Evidence map›Paper›PMID 25462194›Full record

ReviewAgeing research reviews2015

Sleep disorders, obesity, and aging: the role of orexin.

Joshua P Nixon, Vijayakumar Mavanji, Tammy A Butterick, Charles J Billington, Catherine M Kotz, Jennifer A Teske

Open access · greenAbstract readReview
In one paragraph

Review in Ageing research reviews, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 2 pooled it
5.0field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 2 syntheses or guidelines pooled it, 128 citations in OpenAlex.

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  20. Prenatal Effects of Nicotine on Obesity Risks: A Narrative Review.International journal of environmental research and public health · 2022
    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

6 authors at 2 institutions in 1 country.

Joshua P NixonMinneapolis VA Health Care System, One Veterans Drive, Minneapolis, MN 55417, USA; Minnesota Obesity Center, 1334 Eckles Avenue, Saint Paul, MN 55108, USA; University of Minnesota, Department of Food Science and Nutrition, 1334 Eckles Avenue, Saint Paul, MN 55108, USA. Electronic address: nixon049@umn.edu.
Vijayakumar MavanjiMinneapolis VA Health Care System, One Veterans Drive, Minneapolis, MN 55417, USA. Electronic address: mavan001@umn.edu.
Tammy A ButterickMinneapolis VA Health Care System, One Veterans Drive, Minneapolis, MN 55417, USA; University of Minnesota, Department of Food Science and Nutrition, 1334 Eckles Avenue, Saint Paul, MN 55108, USA. Electronic address: butte017@umn.edu.
Charles J BillingtonMinneapolis VA Health Care System, One Veterans Drive, Minneapolis, MN 55417, USA; Department of Medicine, University of Minnesota, 420 Delaware Street SE, Minneapolis, MN 55455, USA; Minnesota Obesity Center, 1334 Eckles Avenue, Saint Paul, MN 55108, USA; University of Minnesota, Department of Food Science and Nutrition, 1334 Eckles Avenue, Saint Paul, MN 55108, USA. Electronic address: billi005@umn.edu.
Catherine M KotzMinneapolis VA Health Care System, One Veterans Drive, Minneapolis, MN 55417, USA; Geriatric Research Education and Clinical Center, One Veterans Drive, Minneapolis, MN 55417, USA; Minnesota Obesity Center, 1334 Eckles Avenue, Saint Paul, MN 55108, USA; University of Minnesota, Department of Food Science and Nutrition, 1334 Eckles Avenue, Saint Paul, MN 55108, USA. Electronic address: kotzx004@umn.edu.
Jennifer A TeskeMinneapolis VA Health Care System, One Veterans Drive, Minneapolis, MN 55417, USA; Minnesota Obesity Center, 1334 Eckles Avenue, Saint Paul, MN 55108, USA; University of Minnesota, Department of Food Science and Nutrition, 1334 Eckles Avenue, Saint Paul, MN 55108, USA; University of Arizona, Department of Nutritional Sciences, 1177 East 4th Street, Shantz Building #332, Tucson, AZ, USA. Electronic address: teskeja@email.arizona.edu.
University of Minnesota · USMinneapolis VA Health Care System · US

Funding

Role of Variability in SPA in Susceptibility to ObesityR01DK100281 · NIDDK · UNIVERSITY OF MINNESOTA · PI KOTZ, CATHERINE M · 2014 to 2017
$1.1M
Enhancing NEAT to Treat ObesityI01RX000441 · VA · MINNEAPOLIS VA MEDICAL CENTER · PI BILLINGTON, CHARLES J., KOTZ, CATHERINE M · 2012 to 2015
–
Orexin Induced Gene and Protein Expression Patterns in the rLHIK2BX001686 · VA · MINNEAPOLIS VA MEDICAL CENTER · PI BUTTERICK, TAMMY ANGALINE · 2013 to 2017
–
BLRD VA IK2 BX001686NIDDK NIH HHS 1R01DK100281-01A1NIDDK NIH HHS R01 DK100281RRD VA I01 RX000441
6 · The paper itself

Abstract

The hypothalamic neuropeptides orexin A and B (hypocretin 1 and 2) are important homeostatic mediators of central control of energy metabolism and maintenance of sleep/wake states. Dysregulation or loss of orexin signaling has been linked to narcolepsy, obesity, and age-related disorders. In this review, we present an overview of our current understanding of orexin function, focusing on sleep disorders, energy balance, and aging, in both rodents and humans. We first discuss animal models used in studies of obesity and sleep, including loss of function using transgenic or viral-mediated approaches, gain of function models using exogenous delivery of orexin receptor agonist, and naturally-occurring models in which orexin responsiveness varies by individual. We next explore rodent models of orexin in aging, presenting evidence that orexin loss contributes to age-related changes in sleep and energy balance. In the next section, we focus on clinical importance of orexin in human obesity, sleep, and aging. We include discussion of orexin loss in narcolepsy and potential importance of orexin in insomnia, correlations between animal and human studies of age-related decline, and evidence for orexin involvement in age-related changes in cognitive performance. Finally, we present a summary of recent studies of orexin in neurodegenerative disease. We conclude that orexin acts as an integrative homeostatic signal influencing numerous brain regions, and that this pivotal role results in potential dysregulation of multiple physiological processes when orexin signaling is disrupted or lost.

Indexed as

Intracellular Signaling Peptides and ProteinsNeuropeptidesObesitySleep Wake DisordersAgingAnimalsDisease Models, AnimalEnergy MetabolismHomeostasisHumansHypothalamusNeurotransmitter AgentsOrexinsSignal TransductionSleepHCRT protein, humanIntracellular Signaling Peptides and ProteinsNeuropeptidesNeurotransmitter AgentsOrexinsAgingEnergy balanceHypocretinObesityOrexinSleep

Identifiers

PMID25462194
PMCPMC4467809
OpenAlexW2055830753

What OpenQuestion holds

Textmetadata
LicenceTDM
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.