Present & Future Role of Molecular Genetic Diagnostics in … · 03/02/2017 · Gene-based...
Transcript of Present & Future Role of Molecular Genetic Diagnostics in … · 03/02/2017 · Gene-based...
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Present & Future Role of Molecular Genetic Diagnostics in ADPKD
Peter C. Harris, PhD!Mayo Clinic, Rochester, MN!
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KDIGO Controversies Conference on Autosomal Dominant Polycystic Kidney Disease
(ADPKD)!!
Edinburgh, Scotland!Friday, January 17, 2014!
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KDIG
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Disclosure of Interests
• Otsuka Pharmaceuticals: Research grant
KDIG
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Mutations to PKD1 or PKD2 cause ADPKD
1 2 3 4 5 6 7 8 910 1112 13 14 15
PKD2 gene
1
PKD1 gene
20 25 3010 155 35 40 46
TSC2
PKD1 transcript!
6!15!13!11!10!9!8!7!6!5!4! 14!12!3!2!1! 20! 24!25!26!27! 29!19!18!17!16! 23! 28! 30!31!21!22! 32! 39!36!37!38!40!41!42!43!44!45! 4!33!34!35!
1kb!
3kb!
1kb!14!13!12!11!10!9!8!7!6!4!3!2!1! 5! 15! PKD2 transcript!
PKD1 gene!!
PKD2 gene!
3kb!
Hughes et al Nat Genet (1995); International Consortium, Cell (1995); Mochizuki et al Science (1996)
PKD1 ~85% families PKD2 ~15% families
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The PKD1 region is duplicated in 16p13.1
P6!
TSC2!PKD1!
12 13.313.213.111.2
11.31213212224 pq 23
ex7-15!ex33! IVS1! ex33!
ex15-16!ex33!
P1,2,4!P3,5!
ex1-IVS1!
HG-repeat! HG-repeat!HG-repeat!
6 PKD1-like pseudogenes; up to 99% identity to PKD1 European Consortium, Cell 1994
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Sequence similarity between PKD1 and the six pseudogenes!
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Sanger screening protocol for ADPKD
• 5 locus specific amplicons cover the duplicated part of PKD1
• PKD1 exons and flanking intronic regions: 46 amplicons
• PKD2 exons and flanking intronic regions: 17 amplicons
• Total 63 amplicons
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High level of allelic heterogeneity in PKD1!
P35!
P3,!P89,!P252!
P179!
P11! P98! P95!
P100!
P225!P99! P234!
P184!
P314!
P236! P164!
P9,P86!
P107,P224,M72!
P2,!P216!
P169,!P200!
P8!
P491,!P373!
P399,!P566!
P408! P398! P18!
P7! P322!P255!
P292!P13,!P404!
P204! P124!P14!
P103!
P267!
P88!
P382!
P241!
P381!
P159!
P366!
P375!
P433!
P206,!P376,!M18!
P293!
P436!
P379!
P438!
P239!
P17,!P17A!
P372!
P602!
P377!
P423! P385!
P386!
P174!
P374!
P243!
P284!
P407!P105,!P187! P117!
P198!
P264!P130!P227!,P344!
P499!
P126,!P449!
P220!
P161!P193!
P228!P135!
P447,P511!P148,P256,!
6!15!13!11!10!9!8!7!6!5!4! 14!12!3!2!1! 20! 24!25!26!27! 29!19!18!17!16! 23! 28! 30!31!21!22! 32! 39!36!37!38!40!41!42!43!44!45! 4!33!34!35!
P157!P352!P285!
M69!
P259!
P501!
M35!
M21!
P611!
M27!
P677!
M24!
M68!
P612!
M32! P442!
P277! M39!
P109! P138!P4!P229!P402! P1,M31! P134! P152! P178!P450! P417!P289!
P118!
P564!
P306!
P559!
P439!
P150!
P341!M76!
M73!
M42!
M77!
M74!P125!
P147!
P301!
M75!
P167!
P190!
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Mutation Types in ADPKD: HALT PKD population
Frameshift 30%
Nonsense 24%
Splicing 10%
Large Del/Dup
2%
InFrame 6%
Missense 28%
PKD1
Frameshifting 28%
Nonsense 41%
Splicing 16%
Large Del/Dup 4%
Missense 11%
PKD2
No mutation identified in ~8% families
Non-definite mutations in 34% PKD1 and 11% PKD2
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Update to ADPKD mutation database
(PKDB): Version 2.95 http://pkdb.mayo.edu !
• Total 2544 variants – PKD1 = 2293 PKD2 = 251
• 1425 Likely Pathogenic mutations (2020 families) – PKD1 = 1250 (1677 families) – PKD2 = 175 (343 families)
• 189 Indeterminate change – PKD1 = 181; PKD2 = 16
• 867 Neutral Polymorphisms – PKD1 = 911 (94%); PKD2 = 58 (6%)
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Diagnostics of ADPKD usually performed by renal imaging!
• Imaging methods can usually accurately diagnose ADPKD in adults!
