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Zpráva o onemocněních · Metabolic
Whole genome sequencing identifies UGT1A1 variants that determine how safely you metabolize chemotherapy drugs, antiretrovirals, and other critical medications.
Zpráva o onemocněních hledá vzácné varianty, o nichž je známo, že způsobují onemocnění, na něž se zpráva zaměřuje.
An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.
Gilbert syndrome is a benign, unconjugated hyperbilirubinemia affecting approximately 2-20% of the general population depending on ethnicity. It is caused by reduced activity of UDP-glucuronosyltransferase 1A1 (UGT1A1), the enzyme responsible for conjugating bilirubin to facilitate excretion. The predominant genetic cause is the UGT1A1*28 polymorphism, consisting of seven TA repeats in the TATA box of the UGT1A1 promoter (instead of the typical six), which reduces enzyme expression to approximately 30% of normal. Clinically, Gilbert syndrome itself is benign: patients develop mild jaundice (typically <6 mg/dL bilirubin), which may transiently worsen with fasting, illness, or stress but poses no health risk.
The critical importance of Gilbert genotyping emerges in pharmacogenomic contexts. UGT1A1*28 homozygotes face severe dose-limiting toxicity with multiple chemotherapy agents and antiretroviral drugs. Variant frequencies vary strikingly by ancestry: approximately 26-31% of Caucasians carry at least one *28 allele, while 42-45% of African Americans and higher percentages of Asian populations carry *28 alleles. Additional UGT1A1 variants exist in specific populations: UGT1A1*6 and *7 in East Asian populations; UGT1A1*5 variants in some populations, each with consequences for drug metabolism.
Understanding UGT1A1 status is essential before prescribing drugs that depend on UGT1A1 for metabolism and clearance. A patient with UGT1A1 homozygous poor metabolizer status must have dose reductions pre-planned before therapy begins, not discovered after severe toxicity develops. Genetic counseling should ensure that any patient diagnosed with Gilbert syndrome or identified through UGT1A1 screening has documentation in their medical record and communicates the result to oncology, infectious disease, and other prescribers of UGT1A1-substrate medications.
UGT1A1 variants differ by ancestry: *28 is most common in Europeans; *6 and *7 predominate in East Asian populations; rare variants in other groups can affect enzyme function.
Autozomálně recesivní
An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.
Co se diagnózou změní
No treatment required for Gilbert syndrome itself; drug dose adjustment for UGT1A1-metabolized medications
Analyzované geny
Známé také jako
familial cholemia; Gilbert disease; Gilbert's syndrome; hyperbilirubinemia type 1
Autozomálně recesivní
Caused by variants in UGT1A1 that severely reduce bilirubin processing, causing persistent and sometimes dangerous jaundice from birth (type 1) or milder lifelong jaundice (type 2).
Co se diagnózou změní
Knowing allows daily phototherapy or liver transplant in type 1, and phenobarbital treatment in type 2, to prevent bilirubin brain damage.
Analyzované geny
Známé také jako
bilirubin UDP glucuronyl transferase deficiency; bilirubin uridinediphosphate glucuronosyltransferase deficiency; bilirubin-UGT deficiency; hereditary unconjugated hyperbilirubinemia; UGT deficiency
Autozomálně recesivní
Caused by variants in ABCC2, which reduce the release of bilirubin into bile and cause mild lifelong jaundice that is usually harmless.
Co se diagnózou změní
Knowing explains raised bilirubin results and can avoid unnecessary investigations; jaundice may worsen with pregnancy or oral contraceptives.
Analyzované geny
Známé také jako
chronic idiopathic jaundice; conjugated hyperbilirubinemia; DJS; Dubin-Sprinz disease; hyperbilirubinemia type 2; Sprinz-Nelson syndrome
Standard pharmacogenomics panels test only *28. They miss ancestry-specific variants and other functional UGT1A1 mutations.
Standard pharmacogenomics panels test UGT1A1*28, the most common variant in European populations. However, this approach misses clinically significant variants in other ancestry groups: UGT1A1*6 and *7, found predominantly in East Asian populations, also substantially reduce enzyme activity and create identical drug metabolism challenges. Patients of African ancestry, Hispanic ancestry, and other non-European populations carry additional rare variants affecting UGT1A1 function. Standard panel testing creates an ancestry-specific blindness, leaving populations outside European descent without complete genetic information. Whole genome sequencing captures the complete UGT1A1 sequence, providing comprehensive variant detection across all populations.
The FDA labeling for irinotecan (a topoisomerase I inhibitor used in colorectal, lung, and ovarian cancer) includes a recommendation for UGT1A1 genotyping: patients who are UGT1A1*28 homozygotes require a 25-30% reduction in irinotecan starting dose to avoid severe neutropenia and diarrhea (grade 3-4 toxicity rates are approximately 3-fold higher in homozygotes without dose reduction). Similarly, UGT1A1*28 homozygotes on atazanavir (a protease inhibitor) experience higher rates of hyperbilirubinemia. A documented UGT1A1 genotype in the medical record prevents dose-limiting toxicity and enables safe, effective therapy continuation.
Jedna souprava, zaslaná domů. Celý váš genom je sekvenován na klinickém standardu používaném pro diagnostická rozhodnutí. Zprávy připravené pro lékaře doručíme do vašeho Genome Manageru během 6–8 týdnů — trvale platné a průběžně aktualizované s vývojem vědy.
Doprava zdarma · Výsledky za 6–8 týdnů
