Evidence map›Paper›PMID 31234301›Full record

ArticleNutrients2019

Lactational High-Fat Diet Exposure Programs Metabolic Inflammation and Bone Marrow Adiposity in Male Offspring.

Hannah Hafner, Eric Chang, Zach Carlson, Allen Zhu, Mita Varghese, Jeremy Clemente, Simin Abrishami, Devika P Bagchi, Ormond A MacDougald, Kanakadurga Singer and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 31 citations in OpenAlex.

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  17. Molecular Interactions between Dietary Lipids and Bone Tissue during Aging.International journal of molecular sciences · 2021
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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

11 authors at 2 institutions in 1 country.

Hannah HafnerDivision of Diabetes, Endocrinology and Metabolism, Department of Pediatrics, University of Michigan Medicine, Ann Arbor, MI 48105, USA. hhafner@med.umich.edu.
Eric ChangDivision of Diabetes, Endocrinology and Metabolism, Department of Pediatrics, University of Michigan Medicine, Ann Arbor, MI 48105, USA. changer@med.umich.edu.ORCID 0000-0001-9898-5773
Zach CarlsonDivision of Diabetes, Endocrinology and Metabolism, Department of Pediatrics, University of Michigan Medicine, Ann Arbor, MI 48105, USA. zcarlson@med.umich.edu.
Allen ZhuDivision of Diabetes, Endocrinology and Metabolism, Department of Pediatrics, University of Michigan Medicine, Ann Arbor, MI 48105, USA. zhual@med.umich.edu.
Mita VargheseDivision of Diabetes, Endocrinology and Metabolism, Department of Pediatrics, University of Michigan Medicine, Ann Arbor, MI 48105, USA. mvarghes@med.umich.edu.
Jeremy ClementeDivision of Diabetes, Endocrinology and Metabolism, Department of Pediatrics, University of Michigan Medicine, Ann Arbor, MI 48105, USA. jerclem@med.umich.edu.
Simin AbrishamiDivision of Diabetes, Endocrinology and Metabolism, Department of Pediatrics, University of Michigan Medicine, Ann Arbor, MI 48105, USA. abrisham@med.umich.edu.
Devika P BagchiDepartment of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48105, USA. dpbagchi@med.umich.edu.ORCID 0000-0002-2258-2289
Ormond A MacDougaldDepartment of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48105, USA. macdouga@med.umich.edu.
Kanakadurga SingerDivision of Diabetes, Endocrinology and Metabolism, Department of Pediatrics, University of Michigan Medicine, Ann Arbor, MI 48105, USA. ksinger@med.umich.edu.ORCID 0000-0001-8278-3800
Brigid GreggDivision of Diabetes, Endocrinology and Metabolism, Department of Pediatrics, University of Michigan Medicine, Ann Arbor, MI 48105, USA. greggb@med.umich.edu.ORCID 0000-0002-1192-2997
Michigan Medicine · USUniversity of Michigan · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Scott Soleimanpour · 2013 to 2026
$24.3M
Pilot and Feasibility (P and F) ProgramP30DK089503 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Kanakadurga Singer · 2010 to 2026
$20.3M
Postdoc Stipend Supplement: Developmental Origins of Metabolic Disorders T32T32DK071212 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON, Kanakadurga Singer · 2005 to 2026
$5.4M
Roles for Wnt Signaling in Adipose TissueR01DK062876 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MACDOUGALD, ORMOND A · 2003 to 2018
$5.1M
The Role of Androgens in Obesity Induced Meta-InflammationR01DK115583 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SINGER, KANAKADURGA · 2018 to 2022
$2.2M
Programming of beta-cells and Glucose Homeostasis by Maternal Metformin ExposureK08DK102526 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GREGG, BRIGID ELLEN · 2015 to 2021
$797k
Mechanisms of hematopoietic stem cell activation in obesityK08DK101755 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SINGER, KANAKADURGA · 2015 to 2018
$644k
Interdisciplinary study of marrow adiposity, mineral metabolism,and energy balancR24DK084970 · NIDDK · MAINEHEALTH · PI HOROWITZ, MARK C, KLIBANSKI, ANNE · 2010 to 2010
$501k
NIDDK NIH HHS K08 DK101755NIDDK NIH HHS K08DK101755NIDDK NIH HHS K08 DK102526NIDDK NIH HHS K08DK102526NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK089503NIDDK NIH HHS R01 DK062876NIDDK NIH HHS R01 DK115583NIDDK NIH HHS R01DK115583NIDDK NIH HHS R24 DK084970NIDDK NIH HHS T32DK071212
6 · The paper itself

Abstract

Overnutrition during critical windows of development plays a significant role in life-long metabolic disease risk. Early exposure to excessive nutrition may result in altered programming leading to increased susceptibility to obesity, inflammation, and metabolic complications. This study investigated the programming effects of high-fat diet (HFD) exposure during the lactation period on offspring adiposity and inflammation. Female C57Bl/6J dams were fed a normal diet or a 60% HFD during lactation. Offspring were weaned onto a normal diet until 12 weeks of age when half were re-challenged with HFD for 12 weeks. Metabolic testing was performed throughout adulthood. At 24 weeks, adipose depots were isolated and evaluated for macrophage profiling and inflammatory gene expression. Males exposed to HFD during lactation had insulin resistance and glucose intolerance as adults. After re-introduction to HFD, males had increased weight gain and worsened insulin resistance and hyperglycemia. There was increased infiltration of pro-inflammatory CD11c

Indexed as

AdiposityLactationMaternal Nutritional Physiological PhenomenaAdipose TissueAge FactorsAnimalsBiomarkersBlood GlucoseBone MarrowDiet, High-FatFemaleHyperglycemiaInflammationInflammation MediatorsInsulin ResistanceMaleBiomarkersBlood GlucoseInflammation Mediatorsadipose tissuedevelopmental programminginflammationlactationmetabolism

Identifiers

PMID31234301
PMCPMC6628038
OpenAlexW2949555388

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.