Respiratio 2020, 2021, 2022; 10, 11, 12 (1-2-3): 15-21
POREĐENJE EFIKASNOSTI DVA TERAPIJSKA REŽIMA NA OPORAVAK INSULINOSEKRETORNE FUNKCIJE U BOLESNIKA SA TIPOM 2 DIJABETESA I SEKUNDARNIM NEUSPJEHOM ORALNE TERAPIJE
COMPARISON OF THE EFFICACY OF TWO THERAPEUTIC REGIMES ON THE RECOVERY OF INSULINOSECRETORIAL FUNCTION IN PATIENTS WITH TYPE 2 DIABETES AND SECONDARY FAILURE OF ORAL THERAPY
Aleksandra Marković*, Gabrijela Malešević *, Milena Brkić**, Ivona Risović * , Valentina
Soldat - Stanković* , Bojana Carić*
Original Research
Naučni članak
Sažetak: Uvod: Sekundarni neuspjeh oralne terapije se definiše kao izostanak povoljnog reagovanja
na oralnu terapiju koja je u prethodnom periodu bolesti bila efikasna. Cilj istraživanja predstavlja
poređenje efekata kratkotrajne insulinske monoterapije i kombinovane terapije (insulin plus metformin)
na insulinosekretornu funkciju i determinsanje režima sa većom efikasnošću u odnosu na ispitivane
parametre.
Metode: U istraživanje je selektovano 75 pacijenata oboljelih od tipa 2 dijabetesa sa potvrđenim
sekundarnim neuspjehom oralne terapije, koji su podijeljeni u dvije grupe na osnovu tjelesne težine, a
svaka grupa je tretirana različitim insulinskim režimima. Pacijenti sa normalnom tjelesnom masom
(grupa A) tretirani su monoinsulinskom intenziviranom konvencionalnom terapijom (tzv. „bazal–bolus“
režim), dok su pacijenti sa povećanom tjelesnom masom (grupa B) tretirani kombinovanom insulinskom
terapijom (bazalni insulin plus metformin) u trajanju od tri mjeseca. Svim ispitanicima su prije, i tri
mjeseca nakon terapijskog režima sa insulinom, rađeni parametri glikoregulacije (HbA1c, glikemija
našte, postprandijalno i cjelodnevni profil), i izračunati homeostatski modeli za procjenu insulinske
sekrecije i rezistencije (HOMA % beta i HOMA IR).
Rezultati: Istraživanja pokazuju poboljšanje glikoregulacije, smanjenjenje IR i poboljšanja
endogenog kapaciteta pankreasa, u obje ispitivane grupe, u odnosu na period prije uključenja insulinske
terapije. Grupa A: glikemija našte (9,5 vs 6,1,p<0,001), postprandijalna (11,6 vs 6,9, p<0,001), HbA1c
(9,0 vs 6,7, p<0,001), HOMA % beta (39,03 vs 83,42, p<0,001), HOMA IR (4,87 vs2,45,p<0,001). Grupa
B: glikemija našte (9,4 vs 6,3, p<0,001), postprandijalna (11,6vs 6,9,p<0,001), HbA1c (9,0vs6,7,
p<0,001), HOMA % beta (54,8 vs 96,92, p<0,001), HOMA IR (7,27 vs 3,38, p<0,001)
Zaključak: Nije bilo značajnih razlika u pogledu efikasnosti na insulinosekretornu funkciju,
insulinsku rezistenciju i glikoregulaciju između dvije ispitivane grupe, odnosno oba terapijska režima su
bili podjednako efikasni.
Ključne riječi: sekundarni neuspjeh, diabetes mellitus tip 2, HOMA % beta, HOMA IR.
