Investigation of the Relationship Between Fok1 and Col1A1 Gene Polymorphisms and Development of Treatment-Related Bone Complications in Children with Acute Lymphoblastic Leukemia

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Erdem M., TÜFEKÇİ Ö., KIZILDAĞ S., YILMAZ Ş., Kizmazoglu D., Filibeli B. E., ...Daha Fazla

TURKISH JOURNAL OF HEMATOLOGY, cilt.36, sa.1, ss.12-18, 2019 (SCI-Expanded) identifier identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 36 Sayı: 1
  • Basım Tarihi: 2019
  • Doi Numarası: 10.4274/tjh.galenos.2018.2018.0221
  • Dergi Adı: TURKISH JOURNAL OF HEMATOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.12-18
  • Anahtar Kelimeler: Acute lymphoblastic leukemia, Bone mineral density, Genetic polymorphism, Osteonecrosis, Osteoporosis, RAY ABSORPTIOMETRY INTERPRETATION, SP1 BINDING-SITE, VITAMIN-D, MINERAL DENSITY, AVASCULAR NECROSIS, OSTEONECROSIS, CHILDHOOD, ADOLESCENTS, CALCIUM, RISK
  • Dokuz Eylül Üniversitesi Adresli: Evet

Özet

Objective: In acute lymphoblastic leukemia (ALL), various clinical risk factors and genetic predispositions contribute to the development of bone complications during and after chemotherapy. In this study, we aimed to investigate whether vitamin D receptor (VDR) Fok1 and collagen protein Col1A1 Sp1-binding site gene polymorphisms, which are important in bone mineral and matrix formation, have effects on the development of bone abnormalities in childhood ALL survivors.