Evidence map›Paper›PMID 22102895›Full record

ArticlePloS one2011

Altered islet composition and disproportionate loss of large islets in patients with type 2 diabetes.

German Kilimnik, Billy Zhao, Junghyo Jo, Vipul Periwal, Piotr Witkowski, Ryosuke Misawa, Manami Hara

Abstract readComparative Study
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
–field-weighted citation impact
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

85 citing papers in PubMed.

  1. Review
  2. Article
  3. The nerve center of organ engineering.Nature communications · 2025
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  9. Article
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  12. Review
  13. Article
  14. Article
  15. Disrupted glucose homeostasis and glucagon and insulin secretion defects in Robo βKO mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  16. Article
  17. Article
  18. Observational
  19. Review
  20. Liraglutide increases islet CaDiabetes, obesity & metabolism · 2022
    Article

25 more citing papers are in PubMed but not listed here.

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.

German KilimnikDepartment of Medicine, The University of Chicago, Chicago, Illinois, United States of America.
Billy Zhao
Junghyo Jo
Vipul Periwal
Piotr Witkowski
Ryosuke Misawa
Manami Hara

Funding

Coordinating Center for Beta Cell Biology ConsortiumU01DK072473 · NIDDK · VANDERBILT UNIVERSITY · PI MAGNUSON, MARK A · 2005 to 2014
$61.0M
ULTRASTRUCTURE AND CYTOMORPHOLOGY COREP30DK042086 · NIDDK · UNIVERSITY OF CHICAGO · PI LIU, CAMBRIAN YANGSHAO · 1990 to 2025
$29.8M
TRANSGENIC COREP60DK020595 · NIDDK · UNIVERSITY OF CHICAGO · PI BELL, GRAEME I · 1985 to 2012
$25.5M
Pilot and Feasibility ProgramP30DK020595 · NIDDK · UNIVERSITY OF CHICAGO · PI Matthew J Brady · 2013 to 2026
$20.9M
Role of the environmental cues for beta-cell differentiation from ES cellsR56DK081527 · NIDDK · UNIVERSITY OF CHICAGO · PI HARA, MANAMI · 2008 to 2009
$462k
Intramural NIH HHSNIDDK NIH HHS DK-042086NIDDK NIH HHS DK-072473NIDDK NIH HHS DK-081527NIDDK NIH HHS DK-20595NIDDK NIH HHS P30 DK020595NIDDK NIH HHS P30 DK042086NIDDK NIH HHS P60 DK020595NIDDK NIH HHS R56 DK081527NIDDK NIH HHS U01 DK072473
6 · The paper itself

Abstract

Human islets exhibit distinct islet architecture with intermingled alpha- and beta-cells particularly in large islets. In this study, we quantitatively examined pathological changes of the pancreas in patients with type 2 diabetes (T2D). Specifically, we tested a hypothesis that changes in endocrine cell mass and composition are islet-size dependent. A large-scale analysis of cadaveric pancreatic sections from T2D patients (n = 12) and non-diabetic subjects (n = 14) was carried out combined with semi-automated analysis to quantify changes in islet architecture. The method provided the representative islet distribution in the whole pancreas section that allowed us to examine details of endocrine cell composition in individual islets. We observed a preferential loss of large islets (>60 µm in diameter) in T2D patients compared to non-diabetic subjects. Analysis of islet cell composition revealed that the beta-cell fraction in large islets was decreased in T2D patients. This change was accompanied by a reciprocal increase in alpha-cell fraction, however total alpha-cell area was decreased along with beta-cells in T2D. Delta-cell fraction and area remained unchanged. The computer-assisted quantification of morphological changes in islet structure minimizes sampling bias. Significant beta-cell loss was observed in large islets in T2D, in which alpha-cell ratio reciprocally increased. However, there was no alpha-cell expansion and the total alpha-cell area was also decreased. Changes in islet architecture were marked in large islets. Our method is widely applicable to various specimens using standard immunohistochemical analysis that may be particularly useful to study large animals including humans where large organ size precludes manual quantitation of organ morphology.

Indexed as

AdolescentAdultAgedAged, 80 and overCase-Control StudiesDiabetes Mellitus, Type 2FemaleHumansImage Processing, Computer-AssistedImmunoenzyme TechniquesIslets of LangerhansMaleMiddle AgedOrgan SizePancreasYoung Adult

Identifiers

PMID22102895
PMCPMC3216964

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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.