Evidence map›Paper›PMID 19401372›Full record

ArticleThe Journal of clinical endocrinology and metabolism2009

The effect of age on insulin sensitivity and insulin secretion in first-degree relatives of type 1 diabetic patients: a population analysis.

Xiaosu Ma, Dorothy Becker, Vincent C Arena, Paolo Vicini, Carla Greenbaum

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. 5α-reductase type 1 modulates insulin sensitivity in men.The Journal of clinical endocrinology and metabolism · 2014
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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

5 authors at 3 institutions in 1 country.

Xiaosu MaDepartment of Bioengineering, University of Washington, Seattle, Washington 98195, USA.
Dorothy Becker
Vincent C Arena
Paolo Vicini
Carla Greenbaum
University of Pittsburgh · USUniversity of Washington · USBenaroya Research Institute

Funding

University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
JUVENILE DIABETES MELLITUS EPIDEMIOLOGY &ETIOLOGYR01DK024021 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BECKER, DOROTHY J · 1986 to 2013
$7.1M
WATER PRECAUTIONS AND TYMPANOSTOMY TUBESM01RR000084 · NCRR · CHILDREN'S HOSP PITTSBURGH/UPMC HLTH SYS · PI PERLMUTTER, DAVID H · 1985 to 2006
$5.6M
Resource Facility for Population KineticsP41EB001975 · NIBIB · UNIVERSITY OF WASHINGTON · PI FOSTER, DAVID M · 2003 to 2007
$4.9M
NCATS NIH HHS UL1 TR000005NCRR NIH HHS M01 RR000084NCRR NIH HHS M01 RR00084NIBIB NIH HHS 2 P41 EB001975NIBIB NIH HHS P41 EB001975NIDDK NIH HHS 5 R01 DK024021-27NIDDK NIH HHS R01 DK024021
6 · The paper itself

Abstract

contextUnderstanding the role of insulin resistance in type 1 diabetes may lead to new prevention strategies. Estimates of insulin resistance in first-degree relatives of those with type 1 diabetes may be obtained using the minimal model of glucose kinetics incorporating a population approach.

objectiveThe objective of the study was to explore parameters contributing to glucose homeostasis in a cross-sectional study of first-degree relatives across a wide age range.

designInsulin sensitivity (SI) was assessed using the minimal model of glucose kinetics after an oral glucose tolerance test combined with nonlinear mixed-effects modeling. Beta-cell function was measured from the insulinogenic index at 30 min (IGI(30)). Disposition index (DI) was estimated as the product of SI and IGI(30).

settingThe study was conducted at an academic center. SUBJECTS: Subjects included 1241 first-degree relatives (aged 2-75 yr).

resultsSI was found to be negatively correlated with age, whereas IGI(30) increased until young adulthood. The increase IGI(30) was apparently insufficient to compensate for the insulin resistance because DI decreased linearly at the rate of 0.035 (10(-2) min(-1) mmol(-1) liter per year) after young adulthood. Both IGI(30) and DI were significantly lower in those with vs. without autoantibodies, whereas there was no difference between these groups with respect to SI.

conclusionsBeta-cell function, adjusted for age-related insulin resistance, decreases throughout life in first-degree relatives. This deterioration may be exacerbated in the presence of autoantibodies. Oral glucose tolerance test data combined with a nonlinear mixed-effect modeling population approach may be a useful technique to evaluate SI and secretion in a population.

Indexed as

Diabetes Mellitus, Type 1FamilyAdolescentAdultAgedAge DistributionAge FactorsChildChild, PreschoolFemaleHumansInsulinInsulin ResistanceInsulin SecretionMaleMiddle AgedInsulin

Identifiers

PMID19401372
PMCPMC2708949
OpenAlexW1990014214

What OpenQuestion holds

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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.