Evidence map›Paper›PMID 27667744›Full record

ArticleDiabetes/metabolism research and reviews2017

Carboxylated and undercarboxylated osteocalcin in metabolic complications of human obesity and prediabetes.

Urszula Razny, Danuta Fedak, Beata Kiec-Wilk, Joanna Goralska, Anna Gruca, Anna Zdzienicka, Malgorzata Kiec-Klimczak, Bogdan Solnica, Alicja Hubalewska-Dydejczyk, Malgorzata Malczewska-Malec

Open access · hybridAbstract read
In one paragraph

Article in Diabetes/metabolism research and reviews, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  6. Crosstalk between bone and brain in Alzheimer's disease: Mechanisms, applications, and perspectives.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
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  8. Recovery from FOLFOX chemotherapy-induced systemic and skeletal muscle metabolic dysfunction in mice.American journal of physiology. Endocrinology and metabolism · 2023
    Article
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  15. Observational
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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 1 institution in 1 country.

Urszula RaznyDepartment of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
Danuta FedakDepartment of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
Beata Kiec-WilkDepartment of Metabolic Diseases, Jagiellonian University Medical College, Krakow, Poland.
Joanna GoralskaDepartment of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
Anna GrucaDepartment of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
Anna ZdzienickaDepartment of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
Malgorzata Kiec-KlimczakDepartment of Endocrinology, Jagiellonian University Medical College, Krakow, Poland.
Bogdan SolnicaDepartment of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
Alicja Hubalewska-DydejczykDepartment of Endocrinology, Jagiellonian University Medical College, Krakow, Poland.
Malgorzata Malczewska-MalecDepartment of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.ORCID 0000-0002-3522-0711
Jagiellonian University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCarboxylated osteocalcin (Gla-OC) participates in bone remodeling, whereas the undercarboxylated form (Glu-OC) takes part in energy metabolism. This study was undertaken to compare the blood levels of Glu-OC and Gla-OC in nonobese, healthy obese, and prediabetic volunteers and correlate it with the metabolic markers of insulin resistance and early markers of inflammation.

methodsNonobese (body mass index [BMI] <30 kg/m

resultsGla-OC in obese patients was significantly lower compared to nonobese ones (11.36 ± 0.39 vs 12.69 ± 0.90 ng/mL, P = .048) and weakly correlated with hsCRP (r = -0.18, P = .042), visfatin concentration (r = -0.19, P = .033), and BMI (r = -0.17, P = .047). Glu-OC was negatively associated with fasting insulin levels (r = -0.18, P = .049) and reduced in prediabetic individuals compared with healthy obese volunteers (3.04 ± 0.28 vs 4.48 ± 0.57, P = .025).

conclusionsDecreased blood concentration of Glu-OC may be a selective early symptom of insulin resistance in obesity, whereas the decreased level of Gla-OC seems to be associated with the appearance of early markers of low grade inflammation accompanying obesity.

Indexed as

Insulin ResistanceAdultAgedBiomarkersBlood GlucoseCarboxylic AcidsEnergy MetabolismFemaleFollow-Up StudiesHumansInflammationMaleMetabolic DiseasesMiddle AgedObesityOsteocalcinBiomarkersBlood GlucoseCarboxylic AcidsOsteocalcincarboxylated osteocalcinobesityprediabetesundercarboxylated osteocalcin

Identifiers

PMID27667744
PMCPMC6681168
OpenAlexW2524981617

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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.