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Significance of fructosamine in the diagnosis of carbohydrate metabolism disorders in children with cystic fibrosis

https://doi.org/10.21518/2079-701X-2022-16-1-226-234

Abstract

Introduction. Cystic fibrosis associated (related) diabetes mellitus (CFDM) is one of the most common severe complications of cystic fibrosis. Today, the issue of the goodness of a single measurement of fasting blood glucose, glycated hemoglobin and fructosamine to assess the degree of carbohydrate metabolism disorders in children with cystic fibrosis is a subject of debate. The gold standard for diagnosing carbohydrate metabolism disorders (impaired fasting glycemia, various pre-diabetic conditions, diabetes mellitus) is the oral glucose tolerance test. Data about the diagnostic value of fructosamine for predicting CFDM aren’t dispositive. No credible studies of fructosamine in children with cystic fibrosis have been found in the Russian medical literature.
Aim. To determine the diagnostic informative value of the blood fructosamine and other single-measured glycemic marker levels in the early diagnosis of carbohydrate metabolism disorders at the pre-diabetes stage in children with cystic fibrosis.
Materials and methods. The results of laboratory tests and instrumental examinations of 87 children with cystic fibrosis aged 5–18 years were reviewed. A cross-sectional study of fructosamine, fasting blood sugar and glycated hemoglobin level (some patients underwent an oral glucose tolerance test), and liver fibroelastometry were also performed.
Results and discussion. An increase in the fructosamine level was observed, which indicates a possible CFDM in children (p = 0.049): CFDM is highly likely, if the level of fructosamine is ≥255.5 µmol/l (reference ranges for children are 272–285 µmol/l; sensitivity = 57.1%, specificity = 85.2%). It has been found that children with cystic fibrosis and liver cirrhosis have increased fructosamine levels: cut-off = 253.0 µmol/l (Sn – 70.0%, Sp – 85.2%).
Conclusion. The fructosamine level, a single determination of fasting blood glucose and glycated hemoglobin are not informative markers for the diagnosis of pre-diabetic conditions in cystic fibrosis in children. It is important to bear in mind that concomitant liver cirrhosis can affect the fructosamine levels. CFDM can be diagnosed at the lower fructosamine level, despite the generally accepted ranges.

About the Authors

N. V. Liabina
National Medical Research Center for Children’s Health
Russian Federation

Pediatrician, Pulmonology Department, Postgraduate Student

2, Bldg. 1, Lomonosov Ave., Moscow, 119926, Russia 



O. I. Simonova
National Medical Research Center for Children’s Health; Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation

 Dr. Sci. (Med.), Head of Pulmonology Department; Professor of Department of Pediatrics and Pediatric Rheumatology

2, Bldg. 1, Lomonosov Ave., Moscow, 119926, Russia

8, Bldg. 2, Trubetskaya St., Moscow, 119991, Russia 



I. V. Shirokova
National Medical Research Center for Children’s Health
Russian Federation

 Cand. Sci. (Med.), Endocrinologist, Consulting and Outpatient Department

2, Bldg. 1, Lomonosov Ave., Moscow, 119926, Russia 



E. L. Semikina
National Medical Research Center for Children’s Health; Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation

 Dr. Sci. (Med.), Lead Research Associate, Head of Laboratory Department; Professor of Department of Pediatrics and Pediatric Rheumatology, Doctor of Clinical Laboratory Diagnostics

2, Bldg. 1, Lomonosov Ave., Moscow, 119926, Russia

8, Bldg. 2, Trubetskaya St., Moscow, 119991, Russia 



E. F. Mavrikidi
National Medical Research Center for Children’s Health
Russian Federation

 Doctor of Clinical Diagnostic Laboratory with Express Diagnostics Group

2, Bldg. 1, Lomonosov Ave., Moscow, 119926, Russia 



I. I. Kondrakhina
National Medical Research Center for Children’s Health
Russian Federation

Doctor of Clinical Diagnostic Laboratory with Express Diagnostics Group

2, Bldg. 1, Lomonosov Ave., Moscow, 119926, Russia 



Yu. V. Gorinova
National Medical Research Center for Children’s Health
Russian Federation

Cand. Sci. (Med.), Senior Research Associate, Paediatric Rare and Genetic Disorders’ Lab, Pulmonologist

2, Bldg. 1, Lomonosov Ave., Moscow, 119926, Russia 



V. A. Kerimova
Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation

Resident Physician

8, Bldg. 2, Trubetskaya St., Moscow, 119991, Russia 



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Review

For citations:


Liabina NV, Simonova OI, Shirokova IV, Semikina EL, Mavrikidi EF, Kondrakhina II, Gorinova YV, Kerimova VA. Significance of fructosamine in the diagnosis of carbohydrate metabolism disorders in children with cystic fibrosis. Meditsinskiy sovet = Medical Council. 2022;(1):226-234. (In Russ.) https://doi.org/10.21518/2079-701X-2022-16-1-226-234

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ISSN 2079-701X (Print)
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