La enfermedad de Parkinson (EP) es el segundo trastorno neurodegenerativo más común, que afecta al 2-3% de la población mayor de 65 años. Clásicamente, se caracteriza por tres síntomas motores: rigidez muscular, temblor en reposo y bradicinesia, pero también presenta numerosos síntomas no motores. La pérdida neuronal en la sustancia negra, que...
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July 29, 2022 (v1)PublicationUploaded on: December 4, 2022
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November 3, 2022 (v1)Publication
Knowledge of genomic features specific to the human lineage may provide insights into brain-related diseases. We leverage high-depth whole genome sequencing data to generate a combined annotation identifying regions simultaneously depleted for genetic variation (constrained regions) and poorly conserved across primates. We propose that these...
Uploaded on: March 24, 2023 -
May 23, 2023 (v1)Publication
Background: Hyperhomocysteinemia is considered an independent risk factor for cognitive impairment. Objective: To study the correlation between homocysteine levels and cognitive impairment in patients with PD. Methods: We conducted a case–control study that included 246 patients with PD, of whom 32 were cognitively impaired. The levels of...
Uploaded on: May 26, 2023 -
September 30, 2022 (v1)Publication
A prodromal phase of Parkinson's disease (PD) may precede motor manifestations by decades. PD patients' siblings are at higher risk for PD, but the prevalence and distribution of prodromal symptoms are unknown. The study objectives were (1) to assess motor and non-motor features estimating prodromal PD probability in PD siblings recruited...
Uploaded on: March 24, 2023 -
March 31, 2023 (v1)Publication
Genome-wide association studies have generated an increasing number of common genetic variants associated with neurological and psychiatric disease risk. An improved under- standing of the genetic control of gene expression in human brain is vital considering this is the likely modus operandum for many causal variants. However, human brain...
Uploaded on: April 14, 2023 -
November 22, 2022 (v1)Publication
Brain cholesterol metabolism has been described as altered in Parkinson's disease (PD) patients. Serum lipid levels have been widely studied in PD with controversial results among different populations and age groups. The present study is aimed at determining if the serum lipid profile could be influenced by the genetic background of PD...
Uploaded on: March 24, 2023 -
September 30, 2022 (v1)Publication
Advanced age represents one of the major risk factors for Parkinson's Disease. Recent biomedical studies posit a role for microRNAs, also known to be remodelled during ageing. However, the relationship between microRNA remodelling and ageing in Parkinson's Disease, has not been fully elucidated. Therefore, the aim of the present study is to...
Uploaded on: March 24, 2023 -
October 25, 2022 (v1)Publication
Parkinson's disease (PD) is the neurological disorder showing the greatest rise in prevalence from 1990 to 2016. Despite clinical definition criteria and a tremendous effort to develop objective biomarkers, precise diagnosis of PD is still unavailable at early stage. In recent years, an increasing number of studies have used omic methods to...
Uploaded on: December 4, 2022 -
May 8, 2023 (v1)Publication
Transcriptomics in Parkinson's disease (PD) offers new insights into the molecular mechanism of PD pathogenesis. Several pathways, such as inflammation and protein degradation, have been identified by differential gene expression analysis. Our aim was to identify gene expression differences underlying the disease etiology and the discovery of...
Uploaded on: May 10, 2023 -
November 29, 2022 (v1)Publication
Parkinson's disease is a neurodegenerative movement disorder that currently has no disease-modifying treatment, partly owing to inefficiencies in drug target identification and validation. We use Mendelian randomization to investigate over 3,000 genes that encode druggable proteins and predict their efficacy as drug targets for Parkinson's...
Uploaded on: December 4, 2022 -
October 3, 2022 (v1)Publication
Long runs of homozygosity (ROH) are contiguous stretches of homozygous genotypes, which are a footprint of inbreeding and recessive inheritance. The presence of recessive loci is suggested for Alzheimer's disease (AD); however, their search has been poorly assessed to date. To investigate homozygosity in AD, here we performed a finescale ROH...
Uploaded on: March 24, 2023 -
November 14, 2022 (v1)Publication
ARTICLE Common variants in Alzheimer's disease and risk stratification by polygenic risk scores Genetic discoveries of Alzheimer's disease are the drivers of our understanding, and together with polygenetic risk stratification can contribute towards planning of feasible and efficient preventive and curative clinical trials. We first perform a...
Uploaded on: March 24, 2023