Metabolic and clinical events preceding diabetes mellitus onset in cystic fibrosis

Cucinotta D, Arrigo T, De Luca F, Di Benedetto A, Lombardo F, Scoglio R, Sferlazzas C, Magazzú G. Metabolic and clinical events preceding diabetes mellitus onset in cystic fibrosis. Eur J Endocrinol 1996;134:731–6. ISSN 0804–4643 Serial assessments of glucose tolerance, of glucose and insulin areas...

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Veröffentlicht in:European journal of endocrinology 1996-06, Vol.134 (6), p.731-736
Hauptverfasser: CUCINOTTA, D, ARRIGO, T, DE LUCA, F, DI BENEDETTO, A, LOMBARDO, F, SCOGLIO, R, SFERLAZZAS, C, MAGAZZU, G
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container_end_page 736
container_issue 6
container_start_page 731
container_title European journal of endocrinology
container_volume 134
creator CUCINOTTA, D
ARRIGO, T
DE LUCA, F
DI BENEDETTO, A
LOMBARDO, F
SCOGLIO, R
SFERLAZZAS, C
MAGAZZU, G
description Cucinotta D, Arrigo T, De Luca F, Di Benedetto A, Lombardo F, Scoglio R, Sferlazzas C, Magazzú G. Metabolic and clinical events preceding diabetes mellitus onset in cystic fibrosis. Eur J Endocrinol 1996;134:731–6. ISSN 0804–4643 Serial assessments of glucose tolerance, of glucose and insulin areas during an oral glucose tolerance test (OGTT) and of clinical parameters as well were evaluated retrospectively in seven diabetic cystic fibrosis patients (study group) during the 4–6.3 years that preceded diabetes mellitus diagnosis. The same metabolic and clinical parameters were also evaluated in seven age-matched patients who did not develop diabetes during a similar observation period (control group). In the study group, glucose tolerance was impaired in all patients but one since the first OGTT and glucose areas progressively increased over time, whereas in the control group glucose tolerance remained stable during the whole observation period. A significant and progressive blunting of insulin secretion occurred over time in both groups. Insulin secretion, however, was reduced but not exhausted at diabetes diagnosis. Neither modification of glycosylated haemoglobin levels over time nor serum islet cell antibodies at diabetes onset were observed in the study group. The overall clinical course of the disease was not different in either group and remained stable during the observation period. These results indicate that in cystic fibrosis diabetes mellitus onset is preceded by a long-standing deterioration of glucose tolerance, whilst insulin secretion progressively declines over time, irrespectively of glucose tolerance status. The prediabetic worsening of glucose tolerance is not necessarily linked to a worsening of overall clinical status. Filippo De Luca, Istituto di Clinica Pediatrica, Policlinico Universitario, 98100 Messina, Italy
doi_str_mv 10.1530/eje.0.1340731
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Metabolic and clinical events preceding diabetes mellitus onset in cystic fibrosis. Eur J Endocrinol 1996;134:731–6. ISSN 0804–4643 Serial assessments of glucose tolerance, of glucose and insulin areas during an oral glucose tolerance test (OGTT) and of clinical parameters as well were evaluated retrospectively in seven diabetic cystic fibrosis patients (study group) during the 4–6.3 years that preceded diabetes mellitus diagnosis. The same metabolic and clinical parameters were also evaluated in seven age-matched patients who did not develop diabetes during a similar observation period (control group). In the study group, glucose tolerance was impaired in all patients but one since the first OGTT and glucose areas progressively increased over time, whereas in the control group glucose tolerance remained stable during the whole observation period. A significant and progressive blunting of insulin secretion occurred over time in both groups. Insulin secretion, however, was reduced but not exhausted at diabetes diagnosis. Neither modification of glycosylated haemoglobin levels over time nor serum islet cell antibodies at diabetes onset were observed in the study group. The overall clinical course of the disease was not different in either group and remained stable during the observation period. These results indicate that in cystic fibrosis diabetes mellitus onset is preceded by a long-standing deterioration of glucose tolerance, whilst insulin secretion progressively declines over time, irrespectively of glucose tolerance status. The prediabetic worsening of glucose tolerance is not necessarily linked to a worsening of overall clinical status. 