Araştırma Makalesi

Endocan Levels in Children with Polycystic Kidney Disease

Cilt: 16 Sayı: 4 7 Temmuz 2022
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Endocan Levels in Children with Polycystic Kidney Disease

Öz

Objective: Autosomal dominant polycystic kidney disease (ADPKD) is a common renal disorder that is characterized by hypertension and renal failure. Recently, it has been emphasized that endocan which is an endothelial dysfunction biomarker, could increase in many renal diseases. High endocan levels have also been reported in hypertensive ADPKD adult patients with renal failure. However, studies are limited on children. In this study, we investigated the serum endocan levels in normotensive ADPKD children with normal renal function.

Material and Methods: The study consisted of 20 ADPKD children without hypertension and renal failure as a patient group, and 20 healthy age- and sex-matched children as a control group. Serum endocan levels were determined by enzyme-linked immunosorbent assay techniques and compared between the two groups.

Results: The mean age of patients was 9.9±4.12 years, and the mean age of the control group was 10.2±3.83 years. There was no significant difference between the two groups in terms of gender, age, and BMI (p=0.751, p=0.813, p=0.781, respectively). The leukocyte (p=0.449), hemoglobin (p=0.337), platelets (p=0.134), serum uric acid (p=0.671) and serum creatinine (p=0.074) levels, eGFR (p=0.459) were not significantly differed between groups. The mean serum endocan level in the PKD group was 345.8±169.5 pg/ml, and in the control group was 448.61±258.2 pg/ml. Serum endocan levels did not change between groups (p=0.159).

Conclusion: Unlike the adult ADPKD patients, this study suggested that serum endocan level was normal in children with ADPKD without hypertension and renal failure.

Anahtar Kelimeler

Destekleyen Kurum

Ankara Doşkapı Çocuk hematoloji ve onkoloji hastanesi etik kurul

Proje Numarası

2019-155

Kaynakça

  1. 1. Torres VE, Harris PC, Pirson Y. Autosomal dominant polycystic kidney disease. Lancet 2007; 369: 1287–301.
  2. 2. Harris PC, Torres VE. Polycystic kidney disease. Annu Rev Med 2009; 60: 321–37.
  3. 3. Rahbari-Oskoui F, Williams O, Chapman A. Mechanisms and management of hypertension in autosomal dominant polycystic kidney disease. Nephrol Dial Transplant 2014; 29: 2194–201.
  4. 4. Karihaloo A, Koraishy F, Huen SC, Lee Y,Merrick D, Caplan MJ, et al. Macrophages promote cyst growth in polycystic kidney disease. J Am Soc Nephrol 2011; 22: 1809–14.
  5. 5. Hiesberger T, Gourley E, Erickson A, Koulen P, Ward CJ, Masyuk TV. et al. Proteolytic cleavage and nuclear translocation of fibrocystin is regulated by intracellular Ca2+ and activation of protein kinase C. J Biol Chem 2006; 281: 34357–64.
  6. 6. Raptis V, Bakogiannis C, Loutradis C, Boutou AK, Lampropoulou I, Intzevidou E. et al. Levels of Endocan, Angiopoietin-2, and Hypoxia Inducible Factor-1a in patients with autosomal dominant polycystic kidney disease and different levels of renal fuction. Am J Nephrol 2018; 47: 231–8.
  7. 7. Messchendorp AL, MEijer E, Boertien WE, Engels GE, Casteleijn NF, Spithoven EM. et al. Urinary biomarkers to identify autosomal dominant polycystic kidney disease patients with a high likelihood of disease progression. Kidney Int Rep 2018; 3: 291-301.
  8. 8. Lassalle P, Molet S, Janin A, Heyden JV, Tavernier J, Fiers W. et al. ESM-1 is a novel human endothelial cell-specific molecule expressed in lung and regulated by cytokines. J Biol Chem 1996; 271: 20458–64.

Ayrıntılar

Birincil Dil

İngilizce

Konular

Klinik Tıp Bilimleri

Bölüm

Araştırma Makalesi

Yayımlanma Tarihi

7 Temmuz 2022

Gönderilme Tarihi

2 Ekim 2021

Kabul Tarihi

2 Kasım 2021

Yayımlandığı Sayı

Yıl 2022 Cilt: 16 Sayı: 4

Kaynak Göster

APA
Aydın, Z., Aygar, İ. S., Bayrakçı, U. S., İnözü, M., & Çaycı, F. Ş. (2022). Endocan Levels in Children with Polycystic Kidney Disease. Türkiye Çocuk Hastalıkları Dergisi, 16(4), 313-317. https://doi.org/10.12956/tchd.1002968
AMA
1.Aydın Z, Aygar İS, Bayrakçı US, İnözü M, Çaycı FŞ. Endocan Levels in Children with Polycystic Kidney Disease. Türkiye Çocuk Hast Derg. 2022;16(4):313-317. doi:10.12956/tchd.1002968
Chicago
Aydın, Zehra, İsmail Selçuk Aygar, Umut Selda Bayrakçı, Mihriban İnözü, ve Fatma Şemsa Çaycı. 2022. “Endocan Levels in Children with Polycystic Kidney Disease”. Türkiye Çocuk Hastalıkları Dergisi 16 (4): 313-17. https://doi.org/10.12956/tchd.1002968.
EndNote
Aydın Z, Aygar İS, Bayrakçı US, İnözü M, Çaycı FŞ (01 Temmuz 2022) Endocan Levels in Children with Polycystic Kidney Disease. Türkiye Çocuk Hastalıkları Dergisi 16 4 313–317.
IEEE
[1]Z. Aydın, İ. S. Aygar, U. S. Bayrakçı, M. İnözü, ve F. Ş. Çaycı, “Endocan Levels in Children with Polycystic Kidney Disease”, Türkiye Çocuk Hast Derg, c. 16, sy 4, ss. 313–317, Tem. 2022, doi: 10.12956/tchd.1002968.
ISNAD
Aydın, Zehra - Aygar, İsmail Selçuk - Bayrakçı, Umut Selda - İnözü, Mihriban - Çaycı, Fatma Şemsa. “Endocan Levels in Children with Polycystic Kidney Disease”. Türkiye Çocuk Hastalıkları Dergisi 16/4 (01 Temmuz 2022): 313-317. https://doi.org/10.12956/tchd.1002968.
JAMA
1.Aydın Z, Aygar İS, Bayrakçı US, İnözü M, Çaycı FŞ. Endocan Levels in Children with Polycystic Kidney Disease. Türkiye Çocuk Hast Derg. 2022;16:313–317.
MLA
Aydın, Zehra, vd. “Endocan Levels in Children with Polycystic Kidney Disease”. Türkiye Çocuk Hastalıkları Dergisi, c. 16, sy 4, Temmuz 2022, ss. 313-7, doi:10.12956/tchd.1002968.
Vancouver
1.Zehra Aydın, İsmail Selçuk Aygar, Umut Selda Bayrakçı, Mihriban İnözü, Fatma Şemsa Çaycı. Endocan Levels in Children with Polycystic Kidney Disease. Türkiye Çocuk Hast Derg. 01 Temmuz 2022;16(4):313-7. doi:10.12956/tchd.1002968

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