Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Mar 29;19(7):4069.
doi: 10.3390/ijerph19074069.

Cystic Fibrosis-Related Diabetes in Poland

Affiliations

Cystic Fibrosis-Related Diabetes in Poland

Marta Rachel et al. Int J Environ Res Public Health. .

Abstract

Cystic fibrosis (CF) is the most common autosomal recessive inherited monogenic disease in Caucasians. As medical technology progresses and the quality of patient care improves, the survival time of patients with CF has increased, which results in more frequent comorbidities such as cystic fibrosis-related diabetes (CFRD). CFRD is the result of abnormal glucose metabolism characterized primarily by insulin deficiency, exacerbated periodically by insulin resistance. The aim of our study was to analyze the epidemiology of patients with CFRD in Poland on the basis of data collected from six CF treatment centers. Analyses were performed on 1157 CF patients who were treated at one of the six CF care centers. CFRD was diagnosed according to standard criteria. All data including demographics, types of CFTR mutations, CFRD duration, and microorganisms in the sputum were obtained from the patients' medical history. Our study indicates that the prevalence of CFRD in Poland is 12.9%. CFRD was most often diagnosed between the ages of 11 and 20 (60% of patients), while 23% of patients were diagnosed between 21 and 30 years of age. Furthermore, we observed that approximately 3-5% of patients under the age of 10 had CFRD. We found out that the type of mutation did not affect the frequency of CFRD development. Factors that increased the risk of developing CFRD include underweight and chronic Pseudomonas aeruginosa infection. Due to the extended lifespan of CF patients, the number of CFRD patients is currently increasing. We believe that the results of our study may complement information from other studies or may be useful in planning health policy in Poland.

Keywords: F508del mutation; cystic fibrosis-related diabetes; diabetes; prevalence.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Flowchart of the study recruitment process.
Figure 2
Figure 2
Age of CFRD diagnosis by sex group.
Figure 3
Figure 3
Percentage of chronic infections in CFRD patients by sex and age group.

Similar articles

Cited by

References

    1. Scotet V., Gutierrez H., Farrell P.M. Newborn screening for CF across the globe—Where is it worthwhile? Int. J. Neonatal Screen. 2020;6:18. doi: 10.3390/ijns6010018. - DOI - PMC - PubMed
    1. Keogh R.H., Tanner K., Simmonds N.J., Bilton D. The changing demography of the cystic fibrosis population: Forecasting future numbers of adults in the UK. Sci. Rep. 2020;10:10660. doi: 10.1038/s41598-020-67353-3. - DOI - PMC - PubMed
    1. Rachel M., Topolewicz S., Śliwczyński A., Galiniak S. Managing Cystic Fibrosis in Polish Healthcare. Int. J. Environ. Res. Public Health. 2020;17:7630. doi: 10.3390/ijerph17207630. - DOI - PMC - PubMed
    1. Jackson A.D., Goss C.H. Epidemiology of CF: How registries can be used to advance our understanding of the CF population. J. Cyst. Fibros. 2018;17:297–305. doi: 10.1016/j.jcf.2017.11.013. - DOI - PubMed
    1. Simmonds N.J., Cullinan P., Hodson M.E. Growing old with cystic fibrosis—The characteristics of long-term survivors of cystic fibrosis. Respir. Med. 2009;103:629–635. doi: 10.1016/j.rmed.2008.10.011. - DOI - PubMed