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DOI 10.1159/000542942

Медицинская библиотека · American journal of nephrology · 2024

Clinical Implementation of Nephrologist-Led Genomic Testing for Glomerular Diseases in Singapore: Rationale and Protocol.

Lim Cynthia, Lim Ru Sin, Choo Jason, Leow Esther Huimin, Chan Gek Cher, Zhang Yaochun, Ng Jun Li, Chin Hui-Lin, Tan Ee Shien, Goh Jeannette, Gandhi Naline, Ng Yong Hong, Than Mya, Ganesan Indra, Chong Siew Le, Yap Celeste, Chao Sing Ming, Cham Breana, Kam Sylvia, Lim Jiin Ying, Mok Irene, Tan Hui Zhuan, Kwek Jia Liang, Lee Tung Lin, Wang Ziyin, Goh Su Mein, Lim Regina, Yeo See Cheng, Teo Boon Wee, Da Yi, Matchar David, Ng Kar Hui

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Аннотация

INTRODUCTION

The early diagnosis and appropriate treatment of monogenic glomerular diseases can reduce kidney failure, avoid unnecessary investigations such as kidney biopsies and ineffective treatment with immunosuppressants, guide transplant decisions, and inform the genetic risks of their family members. Yet, genetic testing for kidney disease is underutilized in Singapore. We aimed to implement a nephrologist-led genetic service and evaluate the acceptance, adoption, utility, and cost-effectiveness of genetic testing for monogenic glomerular disease in Singapore.

METHODS

We will perform a prospective, multi-centre, type II hybrid effectiveness-implementation study with a post-design to evaluate both implementation and clinical outcomes of nephrologist-led genetic testing for suspected genetic glomerular kidney diseases. The multi-disciplinary implementation team will train "genetic nephrologists" to provide pre- and post-test counselling, order targeted exome panel sequencing for suspected glomerular kidney diseases (persistent microscopic haematuria and/or albuminuria or proteinuria in the absence of known causes, steroid-resistant primary nephrotic syndrome, apparent familial IgA nephropathy, or chronic kidney disease with no apparent cause), and interpret genetic test results; create workflows for patient referral, evaluation and management, and discuss genetic results at regular genomic board meetings. The outcomes are acceptance, appropriateness and adoption among patients and nephrologists, utility (proportion of patients who received genetic testing and have a confirmed diagnosis of genetic glomerular disease), and cost-effectiveness.

CONCLUSION

This study will create and evaluate a nephrologist-led genetic service, develop an efficient variant curation process, and inform future recommendations on the optimal referral and genetic testing strategy for monogenic glomerular disease in Singapore. This will facilitate the future mainstreaming of genetic testing that will enable precision medicine in kidney care.

Для цитирования: Lim Cynthia, Lim Ru Sin, Choo Jason, Leow Esther Huimin, Chan Gek Cher, Zhang Yaochun, Ng Jun Li, Chin Hui-Lin, Tan Ee Shien, Goh Jeannette, Gandhi Naline, Ng Yong Hong, Than Mya, Ganesan Indra, Chong Siew Le, Yap Celeste, Chao Sing Ming, Cham Breana, Kam Sylvia, Lim Jiin Ying, Mok Irene, Tan Hui Zhuan, Kwek Jia Liang, Lee Tung Lin, Wang Ziyin, Goh Su Mein, Lim Regina, Yeo See Cheng, Teo Boon Wee, Da Yi, Matchar David, Ng Kar Hui. Clinical Implementation of Nephrologist-Led Genomic Testing for Glomerular Diseases in Singapore: Rationale and Protocol.. American journal of nephrology. 2024. DOI: 10.1159/000542942.

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