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PRJNA576887 SRP225705

Gut microbiota in IBD & circadian rest-activity disruption

Circadian Misalignment as a disease risk factor in Inflammatory Bowel Disease

Cross-sectional study of 41 stool samples from USA patients with ulcerative colitis or Crohn's disease, examining links between circadian rest-activity misalignment, intestinal permeability, and gut microbiota composition. machine-written summary

41 samples · 41 runs · US · Age unknown · 2020 · 2.10 Gbp / sample

Sources
✓Sequence archive 164○Abstract / description✓Full text 41○Supplementary tables–External resources–User contribution–Human verified

Checked this project's papers and archive records yourself? Mark it human-verified.

what each source gave
✓ Sequence archive164 sample values (collection date, country, health condition, health condition detail)
○ Abstract / descriptionread; no usable statement
✓ Full text41 sample values (location locality) · PMC8900134
○ Supplementary tablesfiles read; no table could be matched to the samples
– External resourcesnot covered by the external resources we ingest
– User contributionnothing uploaded yet
– Human verifiednot yet checked by a person · I checked this project — verify it
Samples at a glance
1 country
Age
unknown41
Condition
ulcerative_colitis21
crohns_disease20
Country
US41
Body site
primary41
Sequencing depth per sample · this project all projects
all projects, 0–0.03 Gbp: 25,080 samples (4 %)all projects, 0.03–0.1 Gbp: 17,066 samples (3 %)all projects, 0.1–0.3 Gbp: 29,179 samples (5 %)all projects, 0.3–1 Gbp: 47,044 samples (8 %)all projects, 1–3 Gbp: 124,983 samples (22 %)this project, 1–3 Gbp: 41 samplesall projects, 3–10 Gbp: 253,728 samples (44 %)all projects, 10–30 Gbp: 72,533 samples (13 %)all projects, 30–100 Gbp: 3,024 samples (1 %)all projects, 100–300 Gbp: 106 samples (0 %)all projects, ≥ 300 Gbp: 9 samples (0 %)project median 2.10 Gbp per sample0130Gbp
Community composition
Blautia_A 11.0%Faecalibacterium 8.5%Bifidobacterium 6.9%Roseburia 6.6%Bacteroides 4.9%Anaerostipes 3.3%Collinsella 2.8%Phocaeicola 2.7%Hominenteromicrobium 2.5%Streptococcus 1.9%Gemmiger 1.8%Mediterraneibacter 1.7%not assigned to a genus 7.2%other genera 38.3%

Genera, mean relative abundance over 37 profiled gut samples of this project (Sandpiper SingleM profiles, GTDB R232; low-depth and non-metagenome profiles left out).

Field coverage
fieldsamplescoverageR1R2R3R4
age_category0 0%
country41 100%41
health_condition41 100%41
subject_id0 0%
collection_date41 100%41
detailed_location41 100%
health_condition_detail41 100%41
location_locality41 100%41
Papers (1)
  • Disrupted Circadian Rest-Activity Cycles in Inflammatory Bowel Disease Are Associated With Aggressive Disease Phenotype, Subclinical Inflammation, and Dysbiosis. 2021 PMID 35265631 PMC8900134 own_data
Details
Archive description

Crohn’s Disease (CD) and Ulcerative Colitis (UC), collectively known as inflammatory bowel disease (IBD), are two of the most significant chronic conditions of the gastrointestinal tract (GIT). IBD is typically diagnosed at an early age, has no known cure, and has a chronic relapsing and remitting disease course that includes disabling symptoms during periodic flare ups. IBD affects over 1.5 million individuals in the US with an estimated direct cost of $6.1 billion.(1) IBD has a highly variable disease course, and identifying factors to avoid disease flare is essential to avoid complications such as</p><p>hospitalization and surgery. Recently there has been compelling evidence that IBD subjects commonly have disrupted sleep, and disrupted sleep leads to a more aggressive disease course.(2, 3) Sleep and multiple biological processes in the body are orchestrated by the central circadian clock located in the suprachiasmatic nucleus. We have shown that disruption of the light:dark cycle, or circadian misalignment, can be a risk factor for increased intestinal permeability, dysbiosis, and mucosal inflammation, all of which are known risk factors for disease flare in IBD. However, whether circadian misalignment is prevalent in IBD or if it is a factor in promoting disease flare is a gap in our current knowledge. Microbiome analysis will be conducted to determine these primary outcome measures.

How this project entered the registry

Classified as human gut / stool shotgun DNA metagenome of age unknown by sonnet_x2 with confidence 0.65. Assay shotgun_dna.

  • host run.host_tax_id · “9606”
  • body site study.description · “chronic conditions of the gastrointestinal tract”
Evidence examples (one per field × route)
samplefieldvaluerouteconf.sourcequote
SAMN13012336collection_date2018R10.90biosample.attribute:collection_date2018
SAMN13012336countryUSR10.90sample.attr.geo_loc_nameUSA
SAMN13012336health_conditionulcerative_colitisR10.90biosample_attrUlcerative Colitis
SAMN13012336health_condition_detailUlcerative ColitisR10.90sample.attr.host_diseaseUlcerative Colitis
SAMN13012336location_localityChicagoR30.70paper.fulltext.methodsRush University Medical Center
Sequencing

41 runs over 41 samples · mean 2.07 Gbp per run (median 2.10 Gbp, total 84.78 Gbp; 41 runs with a base count) · layout PAIRED 41 · platform ILLUMINA 41 · models Illumina HiSeq 4000 (41) · 90% of runs with a Sandpiper profile · first public 2020-11-02

Authors (13)

Swanson GR first · Kochman N · Amin J · Chouhan V · Yim W · Engen PA · Shaikh M · Naqib A · Tran L · Voigt RM · Forsyth CB · Green SJ · Keshavarzian A last

Downloads

PRJNA576887.csv.gz (1.8 KB) · parquet (70.5 KB) — all 41 samples, every field with route and confidence · PRJNA576887_determinations.csv.gz (1.6 KB) — 205 evidence rows

Samples (41 · every field this project has values for · hover a cell for its source)
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