Evidence map›Paper›PMID 40953842›Full record

Trial reportBMJ open diabetes research & care2025

Skeletal health in adolescents with poorly controlled type 1 diabetes: results from a randomized controlled trial.

Mari-Anne Pulkkinen, Tero Varimo, Sanna Toiviainen-Salo, Taina H Härkönen, Saila Laakso, Anna-Kaisa Tuomaala, Matti Hero

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in BMJ open diabetes research & care, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Mari-Anne PulkkinenChildren's Hospital, Pediatric Research Center, Helsinki University Hospital, Helsinki, Uusimaa, Finland.ORCID http://orcid.org/0000-0003-2836-1046
Tero VarimoChildren's Hospital, Pediatric Research Center, Helsinki University Hospital, Helsinki, Uusimaa, Finland.ORCID http://orcid.org/0000-0002-6294-4563
Sanna Toiviainen-SaloChildren's Hospital, Pediatric Research Center, Helsinki University Hospital, Helsinki, Uusimaa, Finland.
Taina H HärkönenResearch Program for Clinical and Molecular Metabolism, Faculty of Medicine, University of Helsinki, Helsinki, Uusimaa, Finland.
Saila LaaksoChildren's Hospital, Pediatric Research Center, Helsinki University Hospital, Helsinki, Uusimaa, Finland.
Anna-Kaisa TuomaalaChildren's Hospital, Pediatric Research Center, Helsinki University Hospital, Helsinki, Uusimaa, Finland.ORCID http://orcid.org/0000-0001-8081-188X
Matti HeroChildren's Hospital, Pediatric Research Center, Helsinki University Hospital, Helsinki, Uusimaa, Finland matti.hero@helsinki.fi.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPoorly controlled type 1 diabetes (T1D) has been associated with impaired bone health, but the mechanisms remain unclear. We aimed to investigate whether changes in glycemic control and glucose variability are associated with skeletal health and to evaluate the roles of insulin-like growth factor I (IGF-I) and advanced glycation end-products (AGEs) in bone mineral accrual. RESEARCH DESIGN AND

methodsThis longitudinal study included adolescents with poorly controlled T1D (HbA1c >9%/75 mmol/mol), who underwent dual-energy X-ray absorptiometry (DXA) at baseline and after 12 months. Glycemic control was assessed using glycohemoglobin (HbA1c), continuous glucose monitoring (CGM) parameters, and glycemic load. Serum IGF-I and AGEs, specifically methyl-glyoxal-hydro-imidazolone (MG-HI), were measured. Correlation analyses and linear regression models were used to evaluate the associations between glycemic markers, IGF-I, AGEs and bone parameters.

resultsAltogether, 37 adolescents (48.6 % female) with T1D, with mean HbA1c 9.9% (85 mmol/mol), were followed up from mean age of 14.3 for 12 months. DXA-derived bone mineral density (BMD) z-scores at lumbar spine, proximal femur, and total body less head were approximately 0.5 SDS lower than reference values (p=0.005-0.04). The only significant change in BMD z-scores during the 12-month follow-up was an increase in proximal femur in girls. In the whole group, an increase in IGF-1 was associated with BMD accrual, while changes in HbA1c, time in range, or MG-HI were not. No vertebral fractures were detected.

conclusionsDespite lower BMD in adolescents with poorly controlled T1D, neither changes in glycemic control nor MG-HI levels correlated significantly with bone health measures, while increase of IGF-1 was associated with BMD accrual. Future studies should explore alternative AGEs and use advanced bone imaging techniques to better understand skeletal fragility in T1D.

Indexed as

Bone DensityDiabetes Mellitus, Type 1Absorptiometry, PhotonAdolescentBiomarkersBlood GlucoseChildFemaleFollow-Up StudiesGlycated HemoglobinGlycation End Products, AdvancedGlycemic ControlHumansInsulin-Like Growth Factor ILongitudinal StudiesMaleBiomarkersBlood GlucoseGlycated HemoglobinGlycation End Products, Advancedhemoglobin A1c protein, humanIGF1 protein, humanInsulin-Like Growth Factor IAGEsBone DensityDiabetes Mellitus, Type 1IGF-I

Identifiers

PMID40953842
PMCPMC12434736

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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.