Evidence map›Paper›PMID 41854838›Full record

ReviewDrugs & aging2026

Managing Bone Fragility in Older Adults with Diabetes: Pathophysiology, Assessment, and Therapeutic Considerations.

Gulistan Bahat, Tugba Erdogan, Savas Ozturk, Ozlem Soyluk Selcukbiricik, Serdar Ozkok, Dilek Gogas Yavuz, Mehmet Akif Karan, Jean-Yves Reginster

Abstract readReview
In one paragraph

Review in Drugs & aging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Observational
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

8 authors.

Gulistan BahatDivision of Geriatrics, Department of Internal Medicine, Istanbul Medical Faculty, Istanbul University, Capa, 34390, Istanbul, Turkey. gbahatozturk@yahoo.com.ORCID 0000-0001-6039-5866
Tugba ErdoganDivision of Geriatrics, Department of Internal Medicine, Istanbul Medical Faculty, Istanbul University, Capa, 34390, Istanbul, Turkey.ORCID 0000-0001-8690-0189
Savas OzturkDivision of Nephrology, Department of Internal Medicine, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.ORCID 0000-0002-0961-3810
Ozlem Soyluk SelcukbiricikDivision of Endocrinology and Metabolism, Department of Internal Medicine, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.ORCID 0000-0003-0732-4764
Serdar OzkokDivision of Geriatrics, Department of Internal Medicine, Istanbul Medical Faculty, Istanbul University, Capa, 34390, Istanbul, Turkey.ORCID 0000-0002-0994-1152
Dilek Gogas YavuzDivision of Endocrinology and Metabolism, Department of Internal Medicine, Marmara University School of Medicine, Istanbul, Turkey.ORCID 0000-0002-0075-6313
Mehmet Akif KaranDivision of Geriatrics, Department of Internal Medicine, Istanbul Medical Faculty, Istanbul University, Capa, 34390, Istanbul, Turkey.ORCID 0000-0002-9080-404X
Jean-Yves ReginsterProtein Research Chair, Biochemistry Department, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia.ORCID 0000-0001-6290-752X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Older adults with diabetes mellitus, encompassing both type 1 diabetes (T1D) and type 2 diabetes (T2D), face a substantially elevated risk of fragility fractures, contributing significantly to morbidity and mortality in this vulnerable population. The underlying pathophysiology differs between the two types: T1D is typically characterized by reduced bone mineral density (BMD) stemming from insulinopenia, whereas T2D often presents with normal or even high BMD but compromised bone quality due to factors, including altered microarchitecture, accumulation of advanced glycation end products (AGEs), and low bone turnover. These distinct mechanisms create challenges for accurate fracture risk assessment, as standard tools such as dual-energy X-ray absorptiometry (DXA)-measured BMD and the Fracture Risk Assessment Tool (FRAX) often underestimate the true risk, particularly in T2D. Effective management necessitates a comprehensive, individualized approach. This includes optimizing glycemic control while minimizing hypoglycemia, implementing lifestyle modifications such as adequate nutrition (calcium, vitamin D, protein) and appropriate exercise, and crucially, proactive fall prevention strategies. Careful consideration must be given to the selection of antidiabetic medications, avoiding agents known to harm bone (e.g., thiazolidinediones) and preferring those with neutral or potentially beneficial skeletal effects (e.g., metformin, dipeptidyl peptidase-4 inhibitors [DPP-4i], glucagon-like peptide-1 receptor agonists [GLP-1 RAs]). Osteoporosis pharmacotherapies, including antiresorptive (bisphosphonates, denosumab) and anabolic agents (teriparatide, abaloparatide, romosozumab), appear effective in patients with diabetes largely on the basis of post hoc analyses and observational data, although evidence specific to this population remains limited. Integrating geriatric principles, such as assessing frailty and polypharmacy, is essential for optimizing care and improving outcomes for older adults with diabetes and bone fragility.

Indexed as

Diabetes Mellitus, Type 1Diabetes Mellitus, Type 2Fractures, BoneAged, 80 and overBone DensityHumansHypoglycemic AgentsHypoglycemic Agents

Identifiers

PMID41854838
PMCPMC13038465

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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 Socratic graph.