Evidence map›Paper›PMID 34234512›Full record

ArticleJournal of inflammation research2021

Study on the Clinical Significance of ACE2 and Its Age-Related Expression.

Jie Gu, JiangWen Yin, MengJie Zhang, JinHui Li, YeMing Wu, Jun Chen, HongJun Miao

Open access · goldAbstract read
In one paragraph

Article in Journal of inflammation research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 16 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

7 authors at 3 institutions in 1 country.

Jie Gu *Department of Emergency/Critical care Medicine, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, 210008, People's Republic of China.
JiangWen Yin *Department of Emergency/Critical care Medicine, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, 210008, People's Republic of China.
MengJie Zhang *Department of Emergency/Critical care Medicine, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, 210008, People's Republic of China.
JinHui LiDepartment of Emergency/Critical care Medicine, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, 210008, People's Republic of China.
YeMing WuCenter of Interventional Radiology and Vascular Surgery, Department of Radiology, Zhongda Hospital, Medical School of Southeast University, Nanjing, Jiangsu Province, 210009, People's Republic of China.
Jun ChenDepartment of Emergency/Critical care Medicine, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, 210008, People's Republic of China.
HongJun MiaoDepartment of Emergency/Critical care Medicine, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, 210008, People's Republic of China.
Second Affiliated Hospital of Nanjing Medical University · CNNanjing Medical University · CNZhongda Hospital Southeast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundACE2 plays a particular role in the changes in multiple organ functions. However, whether ACE2 expression differs at different ages and whether it plays a role in infection-related organ dysfunction remains unclear.

methodsFemale and male C57BL/6 mice in four different age groups were included in this study. Immunohistochemical and Western blot analyses were performed to evaluate ACE2 expression characteristics in lung tissues. At the same time, we detected the changes of ACE2 in human blood of different ages and evaluated its clinical significance in sepsis-associated organ dysfunction (SAOD).

resultsThis study indicated that ACE2 is expressed differently in mouse lung tissues at four different ages (P < 0.05). The peak expression distribution of ACE2 in lung tissues was in the newborn and middle-aged cohorts (P < 0.05). Infants younger than one year had a significantly higher concentration of ACE2 in serum and enhanced susceptibility compared with other ages (P < 0.05). Serum APTT, D-dimer, LDH, and PCT, as well as ACE2 in sepsis and SAOD groups, were statistically significant (P < 0.05) and were related to an increased risk of SAOD. There was a positive correlation between ACE2 and D-dimer (P < 0.05).

conclusionThe levels of ACE2 expression varied in different age groups. It tends to be higher in infants and young children. This result suggests that young children are more susceptible to infection. Moreover, a cutoff value for the ACE2 level >1551.15 pg/mL and D-dimer >984.5 U/L should be considered a warning sign of infection-associated organ dysfunction and guide the clinician in evaluating the patient's multiple organ function.

Indexed as

ACE2clinical significanceinfectionorgan dysfunctionSAOD

Identifiers

PMID34234512
PMCPMC8256825
OpenAlexW3173521313

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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.