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Correlation between the serum concentration of vitamin A and disease severity in patients carrying p.G90D in RHO, the most frequent gene associated with dominant retinitis pigmentosa : implications for therapy with vitamin A
ID
Krašovec, Tjaša
(
Avtor
),
ID
Kobal, Nina
(
Avtor
),
ID
Šuštar Habjan, Maja
(
Avtor
),
ID
Volk, Marija
(
Avtor
),
ID
Hawlina, Marko
(
Avtor
),
ID
Fakin, Ana
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(3,94 MB)
MD5: FBBF024AF41F929E21A4738D866661FB
URL - Izvorni URL, za dostop obiščite
https://www.mdpi.com/1422-0067/24/1/780
Galerija slik
Izvleček
The pathogenic variant p.G90D in RHO is believed to be responsible for a spectrum of phenotypes, including congenital stationary blindness (for the purpose of this study termed night blindness without degeneration; NBWD), Sector RP, Pericentral RP, and Classic RP. We present a correlation between the serum concentration of vitamin A and disease severity in patients with this variant. This prospective study involved 30 patients from 7 families (17 male; median age 46 years, range 8–73). Full ophthalmological examination including visual acuity, Goldmann perimetry, slit-lamp exam, optical coherence tomography, fundus autofluorescence, and electrophysiology was performed to determine the presenting phenotype. The serum concentration of vitamin A was determined from a fasting blood sample taken on the day of the exam, where it was found that 23.3% (7/30) of patients had NBWD, 13.3% (4/30) had Sector RP, 3.3% (1/30) had Pericentral RP, and 60% (18/30) had Classic RP. Multiple logistic regression revealed a significantly higher probability of having a milder phenotype (NBWD or Sector RP) in association with younger age (p < 0.05) and a higher concentration of vitamin A (p < 0.05). We hypothesize that vitamin A in its 11-cis-retinal form plays a role in stabilizing the constitutively active p.G90D rhodopsin and its supplementation could be a potential treatment strategy for p.G90D RHO patients.
Jezik:
Angleški jezik
Ključne besede:
retinitis pigmentosa
,
RP
,
vitamin A
,
CSNB
,
NBWD
,
congenital stationary night blindness
,
rhodopsin
,
RHO
,
sector RP
,
treatment
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2023
Št. strani:
14 str.
Številčenje:
Vol. 24, iss. 1, art. 780
PID:
20.500.12556/RUL-155549
UDK:
617.7
ISSN pri članku:
1422-0067
DOI:
10.3390/ijms24010780
COBISS.SI-ID:
147522819
Datum objave v RUL:
05.04.2024
Število ogledov:
514
Število prenosov:
176
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Objavi na:
Gradivo je del revije
Naslov:
International journal of molecular sciences
Skrajšan naslov:
Int. j. mol. sci.
Založnik:
MDPI
ISSN:
1422-0067
COBISS.SI-ID:
2779162
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
pigmentni retinitis
,
RP
,
vitamin A
,
CSNB
,
NBWD
,
prirojena stacionarna nočna slepota
,
rodopsin
,
RHO
,
sektor RP
,
zdravljenje
Projekti
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
J3-1750
Naslov:
Priprava pogojev za gensko zdravljenje dednih očesnih bolezni
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