| dc.date.accessioned |
2022-08-24T09:47:07Z |
|
| dc.date.available |
2022-08-24T09:47:07Z |
|
| dc.date.issued |
2022-08-24 |
|
| dc.identifier.uri |
http://hdl.handle.net/123456789/42770 |
|
| dc.title |
Explaining the Link Between Dyslexia Susceptibility Genes DYX1C1, DCDC2 and KIAA0319 and Variation in Brain Activity in the Middle Temporal Gyrus, Intraparietal Sulcus and Inferior Frontal Gyrus during reading tasks |
en |
| ethesis.faculty |
Lääketieteellinen tiedekunta |
fi |
| ethesis.faculty |
Faculty of Medicine |
en |
| ethesis.faculty |
Medicinska fakulteten |
sv |
| ethesis.faculty.URI |
http://data.hulib.helsinki.fi/id/a4d5aaa2-b5aa-41a7-ba4c-e5e0df7a902d |
|
| ethesis.university.URI |
http://data.hulib.helsinki.fi/id/50ae46d8-7ba9-4821-877c-c994c78b0d97 |
|
| ethesis.university |
Helsingin yliopisto |
fi |
| ethesis.university |
University of Helsinki |
en |
| ethesis.university |
Helsingfors universitet |
sv |
| dct.creator |
Rinne, Nea |
|
| dct.issued |
2022 |
|
| dct.abstract |
Aims:
Reading ability is a fundamental skill in the modern society, yet some individuals have difficulties in learn-ing to read and write. There is a lot of variability in reading skills, and one reason that can cause reading difficulty is a neurodevelopmental disorder called dyslexia. It is the most common learning disability, and the core deficit in dyslexia lies in word decoding, which is the process of connecting letter combinations into their corresponding auditory representations. Dyslexia is familial and is recognized to have strong genetic background. A dozen dyslexia susceptibility genes have been suggested, but DYX1C1, DCDC2 and KIAA0319 have been associated with dyslexia most commonly. The function of these genes is however not yet fully understood. In previous studies variation in these genes have been linked to struc-tural brain alterations in left hemispheric regions where language is mostly processed. The aim of this study was to examine the connection between dyslexia susceptibility genes DCDC2, DYX1C1 and KI-AA0319 and variation in brain activity during reading tasks in the left middle temporal gyrus (MTG), infe-rior Frontal Gyrus (IFG) and intraparietal sulcus (IPS), by combining functional magnetic resonance imag-ing data and genetic data in a neurotypical population. Previous studies have reported that weaker reading skills are associated with decreased brain activity in these regions, and reading incongruent sentences has been associated with increased brain activity in the left IFG and MTG.
Methods:
During fMRI, participants were presented with sentences with illogical and logical endings, and judged them as either congruent or incongruent, in distracted and undistracted conditions. Auditory speech stimuli were used as distractor. Regions of Interest analyses were conducted to examine brain activation in the aforementioned brain regions during distracted and non-distracted reading separately for different allelic groups in single nucleotide polymorphisms of the three genes.
Results and Conclusions:
DYX1C1 showed significant interaction with brain activation in the IPS. A significant interaction of DCDC2 with logic was found in the IFG and IPS showing that individuals carrying susceptibility alleles have reduced brain activation when reading incongruent sentences. Additionally, DCDC2 showed inter-action with distraction in the IFG, as individuals carrying susceptibility alleles had reduced brain activa-tion when a speech distractor was presented. In the MTG, there was a significant interaction of DCDC2 with logic and distractor showing that in different allelic groups, speech distractor modulated the activa-tion elicited by incongruent sentences in different ways.
These results provide a link between variation in dyslexia susceptibility genes and brain activation during reading. Previous studies have mostly linked dyslexia susceptibility genes to structural brain alterations, and dyslexia and lower reading skills have been linked to variation in brain activity. The current study therefore expands the current understanding of genetic basis on reading and linguistic processing. |
en |
| dct.subject |
Dyslexia |
|
| dct.subject |
fMRI |
|
| dct.subject |
DYX1C1 |
|
| dct.subject |
DCDC2 |
|
| dct.subject |
KIAA0319 |
|
| dct.subject |
intraparietal sulcus (IPS) |
|
| dct.subject |
inferior frontal gyrus (IFG) |
|
| dct.subject |
middle temporal gyrus (MTG) |
|
| ethesis.language.URI |
http://data.hulib.helsinki.fi/id/languages/eng |
|
| ethesis.language |
englanti |
fi |
| ethesis.language |
English |
en |
| ethesis.language |
engelska |
sv |
| ethesis.supervisor |
Patrik Wikman |
und |
| ethesis.thesistype |
pro gradu -tutkielmat |
fi |
| ethesis.thesistype |
master's thesis |
en |
| ethesis.thesistype |
pro gradu-avhandlingar |
sv |
| ethesis.thesistype.URI |
http://data.hulib.helsinki.fi/id/thesistypes/mastersthesis |
|
| dct.identifier.ethesis |
E-thesisID:c9fdb612-f5ce-4231-8df7-f9acf0c27741 |
|
| ethesis-internal.timestamp.reviewStep |
2022-06-10 14:21:00:649 |
|
| dct.identifier.urn |
URN:NBN:fi:hulib-202208243343 |
|
| ethesis.discipline.med |
Psykologia
|
und |
| ethesis.discipline.med |
Neuroscience |
und |
| ethesis.facultystudyline |
Neuroscience and psychobiology |
fi |
| ethesis.facultystudyline |
Neuroscience and psychobiology |
en |
| ethesis.facultystudyline |
Neuroscience and psychobiology |
sv |
| ethesis.facultystudyline.URI |
http://data.hulib.helsinki.fi/id/SH_TMED-410 |
|
| ethesis.mastersdegreeprogram |
Translationaalisen lääketieteen maisteriohjelma (Translational Medicine) |
fi |
| ethesis.mastersdegreeprogram |
Master's Programme in Translational Medicine |
en |
| ethesis.mastersdegreeprogram |
Magisterprogrammet i translationell medicin |
sv |
| ethesis.mastersdegreeprogram.URI |
http://data.hulib.helsinki.fi/id/MH30_002 |
|
