Evidence map›Paper›PMID 23475416›Full record

ReviewEndocrine reviews2013

Leptin's role in lipodystrophic and nonlipodystrophic insulin-resistant and diabetic individuals.

Hyun-Seuk Moon, Maria Dalamaga, Sang-Yong Kim, Stergios A Polyzos, Ole-Petter Hamnvik, Faidon Magkos, Jason Paruthi, Christos S Mantzoros

Open access · bronzeAbstract readReview
In one paragraph

Review in Endocrine reviews, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 103 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed, 5 pooled it
15.2field-weighted citation impact, top 1% 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

103 citing papers in PubMed, 5 syntheses or guidelines pooled it, 264 citations in OpenAlex.

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  12. Research Progress on Leptin in Metabolic Dysfunction-associated Fatty Liver Disease.Journal of clinical and translational hepatology · 2025
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43 more citing papers are in PubMed but not listed here.

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 3 countries.

Hyun-Seuk MoonDivision of Endocrinology, Diabetes, and Metabolism, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA.
Maria Dalamaga
Sang-Yong Kim
Stergios A Polyzos
Ole-Petter Hamnvik
Faidon Magkos
Jason Paruthi
Christos S Mantzoros
Harvard University · USAristotle University of Thessaloniki · GRBeth Israel Deaconess Medical Center · USChosun University · KRUniversity General Hospital Attikon · GRVA Boston Healthcare System · US

Funding

Physical Health in Midlife:Influences of adversities and relationshipsR01AG032030 · NIA · JUDGE BAKER CHILDREN'S CENTER · PI CROWELL, JUDITH A · 2009 to 2013
$3.1M
NIA NIH HHS AG032030NIA NIH HHS R01 AG032030PHS HHS 58785PHS HHS 79929PHS HHS 81913
6 · The paper itself

Abstract

Leptin is an adipocyte-secreted hormone that has been proposed to regulate energy homeostasis as well as metabolic, reproductive, neuroendocrine, and immune functions. In the context of open-label uncontrolled studies, leptin administration has demonstrated insulin-sensitizing effects in patients with congenital lipodystrophy associated with relative leptin deficiency. Leptin administration has also been shown to decrease central fat mass and improve insulin sensitivity and fasting insulin and glucose levels in HIV-infected patients with highly active antiretroviral therapy (HAART)-induced lipodystrophy, insulin resistance, and leptin deficiency. On the contrary, the effects of leptin treatment in leptin-replete or hyperleptinemic obese individuals with glucose intolerance and diabetes mellitus have been minimal or null, presumably due to leptin tolerance or resistance that impairs leptin action. Similarly, experimental evidence suggests a null or a possibly adverse role of leptin treatment in nonlipodystrophic patients with nonalcoholic fatty liver disease. In this review, we present a description of leptin biology and signaling; we summarize leptin's contribution to glucose metabolism in animals and humans in vitro, ex vivo, and in vivo; and we provide insights into the emerging clinical applications and therapeutic uses of leptin in humans with lipodystrophy and/or diabetes.

Indexed as

Insulin ResistanceSignal TransductionAnimalsDiabetes MellitusHIV-Associated Lipodystrophy SyndromeHumansHypoglycemic AgentsLeptinLipodystrophy, Congenital GeneralizedReceptors, LeptinHypoglycemic AgentsLEPR protein, humanLeptinReceptors, Leptin

Identifiers

PMID23475416
PMCPMC3660716
OpenAlexW2134859900

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.