CSF2, colony stimulating factor 2, 1437

N. diseases: 1028; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 GeneticVariation disease BEFREE Ratios of the main proteins found in PD patient brain inclusions that can be measured in the CSF appear to have value as short- to mid-term predictors of dementia. 30423201 2018
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 GeneticVariation disease BEFREE Three studies on stroke reported mixed findings but were limited due to the small number of patients undergoing CSF examination, whilst neurosyphilis continued to be reported as a common cause of dementia in studies from North Africa. 28859081 2017
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 GeneticVariation disease BEFREE We included 768 patients (subjective cognitive decline (SCD, n = 194), mild cognitive impairment (MCI, n = 127), dementia (AD and non-AD, n = 447) with amyloid-β PET and CSF Aβ<sub>42</sub> measurement within 1 year. 31810489 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 GeneticVariation disease BEFREE Subjects with dementia and Mild Cognitive Impairment (MCI) due to AD have been found to have higher CSF cortisol levels than cognitively healthy controls. 30881301 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 GeneticVariation disease BEFREE A total of 1,081 adults without dementia (375 healthy subjects and 706 individuals with mild cognitive impairment) were recruited from the Alzheimer's Disease Neuroimaging Initiative (ADNI) to test the influence of BDNF Val66Met polymorphism on cognitive impairment, brain structure atrophy, and change in the levels of CSF biomarkers. 30775992 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE The finding that amnestic MCI based on brief neuropsychological assessment is significantly associated with CSF biomarkers for cognitive decline and Alzheimer's disease is in accordance with longitudinal studies that find memory impairment; both in itself and especially in combination with other cognitive deficit to constitute a risk factor for subsequent cognitive decline and dementia. 30614807 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE Performance of the CSF biomarkers was optimal in the asymptomatic versus Alzheimer's disease dementia comparison (AUC ≥0·90 for all except Aβ<sub>1-40</sub> [0·59, 0·45-0·72]). 30172624 2018
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE Granulocyte-macrophage colony-stimulating factor (GM-CSF) is elevated in cerebrospinal fluid in HIV- associated dementia; in addition, therapeutic GM-CSF elevates plasma viral load. 11834953 2002
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE To examine the disparity in practitioner attitudes and clinical practice relating to the use of CSF biomarkers for dementia diagnosis across Europe. 28826189 2017
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE CSF tau and <sup>18</sup>F-AV-1451 have equal performance in early clinical stages of AD, but <sup>18</sup>F-AV-1451 is superior in the dementia stage, and exhibits close to perfect diagnostic performance for mild to moderate AD. 29321235 2018
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE In this multicentre study in clinical settings, we assessed the accuracy of optimized procedures for FDG-PET brain metabolism and CSF classifications in predicting or excluding the conversion to Alzheimer's disease (AD) dementia and non-AD dementias. 29387532 2018
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE Ample evidence is available for phase 1 (identifying useful leads) and phase 2 (assessing the accuracy for AD dementia versus controls) for CSF biomarkers. 28317649 2017
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE A diagnosis of dementia is currently made in terms of probability and is based on clinical evaluation (neuropsycological tests) as well as on the results of morphological imaging investigations (MRI) that can be supported by biohumoral (CSF analysis), and functional imaging only in the case of uncertain diagnosis of disease. 31802055 2020
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE By a survey, we aimed to do a "selfie" of the use and diffusion of CSF biomarkers of dementia in Italy, the standardization of pre-analytical procedures, the harmonization of ranges, and the participation to Quality Control programs. 27911328 2017
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE Predicting clinical decline and conversion to Alzheimer's disease or dementia using novel Elecsys Aβ(1-42), pTau and tTau CSF immunoassays. 31836810 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE We evaluated the prognostic utility of identifying longitudinal neuropsychological decline along with single cognitive exam and Alzheimer's disease (AD) cerebrospinal fluid (CSF) biomarkers in predicting dementia. 31104015 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE However, looking into the multifactorial nature of AD and the overlapping pathology with other forms of dementia, it is important to integrate the core CSF biomarkers with a broader panel of other biomarkers reflecting different aspects of pathology. 30770953 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE Prognostic models were developed by Cox regression with patient characteristics, MRI, and/or CSF biomarkers to predict clinical progression to MCI or dementia. 30987684 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE Applying CSF biomarker ratios, rather than their single values could represent a useful tool, especially for the differential diagnosis of different forms of dementia. 28726050 2017
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE The evaluation of cerebrospinal fluid (CSF) biomarkers for Alzheimer's disease (AD) (β-amyloid, t-tau, p-tau) can be used to estimate the risk of developing dementia in patients at the pre-clinical stages of AD, i.e. subjective cognitive decline (SCD) and mild cognitive impairment (MCI). 30509028 2018
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE AD diagnosis (MCI or dementia) with normal CSF biomarkers is a rare condition. 29318973 2018
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE The progression of mild cognitive impairment (MCI) to Alzheimer's disease (AD) dementia can be predicted by cognitive, neuroimaging, and cerebrospinal fluid (CSF) markers. 29017593 2017
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE Potential predictors included CSF biomarkers, cognitive performance (verbal learning and memory), apolipoprotein E (APOE) ε4 genotype, medial temporal lobe atrophy, family history of dementia, depressive symptoms, and vascular factors, including the Cardiovascular Risk Factors, Aging and Dementia (CAIDE) risk score. 31805990 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE Thereafter, we focused on the four miRNAs that showed group differences and measured their content in neurally derived blood EVs isolated from 63 subjects: 16 patients with early stage dementia and a CSF Aβ42+ tau profile consistent with AD, 16 individuals with mild cognitive impairment (MCI) and an AD CSF profile, and 31 cognitively intact controls with normal CSF Aβ42+ tau levels. 31849573 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.100 Biomarker disease BEFREE We further suggest that among those patients with substantial cervical stenosis (extensive enough to block CSF circulation in the cervical area as identified by cine MRI) appropriate comparative clinical studies could be undertaken to demarcate associations with presenile dementia, sleep disturbance and posterior fossa dysfunction. 30037601 2018