-
Something wrong with this record ?
High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism
K. Rozenkova, J. Malikova, A. Nessa, L. Dusatkova, L. Bjørkhaug, B. Obermannova, P. Dusatkova, J. Kytnarova, I. Aukrust, LA. Najmi, B. Rypackova, Z. Sumnik, J. Lebl, PR. Njølstad, K. Hussain, S. Pruhova,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NT11402
MZ0
CEP Register
Digital library NLK
Full text - Article
Source
NLK
Free Medical Journals
from 1997 to 1 year ago
PubMed
26431509
DOI
10.1210/jc.2015-2763
Knihovny.cz E-resources
- MeSH
- Transcriptional Activation MeSH
- DNA genetics MeSH
- Adult MeSH
- Potassium Channels, Inwardly Rectifying genetics MeSH
- Genetic Variation MeSH
- Hepatocyte Nuclear Factor 1-alpha genetics MeSH
- Hepatocyte Nuclear Factor 4 genetics MeSH
- Cohort Studies MeSH
- Infant MeSH
- Humans MeSH
- Mutation genetics MeSH
- Infant, Newborn MeSH
- Child, Preschool MeSH
- Protein Serine-Threonine Kinases genetics MeSH
- Rubidium Radioisotopes MeSH
- Sulfonylurea Receptors genetics MeSH
- Pedigree MeSH
- Pregnancy MeSH
- Congenital Hyperinsulinism epidemiology genetics MeSH
- Check Tag
- Adult MeSH
- Infant MeSH
- Humans MeSH
- Male MeSH
- Infant, Newborn MeSH
- Child, Preschool MeSH
- Pregnancy MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
CONTEXT: Congenital hyperinsulinism of infancy (CHI) represents a group of heterogeneous disorders characterized by oversecretion of insulin from pancreatic β-cells causing severe hypoglycemia. OBJECTIVE: We studied the distribution of genetic causes of CHI in a Czech population. METHODS: Countrywide collection of patients with CHI included 40 subjects (12 females, median age of diagnosis, 1 wk [interquartile range, 1-612 wk]). We sequenced the ABCC8, KCNJ11, GLUD1, GCK, HADH, UCP2, SLC16A1, HNF4A, and HNF1A genes and investigated structural changes in the ABCC8 gene. We functionally tested novel variants in the ABCC8 gene by Rb(86+) efflux assay and novel variants in the HNF1A gene by transcriptional activation and DNA-binding tests. RESULTS: We found causal mutations in 20 subjects (50%): 19 carried a heterozygous mutation while one patient was homozygous for mutation in the ABCC8 gene. Specifically, we detected 11 mutations (seven novel) in ABCC8, one novel mutation in KCNJ11, five mutations (two novel) in HNF1A, two novel mutations in HNF4A, and one in GCK. We showed a decrease of activation by diazoxide in mutant KATP channels with novel ABCC8 variants by 41-91% (median, 82%) compared with wild-type (WT) channels and reduced transcriptional activity of mutant HNF1A proteins (2.9% for p.Asn62Lysfs93* and 22% for p.Leu254Gln) accompanied by no DNA-binding ability compared with WT HNF1A. CONCLUSION: We detected a higher proportion of heterozygous mutations causing CHI compared with other cohorts probably due to lack of consanguinity and inclusion of milder CHI forms. Interestingly, HNF1A gene mutations represented the second most frequent genetic cause of CHI in the Czech Republic. Based on our results we present a genetic testing strategy specific for similar populations.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc16020244
- 003
- CZ-PrNML
- 005
- 20190821165954.0
- 007
- ta
- 008
- 160722s2015 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1210/jc.2015-2763 $2 doi
- 024 7_
- $a 10.1210/jc.2015-2763 $2 doi
- 035 __
- $a (PubMed)26431509
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Roženková, Klára $u Department of Paediatrics, Second Faculty of Medicine Charles University in Prague and University Hospital in Motol, Prague 150 06, Czech Republic $7 xx0228157
- 245 10
- $a High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism / $c K. Rozenkova, J. Malikova, A. Nessa, L. Dusatkova, L. Bjørkhaug, B. Obermannova, P. Dusatkova, J. Kytnarova, I. Aukrust, LA. Najmi, B. Rypackova, Z. Sumnik, J. Lebl, PR. Njølstad, K. Hussain, S. Pruhova,
- 520 9_
- $a CONTEXT: Congenital hyperinsulinism of infancy (CHI) represents a group of heterogeneous disorders characterized by oversecretion of insulin from pancreatic β-cells causing severe hypoglycemia. OBJECTIVE: We studied the distribution of genetic causes of CHI in a Czech population. METHODS: Countrywide collection of patients with CHI included 40 subjects (12 females, median age of diagnosis, 1 wk [interquartile range, 1-612 wk]). We sequenced the ABCC8, KCNJ11, GLUD1, GCK, HADH, UCP2, SLC16A1, HNF4A, and HNF1A genes and investigated structural changes in the ABCC8 gene. We functionally tested novel variants in the ABCC8 gene by Rb(86+) efflux assay and novel variants in the HNF1A gene by transcriptional activation and DNA-binding tests. RESULTS: We found causal mutations in 20 subjects (50%): 19 carried a