Evidence map›Paper›PMID 28009047›Full record

ArticleClinical and experimental immunology2017

Longitudinal monitoring of gene expression in ultra-low-volume blood samples self-collected at home.

C Speake, E Whalen, V H Gersuk, D Chaussabel, J M Odegard, C J Greenbaum

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03369821 (Understanding Beta-cell Destruction Through the Study of EXtremely Early-onset Type 1 Diabetes), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 20% 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.

NCT03369821 recruitingnot on this map

Understanding Beta-cell Destruction Through the Study of EXtremely Early-onset Type 1 Diabetes (A Musketeers' Memorandum Study)

TypeobservationalSponsorUniversity of ExeterRan2017 to 2028Enrolled300ConditionsType1 Diabetes MellitusArmsBeta Cell Loss and Immune Function, Immune Function with RNAseq
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Blood gene transcript signature profiling in pregnancies resulting in preterm birth: A systematic review.European journal of obstetrics & gynecology and reproductive biology: X · 2020
    Review
  5. Article
  6. Article
  7. Article
  8. Article
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

6 authors at 1 institution.

C SpeakeBenaroya Research Institute, Seattle, WA, USA.
E WhalenBenaroya Research Institute, Seattle, WA, USA.
V H GersukBenaroya Research Institute, Seattle, WA, USA.
D ChaussabelBenaroya Research Institute, Seattle, WA, USA.
J M OdegardBenaroya Research Institute, Seattle, WA, USA.
C J GreenbaumBenaroya Research Institute, Seattle, WA, USA.
Benaroya Research Institute

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Blood transcriptional profiles could serve as biomarkers of clinical changes in subjects at-risk for or diagnosed with diabetes. However, transcriptional variation over time is poorly understood due to the impracticality of frequent longitudinal phlebotomy in large patient cohorts. We have developed a novel transcriptome assessment method that could be applied to fingerstick blood samples self-collected by study volunteers. Fifteen μL of blood from a fingerstick yielded sufficient RNA to analyse > 176 transcripts by high-throughput quantitative polymerase chain reaction (PCR). We enrolled 13 subjects with type 1 diabetes and 14 controls to perform weekly collections at home for a period of 6 months. Subjects returned an average of 24 of 26 total weekly samples, and transcript data were obtained successfully for > 99% of samples returned. A high degree of correlation between fingerstick data and data from a standard 3 mL venipuncture sample was observed. Increases in interferon-stimulated gene expression were associated with self-reported respiratory infections, indicating that real-world transcriptional changes can be detected using this assay. In summary, we show that longitudinal monitoring of gene expression is feasible using ultra-low-volume blood samples self-collected by study participants at home, and can be used to monitor changes in gene expression frequently over extended periods.

Indexed as

Blood Specimen CollectionBlood VolumeAdolescentAdultBiomarkersDiabetes Mellitus, Type 1FemaleGene Expression ProfilingHumansLongitudinal StudiesMalePhlebotomyReal-Time Polymerase Chain ReactionRNASelf CareYoung AdultBiomarkersRNAautoimmunitydiabetestranscriptomics

Identifiers

PMID28009047
PMCPMC5383441
OpenAlexW2565082939

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.