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DOI 10.1093/labmed/lmac062

Медицинская библиотека · Laboratory medicine · 2023

Association of Catalase Gene Polymorphisms with Idiopathic Nephrotic Syndrome in a Chinese Pediatric Population.

Shi Jianrong, Li Wei, Tao Ran, Zhou Dongming, Guo Yajun, Fu Haidong, Sun Anna, Zhang Junfeng, Mao Jianhua

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Аннотация

OBJECTIVE

Our aim was to investigate the association between gene polymorphisms in catalase (CAT), a well-known oxidative stress regulator, and susceptibility to idiopathic nephrotic syndrome (INS) or responses to steroid therapy in a Chinese pediatric population.

METHODS

We analyzed 3 CAT single-nucleotide polymorphisms (SNVs; rs7943316, rs769217, and rs12270780) using multi-polymerase chain reaction combined with next-generation sequencing in 183 INS patients and 100 healthy controls.

RESULTS

For the allele and genotype frequencies of the CAT SNVs, no significant differences were observed between INS patients and controls. Patients with C allele of CAT rs769217 had a higher risk of developing steroid-dependent nephrotic syndrome than the steroid-sensitive nephrotic syndrome patients (P = 0.018; odds ratio = 1.76).

CONCLUSION

Our data suggests that genetic variations in CAT were unlikely to confer susceptibility to INS in Chinese children, whereas the C allele of the CAT rs769217 polymorphism showed a strong association with steroid-dependent responses in Chinese INS children.

Для цитирования: Shi Jianrong, Li Wei, Tao Ran, Zhou Dongming, Guo Yajun, Fu Haidong, Sun Anna, Zhang Junfeng, Mao Jianhua. Association of Catalase Gene Polymorphisms with Idiopathic Nephrotic Syndrome in a Chinese Pediatric Population.. Laboratory medicine. 2023. DOI: 10.1093/labmed/lmac062.

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