Evidence map›Paper›PMID 28396851›Full record

ArticleJournal of diabetes and metabolic disorders2017

Increased circulatory levels of fractalkine (CX3CL1) are associated with inflammatory chemokines and cytokines in individuals with type-2 diabetes.

Sardar Sindhu, Nadeem Akhter, Hossein Arefanian, Areej Abu Al-Roub, Shamsha Ali, Ajit Wilson, Asma Al-Hubail, Shaima Al-Beloushi, Saad Al-Zanki, Rasheed Ahmad

Open access · hybridAbstract read
In one paragraph

Article in Journal of diabetes and metabolic disorders, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Chemokine CX3CL1 (Fractalkine) Signaling and Diabetic Encephalopathy.International journal of molecular sciences · 2024
    Review
  11. Article
  12. The role of inflammation in diabetic kidney disease.The Korean journal of internal medicine · 2021
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Pathobiological and molecular connections involved in the high fructose and high fat diet induced diabetes associated nonalcoholic fatty liver disease.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2020
    Review
  19. Article
  20. 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

10 authors at 1 institution in 1 country.

Sardar SindhuImmunology Unit, P.O. Box 1180, Dasman, 15462 Kuwait ; Animal & Zebrafish Core Facility, Dasman Diabetes Institute (DDI), P.O. Box 1180, Dasman, 15462 Kuwait.
Nadeem AkhterImmunology Unit, P.O. Box 1180, Dasman, 15462 Kuwait.
Hossein ArefanianIslet Biology Unit, P.O. Box 1180, Dasman, 15462 Kuwait.
Areej Abu Al-RoubImmunology Unit, P.O. Box 1180, Dasman, 15462 Kuwait.
Shamsha AliImmunology Unit, P.O. Box 1180, Dasman, 15462 Kuwait.
Ajit WilsonImmunology Unit, P.O. Box 1180, Dasman, 15462 Kuwait.
Asma Al-HubailClinical Laboratory, P.O. Box 1180, Dasman, 15462 Kuwait.
Shaima Al-BeloushiIslet Biology Unit, P.O. Box 1180, Dasman, 15462 Kuwait.
Saad Al-ZankiImmunology Unit, P.O. Box 1180, Dasman, 15462 Kuwait.
Rasheed AhmadImmunology Unit, P.O. Box 1180, Dasman, 15462 Kuwait.
Dasman Diabetes Institute · KW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFractalkine (CX3CL1) is involved in the development of numerous inflammatory conditions including metabolic diseases. However, changes in the circulatory fractalkine levels in type-2 diabetes (T2D) and their relationship with inflammatory chemokines/cytokines remain unclear. The aim of the study was to determine the T2D-associated modulations in plasma fractalkine levels and investigate their relationship with circulatory chemokines/cytokines.

methodsA total of 47 plasma samples were collected from 23 T2D and 24 non-diabetic individuals selected over a wide range of body mass index (BMI). Clinical metabolic parameters were determined using standard commercial kits. Fractalkine and chemokines/cytokines were measured using Luminex X-MAP® technology. C-reactive protein (CRP) was measured by ELISA. The data were compared using unpaired

resultsPlasma fractalkine levels were significantly higher (P = 0.005) in T2D patients (166 ± 14.22 pg/ml) as compared with non-diabetics (118 ± 8.90 pg/ml). In T2D patients, plasma fractalkine levels correlated positively (P ≤ 0.05) with inflammatory chemokines/cytokines including CCL3 (r = 0.52), CCL4 (r = 0.85), CCL11 (r = 0.51), CXCL1 (r = 0.67), G-CSF (r = 0.91), IFN-α2 (r = 0.97), IL-17A (r = 0.79), IL-1β (r = 0.97), IL-12P70 (r = 0.90), TNF-α (r = 0.58), and IL-6 (r = 0.60). In non-diabetic individuals, fractalkine levels correlated (P ≤ 0.05) with those of CCL4 (r = 0.49), IL-1β (r = 0.73), IL-12P70 (r = 0.41), and TNF-α (r = 0.50). Notably, plasma fractalkine levels in T2D patients associated with systemic inflammation (CRP) (r = 0.65, P = 0.02).

conclusionsThe altered plasma fractalkine levels associate differentially with inflammatory chemokines/cytokines in T2D patients which may have implications for T2D immunopathogenesis.

Indexed as

ChemokinesCX3CL1CytokinesFractalkineInflammationObesityType-2 diabetes

Identifiers

PMID28396851
PMCPMC5379731
OpenAlexW2604491855

What OpenQuestion holds

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LicenceCC BY
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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.