Literatura
1. Sushi J, Sanjay K. Developing a definition for Oral Antidiabetic Drug (OAD) Failure. J Pak Med Assoc. 2020; 70(3): 547-551. |
|
|
|
2. Gandhi GY, Mooradian AD. Management of Hyperglycemia in Older Adults with Type 2 Diabetes. Drugs Aging. 2022; 39(1): 39-58. |
|
|
|
3. Bajaj S, Das AK, Kaira S, Sahay R, Saboo B, et al. BE-SMART (Basal Early Strategies to Maximize HbA1c Reduction with Oral Therapy): Expert Opinion. Diabetes Ther. 2019; 10(4): 1189-1204. |
|
|
|
4. Pitocco D, Valle D, Rossi A, Gentilella R. Unmet needs among patients with type 2 diabetes mellitus and secondary failure to oral anti-diabetic agents. J Endocrinol Invest. 2008; 31(4): 371-9. |
|
|
|
5. Chatterje S, Khunti K, Davies MJ. Type 2 diabetes. Lancet. 2017; 389(10085): 2239-51. |
|
|
|
6. Kabadi UM, Kabadi MU, Weber S, Buboloze F. Progressive beta cell failure in type 2 diabetes mellitus: Microvascular Pancreatic isletopathy? J of Diab. Mell. 2015; 21-27. |
|
|
|
7. Kawahito S, Kitahata H, Oshita S. Problem associated with glucose toxicity: roles of hyperglycemia - induced oxidative stress. World J Gastroeneterol.2009; 7(15(33): 4137-4142.4. |
|
|
|
8. Tuccinadri D, Giorgino R, Pieralice S, Watanace M, Maggi D, et al. The utility of assessing C-peptide in patients with insulin-treated type 2 diabetes: a crosssectional study. Acta Diabetol. 2021; 58(4): 411-417. |
|
|
|
9. Nacionalni vodič dobre kliničke prakse. Diabetes mellitus. Beograd. Ministarstvo zdravlja Republike Srbije. 2012. |
|
|
|
10. Ruiz-Mntero PJ, Gonzalez-Fernandez FT, Mikalacki M, Martin-Moya R. The use of anthropometrical variables for detection of homeostatic measurement assessment-insulin resistance (HOMA-IR) in female participants of a physical exercise program. Bratisi Lek Listy. 2021; 122(10): 727-731. |
|
|
|
11. Zheng HL, Xing Y, Li F, Ding W, Ye SD. Effect of short-term intensive insulin therapy on α-cell function in patients with newly diagnosed type 2 diabetes. Medicine (Baltimore). 2020; 99(14): e19685. |
|
|
|
12. Weng J. Short-term intensive insulin therapy could be the preferred option for new onset Type 2 diabetes mellitus patients with HbA1c > 9. Diabetes. 2017; 9(10): 890-893. |
|
|
|
13. Christensen MB, Gaede P, Hommel E, Gotfredsen A, Norgard K. Glycaemic variability and hypoglycaemia are associated with C-peptide levels in insulin-treated type 2 diabetes. Diabetes Metab. 2020; 46(1): 61-65. |
|
|
|
14. Zhang W, Tang Y, Huang J, Yang Y, Yang Q, Hu H. Efficacy of inulin supplementation in improving insulin control, HbA1c and HOMA-IR in patients with type 2 diabetes: a systematic review and metaanalysis of randomized controlled trials. J Clin Biochem Nutr. 2020; 66(3): 176-183. |
|
|
|
15. Wallace TM, Levy JC, Matthews DR. Use and abuse of HOMA modeling. Diabetes Care 2004; 27(6):1487-95. |
|
|
|
16. Tang Q, Li X, Song P, Xu L. Optimal cut-off values for the homeostasis model assessment of insulin resistance (HOMA-IR) and pre-diabetes screening:Developments in research and prospects for the future. Drug Discov Ther. 2015; 9(6): 380-5. |
|
|
|
17. Roscioni SS, Migliorini A, Gegg M, Lickert H. Impact of islet architecture on beta-cell heterogeneity, plasticity and function. Nat RevEndocrinol. 2016; 12: 695-709. doi:10.1038/nrendo.2016.147. |
|
|
|
|
|
18. Adams MT, Blum B. Determinants and dynamics of pancreatic islet architecture. Islets. 2022. 14 (1): 82-100. |
|
|
|
19. Andrews WJ, Vasquez B, Klimes I et al. Insulin therapy in obese, non insulin dependent diabetes induced improvements in insulin action and secretion that are maintained for two weeks after insulin withdrawal. Diabetes. 1984; 33: 634-642. |
|
|
|
20. Campos C. Chronic hyperglycemia and glucose toxicity: pathology and clinical sequel. Postgraduate Medicine. 2012; 124(6). |
|
|
|
21. Wang Z, York NW, Nichols CG, Remedi MS. Pancreatic beta cell dedifferentiation in diabetes and redifferentiation following insulin therapy. Cell Metab. 2014; 19: 872-82. |
|
|
|
22. Mezza T, Cinti F, Cefalo CMA, Pontecorvi A, Kulkani RN, et al. β-Cell Fate in Human Insulin Resistance and Type 2 Diabetes: A Perspective on Islet Plasticity. Diabetes. 2019; 68(6): 1121-1129. |
|
|
|
23. Wang W, Zhang C. Targeting β-cell dedifferentiation and transdifferentiation: opportunities and challenges. Endocr Connect. 2021; 10(8): R213-R228 |
Adresa autora:
Aleksandra Marković
Univerzitetski klinički centar Republike Srpske, Dvanaest beba bb,
Banja Luka
Tel. + 387 65 540 548
E mail: This email address is being protected from spambots. You need JavaScript enabled to view it.
* Univerzitetski Klinički Centar Republike Srpske, Medicinski fakultet
Univerziteta u Banjoj Luci, Republika Srpska, Bosna iHercegovina
**ZU Talmma medic Banja Luka, Medicinski fakultet Univerziteta u
Banjoj Luci, Republika Srpska, Bosna i Hercegovina