Human Leukocyte Antigens-Associated Severe Cutaneous Adverse Drug Reactions in Vietnamese
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USyd Access
Type
ThesisThesis type
Doctor of PhilosophyAuthor/s
NGUYEN, DINH VANAbstract
Severe cutaneous adverse reactions (SCARs)- Stevens-Johnson Syndrome (SJS), Toxic Epidermal Necrolysis (TEN), Drug Rash with Eosinophilia and Systemic Symptoms (DRESS) and Acute Generalized Exanthematous Pustulosis (AGEP), cause high mortality (10-50%) and morbidity (60%). ...
See moreSevere cutaneous adverse reactions (SCARs)- Stevens-Johnson Syndrome (SJS), Toxic Epidermal Necrolysis (TEN), Drug Rash with Eosinophilia and Systemic Symptoms (DRESS) and Acute Generalized Exanthematous Pustulosis (AGEP), cause high mortality (10-50%) and morbidity (60%). Carbamazepine (CBZ) and allopurinol (A), the most common culprits, are strongly associated with specific genotypes: HLA-B*15:02/HLA-A*31:01 with CBZ; HLA-B*58:0 with A-induced SCARs, especially in Asians. Screening for risk alleles prevents CBZ- and A-induced SCARs. Lack of suitable screening methods, unclear patho-mechanisms and poor understanding of co-factors’ role, have to date prevented clinical translation in Vietnam. Aiming to reduce mortality and morbidity from SCARs, it was necessary to establish any associations between HLA genes and A and CBZ-induced SCARs in Vietnamese, then develop simple, rapid and cost-effective assays for risk alleles. To better understand patho-mechanisms and the role of co-factors, gene expression profiling was undertaken in A-induced SCARS. Chapters 4-7, each present novel, cost-effective, rapid real-time-PCR based assays screening for HLA-B*57:01/58:01 (4), HLA-B*58:01 (5), HLA-B*15:02 (6) and HLA-A*31:01/HLA-B*15:02 (7). In Chapter 8, a case control study of 122 patients with SCARs caused by CBZ or A and 120 drug tolerant controls determined genetic susceptibilities. Key findings were: HLA-B*15:02 and HLA-B*58:01 are pharmacogenomic risk factors for CBZ-induced SJS/TEN and A-induced SCARs in Vietnamese. The risk of developing SCARs with A is increased by having HLA-B*58:01, rs3909184 allele A and renal insufficiency. HLA-B*15:02 was confirmed as a major risk factor for CBZ-induced SCARs in Vietnamese. No association was found between HLA-A*31:01 and CBZ-induced SCARs. The single nucleotide polymorphism, rs9263726, in psoriasis susceptibility 1 candidate 1 (PSORS1C1) gene, was identified as a marker for HLA-B*58:01. The restriction fragment length polymorphism (RFLP) method developed will simplify screening. Finally, gene expression profiling study data (Chapter 9) provide insights into patho-mechanisms of A-induced SCARs and a potential role for miR146a as a co-factor in A tolerance in HLA-B*58:01 carriers. Taken together, a framework to enable screening in Vietnam.
See less
See moreSevere cutaneous adverse reactions (SCARs)- Stevens-Johnson Syndrome (SJS), Toxic Epidermal Necrolysis (TEN), Drug Rash with Eosinophilia and Systemic Symptoms (DRESS) and Acute Generalized Exanthematous Pustulosis (AGEP), cause high mortality (10-50%) and morbidity (60%). Carbamazepine (CBZ) and allopurinol (A), the most common culprits, are strongly associated with specific genotypes: HLA-B*15:02/HLA-A*31:01 with CBZ; HLA-B*58:0 with A-induced SCARs, especially in Asians. Screening for risk alleles prevents CBZ- and A-induced SCARs. Lack of suitable screening methods, unclear patho-mechanisms and poor understanding of co-factors’ role, have to date prevented clinical translation in Vietnam. Aiming to reduce mortality and morbidity from SCARs, it was necessary to establish any associations between HLA genes and A and CBZ-induced SCARs in Vietnamese, then develop simple, rapid and cost-effective assays for risk alleles. To better understand patho-mechanisms and the role of co-factors, gene expression profiling was undertaken in A-induced SCARS. Chapters 4-7, each present novel, cost-effective, rapid real-time-PCR based assays screening for HLA-B*57:01/58:01 (4), HLA-B*58:01 (5), HLA-B*15:02 (6) and HLA-A*31:01/HLA-B*15:02 (7). In Chapter 8, a case control study of 122 patients with SCARs caused by CBZ or A and 120 drug tolerant controls determined genetic susceptibilities. Key findings were: HLA-B*15:02 and HLA-B*58:01 are pharmacogenomic risk factors for CBZ-induced SJS/TEN and A-induced SCARs in Vietnamese. The risk of developing SCARs with A is increased by having HLA-B*58:01, rs3909184 allele A and renal insufficiency. HLA-B*15:02 was confirmed as a major risk factor for CBZ-induced SCARs in Vietnamese. No association was found between HLA-A*31:01 and CBZ-induced SCARs. The single nucleotide polymorphism, rs9263726, in psoriasis susceptibility 1 candidate 1 (PSORS1C1) gene, was identified as a marker for HLA-B*58:01. The restriction fragment length polymorphism (RFLP) method developed will simplify screening. Finally, gene expression profiling study data (Chapter 9) provide insights into patho-mechanisms of A-induced SCARs and a potential role for miR146a as a co-factor in A tolerance in HLA-B*58:01 carriers. Taken together, a framework to enable screening in Vietnam.
See less
Date
2018-06-29Licence
The author retains copyright of this thesis. It may only be used for the purposes of research and study. It must not be used for any other purposes and may not be transmitted or shared with others without prior permission.Faculty/School
Faculty of Medicine and Health, Northern Clinical SchoolAwarding institution
The University of SydneyShare