
DO GENE POLYMORPHISMS PLAY A ROLE IN NEWBORN HYPERBILIRUBINEMIA? Hakan N, Aydin M, Ceylaner S, Di̇lli̇ D, Zenci̇roğlu A, Okumuş N *Corresponding Author: Assoc. Prof. Nilay Hakan, MD, Division of Neonatology, Sitki Koçman University School of Medicine, Orhaniye Mah., Haluk Ozsoy Sk., 48000, Muğla / Türkiye, Phone: +90 (252) 214 13 26, Fax: +90 (252) 211 13 45, E-mail: nhakan@hotmail.com page: 51
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REFERENCES
1. Madan A, McMahon JR, Stevenson DK. Neonatal
hyperbilirubinemia. In: Taeusch HW, Ballard RA,
Gleason CA, Editors. Avery’s Diseases of the New-
born, 8th ed. Philadelphia, Elsevier Saunders, 2005.
2. Al-Omran A, Al-Abdi S, Al-Salam Z. Readmission
for neonatal hyperbilirubinemia in an area with a high
prevalence of glucose-6-phosphate dehydrogenase
deficiency: a hospital-based retrospective study. J
Neonatal Perinatal Med. 2017; 10(2): 181-189.
3. Newman TB, Easterling MJ, Goldman ES, Stevenson
DK. Laboratory evaluation of jaundice in newborns.
Frequency, cost, and yield. Am J Dis Child. 1990;
144(3): 364-368.
4. Beutler E, Gelbart T, Demina A. Racial variability
in the UDP-glucuronosyltransferase 1 (UGT1A1)
promoter: a balanced polymorphism for regulation
of bilirubin metabolism? Proc Natl Acad Sci U S A.
1998; 95(14): 8170-8174.
5. Sarici SU, Serdar MA, Korkmaz A, Erdem G, Oran O,
Tekinalp G, et al. Incidence, course, and prediction of
hyperbilirubinemia in near-term and term newborns.
Pediatrics. 2004; 113(4): 775-780.
6. Mei H, Dong X, Wu B, Wang H, Lu Y, Hu L, et
al. Clinical and genetic etiologies of neonatal un-
conjugated hyperbilirubinemia in the china neonatal
genomes project. J Pediatr. 2022 Apr; 243: 53-60.e9.
7. Bhutani VK, Johnson LH, Sivieri EM. Universal new-
born bilirubin screening. Pediatr Res. 1997; 41: 191.
8. Watchko JF, Lin Z. Exploring the genetic architecture
of neonatal hyperbilirubinemia. Semin Fetal Neonatal
Med. 2010; 15(3): 169-175.
9. Liu W, Chang LW, Xie M, Li WB, Rong ZH, Wu L, et
al. Correlation between UGT1A1 polymorphism and
neonatal hyperbilirubinemia of neonates in Wuhan. J
Huazhong Univ Sci Technolog Med Sci. 2017; 37(5):
740-743.
10. Wang J, Yin J, Xue M, Lyu J, Wan Y. Roles of UG-
T1A1 Gly71Arg and TATA promoter polymorphisms
in neonatal hyperbilirubinemia: A meta-analysis.
Gene. 2020; 736: 144409.
11. Kilic I, Koseler A, Cakaloz I, Atalay E. Screening for
G71R mutation of the UDP-glucuronosyltransferase
1 (UGT1A1) gene in neonates with pathologic and
prolonged hyperbilirubinemia in Turkey. Int J Clin
Pharmacol Ther. 2010; 48(8): 504-548.
12. Narter F, Can G, Ergen A, Isbir T, Ince Z, Çoban A.
Neonatal hyperbilirubinemia and G71R mutation of
the UGT1A1 gene in Turkish patients. J Matern Fetal
Neonatal Med. 2011; 24(2): 313-316.
13. Yang H, Wang Q, Zheng L, Lin M, Zheng XB, Lin
F, et al. Multiple genetic modifiers of bilirubin me-
tabolism involvement in significant neonatal hyper-
bilirubinemia in patients of Chinese descent. PLoS
One. 2015; 10(7): e0132034.
14. D’Silva S, Colah RB, Ghosh K, Mukherjee MB.
Combined effects of the UGT1A1 and OATP2 gene
polymorphisms as major risk factor for unconjugated
hyperbilirubinemia in Indian neonates. Gene. 2014;
547(1): 18-22.
15. Wong F, Boo N, Othman A. Risk factors associated
with unconjugated neonatal hyperbilirubinemia in
Malaysian neonates. J Trop Pediatr. 2013; 59(4): 280-
285.
16. Huang MJ, Kua KE, Teng HC, Tang KS, Weng HW,
Huang CS. Risk factors for severe hyperbilirubinemia
in neonates. Pediatr Res. 2004; 56(5): 682-689.
17. Liu J, Long J, Zhang S, Fang X, Luo Y. The impact
of SLCO1B1 genetic polymorphisms on neonatal
hyperbilirubinemia: a systematic review with meta-
analysis. J Pediatr (Rio J). 2013; 89(5): 434-443.
18. Büyükkale G, Turker G, Kasap M, Akpinar G, Arisoy
E, Günlemez A, et al. Neonatal hyperbilirubinemia
and organic anion transporting polypeptide-2 gene
mutations. Am J Perinatol. 2011; 28(8): 619-626.
19. Alencastro de Azevedo L, Reverbel da Silveira T,
Carvalho CG, Martins de Castro S, Giugliani R, Matte
U. UGT1A1, SLCO1B1, and SLCO1B3 polymor-
phisms vs. neonatal hyperbilirubinemia: is there an
association? Pediatr Res. 2012; 72(2): 169-173.
20. Watchko JF, Lin Z, Clark RH, Kelleher AS, Walker
MW, Spitzer AR; Pediatrix Hyperbilirubinemia Study
Group. Complex multifactorial nature of significant
hyperbilirubinemia in neonates. Pediatrics. 2009;
124(5): e868-877.
21. Prachukthum S, Nunnarumit P, Pienvichit P, Chuan-
sumrit A, Songdej D, Kajanachumpol S, et al. Genetic
polymorphisms in Thai neonates with hyperbiliru-
binemia. Acta Paediatr. 2009; 98(7): 1106-1110.
22. Al-Abdi SY. Decreased Glutathione S-transferase
level and neonatal hyperbilirubinemia associated
with glucose-6-phosphate dehydrogenase deficiency:
A perspective review. Am J Perinatol. 2017; 34(3):
305-314.
23. Madlon-Kay DJ. The clinical significance of ABO
blood group incompatibility. Arch Fam Med. 1993;
2(3): 285-287.
24. Muslu N, Dogruer ZN, Eskandari G, Atici A, Kul S,
Atik U. Are glutathione S-transferase gene polymor-
phisms linked to neonatal jaundice? Eur J Pediatr.
2008; 167(1): 57-61.
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