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Metabolic and clinical events preceding diabetes mellitus onset in cystic fibrosis. Eur J Endocrinol 1996;134:731–6. ISSN 0804–4643 Serial assessments of glucose tolerance, of glucose and insulin areas during an oral glucose tolerance test (OGTT) and of clinical parameters as well were evaluated retrospectively in seven diabetic cystic fibrosis patients (study group) during the 4–6.3 years that preceded diabetes mellitus diagnosis. The same metabolic and clinical parameters were also evaluated in seven age-matched patients who did not develop diabetes during a similar observation period (control group). In the study group, glucose tolerance was impaired in all patients but one since the first OGTT and glucose areas progressively increased over time, whereas in the control group glucose tolerance remained stable during the whole observation period. A significant and progressive blunting of insulin secretion occurred over time in both groups. Insulin secretion, however, was reduced but not exhausted at diabetes diagnosis. Neither modification of glycosylated haemoglobin levels over time nor serum islet cell antibodies at diabetes onset were observed in the study group. The overall clinical course of the disease was not different in either group and remained stable during the observation period. These results indicate that in cystic fibrosis diabetes mellitus onset is preceded by a long-standing deterioration of glucose tolerance, whilst insulin secretion progressively declines over time, irrespectively of glucose tolerance status. The prediabetic worsening of glucose tolerance is not necessarily linked to a worsening of overall clinical status. Filippo De Luca, Istituto di Clinica Pediatrica, Policlinico Universitario, 98100 Messina, Italy</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - analysis</subject><subject>CLINICAL STUDIES</subject><subject>Cystic Fibrosis - complications</subject><subject>Cystic Fibrosis - metabolism</subject><subject>Cystic Fibrosis - physiopathology</subject><subject>Diabetes Mellitus - etiology</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Fasting</subject><subject>Glucose Intolerance</subject><subject>Glucose Tolerance Test</subject><subject>Humans</subject><subject>Insulin - metabolism</subject><subject>Insulin Secretion</subject><subject>Medical sciences</subject><subject>Retrospective Studies</subject><issn>0804-4643</issn><issn>1479-683X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LAzEQhoMotVaPHoUcxNvWSZPNbo4ifkFFEAVvSzaZSMp2t-5shf57U1p69TQvzDMfPIxdCpiKXMItLnCaolRQSHHExkIVJtOl_DpmYyhBZUorecrOiBYAImUYsVFZaG2UGrP3Vxxs3TXRcdt67prYRmcbjr_YDsRXPTr0sf3mPtoaByS-xKaJw5p41xIOPLbcbWhI8yHWfUeRztlJsA3hxb5O2Ofjw8f9czZ_e3q5v5tntTQwZLLMxcwpFzx6WzoBmCutC-NsEdCFmRcBZkYWuVWgBXjUzqCWyoA06GsjJ-xmt3fVdz9rpKFaRnLpO9tit6aqKEVZKL0Fsx3o0n_UY6hWfVzaflMJqLYOq-SwSnHnMPFX-8Xreon-QO-lpf71vm8puQq9bV2kAyaFyhVAwuQOq2NHLiafMSS3_xz_A6Jli2M</recordid><startdate>19960601</startdate><enddate>19960601</enddate><creator>CUCINOTTA, D</creator><creator>ARRIGO, T</creator><creator>DE LUCA, F</creator><creator>DI BENEDETTO, A</creator><creator>LOMBARDO, F</creator><creator>SCOGLIO, R</creator><creator>SFERLAZZAS, C</creator><creator>MAGAZZU, G</creator><general>Portland Press</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19960601</creationdate><title>Metabolic and clinical events preceding diabetes mellitus onset in cystic fibrosis</title><author>CUCINOTTA, D ; ARRIGO, T ; DE LUCA, F ; DI BENEDETTO, A ; LOMBARDO, F ; SCOGLIO, R ; SFERLAZZAS, C ; MAGAZZU, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b390t-38512c4cfdeda8c10e546679ca7fecf2d1f029375a40610de6c9e6349039edb93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Blood Glucose - analysis</topic><topic>CLINICAL STUDIES</topic><topic>Cystic Fibrosis - complications</topic><topic>Cystic