Evidence map›Paper›PMID 28631813›Full record

ArticleJournal of cellular physiology2018

High fat diet attenuates hyperglycemia, body composition changes, and bone loss in male streptozotocin-induced type 1 diabetic mice.

Adriana Lelis Carvalho, Victoria E DeMambro, Anyonya R Guntur, Phuong Le, Kenichi Nagano, Roland Baron, Francisco José Albuquerque de Paula, Katherine J Motyl

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 25 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 2 countries.

Adriana Lelis CarvalhoCenter for Clinical and Translational Research, Maine Medical Center Research Institute, Scarborough, Maine.
Victoria E DeMambroCenter for Clinical and Translational Research, Maine Medical Center Research Institute, Scarborough, Maine.
Anyonya R GunturCenter for Clinical and Translational Research, Maine Medical Center Research Institute, Scarborough, Maine.
Phuong LeCenter for Clinical and Translational Research, Maine Medical Center Research Institute, Scarborough, Maine.
Kenichi NaganoDepartment of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, Harvard University, Boston, Massachusetts.
Roland BaronDepartment of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, Harvard University, Boston, Massachusetts.
Francisco José Albuquerque de PaulaDepartment of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, São Paulo, Brazil.
Katherine J MotylCenter for Clinical and Translational Research, Maine Medical Center Research Institute, Scarborough, Maine.ORCID http://orcid.org/0000-0002-8301-8737
Maine Medical Center Research Institute · USHarvard University · USUniversidade de São Paulo · BR

Funding

The role of night shift work in metabolic disorders during and after pregnancyP20GM121301 · NIGMS · MAINEHEALTH · PI Elizabeth Scharnetzki · 2017 to 2026
$25.1M
Interdisciplinary Study of Marrow Adiposity, Mineral Metabolism & Energy BalanceR24DK092759 · NIDDK · MAINEHEALTH · PI HOROWITZ, MARK C, MACDOUGALD, ORMOND A · 2011 to 2019
$13.0M
Progenitor Cell Analysis CoreP30GM106391 · NIGMS · MAINEHEALTH · PI WOJCHOWSKI, DON MICHAEL · 2013 to 2017
$5.7M
Phase III COBRE in Vascular BiologyP30GM103392 · NIGMS · MAINEHEALTH · PI ST. GERMAIN, DONALD L. · 2012 to 2016
$4.7M
TRPM8 is a novel regulator of bone homeostasis through neural and cell-autonomous mechanismsK01AR067858 · NIAMS · MAINEHEALTH · PI MOTYL, KATHERINE JEAN · 2016 to 2020
$613k
Role of MitoNEET in regulating osteoblast bioenergetics and catabolismR03AR068095 · NIAMS · MAINEHEALTH · PI GUNTUR, ANYONYA R · 2016 to 2018
$234k
NIAMS NIH HHS K01 AR067858NIAMS NIH HHS R03 AR068095NIDDK NIH HHS R24 DK092759NIGMS NIH HHS P20 GM121301NIGMS NIH HHS P30 GM103392NIGMS NIH HHS P30 GM106391
6 · The paper itself

Abstract

There is a growing and alarming prevalence of obesity and the metabolic syndrome in type I diabetic patients (T1DM), particularly in adolescence. In general, low bone mass, higher fracture risk, and increased marrow adipose tissue (MAT) are features of diabetic osteopathy in insulin-deficient subjects. On the other hand, type 2 diabetes (T2DM) is associated with normal or high bone mass, a greater risk of peripheral fractures, and no change in MAT. Therefore, we sought to determine the effect of weight gain on bone turnover in insulin-deficient mice. We evaluated the impact of a 6-week high-fat (HFD) rich in medium chain fatty acids or low-fat diet (LFD) on bone mass and MAT in a streptozotocin (STZ)-induced model using male C57BL/6J mice at 8 weeks of age. Dietary intervention was initiated after diabetes confirmation. At the endpoint, lower non-fasting glucose levels were observed in diabetic mice fed with high fat diet compared to diabetic mice fed the low fat diet (STZ-LFD). Compared to euglycemic controls, the STZ-LFD had marked polydipsia and polyphagia, as well as reduced lean mass, fat mass, and bone parameters. Interestingly, STZ-HFD mice had higher bone mass, namely less cortical bone loss and more trabecular bone than STZ-LFD. Thus, we found that a HFD, rich in medium chain fatty acids, protects against bone loss in a T1DM mouse model. Whether this may also translate to T1DM patients who are overweight or obese in respect to maintenance of bone mass remains to be determined through longitudinal studies.

Indexed as

Body CompositionBone RemodelingDiet, High-FatStreptozocinAdiposityAnimalsBiomarkersBlood GlucoseDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Fatty AcidsInsulinKetonesMaleMice, Inbred C57BLOsteoporosisBiomarkersBlood GlucoseFatty AcidsInsulinKetonesStreptozocinbone marrow adipose tissuebone masshigh fat diettype 1 diabetes mellitus

Identifiers

PMID28631813
PMCPMC5673543
OpenAlexW2645317886

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.