Level D· Scientific groundwork from lab and animal studiesNarrative ReviewEurope PMC

Progranulin: at the interface of neurodegenerative and metabolic diseases

Nguyen AD., Nguyen TA., Martens LH., Mitic LL., Farese RV.

Narrative Review on Type 2 Diabetes, Neuroinflammation, Chronic Inflammation, published in Trends Endocrinol Metab (2013) — summary generated from the PubMed abstract.

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Level D· Scientific groundwork from lab and animal studiesEvidence level of this study

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
Read the A–D evidence level guide

This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Narrative Review
Journal
Trends Endocrinol Metab (2013)
Reported sample size
—
Source database
Europe PMC
PMID
24035620
PMCID
PMC3842380
DOI
10.1016/j.tem.2013.08.003
Citations
70

Abstract (original English)

Progranulin is a widely expressed, cysteine-rich, secreted glycoprotein originally discovered for its growth factor-like properties. Its subsequent identification as a causative gene for frontotemporal dementia (FTD), a devastating early-onset neurodegenerative disease, has catalyzed a surge of new discoveries about progranulin function in the brain. More recently, progranulin was recognized as an adipokine involved in diet-induced obesity and insulin resistance, revealing its metabolic function. We review here progranulin biology in both neurodegenerative and metabolic diseases. In particular, we highlight the growth factor-like, trophic, and anti-inflammatory properties of progranulin as potential unifying themes in these seemingly divergent conditions. We also discuss potential therapeutic options for raising progranulin levels to treat progranulin-deficient FTD, as well as the possible consequences of such treatment.

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.
  • • This is a narrative review: it collects no new patient data and does not systematically appraise evidence quality.

Evidence level

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

How we grade evidence
AnimalsHumansNeurodegenerative DiseasesMetabolic DiseasesDiabetes Mellitus, Type 2Insulin ResistanceObesityIntercellular Signaling Peptides and ProteinsFrontotemporal DementiaProgranulins

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