• Imaging diagnostics less reliable in younger adults!• Especially in families with less severe disease!
• PKD2 and hypomorphic PKD1 mutations!!
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Gene-based diagnostics for ADPKD!!• Genetic testing may be helpful when imaging
results are equivocal and firm diagnosis required!• Living related donors!
• Confirming negative diagnosis in young potential donor when imaging results may be unreliable!
• Clarifying the diagnosis in a potential donor when 1 or 2 cysts detected by imaging !
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• Individuals with a negative family history and/or an unusual disease presentation: to clarify the diagnosis!• Early onset ADPKD!• Mild PKD!• Atypical radiological presentation!
• Once therapies available: testing of young patients to obtain a firm diagnosis before starting treatment!
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Cornec-Le Gall 2013 JASN
Knowing the gene and the mutation are of prognostic value in ADPKD!
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Gene-based prognostics in ADPKD!• Gene and mutation data can provide information
about the severity of disease!• Truncating PKD1 mutations associated with more
severe disease!• PKD2 mutations associated with milder disease!• Hypomorphic PKD1 mutations associated with milder
disease!!
• Prognostic information can help patient management!• Planning for ESRD!• Provide reassurance for those with predicted less
severe course!• Select patients for clinical trials!• Select patients treatments!
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Resolve complex ADPKD cases!
• Negative family history!• Determine if disease is ADPKD!
• Especially with mild disease!
• De novo mutation!• Reduced risk in sibs!• Mosaicism – can complicate risk prediction!
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• Early onset cases!• Some due to combinations of ADPKD alleles!
• Of value for avoiding further early onset cases in a family!• Marked intrafamilial variation!
• Allelic/genic combinations!• Mosaicism!
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Hypomorphic PKD1 allele in homozygosity: extreme intrafamilial phenotypic variability
Unusual, reniform kidneys with multiple
small cysts in homozygotes
Consanguineous US family of French origin
homozygous or heterozygous for R3277C
Rossetti et al 2009 KI!
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Family with PKD1 and PKD2 mutation: intrafamilial phenotypic variability
Patients with both mutations have more
severe disease
Gainullin in preparation
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MLPA assay for PKD1 and PKD2
– 3-4% of mutations are large rearrangements
– PKD1 deletion of exons 3-9, 40% mosaic PKD1 PKD2
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Screening for mosaics employing next generation sequencing
Hopp, work in progress
ADPKD patient with mild disease (S.Cr. 1.9 at 77y) and a negative family history was mutation negative by Sanger sequencing NGS analysis identified the nonsense mutation PKD1: p.R4228X at a low level
The variant is at 8% and has a read depth of 5600. The variant is in perfect F/R balance and looks clean in the alignment Control
Patient
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In utero onset ADPKD
• Rarely (
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Early-onset disease associated with co-inheritance of a truncating and hypomorphic PKD1 allele
Rossetti et al 2009 KI!
In utero onset ADPKD
XQ RC
QQ RC
QX RR
QX RR
QX RR
PKD1 Variants
Q2158X R3277C
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Other explanations for early onset ADPKD
• Not all EO cases due to co-inheritance of ADPKD alleles
• Co-inheritance of mutations at other loci may cause EO PKD – HNF1B – PKHD1
• Analysis of candidate panel or whole exome screen may be appropriate in unresolved EO cases
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Bergmann 2011 JASN
Example of combination of PKD1 and HNF1B allele causing EO PKD
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Gene-based diagnostics in ADPKD is complex • Genetic and extreme allelic heterogeneity
– Completely screen PKD1 and PKD2 required • Segmental duplication of PKD1
– Locus specific enrichment required – Exon capture methods unreliable
• Many variants of uncertain significance • Many PKD1 non-truncating changes hypomorphic
– Identification of hypomorphic alleles difficult • Genetic test is expensive and not always informative • Reports often uninformative and difficult to understand
– Clinical testing only available through one vendor in US: – Athena Diagnostics - ~$5000 with MLPA testing – Recent Supreme Court ruling may open US market
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Next-generation sequencing allows rapid analysis of multiple patient samples!
• PKD1 and PKD2 amplified as 14 long-range products!• exon capture unreliable for PKD1 because of genomic duplication !
• Potential for higher throughput and reduced cost!
• Mutation detection rate likely to be comparable!
• Introns, UTRs and promoters could also be screened!
1
5
10
15
20
25
30
35
40
46
Gen1
Gen2-13
Gen13-15
Gen15-21
Gen22-34
Gen33-38
Gen41-46
Gen37-42
Rossetti 2012 JASN
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Mutation-based diagnostics in ADPKD is likely to be more widely employed
• Mutation identified in 90% cases – Definite (truncating) mutations in ~65% families
• Bioinformatic scoring of non-definite mutations increasingly reliable – Recurrent mutations ~50% in recent studies – Mutation database of value
• Identify pathogenic mutations • Highlight hypomorphic changes
• Of diagnostic and prognostic value • Mutation type may in the future influence treatment options
– Similar to cystic fibrosis • Cost of test needs to decrease • Reliability and interpretation of results needs to improve