Evidence map›Paper›PMID 32515825›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2020

In Vivo Quasi-Elastic Light Scattering Eye Scanner Detects Molecular Aging in Humans.

Olga Minaeva, Srikant Sarangi, Danielle M Ledoux, Juliet A Moncaster, Douglas S Parsons, Kevin J Washicosky, Caitlin A Black, Frank J Weng, Maria Ericsson, Robert D Moir and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact, top 100% of its field
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

4 citing papers in PubMed, 0 citations in OpenAlex.

  1. Review
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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

15 authors at 4 institutions in 1 country.

Olga MinaevaMolecular Aging & Development Laboratory, Boston University School of Medicine, Massachusetts.
Srikant SarangiMolecular Aging & Development Laboratory, Boston University School of Medicine, Massachusetts.
Danielle M LedouxDepartment of Ophthalmology, Boston Children's Hospital, Massachusetts.
Juliet A MoncasterMolecular Aging & Development Laboratory, Boston University School of Medicine, Massachusetts.
Douglas S ParsonsMolecular Aging & Development Laboratory, Boston University School of Medicine, Massachusetts.
Kevin J WashicoskyGenetics and Aging Research Unit, Department of Neurology, Massachusetts General Hospital, Charlestown.
Caitlin A BlackDepartment of Ophthalmology, Boston Children's Hospital, Massachusetts.
Frank J WengDepartment of Ophthalmology, Boston Children's Hospital, Massachusetts.
Maria EricssonElectron Microscopy Facility, Harvard Medical School, Boston, Massachusetts.
Robert D MoirGenetics and Aging Research Unit, Department of Neurology, Massachusetts General Hospital, Charlestown.
Yorghos TripodisDepartment of Biostatistics, Boston University School of Public Health, Massachusetts.
John I ClarkDepartment of Biological Structure, University of Washington, Seattle.
Rudolph E TanziGenetics and Aging Research Unit, Department of Neurology, Massachusetts General Hospital, Charlestown.
David G HunterDepartment of Ophthalmology, Boston Children's Hospital, Massachusetts.
Lee E GoldsteinMolecular Aging & Development Laboratory, Boston University School of Medicine, Massachusetts.
Boston University · USBoston Children's Hospital · USHarvard University · USUniversity of Washington · US

Funding

Neuropathology CoreP30AG013846 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI KOWALL, NEIL W. · 1996 to 2020
$29.1M
NIA NIH HHS P30 AG013846
6 · The paper itself

Abstract

The absence of clinical tools to evaluate individual variation in the pace of aging represents a major impediment to understanding aging and maximizing health throughout life. The human lens is an ideal tissue for quantitative assessment of molecular aging in vivo. Long-lived proteins in lens fiber cells are expressed during fetal life, do not undergo turnover, accumulate molecular alterations throughout life, and are optically accessible in vivo. We used quasi-elastic light scattering (QLS) to measure age-dependent signals in lenses of healthy human subjects. Age-dependent QLS signal changes detected in vivo recapitulated time-dependent changes in hydrodynamic radius, protein polydispersity, and supramolecular order of human lens proteins during long-term incubation (~1 year) and in response to sustained oxidation (~2.5 months) in vitro. Our findings demonstrate that QLS analysis of human lens proteins provides a practical technique for noninvasive assessment of molecular aging in vivo.

Indexed as

Dynamic Light ScatteringAdolescentAdultAgingChildChild, PreschoolCross-Sectional StudiesCrystallinsElectrophoresis, Polyacrylamide GelFemaleHumansLens, CrystallineMaleMicroscopy, Electron, TransmissionMiddle AgedOxidation-ReductionCrystallinsCrystallinHumanLensMolecular agingProtein aggregation

Identifiers

PMID32515825
PMCPMC7494032
OpenAlexW2992795055

What OpenQuestion holds

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Registered trials

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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.