Evidence map›Paper›PMID 39777548›Full record

Observational studyCalcified tissue international2025

Serum Pentosidine in Relation to Obesity in Patients with Type 2 Diabetes and Healthy Controls.

Sandra Baumann, Lilian Sewing, Cyril Traechslin, Wilma Verhagen-Kamerbeek, Leticia Grize, Marius Kraenzlin, Christian Meier

Erratum issued Registry-linked trialAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Calcified tissue international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT02551315 (Microarchitecture, Bone Strength and Fracture Risk in Type 2 Diabetes), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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.

NCT02551315 completednot on this map

Microarchitecture, Bone Strength and Fracture Risk in Type 2 Diabetes: the DiabOS Study

TypeobservationalSponsorUniversity Hospital, Basel, SwitzerlandRan2016 to 2020Enrolled274ConditionsType 2 Diabetes Mellitus, Bone Fractures
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Sandra BaumannDivision of Endocrinology and Diabetes, Spital Emmental, Burgdorf, Switzerland.ORCID 0009-0001-3408-4228
Lilian SewingDivision of Endocrinology, Diabetes and Metabolism, University Hospital Basel, Aeschenvorstadt 57, 4051, Basel, Switzerland.
Cyril TraechslinDivision of Endocrinology, Diabetes and Metabolism, University Hospital Basel, Aeschenvorstadt 57, 4051, Basel, Switzerland.
Wilma Verhagen-KamerbeekDivision of Endocrinology, Diabetes and Metabolism, University Hospital Basel, Aeschenvorstadt 57, 4051, Basel, Switzerland.
Leticia GrizeSwiss Tropical and Public Health Institute and University of Basel, Basel, Switzerland.
Marius KraenzlinEndocrine Clinic and Laboratory, Basel, Switzerland.
Christian MeierDivision of Endocrinology, Diabetes and Metabolism, University Hospital Basel, Aeschenvorstadt 57, 4051, Basel, Switzerland. christian.meier@unibas.ch.ORCID 0000-0002-0619-821X

Funding

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 320030 169407
6 · The paper itself

Abstract

Pentosidine (PEN), a surrogate marker of advanced glycation end-product formation, reflects increased non-enzymatic cross-linking in bone collagen, which is thought to be an important determinant of bone fragility in type 2 diabetes mellitus (T2DM). We aimed to investigate serum concentrations of PEN in patients with T2DM and controls without T2DM and to examine its relationship with bone parameters and metabolic state such as glycaemic control, insulin resistance and body weight. In a cross-sectional study-design, data from postmenopausal women and men with T2DM (n = 110) and controls without T2DM (n = 111) were evaluated. Serum PEN was measured using an ELISA-based assay (CSB-E09415h, Cusabio). In addition, biochemical markers of glucose metabolism and bone turnover markers were measured. Bone mineral density (BMD) was assessed by dual-energy X-ray absorptiometry. After adjustment for age, gender and body mass index (BMI), serum PEN was significantly higher in patients with T2DM compared to controls (p = 0.02) and most prominently in women with T2DM (p = 0.09). We found a strong association of serum PEN concentrations with BMI in the entire study population (R = 0.43, p < 0.001) as well as in patients with T2DM (R = 0.28, p < 0.01). While bone turnover markers were significantly decreased, and BMD increased in patients with T2DM, only weak or no associations were observed between these skeletal surrogate markers and serum PEN. We conclude that serum PEN is strongly associated with BMI with highest levels in obese women with T2DM. Adjustment for patient's weight is needed when evaluating serum PEN levels in patients with T2DM.Clinical Trial Information: NCT02551315.

Indexed as

ArginineBone DensityDiabetes Mellitus, Type 2LysineObesityAgedBiomarkersBody Mass IndexCross-Sectional StudiesFemaleHumansMaleMiddle AgedArginineBiomarkersLysinepentosidineBone turnoverObesityPentosidineType 2 diabetes

Identifiers

PMID39777548
PMCPMC11706925

What OpenQuestion holds

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Registered trials

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.