Evidence map›Paper›PMID 25685827›Full record

ArticleBone reports2015

Effects of long-term doxycycline on bone quality and strength in diabetic male DBA/2J mice.

John L Fowlkes, Jeffry S Nyman, R Clay Bunn, Gael E Cockrell, Elizabeth C Wahl, Mallikarjuna R Rettiganti, Charles K Lumpkin, Kathryn M Thrailkill

Open access · goldAbstract read
In one paragraph

Article in Bone reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 12 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

8 authors at 3 institutions in 1 country.

John L FowlkesDepartment of Pediatrics, University of Arkansas for Medical Sciences and Arkansas Children's Hospital Research Institute, Little Rock, AR, 72202.
Jeffry S NymanVA Tennessee Valley Health Care System, Department of Orthopaedic Surgery & Rehabilitation and Center for Bone Biology, Vanderbilt University Medical Center, Nashville, TN 37232; USA.
R Clay BunnDepartment of Pediatrics, University of Arkansas for Medical Sciences and Arkansas Children's Hospital Research Institute, Little Rock, AR, 72202.
Gael E CockrellDepartment of Pediatrics, University of Arkansas for Medical Sciences and Arkansas Children's Hospital Research Institute, Little Rock, AR, 72202.
Elizabeth C WahlDepartment of Pediatrics, University of Arkansas for Medical Sciences and Arkansas Children's Hospital Research Institute, Little Rock, AR, 72202.
Mallikarjuna R RettigantiDepartment of Pediatrics, University of Arkansas for Medical Sciences and Arkansas Children's Hospital Research Institute, Little Rock, AR, 72202.
Charles K LumpkinDepartment of Pediatrics, University of Arkansas for Medical Sciences and Arkansas Children's Hospital Research Institute, Little Rock, AR, 72202.
Kathryn M ThrailkillDepartment of Pediatrics, University of Arkansas for Medical Sciences and Arkansas Children's Hospital Research Institute, Little Rock, AR, 72202.
Arkansas Children's Hospital · USUniversity of Arkansas for Medical Sciences · USVA Tennessee Valley Healthcare System · US

Funding

THE PHYSIOLOGY OF IGFBP DEGRADING PROTEINASES IN BONER01DK055653 · NIDDK · UNIVERSITY OF KENTUCKY · PI FOWLKES, JOHN L · 1999 to 2009
$2.0M
EXTRAMURAL RES FACILITIES CONSTR PROJC06RR016517 · NCRR · ARKANSAS CHILDREN'S HOSP (LITTLE ROCK) · PI BURKS, ARVIL WESLEY · 2001 to 2002
$1.3M
The Insulin/IGF-I Axis in Diabetic OsteopathyR01DK084045 · NIDDK · UNIVERSITY OF KENTUCKY · PI FOWLKES, JOHN L · 2012 to 2015
$1.3M
Aging and Diabetes-Related Factors Compromising Bone Fracture ResistanceI01BX001018 · VA · VETERANS HEALTH ADMINISTRATION · PI NYMAN, JEFFRY STEPHEN · 2011 to 2014
–
BLRD VA I01 BX001018NCRR NIH HHS C06 RR016517NIDDK NIH HHS R01 DK055653NIDDK NIH HHS R01 DK084045
6 · The paper itself

Abstract

In type 1 diabetes, diabetic bone disease (DBD) is characterized by decreased bone mineral density, a state of low bone turnover and an increased risk of fracture. Animal models of DBD demonstrate that acquired alterations in trabecular and cortical bone microarchitecture contribute to decreased bone strength in diabetes. With anti-collagenolytic and anti-inflammatory properties, tetracycline derivatives may prevent diabetes-related decreases in bone strength. To determine if doxycycline, a tetracycline class antibiotic, can prevent the development of DBD in a model of long-term diabetes, male DBA/2J mice, with or without diabetes, were treated with doxycycline-containing chow for 10 weeks (dose range, 28-92 mg/kg/day). Long-term doxycycline exposure was not deleterious to the microarchitecture or biomechanical properties of healthy bone in male DBA/2J mice. Doxycycline treatment also did not prevent or alleviate the deleterious changes in trabecular microarchitecture, cortical structure, and biomechanical properties of bone induced by chronic diabetes.

Indexed as

cortical boneDiabetic bone diseasemicroarchitecturetetracyclinetrabecular bonetype 1 diabetes

Identifiers

PMID25685827
PMCPMC4324548
OpenAlexW2087075569

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.