Fibrosis - metabolism</topic><topic>Cystic Fibrosis - physiopathology</topic><topic>Diabetes Mellitus - etiology</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Fasting</topic><topic>Glucose Intolerance</topic><topic>Glucose Tolerance Test</topic><topic>Humans</topic><topic>Insulin - metabolism</topic><topic>Insulin Secretion</topic><topic>Medical sciences</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CUCINOTTA, D</creatorcontrib><creatorcontrib>ARRIGO, T</creatorcontrib><creatorcontrib>DE LUCA, F</creatorcontrib><creatorcontrib>DI BENEDETTO, A</creatorcontrib><creatorcontrib>LOMBARDO, F</creatorcontrib><creatorcontrib>SCOGLIO, R</creatorcontrib><creatorcontrib>SFERLAZZAS, C</creatorcontrib><creatorcontrib>MAGAZZU, G</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CUCINOTTA, D</au><au>ARRIGO, T</au><au>DE LUCA, F</au><au>DI BENEDETTO, A</au><au>LOMBARDO, F</au><au>SCOGLIO, R</au><au>SFERLAZZAS, C</au><au>MAGAZZU, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolic and clinical events preceding diabetes mellitus onset in cystic fibrosis</atitle><jtitle>European journal of endocrinology</jtitle><addtitle>Eur J Endocrinol</addtitle><date>1996-06-01</date><risdate>1996</risdate><volume>134</volume><issue>6</issue><spage>731</spage><epage>736</epage><pages>731-736</pages><issn>0804-4643</issn><eissn>1479-683X</eissn><abstract>Cucinotta D, Arrigo T, De Luca F, Di Benedetto A, Lombardo F, Scoglio R, Sferlazzas C, Magazzú G. Metabolic and clinical events preceding diabetes mellitus onset in cystic fibrosis. Eur J Endocrinol 1996;134:731–6. ISSN 0804–4643 Serial assessments of glucose tolerance, of glucose and insulin areas during an oral glucose tolerance test (OGTT) and of clinical parameters as well were evaluated retrospectively in seven diabetic cystic fibrosis patients (study group) during the 4–6.3 years that preceded diabetes mellitus diagnosis. The same metabolic and clinical parameters were also evaluated in seven age-matched patients who did not develop diabetes during a similar observation period (control group). In the study group, glucose tolerance was impaired in all patients but one since the first OGTT and glucose areas progressively increased over time, whereas in the control group glucose tolerance remained stable during the whole observation period. A significant and progressive blunting of insulin secretion occurred over time in both groups. Insulin secretion, however, was reduced but not exhausted at diabetes diagnosis. Neither modification of glycosylated haemoglobin levels over time nor serum islet cell antibodies at diabetes onset were observed in the study group. The overall clinical course of the disease was not different in either group and remained stable during the observation period. These results indicate that in cystic fibrosis diabetes mellitus onset is preceded by a long-standing deterioration of glucose tolerance, whilst insulin secretion progressively declines over time, irrespectively of glucose tolerance status. The prediabetic worsening of glucose tolerance is not necessarily linked to a worsening of overall clinical status. Filippo De Luca, Istituto di Clinica Pediatrica, Policlinico Universitario, 98100 Messina, Italy</abstract><cop>Colchester</cop><pub>Portland Press</pub><pmid>8766944</pmid><doi>10.1530/eje.0.1340731</doi><tpages>6</tpages></addata></record>
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ispartof European journal of endocrinology, 1996-06, Vol.134 (6), p.731-736
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE
subjects Adolescent
Adult
Biological and medical sciences
Blood Glucose - analysis
CLINICAL STUDIES
Cystic Fibrosis - complications
Cystic Fibrosis - metabolism
Cystic Fibrosis - physiopathology
Diabetes Mellitus - etiology
Diabetes. Impaired glucose tolerance
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Etiopathogenesis. Screening. Investigations. Target tissue resistance
Fasting
Glucose Intolerance
Glucose Tolerance Test
Humans
Insulin - metabolism
Insulin Secretion
Medical sciences
Retrospective Studies
title Metabolic and clinical events preceding diabetes mellitus onset in cystic fibrosis
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