APOE epsilon status in Hungarian patients with primary progressive multiple sclerosis
PRINCIPLES: Apolipoprotein E (ApoE), an important glycoprotein in the transport, uptake and redistribution of cholesterol, is necessary in nerve tissue repair. The APOE gene (APOE) is involved in neurodegenerative diseases, the best-known association being that between the APOE epsilon4 allele and A...
Elmentve itt :
| Szerzők: | |
|---|---|
| Dokumentumtípus: | Cikk |
| Megjelent: |
2010
|
| Sorozat: | SWISS MEDICAL WEEKLY
140 |
| doi: | 10.4414/smw.2010.13119 |
| mtmt: | 1482468 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/9927 |
| LEADER | 02752nab a2200337 i 4500 | ||
|---|---|---|---|
| 001 | publ9927 | ||
| 005 | 20200127101555.0 | ||
| 008 | 161116s2010 hu o 0|| zxx d | ||
| 022 | |a 1424-7860 | ||
| 024 | 7 | |a 10.4414/smw.2010.13119 |2 doi | |
| 024 | 7 | |a 1482468 |2 mtmt | |
| 040 | |a SZTE Publicatio Repozitórium |b hun | ||
| 041 | |a zxx | ||
| 100 | 1 | |a Losonczi Erika | |
| 245 | 1 | 0 | |a APOE epsilon status in Hungarian patients with primary progressive multiple sclerosis |h [elektronikus dokumentum] / |c Losonczi Erika |
| 260 | |c 2010 | ||
| 300 | |a Paper w13119-6 p | ||
| 490 | 0 | |a SWISS MEDICAL WEEKLY |v 140 | |
| 520 | 3 | |a PRINCIPLES: Apolipoprotein E (ApoE), an important glycoprotein in the transport, uptake and redistribution of cholesterol, is necessary in nerve tissue repair. The APOE gene (APOE) is involved in neurodegenerative diseases, the best-known association being that between the APOE epsilon4 allele and Alzheimer's disease. Multiple sclerosis (MS) is a chronic inflammatory neurological disease. The aim of this study was to assess (multicentre assessment) the possible influence of the APOE gene on the susceptibility of primary progressive MS (PPMS) in Hungary. METHODS: Polymerase chain reaction and restriction fragment length polymorphism were carried out on DNA isolated from 135 volunteers. RESULTS: The number of PPMS patients without the epsilon2 allele was found to be remarkably high, whilst the epsilon2 allele was overrepresented in the RRMS group. A markedly high frequency of the epsilon4 allele was found in the PPMS group and a very low frequency in the HC group. With regards to the clinical parameters, significant differences were observed between the RRMS and PPMS groups. Differences were also detected regarding the EDSS and MSSS scores when the patients were grouped by the presence or absence of the epsilon2 allele. All of the observed differences in the clinical parameters disappeared when the patients were further stratified by the type of MS. CONCLUSIONS: Our findings suggest that the presence of the epsilon2 and epsilon4 alleles may play a role in the development of the disease. However, if any type of the disease has already developed the alleles show no association with the clinical parameters. | |
| 700 | 0 | 1 | |a Bencsik Krisztina |e aut |
| 700 | 0 | 2 | |a Fricska-Nagy Zsanett |e aut |
| 700 | 0 | 2 | |a Honti Viktor |e aut |
| 700 | 0 | 2 | |a Szalczer Estilla |e aut |
| 700 | 0 | 2 | |a Rajda Cecília |e aut |
| 700 | 0 | 2 | |a Illés Zsolt László |e aut |
| 700 | 0 | 2 | |a Mátyás Klotild |e aut |
| 700 | 0 | 2 | |a Rózsa Csilla |e aut |
| 700 | 0 | 2 | |a Csépány Tünde |e aut |
| 700 | 0 | 2 | |a Füvesi Judit |e aut |
| 700 | 0 | 2 | |a Vécsei László |e aut |
| 856 | 4 | 0 | |u http://publicatio.bibl.u-szeged.hu/9927/1/Losonczi_APOE_epsilon_status_u.pdf |z Dokumentum-elérés |