Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Gene polymorphisms involved in manifestation of leucopenia, digestive intolerance, and pancreatitis in azathioprine-treated patients

K. Wroblova, M. Kolorz, M. Batovsky, V. Zboril, J. Suchankova, M. Bartos, B. Ulicny, I. Pav, L. Bartosova

. 2012 ; 57 (9) : 2394-401.

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc13000857
E-zdroje Online Plný text

NLK ProQuest Central od 1997-01-01 do Před 1 rokem
Medline Complete (EBSCOhost) od 2009-07-01 do Před 1 rokem
Nursing & Allied Health Database (ProQuest) od 1997-01-01 do Před 1 rokem
Health & Medicine (ProQuest) od 1997-01-01 do Před 1 rokem
Family Health Database (ProQuest) od 1997-01-01 do Před 1 rokem

BACKGROUND: Approximately 10-28 % of patients experience adverse drug reactions related to treatment with thiopurines. The most serious reaction is myelosuppression, typically manifested as leucopenia, which occurs in approximately 2-5 % of patients. Other adverse drug reactions that often accompany thiopurine therapy are pancreatitis, hepatotoxicity, allergic reactions, digestive intolerance, arthralgia, febrile conditions, and rash. OBJECTIVE: The objective of this study was to assess the relationship between variant alleles of thiopurine S-methyltransferase (SNPs 238G > C, 460G > A and 719A > G), inosine triphosphate diphosphatase (SNPs 94C > A and IVS2 + 21A > C), and xanthine dehydrogenase (837C > T) and the occurrence of adverse drug reactions to azathioprine therapy. METHODS: Genotype was determined for 188 Caucasians diagnosed with inflammatory bowel disease treated with a standard dose of azathioprine (1.4-2.0 mg/kg/day). Allelic variants were determined by PCR-REA and real-time PCR methods. Results were statistically evaluated by use of Fisher's test and by odds ratio calculation. RESULTS: Variant genotype thiopurine S-methyltransferase predisposes to development of leucopenia (P = 0.003, OR = 5, CI 95 %, 1.8058-13.8444). Although not statistically significant, we observed a trend that suggested correlation between the occurrence of digestive intolerance and the variant genotype inosine triphosphate diphosphatase (P = 0.1102; OR 15.63, CI 95 %, 1.162-210.1094), and between the occurrence of pancreatitis and the variant allele xanthine dehydrogenase 837T (P = 0.1124; OR 12,1, CI 95 %, 1.15-126.37). CONCLUSION: The variant genotype thiopurine S-methyltransferase has been associated with the occurrence of leucopenia. The involvement of polymorphisms in inosine triphosphate diphosphatase and xanthine dehydrogenase genes in the development of digestive intolerance and pancreatitis will require further verification.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc13000857
003      
CZ-PrNML
005      
20130115212037.0
007      
ta
008      
130108s2012 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s10620-012-2163-y $2 doi
035    __
$a (PubMed)22535280
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Wroblova, Katerina $u Department of Human Pharmacology and Toxicology, Faculty of Pharmacy, University of Veterinary and Pharmaceutical Sciences Brno, Palackeho 1/3, 612 42 Brno, Czech Republic.
245    10
$a Gene polymorphisms involved in manifestation of leucopenia, digestive intolerance, and pancreatitis in azathioprine-treated patients / $c K. Wroblova, M. Kolorz, M. Batovsky, V. Zboril, J. Suchankova, M. Bartos, B. Ulicny, I. Pav, L. Bartosova
520    9_
$a BACKGROUND: Approximately 10-28 % of patients experience adverse drug reactions related to treatment with thiopurines. The most serious reaction is myelosuppression, typically manifested as leucopenia, which occurs in approximately 2-5 % of patients. Other adverse drug reactions that often accompany thiopurine therapy are pancreatitis, hepatotoxicity, allergic reactions, digestive intolerance, arthralgia, febrile conditions, and rash. OBJECTIVE: The objective of this study was to assess the relationship between variant alleles of thiopurine S-methyltransferase (SNPs 238G > C, 460G > A and 719A > G), inosine triphosphate diphosphatase (SNPs 94C > A and IVS2 + 21A > C), and xanthine dehydrogenase (837C > T) and the occurrence of adverse drug reactions to azathioprine therapy. METHODS: Genotype was determined for 188 Caucasians diagnosed with inflammatory bowel disease treated with a standard dose of azathioprine (1.4-2.0 mg/kg/day). Allelic variants were determined by PCR-REA and real-time PCR methods. Results were statistically evaluated by use of Fisher's test and by odds ratio calculation. RESULTS: Variant genotype thiopurine S-methyltransferase predisposes to development of leucopenia (P = 0.003, OR = 5, CI 95 %, 1.8058-13.8444). Although not statistically significant, we observed a trend that suggested correlation between the occurrence of digestive intolerance and the variant genotype inosine triphosphate diphosphatase (P = 0.1102; OR 15.63, CI 95 %, 1.162-210.1094), and between the occurrence of pancreatitis and the variant allele xanthine dehydrogenase 837T (P = 0.1124; OR 12,1, CI 95 %, 1.15-126.37). CONCLUSION: The variant genotype thiopurine S-methyltransferase has been associated with the occurrence of leucopenia. The involvement of polymorphisms in inosine triphosphate diphosphatase and xanthine dehydrogenase genes in the development of digestive intolerance and pancreatitis will require further verification.
650    _2
$a azathioprin $x škodlivé účinky $x terapeutické užití $7 D001379
650    _2
$a gastrointestinální nemoci $x chemicky indukované $x genetika $7 D005767
650    _2
$a regulace genové exprese $7 D005786
650    _2
$a genetická predispozice k nemoci $7 D020022
650    _2
$a genotyp $7 D005838
650    _2
$a lidé $7 D006801
650    _2
$a imunosupresiva $x škodlivé účinky $x terapeutické užití $7 D007166
650    _2
$a idiopatické střevní záněty $x farmakoterapie $7 D015212
650    _2
$a leukopenie $x chemicky indukované $x genetika $7 D007970
650    _2
$a methyltransferasy $x genetika $x metabolismus $7 D008780
650    _2
$a pankreatitida $x chemicky indukované $x genetika $7 D010195
650    _2
$a polymerázová řetězová reakce $x metody $7 D016133
650    _2
$a polymorfismus genetický $7 D011110
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1#
$a Kolorz, Michal. $7 _BN006015
700    1_
$a Bátovský, Marián, $d 1951- $7 jo2007286430
700    1_
$a Zbořil, Vladimír, $d 1955- $7 mzk2005278248
700    1_
$a Suchankova, Jana
700    1_
$a Bartoš, Milan, $d 1964- $7 xx0037128
700    1_
$a Uličný, Boris
700    1#
$a Páv, Igor. $7 xx0201239
700    1_
$a Bartošová, Ladislava $7 ola2006340376
773    0_
$w MED00009570 $t Digestive diseases and sciences $x 1573-2568 $g Roč. 57, č. 9 (2012), s. 2394-401
856    41
$u https://pubmed.ncbi.nlm.nih.gov/22535280 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20130108 $b ABA008
991    __
$a 20130115212204 $b ABA008
999    __
$a ok $b bmc $g 963639 $s 799021
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2012 $b 57 $c 9 $d 2394-401 $i 1573-2568 $m Digestive diseases and sciences $n Dig Dis Sci $x MED00009570
LZP    __
$a Pubmed-20130108

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...