Evidence map›Paper›PMID 32617858›Full record

ArticleJournal of endocrinological investigation2021

The -514C>T polymorphism in the LIPC gene modifies type 2 diabetes risk through modulation of HDL-cholesterol levels in Mexicans.

M T Guerra-García, H Moreno-Macías, A Ochoa-Guzmán, M L Ordoñez-Sánchez, R Rodríguez-Guillen, P Vázquez-Cárdenas, V M Ortíz-Ortega, M Peimbert-Torres, C A Aguilar-Salinas, M T Tusié-Luna

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of endocrinological investigation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.1field-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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Interaction betweenNutrients · 2023
    Article
  6. Association ofFrontiers in neurology · 2023
    Article
  7. Article
  8. 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

10 authors at 3 institutions in 1 country.

M T Guerra-GarcíaUnit of Molecular Biology and Genomic Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga #15, Belisario Domínguez, Sección XVI, Tlalpan, 14080, Mexico City, Mexico.
H Moreno-MacíasUnit of Molecular Biology and Genomic Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga #15, Belisario Domínguez, Sección XVI, Tlalpan, 14080, Mexico City, Mexico.
A Ochoa-GuzmánUnit of Molecular Biology and Genomic Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga #15, Belisario Domínguez, Sección XVI, Tlalpan, 14080, Mexico City, Mexico.
M L Ordoñez-SánchezUnit of Molecular Biology and Genomic Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga #15, Belisario Domínguez, Sección XVI, Tlalpan, 14080, Mexico City, Mexico.
R Rodríguez-GuillenUnit of Molecular Biology and Genomic Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga #15, Belisario Domínguez, Sección XVI, Tlalpan, 14080, Mexico City, Mexico.
P Vázquez-CárdenasObesity Clinic, Hospital General Dr. Manuel Gea González, Mexico City, Mexico.
V M Ortíz-OrtegaDepartment of Physiology of Nutrition, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
M Peimbert-TorresNature Sciences Department, Universidad Autónoma Metropolitana, Mexico City, Mexico.
C A Aguilar-SalinasDivision of Nutrition, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
M T Tusié-LunaUnit of Molecular Biology and Genomic Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga #15, Belisario Domínguez, Sección XVI, Tlalpan, 14080, Mexico City, Mexico. mttusie@gmail.com.ORCID http://orcid.org/0000-0003-4478-038X
Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MXUniversidad Autónoma Metropolitana · MXHospital General Dr. Manuel Gea Gonzalez · MX

Funding

CONACyT 128877
6 · The paper itself

Abstract

purposeBoth type 2 diabetes (T2D) and low levels of high-density lipoprotein cholesterol (HDL-C) are very prevalent conditions among Mexicans. Genetic variants in the LIPC gene have been associated with both conditions. This study aimed to evaluate the association of the -514C < T (rs1800588) LIPC gene polymorphism with different metabolic traits, particularly the effects of this polymorphism on HDL-C plasma levels and T2D risk.

methodsMediation analysis was used to assess the direct and indirect effects of the -514C>T LIPC gene variant on HDL-C levels, T2D risk, and body mass index (BMI), in 2105 Mexican mestizo participants. We also assessed the functional effect of the -514C>T LIPC variant on the promoter activity of a reporter gene in the HepG2 cell line.

resultsDirect effects show that the -514C>T LIPC polymorphism is significantly associated with increased HDL-C plasma levels (β = 0.03; p < 0.001). The -514C>T variant resulted in an indirect protective effect on T2D risk through increasing HDL-C levels (β = - 0.03; p < 0.001). Marginal direct association between -514C>T and T2D was found (β = 0.08; p = 0.06). Variables directly influencing T2D status were European ethnicity (β = - 7.20; p < 0.001), age (β = 0.04; p < 0.001), gender (β = - 0.15; p = 0.017) and HDL-C (β = - 1.07; p < 0.001). In addition, we found that the -514C>T variant decreases the activity of LIPC promoter by 90% (p < 0.001).

conclusionsThe -514C>T polymorphism was not directly associated with T2D risk. HDL-C acts as a mediator between -514C>T LIPC gene variant and T2D risk in the Mexican population.

Indexed as

Body Mass IndexPolymorphism, Single NucleotidePromoter Regions, GeneticAdolescentAdultAgedBiomarkersCase-Control StudiesCholesterol, HDLDiabetes Mellitus, Type 2FemaleFollow-Up StudiesGenotypeHumansLipaseMaleBiomarkersCholesterol, HDLLipaseLIPC protein, humanHDLHDL-CLIPCrs1800588Type 2 diabetes

Identifiers

PMID32617858
OpenAlexW3040256653

What OpenQuestion holds

Textmetadata
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.