-
Je něco špatně v tomto záznamu ?
FGF21 Levels in Pheochromocytoma/Functional Paraganglioma
J. Klímová, T. Zelinka, J. Rosa, B. Štrauch, D. Haluzíková, M. Haluzík, R. Holaj, Z. Krátká, J. Kvasnička, V. Ďurovcová, M. Matoulek, K. Novák, D. Michalský, J. Widimský, O. Petrák,
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
Grantová podpora
AZV 16-30345A
Ministerstvo Zdravotnictví Ceské Republiky
NV16-30345A
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
NLK
Free Medical Journals
od 2009
PubMed Central
od 2009
Europe PubMed Central
od 2009
ProQuest Central
od 2009-01-01
Open Access Digital Library
od 2009-01-01
Open Access Digital Library
od 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2009
PubMed
30959789
DOI
10.3390/cancers11040485
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
Fibroblast growth factor 21 (FGF21) is a hepatokine with beneficial effects on metabolism. Our aim was to evaluate the relationship between the serum FGF21, and energy and glucose metabolism in 40 patients with pheochromocytoma/functional paraganglioma (PPGL), in comparison with 21 obese patients and 26 lean healthy controls. 27 patients with PPGL were examined one year after tumor removal. Basic anthropometric and biochemical measurements were done. Energy metabolism was measured by indirect calorimetry (Vmax-Encore 29N). FGF21 was measured by ELISA. FGF21 was higher in PPGL than in controls (174.2 (283) pg/mL vs. 107.9 (116) pg/mL; p < 0.001) and comparable with obese (174.2 (283) pg/mL vs. 160.4 (180); p = NS). After tumor removal, FGF21 decreased (176.4 (284) pg/mL vs. 131.3 (225) pg/mL; p < 0.001). Higher levels of FGF21 were expressed, particularly in patients with diabetes. FGF21 positively correlated in PPGL with age (p = 0.005), BMI (p = 0.028), glycemia (p = 0.002), and glycated hemoglobin (p = 0.014). In conclusion, long-term catecholamine overproduction in PPGL leads to the elevation in serum FGF21, especially in patients with secondary diabetes. FGF21 levels were comparable between obese and PPGL patients, despite different anthropometric indices. We did not find a relationship between FGF21 and hypermetabolism in PPGL. Tumor removal led to the normalization of FGF21 and the other metabolic abnormalities.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19029199
- 003
- CZ-PrNML
- 005
- 20190819085026.0
- 007
- ta
- 008
- 190813s2019 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3390/cancers11040485 $2 doi
- 035 __
- $a (PubMed)30959789
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Klímová, Judita $u Third Department of Medicine, Department of Endocrinology and Metabolism of the First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic. Judita.Klimova@vfn.cz.
- 245 10
- $a FGF21 Levels in Pheochromocytoma/Functional Paraganglioma / $c J. Klímová, T. Zelinka, J. Rosa, B. Štrauch, D. Haluzíková, M. Haluzík, R. Holaj, Z. Krátká, J. Kvasnička, V. Ďurovcová, M. Matoulek, K. Novák, D. Michalský, J. Widimský, O. Petrák,
- 520 9_
- $a Fibroblast growth factor 21 (FGF21) is a hepatokine with beneficial effects on metabolism. Our aim was to evaluate the relationship between the serum FGF21, and energy and glucose metabolism in 40 patients with pheochromocytoma/functional paraganglioma (PPGL), in comparison with 21 obese patients and 26 lean healthy controls. 27 patients with PPGL were examined one year after tumor removal. Basic anthropometric and biochemical measurements were done. Energy metabolism was measured by indirect calorimetry (Vmax-Encore 29N). FGF21 was measured by ELISA. FGF21 was higher in PPGL than in controls (174.2 (283) pg/mL vs. 107.9 (116) pg/mL; p < 0.001) and comparable with obese (174.2 (283) pg/mL vs. 160.4 (180); p = NS). After tumor removal, FGF21 decreased (176.4 (284) pg/mL vs. 131.3 (225) pg/mL; p < 0.001). Higher levels of FGF21 were expressed, particularly in patients with diabetes. FGF21 positively correlated in PPGL with age (p = 0.005), BMI (p = 0.028), glycemia (p = 0.002), and glycated hemoglobin (p = 0.014). In conclusion, long-term catecholamine overproduction in PPGL leads to the elevation in serum FGF21, especially in patients with secondary diabetes. FGF21 levels were comparable between obese and PPGL patients, despite different anthropometric indices. We did not find a relationship between FGF21 and hypermetabolism in PPGL. Tumor removal led to the normalization of FGF21 and the other metabolic abnormalities.
