Evidence map›Paper›PMID 27329162›Full record

ArticleCell stress & chaperones2016

Association between circulating inflammatory molecules and alcoholic liver disease in men.

Bao-Ge Qu, Weimin Bi, Yi-Guo Jia, Yuan-Xun Liu, Hui Wang, Ji-Liang Su, Li-Li Liu, Zhong-Dong Wang, Ya-Fei Wang, Xing-Hai Han and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell stress & chaperones, 2016. 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
0.7field-weighted citation impact, top 27% 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, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Growing burden of alcoholic liver disease in China: A review.World journal of gastroenterology · 2019
    Review
  4. 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

13 authors at 2 institutions in 1 country.

Bao-Ge QuDepartment of Gastroenterology, Taishan Hospital, Taian, Shandong, 271000, People's Republic of China. qubaoge@sina.com.
Weimin BiSurgery of Gastroenterology, Taian City's Central Hospital, Taian, Shandong, 271000, People's Republic of China.
Yi-Guo JiaDepartment of Gastroenterology, Taishan Hospital, Taian, Shandong, 271000, People's Republic of China.
Yuan-Xun LiuDepartment of Gastroenterology, Taishan Hospital, Taian, Shandong, 271000, People's Republic of China.
Hui WangDepartment of Gastroenterology, Taishan Hospital, Taian, Shandong, 271000, People's Republic of China.
Ji-Liang SuDepartment of Gastroenterology, Taishan Hospital, Taian, Shandong, 271000, People's Republic of China.
Li-Li LiuDepartment of Gastroenterology, Taishan Hospital, Taian, Shandong, 271000, People's Republic of China.
Zhong-Dong WangDepartment of Gastroenterology, Taishan Hospital, Taian, Shandong, 271000, People's Republic of China.
Ya-Fei WangDepartment of Gastroenterology, Taishan Hospital, Taian, Shandong, 271000, People's Republic of China.
Xing-Hai HanDepartment of Gastroenterology, Taishan Hospital, Taian, Shandong, 271000, People's Republic of China.
Jin-Dun PanDepartment of Gastroenterology, Taishan Hospital, Taian, Shandong, 271000, People's Republic of China.
Guang-Ying RenDepartment of Gastroenterology, Taishan Hospital, Taian, Shandong, 271000, People's Republic of China.
Wen-Juan HuDepartment of Gastroenterology, Taishan Hospital, Taian, Shandong, 271000, People's Republic of China.
Affiliated Hospital of Taishan Medical University · CNTaian City Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The association between alcoholic liver disease (ALD) and the inflammatory response remains controversial. The aim of this study was to explore this association between ALD and inflammation. We enrolled 214 male participants, who were divided into three age-matched groups: ALD (n = 135), chronic alcohol ingestion without ALD (non-ALD; n = 42), and control (n = 37). The BMI was significantly higher in the ALD group than in the non-ALD and control groups (all P = 0.000). Further, the constituent ratio of the liver inflammatory level was significantly higher in the ALD group than in the non-ALD and control groups (P = 0.002 and P = 0.000, respectively). In addition, the median serum ALT, AST, and GGT levels were significantly higher in the ALD group than in the control group (P = 0.023, P = 0.008, and P = 0.000, respectively); these levels were also significantly higher in the ALD group than in the non-ALD group (P = 0.013, P = 0.010, and P = 0.000, respectively). The median serum CRP level was significantly higher in the ALD group than in the non-ALD and control groups (P = 0.006 and P = 0.000, respectively). Further, the median serum TNF-α level was significantly lower in the ALD group than in the non-ALD and control groups (P = 0.004 and P = 0.000, respectively). The median serum sOX40L and HSP70 levels were significantly lower in the ALD group than in the control group (P = 0.008 and P = 0.018, respectively). In addition, the ALT, AST, and GGT levels were positively correlated with the CRP level (r = 0.211, P = 0.002; r = 0.220, P = 0.001 and r = 0.295, P = 0.000, respectively), and the GGT level was negatively correlated with the TNF-α (r = -0.225, P = 0.001), sOX40L (r = -0.165, P = 0.016), and HSP70 levels (r = -0.178, P = 0.009). Further, the Cr level was negatively correlated with the IL-10 level (r = -0.166, P = 0.015). Logistic regression analysis verified that the BMI (OR  =  1.637, 95%CI: 1.374-1.951, P  =  0.000) and GGT level were significantly higher (OR  =  1.039, 95%CI: 1.020-1.059, P  =  0.000) and that the TNF-α (OR  =  0.998, 95%CI: 0.996-1.000, P  =  0.030) and HSP70 levels were significantly lower (OR  =  1.017, 95%CI: 1.003-1.031, P  =  0.029) in the ALD group than in the non-ALD group. Further, the moderate-to-severe ALD patients had a significantly higher serum CRP level (Or =   1.349, 95%CI: 1.066-1.702, P  =  0.013) and significantly lower HSP60 (OR  =  0.965, 95%CI: 0.938-0.993, P  =  0.014) and HSP70 levels (OR  =  0.978, 95%CI: 0.962-0.995, P  =  0.010) than the mild ALD patients. These results suggest that ALD patients may present with obesity, liver damage, and an imbalanced inflammatory immune response, mainly manifesting as decreased levels of immune inflammatory cytokines. In addition, they suggest that certain liver and kidney function parameters and ALD severity are either positively or negatively correlated with certain inflammatory cytokines. Hence, ALD patients may be at increased risks of obesity- and inflammation-related diseases. Accordingly, to control the inflammatory response, preventative measures for patients with this disease should include weight control and protection of liver and kidney function.

Indexed as

AdultAgedCase-Control StudiesCytokinesHumansLiver Diseases, AlcoholicMaleMiddle AgedCytokinesAlcoholic liver diseaseBody mass indexHepatorenal functionInflammatory cytokines

Identifiers

PMID27329162
PMCPMC5003803
OpenAlexW2472163695

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.