Araştırma Makalesi

FGF-23, Inflammation and Iron Metabolism in The Early Stages of Autosomal Dominant Polycystic Kidney Disease

Cilt: 42 Sayı: 2 17 Mart 2020
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FGF-23, Inflammation and Iron Metabolism in The Early Stages of Autosomal Dominant Polycystic Kidney Disease

Öz

To investigate the correlation of Fibroblast Growth Faktör-23 (sFGF-23) with iron status, inflammation and carotid intima-media thickness (CIMT) in the early stages of autosomal dominant polycystic kidney disease (ADPKD). Forty ADPKD patients (24 female) with normal creatinine levels and 40 healthy volunteers (21 female) were included in the study. Serum FGF-23 levels were measured using the ELISA technique. The associations between sFGF-23 with CIMT, hs-CRP, neutrophil lymphocyte ratio (NLR) and iron parameters were evaluated using correlation analysis. Patients’ sFGF-23 levels were significantly higher [245 (182-963) pg/mL; vs. 219.6 (34-494) pg/mL], (P< 0.001). NLR and hs-CRP were also found to be statistically higher in patients than controls (P< 0.001 and P= 0.003, respectively). CIMT was significantly higher in the patient group (P= 0.037). There were statistically significant negative correlations between sFGF-23 and calcium, hemoglobin, hematocrit, serum iron, ferritin, and NLR (P= 0.009, P= 0.035, P= 0.002, P= 0.033, P= 0.017, P= 0.023, respectively), and positive correlations with phosporus, total iron binding capacity and sFGF-23 (P= 0.010, P= 0.049, respectively). There was no statistically significant correlation between sFGF-23 and PTH, hs-CRP and CIMT. In multivariate lineer regression analysis, serum phosphorus level was statistically significiant independent risk factor for the determinantion of sFGF-23 level [B: 0.318, OR:130,662(32,715-228,610), P=0.010]. Our study results support an inverse relationship between sFGF-23 and iron deficiency but no relationship between sFGF-23 and inflammation and atherosclerosis in the early stages of ADPKD.

Anahtar Kelimeler

Kaynakça

  1. References:1. Isakova T, Wahl P, Vargas GS, et al. Fibroblast growth factor 23 is elevated before parathyroid hormone and phosphate in chronic kidney disease. Kidney international. 2011;79:1370–1378.
  2. 2. Lukaszyk E, Lukaszyk M, Koc-Zorawska E, Bodzenta-Lukaszyk A, Malyszko J. Fibroblast growth factor 23, iron and inflammation are they related in early stages of chronic kidney disease? Arch Med Sci. 2017;13, 4: 845–850
  3. 3. Masanobu Kawai. The FGF23/Klotho axis in the regulation of mineral and metabolic homeostasis. Horm Mol Biol Clin Invest. 2016;28(1): 55–67
  4. 4. Scialla JJ, Xie H, Rahman M, et al.; Chronic Renal Insufficiency Cohort (CRIC) Study Investigators. Fibroblast growth factor-23 and cardiovascular events in CKD. J Am Soc Nephrol. 2014;25: 349-60.
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  6. 6. Kocaman O, Oflaz H, Yekeler E, et al. Endothelial dysfunction and increased carotid intima-media thickness in patients with autosomal dominant polycystic kidney disease. Am J Kidney Dis, 2004;43: 854-60.
  7. 7. Pavik I, Jaeger P, Kistler AD, et al. Patients with autosomal dominant polycystic kidney disease have elevated fibroblast growth factor 23 levels and a renal leak of phosphate. Kidney Int. 2011; 79: 234-40.
  8. 8. Munoz Mendoza J, Isakova T, Ricardo AC, et al.; Chronic Renal Insufficiency Cohort. Fibroblast Growth Factor 23 and Inflammation in CKD. Clin J Am Soc Nephrol. 2012;Jul;7(7):1155-62.

Ayrıntılar

Birincil Dil

İngilizce

Konular

Sağlık Kurumları Yönetimi

Bölüm

Araştırma Makalesi

Yayımlanma Tarihi

17 Mart 2020

Gönderilme Tarihi

16 Mart 2019

Kabul Tarihi

11 Nisan 2019

Yayımlandığı Sayı

Yıl 2020 Cilt: 42 Sayı: 2

Kaynak Göster

APA
Doğan, İ., Ocak, B., Eser, B., Kayadibi, H., Özkurt, S., & Kısakol, G. (2020). FGF-23, Inflammation and Iron Metabolism in The Early Stages of Autosomal Dominant Polycystic Kidney Disease. Osmangazi Tıp Dergisi, 42(2), 195-202. https://doi.org/10.20515/otd.540614
AMA
1.Doğan İ, Ocak B, Eser B, Kayadibi H, Özkurt S, Kısakol G. FGF-23, Inflammation and Iron Metabolism in The Early Stages of Autosomal Dominant Polycystic Kidney Disease. Osmangazi Tıp Dergisi. 2020;42(2):195-202. doi:10.20515/otd.540614
Chicago
Doğan, İbrahim, Birol Ocak, Barış Eser, Hüseyin Kayadibi, Sultan Özkurt, ve Gürcan Kısakol. 2020. “FGF-23, Inflammation and Iron Metabolism in The Early Stages of Autosomal Dominant Polycystic Kidney Disease”. Osmangazi Tıp Dergisi 42 (2): 195-202. https://doi.org/10.20515/otd.540614.
EndNote
Doğan İ, Ocak B, Eser B, Kayadibi H, Özkurt S, Kısakol G (01 Mart 2020) FGF-23, Inflammation and Iron Metabolism in The Early Stages of Autosomal Dominant Polycystic Kidney Disease. Osmangazi Tıp Dergisi 42 2 195–202.
IEEE
[1]İ. Doğan, B. Ocak, B. Eser, H. Kayadibi, S. Özkurt, ve G. Kısakol, “FGF-23, Inflammation and Iron Metabolism in The Early Stages of Autosomal Dominant Polycystic Kidney Disease”, Osmangazi Tıp Dergisi, c. 42, sy 2, ss. 195–202, Mar. 2020, doi: 10.20515/otd.540614.
ISNAD
Doğan, İbrahim - Ocak, Birol - Eser, Barış - Kayadibi, Hüseyin - Özkurt, Sultan - Kısakol, Gürcan. “FGF-23, Inflammation and Iron Metabolism in The Early Stages of Autosomal Dominant Polycystic Kidney Disease”. Osmangazi Tıp Dergisi 42/2 (01 Mart 2020): 195-202. https://doi.org/10.20515/otd.540614.
JAMA
1.Doğan İ, Ocak B, Eser B, Kayadibi H, Özkurt S, Kısakol G. FGF-23, Inflammation and Iron Metabolism in The Early Stages of Autosomal Dominant Polycystic Kidney Disease. Osmangazi Tıp Dergisi. 2020;42:195–202.
MLA
Doğan, İbrahim, vd. “FGF-23, Inflammation and Iron Metabolism in The Early Stages of Autosomal Dominant Polycystic Kidney Disease”. Osmangazi Tıp Dergisi, c. 42, sy 2, Mart 2020, ss. 195-02, doi:10.20515/otd.540614.
Vancouver
1.İbrahim Doğan, Birol Ocak, Barış Eser, Hüseyin Kayadibi, Sultan Özkurt, Gürcan Kısakol. FGF-23, Inflammation and Iron Metabolism in The Early Stages of Autosomal Dominant Polycystic Kidney Disease. Osmangazi Tıp Dergisi. 01 Mart 2020;42(2):195-202. doi:10.20515/otd.540614


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