Evidence map›Paper›PMID 23884776›Full record

Observational studyThe Journal of clinical endocrinology and metabolism2013

Longitudinal decline of β-cell function: comparison of a direct method vs a fasting surrogate measure: the Insulin Resistance Atherosclerosis Study.

A Festa, S M Haffner, L E Wagenknecht, C Lorenzo, A J G Hanley

Open access · bronzeAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in The Journal of clinical endocrinology and metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

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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 4 institutions in 2 countries.

A FestaPhD, University of Toronto, 150 College Street, Room 341, Toronto, ON, M5S 3E2. anthony.hanley@utoronto.ca.
S M Haffner
L E Wagenknecht
C Lorenzo
A J G Hanley
Eli Lilly (United States) · USMount Sinai Hospital · CAThe University of Texas Health Science Center at San Antonio · USWake Forest University · US

Funding

ZOLEDRONATE VS AREDIA IN MULTIPLE MYELOMA/BREAST CANCER W /BONE DISORDERSM01RR001346 · NCRR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ESCAMILLA, MICHAEL A · 1985 to 2008
$23.1M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR001120 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, HARGREAVES, KENNETH M · 2013 to 2017
$16.5M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR000149 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A · 2012 to 2013
$6.8M
EPIDEMIOLOGY OF IMPAIRED COAGULANT BALANCE IN DIABETESR01HL058329 · NHLBI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI TRACY, RUSSELL P · 1996 to 2000
$194k
INSULIN RESISTANCE AND ATHEROSCLEROSIS STUDY (IRAS)U01HL047890 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BERGMAN, RICHARD N. · 1991 to 1999
–
INSULIN RESISTANCE AND CARDIOVASCULAR DISEASEU01HL047892 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI REWERS, MARIAN J. · 1991 to 1999
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INSULIN RESISTANCE AND ATHEROSCLEROSIS STUDY (IRAS)U01HL047887 · NHLBI · WAKE FOREST UNIVERSITY · PI WAGENKNECHT, LYNNE E · 1991 to 1999
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INSULIN RESISTANCE AND ATHEROSCLEROSIS STUDY (IRAS)U01HL055208 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI HAFFNER, STEVEN M. · 1995 to 1999
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INSULIN RESISTANCE AND ATHEROSCLEROSIS STUDY (IRAS)U01HL047902 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI SAAD, MOHAMMED F · 1991 to 1999
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INSULIN RESISTANCE, HYPERGLYCEMIA AND ATHEROSCLEROSISU01HL047889 · NHLBI · KAISER FOUNDATION RESEARCH INSTITUTE · PI SELBY, JOE V · 1991 to 1999
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NCATS NIH HHS UL1 TR000149NCATS NIH HHS UL1 TR001120NCRR NIH HHS M01 RR001346NCRR NIH HHS M01 RR01346NCRR NIH HHS M01 RR431NHLBI NIH HHS HL-47887NHLBI NIH HHS HL-47889NHLBI NIH HHS HL-47890NHLBI NIH HHS HL-47892NHLBI NIH HHS HL-55208NHLBI NIH HHS R01-HL-58329NHLBI NIH HHS U01 HL047892NHLBI NIH HHS U01 HL047902
6 · The paper itself

Abstract

contextβ-Cell function (BCF) declines over the course of type 2 diabetes, but little is known about BCF changes across glucose tolerance status (GTS) categories, and comparisons of direct vs surrogate measures.

objectiveTo assess longitudinal changes in BCF across GTS.

designThe Insulin Resistance Atherosclerosis Study is a multicenter, observational, epidemiologic study.

settingFour clinical centers in the US that could identify subjects likely to have impaired fasting glucose (IFG) or impaired glucose tolerance (IGT). PATIENTS: We compared longitudinal changes in BCF in 1052 subjects over 5 years. Subjects were categorized according to baseline GTS: normal glucose tolerance (NGT: n = 547), impaired fasting glucose or impaired glucose tolerance (IFG/IGT: n = 341), and newly diagnosed type 2 diabetes (n = 164).

interventionsNone.

main outcome measuresBCF was assessed from a frequently sampled iv glucose tolerance test (AIR, acute insulin response), and the homeostasis model assessment of BCF (HOMA B).

resultsNGT and IFG/IGT subjects increased their insulin secretion over time, whereas those with type 2 diabetes experienced either decline or little change in BCF. After adjustment for demographic variables and change in insulin resistance, change in HOMA B underestimated the magnitude of changes in BCF, as assessed by change in AIR. Relative to NGT, the 5-year change in insulin secretion in IFG/IGT and type 2 diabetes was 31% and 70% lower (by HOMA B) and 50% and 80% lower (by AIR).

conclusionsThe decline in BCF over time in IFG/IGT and type 2 diabetes may be more pronounced than previously estimated; HOMA B may underestimate this decline significantly.

Indexed as

AdultAgedAtherosclerosisBlood GlucoseDiabetes Mellitus, Type 2FastingFemaleGlucose IntoleranceGlucose Tolerance TestHumansInsulin ResistanceInsulin-Secreting CellsLongitudinal StudiesMaleMiddle AgedPrediabetic StateBlood Glucose

Identifiers

PMID23884776
PMCPMC3790620
OpenAlexW2104169421

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.