Public health impact of poor sleep on COVID-19, influenza and upper respiratory infections
This article has been Reviewed by the following groups
Listed in
- Evaluated articles (ScreenIT)
Abstract
Article activity feed
-
-
SciScore for 10.1101/2022.02.16.22271055: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
NIH rigor criteria are not applicable to paper type.Table 2: Resources
Antibodies Sentences Resources Diagnoses were primarily by PCR (N=3,424), with a small proportion of samples diagnosed through antigen testing (N=9), or antibody testing (N=6), and 57 samples with a missing diagnosis type. antigen testing ( N=9) ,suggested: NoneSoftware and Algorithms Sentences Resources When a study participant is recruited, their entire medical record is linked into the FinnGen database and not just subsequent healthcare provider visits, allowing a detailed understanding of their medical history. FinnGensuggested: (Open Targets Genetics Portal, RRID:SCR_021701)Samples were genotyped using Illumina and Affymetrix … SciScore for 10.1101/2022.02.16.22271055: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
NIH rigor criteria are not applicable to paper type.Table 2: Resources
Antibodies Sentences Resources Diagnoses were primarily by PCR (N=3,424), with a small proportion of samples diagnosed through antigen testing (N=9), or antibody testing (N=6), and 57 samples with a missing diagnosis type. antigen testing ( N=9) ,suggested: NoneSoftware and Algorithms Sentences Resources When a study participant is recruited, their entire medical record is linked into the FinnGen database and not just subsequent healthcare provider visits, allowing a detailed understanding of their medical history. FinnGensuggested: (Open Targets Genetics Portal, RRID:SCR_021701)Samples were genotyped using Illumina and Affymetrix chip arrays (Illumina Inc., San Diego, and Thermo Fisher Scientific, Santa Clara, CA, USA) and imputed to GRCh38/hg38 using Beagle v4.153 with the SISu v3.0 reference panel, consisting of 3,775 whole genome-sequenced Finnish individuals54 (see https://dx.doi.org/10.17504/protocols.io.nmndc5e for the complete imputation and QC protocol). Beaglesuggested: (BEAGLE, RRID:SCR_001789)These GWA analyses were performed using REGENIE55 v2.0.2 and in the model-building step (step 1) were adjusted for age at follow-up end (2019/12/31) or death, sex, genotyping batch and the first 10 genetic principal components. REGENIE55suggested: NoneWe performed this analysis using the Python module “lifelines” (v0.26.0)56 with Python (v3.8.11 for FinnGen, v3.7.11 for UK Biobank). Pythonsuggested: (IPython, RRID:SCR_001658)Results from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).
Results from LimitationRecognizer: We detected the following sentences addressing limitations in the study:We note the following limitations, welcome feedback from the scientific community and will aim to address some of these issues in future studies in this line of research. First of all, FinnGen endpoints were identified using hospital records only, and consequently results of survival analyses are biased towards more serious cases of the prior (insomnia) endpoint. In comparison, in the UK Biobank diagnoses were captured in hospital and primary care data. It is therefore possible that the differences in hazard ratio we see between the two cohorts represent a) greater statistical power due to more severe insomnia diagnosis, b) a real difference in effect of insomnia on more severe (FinnGen) and less severe (UK Biobank) respiratory infections, c) differences between the cohort demographics or d) a combination of these factors. Confounding this issue is that the UK Biobank suffers from ascertainment bias, resulting in a cohort that is, on average, healthier and less socioeconomically deprived than the general UK population48 and it is likely, though not yet reported, that the FinnGen study also suffers from this bias. The insomnia prevalence that we observed (0.9% in FinnGen and 3.8% in UKB; Supp Table 5) point to low ascertainment in these cohorts compared to estimates of insomnia prevalence (7.9% in the UK49 and up to 11.7% in Finland50). While ascertainment bias has been shown to exaggerate the effects of a prior endpoint on survival time51, it is not currently known how this a...
Results from TrialIdentifier: No clinical trial numbers were referenced.
Results from Barzooka: We did not find any issues relating to the usage of bar graphs.
Results from JetFighter: We did not find any issues relating to colormaps.
Results from rtransparent:- Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
- Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
- No protocol registration statement was detected.
Results from scite Reference Check: We found no unreliable references.
-