Evidence map›Paper›PMID 32069304›Full record

ArticlePloS one2020

Irisin and markers of metabolic derangement in non-diabetic Caucasian subjects with stage I-II obesity during early aging.

Jonica Campolo, Ettore Corradi, Alice Rizzardi, Marina Parolini, Cinzia Dellanoce, Maria Luisa Di Guglielmo, Patrizia Tarlarini, Marina Cattaneo, Maria Giovanna Trivella, Renata De Maria

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Jonica CampoloCardioThoracic and Vascular Department, CNR Institute of Clinical Physiology, Milan, Italy.ORCID 0000-0002-1711-6216
Ettore CorradiClinical Nutritional Unit, Medical Department, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
Alice RizzardiCardioThoracic and Vascular Department, CNR Institute of Clinical Physiology, Milan, Italy.
Marina ParoliniCardioThoracic and Vascular Department, CNR Institute of Clinical Physiology, Milan, Italy.
Cinzia DellanoceCardioThoracic and Vascular Department, CNR Institute of Clinical Physiology, Milan, Italy.
Maria Luisa Di GuglielmoCardioThoracic and Vascular Department, CNR Institute of Clinical Physiology, Milan, Italy.
Patrizia TarlariniClinical Nutritional Unit, Medical Department, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
Marina CattaneoClinical Nutritional Unit, Medical Department, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
Maria Giovanna TrivellaCardioThoracic and Vascular Department, CNR Institute of Clinical Physiology, Milan, Italy.
Renata De MariaCardioThoracic and Vascular Department, CNR Institute of Clinical Physiology, Milan, Italy.
Istituto di Fisiologia Clinica · ITAzienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Irisin concentrations are decreased in subjects with overt diabetes and upregulated in those with obesity or impaired fasting glucose. However, gender-balanced data in older populations, in whom risk factors commonly culminate in overt cardiovascular disease, are scarce. We assessed in non-diabetic Caucasian subjects with stage I-II obesity in the early aging range (50 to 70 years), the relationship between irisin, body composition and markers of metabolic derangement by gender. In 60 (31 women, 29 men) non-diabetics with a body mass index ≥30 - ≤40 kg/m2, we measured anthropometrics and body composition (Air Displacement Plethysmography). We assayed lipid and glucose profile by routine methods, plasma irisin by ELISA and measured insulin resistance by the HOMA index. Irisin levels were higher in women than in men (161 [105-198]) vs 83 [33-115] ng/ml, P<0.001), and correlated directly with HOMA index in both (rho 0.735, P<0.001 M, rho 0.452, P = 0.011 F). Sex differences were maintained across insulin resistance severity stages. In men, irisin concentrations correlated directly with body mass index (rho 0.755, P<0.001), waist circumference (rho 0.623, P<0.001), fat mass index (rho 0.762, P<0.001), glucose (rho 0.408, P = 0.028), the fatty liver index (rho 0.705, P<0.001) and FINDRISC score (rho 0.536, P = 0.003). Among non-diabetic Caucasian subjects with obesity in the early stages of aging, irisin levels reflect the amount of body fat and insulin resistance severity, independently of between-gender differences in the adipomyokine concentrations and are associated with markers of visceral adiposity in men but not in women.

Indexed as

White PeopleAgedAgingBiomarkersExerciseFemaleFibronectinsHumansMaleMiddle AgedObesitySex CharacteristicsBiomarkersFibronectinsFNDC5 protein, human

Identifiers

PMID32069304
PMCPMC7028288
OpenAlexW3006721935

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Registered trials

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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.