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Zelinka, Tomáš $u Third Department of Medicine, Department of Endocrinology and Metabolism of the First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic. Tomas.Zelinka@vfn.cz.
- 700 1_
- $a Rosa, Ján $u Third Department of Medicine, Department of Endocrinology and Metabolism of the First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic. Jan.Rosa@vfn.cz.
- 700 1_
- $a Štrauch, Branislav $u Third Department of Medicine, Department of Endocrinology and Metabolism of the First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic. Branislav.Strauch@vfn.cz.
- 700 1_
- $a Haluzíková, Denisa $u Institute of Sports Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, 120 00 Prague, Czech Republic. Denisa.Haluzikova@vfn.cz.
- 700 1_
- $a Haluzík, Martin $u Centre for Experimental Medicine and Diabetes Centre, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic. martin.haluzik@ikem.cz. Institute for Medical Biochemistry and Laboratory Diagnostics, Charles University and General University Hospital in Prague, 128 08 Prague, Czech Republic. martin.haluzik@ikem.cz.
- 700 1_
- $a Holaj, Robert $u Third Department of Medicine, Department of Endocrinology and Metabolism of the First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic. Robert.Holaj@vfn.cz.
- 700 1_
- $a Krátká, Zuzana $u Third Department of Medicine, Department of Endocrinology and Metabolism of the First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic. Zuzana.Kratka@vfn.cz.
- 700 1_
- $a Kvasnička, Jan $u Third Department of Medicine, Department of Endocrinology and Metabolism of the First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic. Jan.Kvasnicka3@vfn.cz.
- 700 1_
- $a Ďurovcová, Viktorie $u Third Department of Medicine, Department of Endocrinology and Metabolism of the First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic. viktoria.durovcova@gmail.com.
- 700 1_
- $a Matoulek, Martin $u Third Department of Medicine, Department of Endocrinology and Metabolism of the First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic. martin.matoulek@vstj.cz.
- 700 1_
- $a Novák, Květoslav $u Department of Urology of the First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic. Kvetoslav.Novak@vfn.cz.
- 700 1_
- $a Michalský, David $u First Department of Surgery of the First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic. david.michalsky@vfn.cz.
- 700 1_
- $a Widimský, Jiří $u Third Department of Medicine, Department of Endocrinology and Metabolism of the First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic. Jiri.Widimsky@vfn.cz.
- 700 1_
- $a Petrák, Ondřej $u Third Department of Medicine, Department of Endocrinology and Metabolism of the First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic. Ondrej.Petrak@vfn.cz.
- 773 0_
- $w MED00173178 $t Cancers $x 2072-6694 $g Roč. 11, č. 4 (2019)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/30959789 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20190813 $b ABA008
- 991 __
- $a 20190819085300 $b ABA008
- 999 __
- $a ind $b bmc $g 1434348 $s 1067659
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 11 $c 4 $e 20190405 $i 2072-6694 $m Cancers $n Cancers $x MED00173178
- GRA __
- $a AZV 16-30345A $p Ministerstvo Zdravotnictví Ceské Republiky
- GRA __
- $a NV16-30345A $p MZ0
- LZP __
- $a Pubmed-20190813