heterozygous mutation while one patient was homozygous for mutation in the ABCC8 gene. Specifically, we detected 11 mutations (seven novel) in ABCC8, one novel mutation in KCNJ11, five mutations (two novel) in HNF1A, two novel mutations in HNF4A, and one in GCK. We showed a decrease of activation by diazoxide in mutant KATP channels with novel ABCC8 variants by 41-91% (median, 82%) compared with wild-type (WT) channels and reduced transcriptional activity of mutant HNF1A proteins (2.9% for p.Asn62Lysfs93* and 22% for p.Leu254Gln) accompanied by no DNA-binding ability compared with WT HNF1A. CONCLUSION: We detected a higher proportion of heterozygous mutations causing CHI compared with other cohorts probably due to lack of consanguinity and inclusion of milder CHI forms. Interestingly, HNF1A gene mutations represented the second most frequent genetic cause of CHI in the Czech Republic. Based on our results we present a genetic testing strategy specific for similar populations.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a předškolní dítě $7 D002675
- 650 _2
- $a kohortové studie $7 D015331
- 650 _2
- $a vrozený hyperinzulinismus $x epidemiologie $x genetika $7 D044903
- 650 _2
- $a DNA $x genetika $7 D004247
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a genetická variace $7 D014644
- 650 _2
- $a hepatocytární jaderný faktor 1-alfa $x genetika $7 D051538
- 650 _2
- $a hepatocytární jaderný faktor 4 $x genetika $7 D051557
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a kojenec $7 D007223
- 650 _2
- $a novorozenec $7 D007231
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a mutace $x genetika $7 D009154
- 650 _2
- $a rodokmen $7 D010375
- 650 _2
- $a draslíkové kanály dovnitř usměrňující $x genetika $7 D024661
- 650 _2
- $a těhotenství $7 D011247
- 650 _2
- $a protein-serin-threoninkinasy $x genetika $7 D017346
- 650 _2
- $a radioizotopy rubidia $7 D012414
- 650 _2
- $a receptory sulfonylurey $x genetika $7 D064233
- 650 _2
- $a aktivace transkripce $7 D015533
- 651 _2
- $a Česká republika $x epidemiologie $7 D018153
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Malíková, Jana $7 xx0158263 $u Department of Paediatrics, Second Faculty of Medicine Charles University in Prague and University Hospital in Motol, Prague 150 06, Czech Republic
- 700 1_
- $a Nessa, Azizun
- 700 1_
- $a Dušátková, Lenka, $u Department of Paediatrics, Second Faculty of Medicine Charles University in Prague and University Hospital in Motol, Prague 150 06, Czech Republic $d 1985- $7 xx0207024
- 700 1_
- $a Bjørkhaug, Lise
- 700 1_
- $a Obermannová, Barbora $u Department of Paediatrics, Second Faculty of Medicine Charles University in Prague and University Hospital in Motol, Prague 150 06, Czech Republic $7 xx0173310
- 700 1_
- $a Dušátková, Petra, $u Department of Paediatrics, Second Faculty of Medicine Charles University in Prague and University Hospital in Motol, Prague 150 06, Czech Republic $d 1983- $7 xx0152579
- 700 1_
- $a Kytnarová, Jitka, $u Department of Paediatrics, First Faculty of Medicine (J.K.), Charles University in Prague and the General University Hospital in Prague, Prague 121 08, Czech Republic $d 1964- $7 nlk20040146963
- 700 1_
- $a Aukrust, Ingvild $7 gn_A_00010103
- 700 1_
- $a Najmi, Laeya A
- 700 1_
- $a Rypáčková, Blanka $u Second Department of Internal Medicine FNKV, Third Faculty of Medicine, Charles University in Prague, Prague 100 00, Czech Republic $7 xx0171714
- 700 1_
- $a Šumník, Zdeněk, $u Department of Paediatrics, Second Faculty of Medicine Charles University in Prague and University Hospital in Motol, Prague 150 06, Czech Republic $d 1970- $7 xx0036973
- 700 1_
- $a Lebl, Jan, $u Department of Paediatrics, Second Faculty of Medicine Charles University in Prague and University Hospital in Motol, Prague 150 06, Czech Republic $d 1955- $7 jn19990010093
- 700 1_
- $a Njølstad, Pål R
- 700 1_
- $a Hussain, Khalid
- 700 1_
- $a Průhová, Štěpánka, $u Department of Paediatrics, Second Faculty of Medicine Charles University in Prague and University Hospital in Motol, Prague 150 06, Czech Republic $d 1974- $7 mzk2004252387
- 773 0_
- $w MED00002582 $t The Journal of clinical endocrinology and metabolism $x 1945-7197 $g Roč. 100, č. 12 (2015), s. E1540-9
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/26431509 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20160722 $b ABA008
- 991 __
- $a 20190821170232 $b ABA008
- 999 __
- $a ok $b bmc $g 1154914 $s 944772
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2015 $b 100 $c 12 $d E1540-9 $e 20151002 $i 1945-7197 $m The Journal of clinical endocrinology and metabolism $n J Clin Endocrinol Metab $x MED00002582
- GRA __
- $a NT11402 $p MZ0
- LZP __
- $a Pubmed-20160722