Evidence map›Paper›PMID 25666530›Full record

ArticleInternational journal of obesity (2005)2015

Adipose tissue morphology predicts improved insulin sensitivity following moderate or pronounced weight loss.

D Eriksson-Hogling, D P Andersson, J Bäckdahl, J Hoffstedt, S Rössner, A Thorell, E Arner, P Arner, M Rydén

Abstract read
PubMed Publisher
In one paragraph

Article in International journal of obesity (2005), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
8.0field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Capsinoids treatment reduces steatosis with consequent attenuation in the progression of metabolic dysfunction-associated steatotic liver disease in obese rats.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. 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

9 authors at 2 institutions in 1 country.

D Eriksson-HoglingDepartment of Medicine (H7), Karolinska Institutet, Karolinska University Hospital, Karolinska University Hospital, Huddinge, Stockholm, Sweden.
D P AnderssonDepartment of Medicine (H7), Karolinska Institutet, Karolinska University Hospital, Karolinska University Hospital, Huddinge, Stockholm, Sweden.
J BäckdahlDepartment of Medicine (H7), Karolinska Institutet, Karolinska University Hospital, Karolinska University Hospital, Huddinge, Stockholm, Sweden.
J HoffstedtDepartment of Medicine (H7), Karolinska Institutet, Karolinska University Hospital, Karolinska University Hospital, Huddinge, Stockholm, Sweden.
S RössnerDepartment of Medicine (H7), Karolinska Institutet, Karolinska University Hospital, Karolinska University Hospital, Huddinge, Stockholm, Sweden.
A ThorellDepartment of Surgery, Karolinska Institutet, Ersta Hospital, Stockholm, Sweden.
E ArnerDepartment of Medicine (H7), Karolinska Institutet, Karolinska University Hospital, Karolinska University Hospital, Huddinge, Stockholm, Sweden.
P ArnerDepartment of Medicine (H7), Karolinska Institutet, Karolinska University Hospital, Karolinska University Hospital, Huddinge, Stockholm, Sweden.
M RydénDepartment of Medicine (H7), Karolinska Institutet, Karolinska University Hospital, Karolinska University Hospital, Huddinge, Stockholm, Sweden.
Karolinska University Hospital · SEKarolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCross-sectional studies show that white adipose tissue hypertrophy (few, large adipocytes), in contrast to hyperplasia (many, small adipocytes), associates with insulin resistance and increased risk of developing type 2 diabetes. We investigated if baseline adipose cellularity could predict improvements in insulin sensitivity following weight loss.

methodsPlasma samples and subcutaneous abdominal adipose biopsies were examined in 100 overweight or obese individuals before and 10 weeks after a hypocaloric diet (7±3% weight loss) and in 61 obese subjects before and 2 years after gastric by-pass surgery (33±9% weight loss). The degree of adipose tissue hypertrophy or hyperplasia (termed the morphology value) in each individual was calculated on the basis of the relationship between fat cell volume and total fat mass. Insulin sensitivity was determined by homeostasis model assessment-estimated insulin resistance (HOMAIR).

resultsIn both cohorts at baseline, subjects with hypertrophy displayed significantly higher fasting plasma insulin and HOMAIR values than subjects with hyperplasia (P<0.0001), despite similar total fat mass. Plasma insulin and HOMAIR were normalized in both cohorts following weight loss. The improvement (delta insulin or delta HOMAIR) was more pronounced in individuals with hypertrophy, irrespective of whether adipose morphology was used as a continuous (P=0.0002-0.027) or nominal variable (P=0.002-0.047). Absolute adipocyte size associated (although weaker than morphology) with HOMAIR improvement only in the surgery cohort. Anthropometric measures at baseline (fat mass, body mass index, waist-to-hip ratio or waist circumference) showed no significant association with delta insulin or delta HOMAIR.

conclusionsIn contrast to anthropometric variables or fat cell size, subcutaneous adipose morphology predicts improvement in insulin sensitivity following both moderate and pronounced weight loss in overweight/obese subjects.

Indexed as

Bariatric SurgeryDiet, ReducingWeight LossAdipocytesAdipose Tissue, WhiteAdultBlood GlucoseBody Mass IndexCell EnlargementCohort StudiesDiabetes Mellitus, Type 2FemaleHumansInflammationMaleObesityBlood Glucose

Identifiers

PMID25666530
OpenAlexW2019559943

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.