Evidence map›Paper›PMID 40658501›Full record

Observational studyRevista medica del Instituto Mexicano del Seguro Social2025

Comprehensive study of associated factors with Type 2 Diabetes in Mexico: protocol.

Aldo Ferreira-Hermosillo, Rodolfo Rivas-Ruiz, Ivonne Analí Roy-García, Eduardo Antonio Ferat-Osorio, Octavio Castro-Escamilla, Keiko Taniguchi-Ponciano, Daniel Marrero-Rodríguez, Amelia Irene Rodríguez-Jiménez, Patricia Pérez-Zataray, Jose Luis Cevallos-Rivera and 8 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Revista medica del Instituto Mexicano del Seguro Social, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Aldo Ferreira-HermosilloInstituto Mexicano del Seguro Social, Centro Médico Nacional Siglo XXI, Hospital de Especialidades "Dr. Bernardo Sepúlveda Gutiérrez", Unidad de Investigación Médica en Enfermedades Endocrinas. Ciudad de México, México.ORCID 0000-0002-5159-9856
Rodolfo Rivas-RuizInstituto Mexicano del Seguro Social, Coordinación de Investigación en Salud, División de investigación Clínica. Ciudad de México, México.ORCID 0000-0002-5967-7222
Ivonne Analí Roy-GarcíaInstituto Mexicano del Seguro Social, Coordinación de Investigación en Salud, División de investigación Clínica. Ciudad de México, México.ORCID 0000-0002-1859-3866
Eduardo Antonio Ferat-OsorioInstituto Mexicano del Seguro Social, Coordinación de Investigación en Salud, División de investigación Clínica. Ciudad de México, México.ORCID 0000-0001-5361-7854
Octavio Castro-EscamillaInstituto Mexicano del Seguro Social, Coordinación de Investigación en Salud, División de investigación Clínica. Ciudad de México, México.ORCID 0000-0002-4061-4854
Keiko Taniguchi-PoncianoInstituto Mexicano del Seguro Social, Centro Médico Nacional Siglo XXI, Hospital de Especialidades "Dr. Bernardo Sepúlveda Gutiérrez", Unidad de Investigación Médica en Enfermedades Endocrinas. Ciudad de México, México.ORCID 0000-0003-1623-7398
Daniel Marrero-RodríguezInstituto Mexicano del Seguro Social, Centro Médico Nacional Siglo XXI, Hospital de Especialidades "Dr. Bernardo Sepúlveda Gutiérrez", Unidad de Investigación Médica en Enfermedades Endocrinas. Ciudad de México, México.ORCID 0000-0001-5311-6654
Amelia Irene Rodríguez-JiménezInstituto Mexicano del Seguro Social, Unidad de Medicina Familiar No. 10. San Buenaventura, Coahuila, México.ORCID 0009-0009-4439-6231
Patricia Pérez-ZatarayInstituto Mexicano del Seguro Social, Unidad de Medicina Familiar No. 181. Los Sabinos, Jalisco, México.ORCID 0009-0004-9180-4801
Jose Luis Cevallos-RiveraInstituto Mexicano del Seguro Social, Unidad de Medicina Familiar No. 30. Perote, Veracruz, México.ORCID 0009-0009-1129-3076
Jorge A Hernández-CasildoInstituto Mexicano del Seguro Social, División de Innovación y Modelos de Financiamiento. Ciudad de México, México.ORCID 0000-0003-1692-9917
José Félix Saavedra-RamírezInstituto Mexicano del Seguro Social, División de Innovación y Modelos de Financiamiento. Ciudad de México, México.ORCID 0009-0008-4898-9598
Víctor G Cruz-MoralesInstituto Mexicano del Seguro Social, División de Innovación y Modelos de Financiamiento. Ciudad de México, México.ORCID 0009-0006-1144-2607
Omar Livio Peralta-MéndezInstituto Mexicano del Seguro Social, Dirección de Planeación para la Transformación Institucional. Ciudad de México, México.ORCID 0009-0008-8530-4957
Alejandro M Vargas-GarcíaInstituto Mexicano del Seguro Social, Dirección de Planeación para la Transformación Institucional. Ciudad de México, México.ORCID 0009-0002-2564-0496
Asa Christina LaurellInstituto Mexicano del Seguro Social, Dirección de Planeación para la Transformación Institucional. Ciudad de México, México.ORCID 0009-0009-0168-3089
Rosana PelayoInstituto Mexicano del Seguro Social, Unidad de Educación e Investigación en Salud. Ciudad de México, México.ORCID 0000-0003-3401-9757
Laura C BonifazInstituto Mexicano del Seguro Social, Coordinación de Investigación en Salud. Ciudad de México, México.ORCID 0000-0001-8482-5648

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the main goals in the treatment of patients with type 2 diabetes (T2D) is the prevention of its complications. Most existing studies have evaluated a limited and isolated number of inflammatory molecules and metabolic factors, and only rarely have clinical and lifestyle variables been jointly considered. The objective of this study is to describe the protocol design for a comprehensive assessment of patients with T2D, considering glycemic control and the development of complications. A cross-sectional, observational, and multicenter study was conducted in three primary care units located in the states of Coahuila, Jalisco, and Veracruz. Glycemic dysregulation will be assessed by measuring glycated hemoglobin, while diabetic nephropathy will be identified through alterations in the glomerular filtration rate. Additionally, clinical and biochemical parameters, lifestyle habits, physical condition, type of treatment, treatment adherence, and nutritional aspects will be evaluated. Furthermore, transcriptomic analysis using RNA-Seq will be performed to identify the genes that best stratify and distinguish patients with glycemic dysregulation, metabolic alterations, and diabetic nephropathy through principal component analysis and ROC curves based on relative RNA expression. To determine clinical factors associated with the link between molecular profiles and glycemic dysregulation, multiple logistic regression models will be developed to identify a pathological molecular signature characteristic of the disease.

Indexed as

Diabetes Mellitus, Type 2Blood GlucoseCross-Sectional StudiesDiabetic NephropathiesFemaleGlycated HemoglobinGlycemic ControlHumansMaleMexicoPrimary Health CareBlood GlucoseGlycated HemoglobinDiabetes Mellitus, Type 2Diabetic NepGenesGlycated HemoglobinGlycemic ControlTranscriptome

Identifiers

PMID40658501
PMCPMC12303611

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.