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Makale detayı · 2018 · article

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome

YÖKSİS OpenAlex Açık erişim · green Üst %1
Yıl2018
Atıf239OpenAlex
Atıf211Semantic Scholar · 16 etkili
Yüzdelik%99,3
FWCI11,311,00 = dünya ortalaması
Scopus (SJR)Q1
WoS (JCR)Q1

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıClinical Journal of the American Society of Nephrology
  • Katalog eşleşmesi (ISSN)Clinical Journal of the American Society of Nephrology
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

OpenAlex İngilizce

Background and objectives Steroid-resistant nephrotic syndrome overwhelmingly progresses to ESRD. More than 30 monogenic genes have been identified to cause steroid-resistant nephrotic syndrome. We previously detected causative mutations using targeted panel sequencing in 30% of patients with steroid-resistant nephrotic syndrome. Panel sequencing has a number of limitations when compared with whole exome sequencing. We employed whole exome sequencing to detect monogenic causes of steroid-resistant nephrotic syndrome in an international cohort of 300 families. Design, setting, participants, & measurements Three hundred thirty-five individuals with steroid-resistant nephrotic syndrome from 300 families were recruited from April of 1998 to June of 2016. Age of onset was restricted to <25 years of age. Exome data were evaluated for 33 known monogenic steroid-resistant nephrotic syndrome genes. Results In 74 of 300 families (25%), we identified a causative mutation in one of 20 genes known to cause steroid-resistant nephrotic syndrome. In 11 families (3.7%), we detected a mutation in a gene that causes a phenocopy of steroid-resistant nephrotic syndrome. This is consistent with our previously published identification of mutations using a panel approach. We detected a causative mutation in a known steroid-resistant nephrotic syndrome gene in 38% of consanguineous families and in 13% of nonconsanguineous families, and 48% of children with congenital nephrotic syndrome. A total of 68 different mutations were detected in 20 of 33 steroid-resistant nephrotic syndrome genes. Fifteen of these mutations were novel. NPHS1 , PLCE1 , NPHS2 , and SMARCAL1 were the most common genes in which we detected a mutation. In another 28% of families, we detected mutations in one or more candidate genes for steroid-resistant nephrotic syndrome. Conclusions Whole exome sequencing is a sensitive approach toward diagnosis of monogenic causes of steroid-resistant nephrotic syndrome. A molecular genetic diagnosis of steroid-resistant nephrotic syndrome may have important consequences for the management of treatment and kidney transplantation in steroid-resistant nephrotic syndrome.

Konular

Atıflar

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Yerel katalogda bu makaleye atıf yapan 26 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. 2022 Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiencyAtıf 67 · OpenAlex
  2. 2022 Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiencyAtıf 67 · OpenAlex
  3. 2022 Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiencyAtıf 67 · OpenAlex
  4. 2020 Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet–ESPN inherited glomerulopathy working groupAtıf 41 · OpenAlex
  5. 2020 Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet–ESPN inherited glomerulopathy working groupAtıf 41 · OpenAlex
  6. 2020 COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndromeAtıf 22 · OpenAlex
  7. 2020 COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndromeAtıf 22 · OpenAlex
  8. 2020 COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndromeAtıf 22 · OpenAlex
  9. 2023 A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literatureAtıf 17 · OpenAlex
  10. 2023 A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literatureAtıf 17 · OpenAlex

Yazarlar

58
  1. Jillian K Warejko 1
  2. Tan WEIZHEN 2
  3. Daga ANKANA 3
  4. DAVID SCAPIRO 4
  5. SHERLEE SHRIL 5
  6. SWETLANA LOVRIC 6
  7. SHAIZA ASHRAF 7
  8. Jia Rao 8
  9. Tobias Hermle 9
  10. Tilman Jobst-Schwan 10
  11. Eugen WIDMEIER 11
  12. Amar J Majmundar 12
  13. Ronen Schneider 13
  14. HUEN YONG GEE 14
  15. J Magdalena Schmidt 15
  16. Asaf Vivante 16
  17. Amelie T van der Ven 17
  18. Hadas Ityel 18
  19. Jing Chen 19
  20. CAROLINE E SADOWSKI 20
  21. STEFAN KOHL 21
  22. WERNER L PABST 22
  23. Makiko Nakayama 23
  24. MICHEAL JG SOMERS 24
  25. Nancy M Rodig 25
  26. Ghaleb Daouk 26
  27. Michelle Baum 27
  28. DEBORAH R STEIN 28
  29. Michael A FERGUSON 29
  30. Avram Z TRAUM 30
  31. NEVEEN A SOLIMAN 31
  32. JAMEEELA A KARI 32
  33. SHERIF EL DESOKY 33
  34. HANAN M FATHY 34
  35. MARTIN ZENKER 35
  36. SEVCAN AZİME BAKKALOĞLU EZGÜ GAZİ ÜNİVERSİTESİ 36
  37. DIRK E MÜLLER WEIFEL 37
  38. ZEKİYE AYTÜL NOYAN 38
  39. FATİH ÖZALTIN 39
  40. Melisa A CADNAPAPHORNCHAI 40
  41. Seema HASHMI 41
  42. JEFFREY HOPCIAN 42
  43. JEFFREY B KOPP 43
  44. DETLEF BOCKENHAUER 44
  45. Radovan BOGDANOVIC 45
  46. Natasa STAJIC 46
  47. GIL CHERNIN 47
  48. Robert ETTENGER 48
  49. Henry FEHRENBACH 49
  50. MARKUS J KEMPER 50
  51. REYNER LOZA MUNARRIZ 51
  52. Rainer BÜSCHER 52
  53. ERKİN SERDAROĞLU SAĞLIK BİLİMLERİ ÜNİVERSİTESİ 53
  54. Velibor TASIC 54
  55. Shrikant MANE 55
  56. RICHARD P LIFTON 56
  57. Daniela A BRAUN 57
  58. FRIEDHELM HILDEBRANDT 58