Evidence map›Paper›PMID 10480626›Full record

Trial reportDiabetes1999

Genetic and physiologic analysis of the role of uncoupling protein 3 in human energy homeostasis.

W K Chung, A Luke, R S Cooper, C Rotini, A Vidal-Puig, M Rosenbaum, M Chua, G Solanes, M Zheng, L Zhao and 15 more

Abstract readClinical TrialControlled Clinical Trial
In one paragraph

Trial report in Diabetes, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

9 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. The role of uncoupling protein 3 in human physiology.The Journal of clinical investigation · 2003
    Review
  8. Article
  9. The long isoform uncoupling protein-3 (UCP3L) in human energy homeostasis.International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity · 1999
    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

25 authors at 1 institution in 1 country.

W K ChungDepartment of Pediatrics and Medicine, Naomi Berrie Diabetes Center, Columbia University College of Physicians and Surgeons, New York, New York, USA.
A Luke
R S Cooper
C Rotini
A Vidal-Puig
M Rosenbaum
M Chua
G Solanes
M Zheng
L Zhao
C LeDuc
A Eisberg
F Chu
E Murphy
M Schreier
L Aronne
S Caprio
B Kahle
D Gordon
S M Leal
R Goldsmith
A L Andreu
C Bruno
S DiMauro
R L Leibel
Columbia University · US

Funding

RESEARCH TRAININGP30DK026687 · NIDDK · ST. LUKE'S-ROOSEVELT INST FOR HLTH SCIS · PI Anthony W Ferrante, DYMPNA GALLAGHER · 1986 to 2026
$33.0M
The molecular genetic analysis of human obesityR01DK052431 · NIDDK · ROCKEFELLER UNIVERSITY · PI CHUNG, WENDY K, LEIBEL, RUDOLPH L · 1996 to 2020
$11.6M
GENETICS OF HYPERTENSION IN BLACKSR01HL053353 · NHLBI · LOYOLA UNIVERSITY CHICAGO · PI COOPER, RICHARD STANLEY · 1995 to 2013
$8.3M
OBESITY RESEARCH CENTER TRAINING PROGRAMT32DK007559 · NIDDK · ST. LUKE'S-ROOSEVELT INST FOR HLTH SCIS · PI DYMPNA GALLAGHER · 1989 to 2026
$4.3M
Glucose-Sensing by Neurons: Its Importance and the Role of UCP2R37DK053477 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI LOWELL, BRADFORD B · 2007 to 2016
$4.2M
UCPs:Regulators of Intracelluar Energy HomeostasisR01DK053477 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI LOWELL, BRADFORD B · 1998 to 2006
$2.6M
LINKAGE ANALYSIS METHODS FOR HUMAN GENE MAPPINGR01HG000008 · NHGRI · ROCKEFELLER UNIVERSITY · PI OTT, JURG · 1990 to 2004
$1.2M
ENERGY HOMEOSTASIS IN HUMAN OBESITYR01DK030583 · NIDDK · ROCKEFELLER UNIVERSITY · PI LEIBEL, RUDOLPH L · 1986 to 2001
$514k
NHGRI NIH HHS R01 HG000008NHLBI NIH HHS R01 HL053353NIDDK NIH HHS DK30583NIDDK NIH HHS DK52431NIDDK NIH HHS P30 DK026687NIDDK NIH HHS R01 DK052431NIDDK NIH HHS R01 DK053477NIDDK NIH HHS R37 DK053477NIDDK NIH HHS T32 DK007559NIDDK NIH HHS T32DK07559
6 · The paper itself

Abstract

By virtue of its potential effects on rates of energy expenditure, uncoupling protein 3 (UCP3) is an obesity candidate gene. We identified nine sequence variants in UCP3, including Val9Met, Val102Ile, Arg282Cys, and a splice site mutation in the intron between exons 6 and 7. The splice mutation results in an inability to synthesize mRNA for the long isoform (UCP3L) of UCP3. Linkage (sib pair), association, and transmission disequilibrium testing studies on 942 African-Americans did not suggest a significant effect of UCP3 on body composition in this group. In vastus lateralis skeletal muscle of individuals homozygous for the splice mutation, no UCP3L mRNA was detectable; the short isoform (UCP3S) was present in an increased amount. In this muscle, we detected no alterations of in vitro mitochondrial coupling activity, mitochondrial respiratory enzyme activity, or systemic oxygen consumption or respiratory quotient at rest or during exercise. These genetic and physiologic data suggest the following possibilities: UCP3S has uncoupling capabilities equivalent to UCP3L; other UCPs may compensate for a deficiency of bioactive UCP3L; UCP3L does not function primarily as a mitochondrial uncoupling protein.

Indexed as

MitochondriaAlternative SplicingAsian PeopleBlack or African AmericanBlack PeopleCarrier ProteinsEnergy MetabolismGenetic LinkageHispanic or LatinoHomeostasisHumansIon ChannelsLinkage DisequilibriumMitochondrial ProteinsUncoupling Protein 3White PeopleCarrier ProteinsIon ChannelsMitochondrial ProteinsUCP3 protein, humanUncoupling Protein 3

Identifiers

PMID10480626
PMCPMC6155469
OpenAlexW2102547070

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.