,Lunds universitet,Pediatrik, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Paediatrics (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine
de Monestrol, I (författare)
Karolinska Institutet
Hjelte, L (författare)
Karolinska Institutet
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Johannesson, Marie (författare)
Uppsala universitet,Institutionen för kvinnors och barns hälsa,Övrig pediatrisk forskning/Nordvall
Kornfält, Ragnhild (författare)
Lund University,Lunds universitet,Pediatrik, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Paediatrics (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine
Lindblad, A (författare)
Strandvik, B (författare)
Wahlgren, Lars (författare)
Lund University,Lunds universitet,Statistiska institutionen,Ekonomihögskolan,Department of Statistics,Lund University School of Economics and Management, LUSEM
Holmberg, Lars (författare)
Lund University,Lunds universitet,Pediatrik, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Paediatrics (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine
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 (creator_code:org_t)
2002-05-03
2002
Engelska.
Ingår i: Pediatric Pulmonology. - : Wiley. - 8755-6863 .- 1099-0496. ; 33:6, s. 483-491
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The severity of lung disease in cystic fibrosis (CF) may be related to the type of mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, and to environmental and immunological factors. Since pulmonary disease is the main determinant of morbidity and mortality in CF, it is important to identify factors that can explain and predict this variation. The aim of this longitudinal study of the whole Swedish CF population over age 7 years was to correlate genetic and clinical data with the rate of decline in pulmonary function. The statistical analysis was performed using the mixed model regression method, supplemented with calculation of relative risks for severe lung disease in age cohorts.The severity of pulmonary disease was to some extent predicted by CFTR genotype. Furthermore, the present investigation is the first long-term study showing a significantly more rapid deterioration of lung function in patients with concomitant diabetes mellitus. Besides diabetes mellitus, pancreatic insufficiency and chronic Pseudomonas colonization were found to be negative predictors of pulmonary function. In contrast to several other reports, we found no significant differences in lung function between genders. Patients with pancreatic sufficiency have no or only a slight decline of lung function with age once treatment is started, but an early diagnosis in this group is desirable.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)

Nyckelord

Cystic Fibrosis : physiopathology
Cystic Fibrosis : surgery
Cystic Fibrosis Transmembrane Conductance Regulator : genetics
Disease Progression
Female
Human
Longitudinal Studies
Lung : physiopathology
Male
Lung Transplantation
Mutation
Predictive Value of Tests
Regression Analysis
Support
Risk Factors
Non-U.S. Gov't
Cystic Fibrosis : microbiology
Preschool
Child
Alleles
Adult
Adolescence
MEDICINE

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