Evidence map›Paper›PMID 34517295›Full record

Observational studyBlood cells, molecules & diseases2021

COVID-19 induces proatherogenic alterations in moderate to severe non-comorbid patients: A single-center observational study.

Louise F Kimura, Morena B Sant'Anna, Sonia A Andrade, Matteo C Ebram, Cristiane F G Lima, Rosa M G Celano, Ruy F M Viégas, Gisele Picolo

Open access · greenAbstract readComparative StudyObservational Study
In one paragraph

Observational study in Blood cells, molecules & diseases, 2021. 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
0.5field-weighted citation impact, top 34% 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, 9 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Louise F KimuraLaboratory of Pain and Signaling, Butantan Institute, Avenida Vital Brazil 1500, São Paulo, SP 05503-900, Brazil. Electronic address: louise.vieira@esib.butantan.gov.br.
Morena B Sant'AnnaLaboratory of Pain and Signaling, Butantan Institute, Avenida Vital Brazil 1500, São Paulo, SP 05503-900, Brazil. Electronic address: morena.santanna@esib.butantan.gov.br.
Sonia A AndradeLaboratory of Pain and Signaling, Butantan Institute, Avenida Vital Brazil 1500, São Paulo, SP 05503-900, Brazil. Electronic address: sonia.andrade@butantan.gov.br.
Matteo C EbramLaboratory of Pain and Signaling, Butantan Institute, Avenida Vital Brazil 1500, São Paulo, SP 05503-900, Brazil. Electronic address: matteo.celano@fm.usp.br.
Cristiane F G LimaLaboratory of Pain and Signaling, Butantan Institute, Avenida Vital Brazil 1500, São Paulo, SP 05503-900, Brazil. Electronic address: cristiane.lima@esib.butantan.gov.br.
Rosa M G CelanoUniversity of Taubaté (UNITAU), Rua Quatro de Março, 432, Taubaté, SP 12020-270, Brazil. Electronic address: ebramcelano@uol.com.br.
Ruy F M ViégasUniversity of Taubaté (UNITAU), Rua Quatro de Março, 432, Taubaté, SP 12020-270, Brazil. Electronic address: ruyfelipe@endocard.com.br.
Gisele PicoloLaboratory of Pain and Signaling, Butantan Institute, Avenida Vital Brazil 1500, São Paulo, SP 05503-900, Brazil. Electronic address: gisele.picolo@butantan.gov.br.
Instituto Butantan · BRUniversidade de Taubaté · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with COVID-19 can be asymptomatic or present mild to severe symptoms, leading to respiratory and cardiovascular complications and death. Type 2 diabetes mellitus (T2DM) and obesity are considered risk factors for COVID-19 poor prognosis. In parallel, COVID-19 severe patients exhibit dyslipidemia and alterations in neutrophil to lymphocyte ratio (NLR) associated with disease severity and mortality. To investigate whether such alterations are caused by the infection or results from preexisting comorbidities, this work analyzed dyslipidemia and the hemogram profile of COVID-19 patients according to the severity and compared with patients without T2DM or obesity comorbidities. Dyslipidemia, with a marked decrease in HDL levels, and increased NLR accompanied the disease severity, even in non-T2DM and non-obese patients, indicating that COVID-19 causes the observed alterations. Because decreased hemoglobin is involved in COVID-19 severity, and hemoglobin concentration is associated with metabolic diseases, the erythrogram of patients was also evaluated. We verified a drop in hemoglobin and erythrocyte number in severe patients, independently of T2DM and obesity, which may explain in part the need for artificial ventilation in severe cases. Thus, the control of such parameters (especially HDL levels, NLR, and hemoglobin concentration) could be a good strategy to prevent COVID-19 complications and death.

Indexed as

Leukocyte CountSARS-CoV-2AdultAgedAnemiaAtherosclerosisComorbidityCOVID-19Diabetes Mellitus, Type 2DyslipidemiasErythrocyte CountHemoglobinsHumansHypoxiaLipoproteins, HDLLymphocyte CountHemoglobinsLipoproteins, HDLCOVID-19DyslipidemiaHemoglobin concentrationNeutrophil to lymphocyte ratioSARS-CoV-2

Identifiers

PMID34517295
PMCPMC8426321
OpenAlexW3200371676

What OpenQuestion holds

Textmetadata
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.