1ST-PHASE INSULIN RELEASE IN ADULT CYSTIC-FIBROSIS PATIENTS - CORRELATION WITH CLINICAL AND BIOLOGICAL PARAMETERS

被引:24
作者
DESCHEPPER, J [1 ]
HACHIMIIDRISSI, S [1 ]
SMITZ, J [1 ]
DAB, I [1 ]
LOEB, H [1 ]
机构
[1] VRIJE UNIV BRUSSELS,ACAD ZIEKENHUIS KINDEREN,DEPT RIA,B-1090 BRUSSELS,BELGIUM
关键词
CYSTIC FIBROSIS; INSULIN; GLUCOSE TOLERANCE;
D O I
10.1159/000182555
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adult patients with cystic fibrosis (CF) are at high risk for developing insulin-dependent diabetes mellitus. Therefore, the fast insulin release (FIR) to intravenously administered glucose was measured in 23 adult CF patients. The influence of the clinical parameters and type of gene deletion on the amplitude of the FIR, defined by the sum of the 1st- and 3rd-minute insulin concentrations was analyzed. In 11 of the 18 normoglycemic patients with exocrine pancreatic insufficiency and the 3 nontreated diabetic CF patients studied, an FIR value lower than the 3rd percentile was found. The female patients had higher mean FIR values than the male patients (62.8 +/- 39.6 vs. 27.9 +/- 17.9 mU/l; p < 0.05). No influence of age, body mass index, or pulmonary or liver involvement on the FIR was found. Subjects heterozygous for the delta F508 deletion had a similar insulin response as homozygous patients. The FIR level correlated negatively with the basal glucose level (r = 0.4; p < 0.001). In conclusion, 61% of the adult nondiabetic CF patients with exocrine pancreatic insufficiency presented a loss in acute insulin response, which could not be predicted by clinical or genetic parameters.
引用
收藏
页码:260 / 263
页数:4
相关论文
共 16 条
[1]   ORAL GLUCOSE-TOLERANCE TESTING IN CYSTIC-FIBROSIS - CORRELATIONS WITH CLINICAL-PARAMETERS AND GLYCOSYLATED HEMOGLOBIN DETERMINATIONS [J].
DESCHEPPER, J ;
DAB, I ;
DERDE, MP ;
LOEB, H .
EUROPEAN JOURNAL OF PEDIATRICS, 1991, 150 (06) :403-406
[2]   DIABETES-MELLITUS ASSOCIATED WITH CYSTIC-FIBROSIS [J].
FINKELSTEIN, SM ;
WIELINSKI, CL ;
ELLIOTT, GR ;
WARWICK, WJ ;
BARBOSA, J ;
WU, SC ;
KLEIN, DJ .
JOURNAL OF PEDIATRICS, 1988, 112 (03) :373-377
[3]  
HANDWERGER S, 1969, NEW ENGL J MED, V281, P452
[4]   ENDOCRINE PANCREAS IN CYSTIC-FIBROSIS - AN IMMUNOHISTOCHEMICAL STUDY [J].
IANNUCCI, A ;
MUKAI, K ;
JOHNSON, D ;
BURKE, B .
HUMAN PATHOLOGY, 1984, 15 (03) :278-284
[5]   SEVERITY OF CYSTIC-FIBROSIS IN PATIENTS HOMOZYGOUS AND HETEROZYGOUS FOR DELTA-F508 MUTATION [J].
JOHANSEN, HK ;
NIR, M ;
HOIBY, N ;
KOCH, C ;
SCHWARTZ, M .
LANCET, 1991, 337 (8742) :631-634
[6]  
KUGLIN B, 1989, ARZTL LAB, V35, P135
[7]   INFLUENCE OF THE DEVELOPMENT OF DIABETES-MELLITUS ON CLINICAL STATUS IN PATIENTS WITH CYSTIC-FIBROSIS [J].
LANNG, S ;
THORSTEINSSON, B ;
NERUP, J ;
KOCH, C .
EUROPEAN JOURNAL OF PEDIATRICS, 1992, 151 (09) :684-687
[8]   GLUCOSE-TOLERANCE IN CYSTIC-FIBROSIS [J].
LANNG, S ;
THORSTEINSSON, B ;
ERICHSEN, G ;
NERUP, J ;
KOCH, C .
ARCHIVES OF DISEASE IN CHILDHOOD, 1991, 66 (05) :612-616
[9]   BLOOD GLUCOSE AND SERUM INSULIN LEVELS IN CHILDREN WITH CYSTIC FIBROSIS [J].
MILNER, AD .
ARCHIVES OF DISEASE IN CHILDHOOD, 1969, 44 (235) :351-&
[10]   PANCREATIC ENDOCRINE FUNCTION IN CYSTIC-FIBROSIS [J].
MORAN, A ;
DIEM, P ;
KLEIN, DJ ;
LEVITT, MD ;
ROBERTSON, RP .
JOURNAL OF PEDIATRICS, 1991, 118 (05) :715-723