CFTR pathogenic variants spectrum in a cohort of Mexican patients with cystic fibrosis

被引:1
作者
Martinez-Hernandez, Angelica [1 ]
Mendoza-Caamal, Elvia C. [2 ]
Mendiola-Vidal, Namibia G. [1 ,3 ]
-Olmos, Francisco Barajas [1 ]
Villafan-Bernal, Jose Rafael [1 ,3 ]
Jimenez-Ruiz, Juan Luis [1 ]
Monge-Cazares, Tulia [1 ]
Garcia-Ortiz, Humberto [1 ]
Contreras-Cubas, Cecilia [1 ]
Centeno-Cruz, Federico [1 ]
Alaez-Verson, Carmen [3 ,5 ]
Ortega-Torres, Soraya [4 ,6 ]
Luna-Castaneda, Adriana del C. [7 ]
Baca, Vicente [6 ,8 ]
Lezana, Jose Luis [9 ,10 ,11 ]
Orozco, Lorena [1 ]
机构
[1] Inst Nacl Med Genom, Immunogen & Metab Dis Lab, Mexico City 14610, Mexico
[2] Inst Nacl Med Genom, Clin Area, Mexico City 14610, Mexico
[3] Maestria Ciencias Med, Ciencias Med, Sede HGGEA, UNAM, Mexico City 04510, Mexico
[4] Consejo Nacl Humanidades Ciencia & Tecnol CONAHCYT, Mexico City 03940, Mexico
[5] Inst Nacl Med Genom, Genom Diagnost Lab, Mexico City 14610, Mexico
[6] Univ Nacl Autonoma Mexico, Fac Med, Curso Alta Especial Med Genom, Inst Nacl Med Genom, Mexico City 04510, Mexico
[7] Hosp Pediat Mexico City, Neumol Dept, CMN Siglo XXI IMSS, Mexico City 06720, Mexico
[8] Hosp Pediat Mexico City, Rheumatol Dept, CMN Siglo XXI IMSS, Mexico City 06720, Mexico
[9] Hosp Infantil Mexico Dr Federico Gomez, Cyst Fibrosis Clin, Mexico City 06720, Mexico
[10] Hosp Infantil Mexico Dr Federico Gomez, Pulm Physiol Lab, Mexico City 06720, Mexico
[11] Asociac Mexicana Fibrosis Quist AC, Mexico City 03700, Mexico
关键词
Pathogenic variants; Mexican populations; Next-generation sequencing (NGS); Three-dimensional protein structure; Novel variants; Complex allele; CFTR; Cystic fibrosis; CFTR GENE; ASSOCIATION; FREQUENCY;
D O I
10.1016/j.heliyon.2024.e28984
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Molecular diagnosis of cystic fibrosis (CF) is challenging in Mexico due to the population's high genetic heterogeneity. To date, 46 pathogenic variants (PVs) have been reported, yielding a detection rate of 77%. We updated the spectrum and frequency of PVs responsible for this disease in mexican patients. Methods: We extracted genomic DNA from peripheral blood lymphocytes obtained from 297 CF patients and their parents. First, we analyzed the five most frequent PVs in the Mexican population using PCR-mediated site-directed mutagenesis. In patients with at least one identified allele, CFTR sequencing was performed using next-generation sequencing tools and multiplex ligation-dependent probe amplification. For variants not previously classified as pathogenic, we used a combination of in silico prediction, CFTR modeling, and clinical characteristics to determine a genotype-phenotype correlation. Results: We identified 95 PVs, increasing the detection rate to 87.04%. The most frequent variants were p.(PheF508del) (42.7%), followed by p.(Gly542*) (5.6%), p.(Ser945Leu) (2.9%), p.(Trp1204*) and p.(Ser549Asn) (2.5%), and CFTRdel25-26 and p.(Asn386Ilefs*3) (2.3%). The remaining variants had frequencies of <2.0%, and some were exclusive to one family. We identified 10 novel PVs localized in different exons (frequency range: 0.1-0.8%), all of which produced structural changes, deletions, or duplications in different domains of the protein, resulting in dysfunctional ion flow. The use of different in silico software and American College of Medical Genetics and Genomics (ACMG) and the Association for Molecular Pathology (AMP) criteria allowed us to assume that all of these PVs were pathogenic, causing a severe phenotype. Conclusions: In a highly heterogeneous population, combinations of different tools are needed to identify the variants responsible for CF and enable the establishment of appropriate strategies for CF diagnosis, prevention, and treatment.
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