Evidence map›Paper›PMID 31376643›Full record

ArticleNeuroImage. Clinical2019

Prediction of fast decline in amyloid positive mild cognitive impairment patients using multimodal biomarkers.

Hyemin Jang, Jongyun Park, Sookyoung Woo, Seonwoo Kim, Hee Jin Kim, Duk L Na, Samuel N Lockhart, Yeshin Kim, Ko Woon Kim, Soo Hyun Cho and 4 more

Abstract read
In one paragraph

Article in NeuroImage. Clinical, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Yonsei medical journal · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Hyemin JangDepartment of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, South Korea.
Jongyun ParkSchool of Biomedical Engineering, Korea University, Seoul, South Korea.
Sookyoung WooStatistics and data center, Samsung Medical Center, Seoul, South Korea.
Seonwoo KimStatistics and data center, Samsung Medical Center, Seoul, South Korea.
Hee Jin KimDepartment of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, South Korea.
Duk L NaDepartment of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, South Korea.
Samuel N LockhartDepartment of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Yeshin KimDepartment of Neurology, Kangwon National University Hospital, Kangwon National University College of Medicine, Chuncheon, South Korea.
Ko Woon KimDepartment of Neurology, Chonbuk National University Hospital, Chonbuk National University Medical school, Jeonju, South Korea.
Soo Hyun ChoDepartment of Neurology, Chonnam National University Hospital, Gwangju, South Korea.
Seung Joo KimDepartment of Neurology, Gyeongsang University Hospital, Changwon, South Korea.
Joon-Kyung SeongSchool of Biomedical Engineering, Korea University, Seoul, South Korea. Electronic address: jkseong@korea.ac.kr.
Sang Won SeoDepartment of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, South Korea; Neuroscience Center, Samsung Medical Center, Seoul, South Korea; Samsung Alzheimer Research Center, Samsung Medical Center, Seoul, South Korea; Center for Clinical Epidemiology, Samsung Medical Center, Seoul, South Korea. Electronic address: sw72.seo@samsung.com.
Alzheimer’s Disease Neuroimaging Initiative

Funding

Wake Forest Alzheimer's Disease Core CenterP30AG049638 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI RAPP, STEPHEN R · 2016 to 2020
$12.2M
NIA NIH HHS P30 AG049638
6 · The paper itself

Abstract

It may be possible to classify patients with Aβ positive (+) mild cognitive impairment (MCI) into fast and slow decliners according to their biomarker status. In this study, we aimed to develop a risk prediction model to predict fast decline in the Aβ+ MCI population using multimodal biomarkers. We included 186 Aβ+ MCI patients who underwent florbetapir PET, brain MRI, cerebrospinal fluid (CSF) analyses, and FDG PET at baseline. We defined conversion to dementia within 3 years (= fast decline) as the outcome. The associations of potential covariates (MCI stage, APOE4 genotype, corrected hippocampal volume (HV), FDG PET SUVR, AV45 PET SUVR, CSF Aβ, total tau (t-tau), and phosphorylated tau (p-tau)) with the outcome were tested and nomograms were constructed using logistic regression models in the training dataset (n=124, n of fast decliners=52). The model was internally validated with the testing dataset (n=62, n of fast decliners=22). The multivariable analysis (including CSF t-tau) showed that MCI stage (late MCI vs. early MCI; OR 15.88, 95% CI 4.59, 54.88), APOE4 (OR 5.65, 95% CI 1.52, 20.98), corrected HV*1000 (OR 0.22, 95% CI 0.09, 0.57), FDG SUVR*10 (OR 0.43, 95% CI 0.27, 0.71), and log

Indexed as

Disease ProgressionAgedAged, 80 and overAlzheimer DiseaseAmyloid beta-PeptidesBiomarkersCognitive DysfunctionFemaleFollow-Up StudiesHumansMagnetic Resonance ImagingMaleMiddle AgedPositron-Emission TomographyPredictive Value of Teststau ProteinsAmyloid beta-PeptidesBiomarkersMAPT protein, humantau ProteinsAlzheimer's diseaseAmyloidConversion to dementiaMild cognitive impairmentMultimodal biomarkersNomogram

Identifiers

PMID31376643
PMCPMC6677900

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.