Evidence map›Paper›PMID 18196243›Full record

ArticleRheumatology international2008

Serum leptin in systemic lupus erythematosus.

M Wisłowska, M Rok, K Stepień, A Kuklo-Kowalska

Abstract read
PubMed Publisher
In one paragraph

Article in Rheumatology international, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 32% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Emerging role of leptin in rheumatoid arthritis.Clinical and experimental immunology · 2014
    Pooled it
  2. Article
  3. Review
  4. Cardiovascular disease in systemic lupus erythematosus.Rheumatology and immunology research · 2021
    Review
  5. Article
  6. The role of leptin in selected skin diseases.Lipids in health and disease · 2020
    Review
  7. Article
  8. Article
  9. What is the role of adipokines in myasthenia gravis?Therapeutics and clinical risk management · 2018
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Pathogenesis and treatment of atherosclerosis in lupus.Rheumatic diseases clinics of North America · 2014
    Review
  16. Article
  17. Adipokines, metabolic syndrome and rheumatic diseases.Journal of immunology research · 2014
    Review
  18. Article
  19. Article
  20. The role of adipokines in connective tissue diseases.European journal of nutrition · 2012
    Review
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

4 authors at 1 institution in 1 country.

M WisłowskaDepartment of Rheumatology, Central Clinical Hospital, Wołoska 137, 02-507 Warsaw, Poland. mwislowska@wp.Pl
M Rok
K Stepień
A Kuklo-Kowalska
Central Clinical Hospital · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leptin, a peptide hormone, plays an essential role in the regulation of body weight, the endocrine function, reproduction, the immune response and inflammation. The immune system, in turn, modifies leptin's production. Systemic lupus erythematosus (SLE) is an autoimmunological disease characterized by widespread inflammation with possible involvement of each body organ and system. In this study, we assessed serum leptin levels in SLE patients and the control group in search for correlations between leptin concentrations and other markers' level, the activity of the disease, its duration, the age of the patients and their bone mineral density. Blood samples were collected from 30 SLE and 30 control group women. Each SLE patient was matched with one from the control for age (+/-1 year) and the body mass index (BMI; +/-1). Serum leptin levels were determined using the DRG Leptin ELISA Kit. Serum leptin levels in SLE patients ranged from 1.8 to 66.3 ng/ml (median value 7.5), and in control group it was 8.8 ng/ml (0.7-39.2) (NS). In SLE, serum leptin levels (after the logarithmic transformation) correlated with BMI (r = 0.89, P < 0.0001), the age (r = 0.34, P < 0.01) and the patients' disease duration (r = 0.59, P < 0.0005). Serum leptin levels in SLE patients with arthritis (P < 0.05) and central nervous system (CNS) involvement (P = 0.05) were significantly lower in comparison with serum leptin levels in SLE patients without arthritis and CNS involvement. No correlation was found between serum leptin levels and the T-score. In the control group, the logarithmic transformation of serum leptin levels positively correlated with BMI (r = 0.52, P < 0.05). No differences in serum leptin levels were shown between SLE patients and the control group. However, we found correlation between BMI and serum leptin levels in both groups. Furthermore, serum leptin levels in SLE patients with arthritis and CNS involvement were significantly lower in comparison with SLE patients without arthritis and CNS involvement, which suggests that active chronic inflammation may lower plasma leptin concentrations.

Indexed as

AdultBody Mass IndexCase-Control StudiesFemaleHumansLeptinLupus Erythematosus, SystemicMiddle AgedSeverity of Illness IndexLeptin

Identifiers

PMID18196243
OpenAlexW2028105069

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.