Evidence map›Paper›PMID 30301129›Full record

ReviewNutrients2018

Ironing out the Details: Untangling Dietary Iron and Genetic Background in Diabetes.

Mario A Miranda, Heather A Lawson

Open access · goldAbstract readReview
In one paragraph

Review in Nutrients, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Iron Homeostasis and Energy Metabolism in Obesity.Clinical nutrition research · 2022
    Review
  3. Review
  4. Article
  5. Article
  6. Leptin Receptor-DeficientFrontiers in nutrition · 2021
    Article
  7. Article
  8. Article
  9. Article
  10. Article
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

2 authors at 1 institution in 1 country.

Mario A MirandaDepartment of Genetics, Washington University School of Medicine, Campus Box 8232, 660 South Euclid Ave, Saint Louis, MO 63110, USA. mario.miranda@wustl.edu.
Heather A LawsonDepartment of Genetics, Washington University School of Medicine, Campus Box 8232, 660 South Euclid Ave, Saint Louis, MO 63110, USA. hlawson@genetics.wustl.edu.
Washington University in St. Louis · US

Funding

NIH HHS NHGRI-T32-HG000045NIH HHS NIDDK-K01DK095003
6 · The paper itself

Abstract

The search for genetic risk factors in type-II diabetes has been hindered by a failure to consider dietary variables. Dietary nutrients impact metabolic disease risk and severity and are essential to maintaining metabolic health. Genetic variation between individuals confers differences in metabolism, which directly impacts response to diet. Most studies attempting to identify genetic risk factors in disease fail to incorporate dietary components, and thus are ill-equipped to capture the breadth of the genome's impact on metabolism. Understanding how genetic background interacts with nutrients holds the key to predicting and preventing metabolic diseases through the implementation of personalized nutrition. Dysregulation of iron homeostasis is associated with type-II diabetes, but the link between dietary iron and metabolic dysfunction is poorly defined. High iron burden in adipose tissue induces insulin resistance, but the mechanisms underlying adipose iron accumulation remain unknown. Hepcidin controls dietary iron absorption and distribution in metabolic tissues, but it is unknown whether genetic variation influencing hepcidin expression modifies susceptibility to dietary iron-induced insulin resistance. This review highlights discoveries concerning the axis of iron homeostasis and adipose function and suggests that genetic variation underlying dietary iron metabolism is an understudied component of metabolic disease.

Indexed as

Diabetes Mellitus, Type 2DietEpigenesis, GeneticGenetic VariationAdipose TissueGene Expression RegulationGenomeHepcidinsHomeostasisHumansInsulin ResistanceIronIron, DietaryPrecision MedicineHepcidinsIronIron, Dietaryadiposediabetesdietgene-environment interaction (GEI)hepcidininsulin sensitivityiron

Identifiers

PMID30301129
PMCPMC6213605
OpenAlexW2895582981

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.