Evidence map›Paper›PMID 19171928›Full record

ReviewToxicologic pathology2009

The role of protease inhibitors in the pathogenesis of HIV-associated lipodystrophy: cellular mechanisms and clinical implications.

Oliver P Flint, Mustafa A Noor, Paul W Hruz, Phil B Hylemon, Kevin Yarasheski, Donald P Kotler, Rex A Parker, Aouatef Bellamine

Open access · bronzeAbstract readReview
In one paragraph

Review in Toxicologic pathology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
9.7field-weighted citation impact, top 2% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 97 citations in OpenAlex.

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  12. Expert Panel Review on Nonalcoholic Fatty Liver Disease in Persons With Human Immunodeficiency Virus.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2022
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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

8 authors at 6 institutions in 1 country.

Oliver P FlintPharmaceutical Research and Development, Bristol-Myers Squibb Company, Princeton, New Jersey 08543, USA. oliver.flint@bms.com
Mustafa A Noor
Paul W Hruz
Phil B Hylemon
Kevin Yarasheski
Donald P Kotler
Rex A Parker
Aouatef Bellamine
Bristol-Myers Squibb (United States) · USWashington University in St. Louis · USColumbia University · USGlaxoSmithKline (United States) · USPrinceton University · USVirginia Commonwealth University · US

Funding

Myocardial Function /FFA Metabolism in HIV Metabolic SynR01DK059531 · NIDDK · WASHINGTON UNIVERSITY · PI YARASHESKI, KEVIN E · 2000 to 2008
$3.8M
PROTEIN TURNOVER AND ANABOLIC INTERVENTIONS IN AIDSR01DK049393 · NIDDK · WASHINGTON UNIVERSITY · PI YARASHESKI, KEVIN E · 1994 to 2008
$2.2M
Yoga for the Management of HIV-Metabolic SyndromesR21AT003083 · NCCIH · WASHINGTON UNIVERSITY · PI YARASHESKI, KEVIN E · 2005 to 2007
$604k
EXERCISE AND PIOGLITAZONE FOR HIV CARDIOMETABOLIC SYNDROMESR56DK049393 · NIDDK · WASHINGTON UNIVERSITY · PI YARASHESKI, KEVIN E · 2009 to 2009
$500k
Characterizing the HIV-Muscle Mitochondrial ProteomeR21DK074345 · NIDDK · WASHINGTON UNIVERSITY · PI YARASHESKI, KEVIN E · 2005 to 2006
$415k
NCCIH NIH HHS R21 AT003083NIDDK NIH HHS R01 DK049393NIDDK NIH HHS R01 DK059531NIDDK NIH HHS R21 DK074345NIDDK NIH HHS R56 DK049393
6 · The paper itself

Abstract

Metabolic complications associated with HIV infection and treatment frequently present as a relative lack of peripheral adipose tissue associated with dyslipidemia and insulin resistance. In this review we explain the connection between abnormalities of intermediary metabolism, observed either in vitro or in vivo, and this group of metabolic effects. We review molecular mechanisms by which the HIV protease inhibitor (PI) class of drugs may affect the normal stimulatory effect of insulin on glucose and fat storage. We then propose that both chronic inflammation from HIV infection and treatment with some drugs in this class trigger cellular homeostatic stress responses with adverse effects on intermediary metabolism. The physiologic outcome is such that total adipocyte storage capacity is decreased, and the remaining adipocytes resist further fat storage. The excess circulating and dietary lipid metabolites, normally "absorbed" by adipose tissue, are deposited ectopically in lean (muscle and liver) tissue, where they impair insulin action. This process leads to a pathologic cycle of lipotoxicity and lipoatrophy and a clinical phenotype of body fat distribution with elevated waist-to-hip ratio similar to the metabolic syndrome.

Indexed as

AdipocytesAdipose TissueAnimalsCells, CulturedDyslipidemiasGlucoseHIV-Associated Lipodystrophy SyndromeHIV InfectionsHIV Protease InhibitorsHumansInsulinInsulin ResistanceInsulin-Secreting CellsMetabolic SyndromeGlucoseHIV Protease InhibitorsInsulin

Identifiers

PMID19171928
PMCPMC3170409
OpenAlexW2102679591

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.