Profile of the Immune and Inflammatory Response in Individuals With Prediabetes and Type 2 Diabetes

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Profile of the Immune and Inflammatory Response in Individuals With Prediabetes and Type 2 Diabetes. / Grossmann, Vera; Schmitt, Volker H; Zeller, Tanja; Panova-Noeva, Marina; Schulz, Andreas; Laubert-Reh, Dagmar; Juenger, Claus; Schnabel, Renate B; Abt, Tobias G J; Laskowski, Rafael; Wiltink, Jörg; Schulz, Eberhard; Blankenberg, Stefan; Lackner, Karl J; Münzel, Thomas; Wild, Philipp S.

In: DIABETES CARE, Vol. 38, No. 7, 07.2015, p. 1356-1364.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Grossmann, V, Schmitt, VH, Zeller, T, Panova-Noeva, M, Schulz, A, Laubert-Reh, D, Juenger, C, Schnabel, RB, Abt, TGJ, Laskowski, R, Wiltink, J, Schulz, E, Blankenberg, S, Lackner, KJ, Münzel, T & Wild, PS 2015, 'Profile of the Immune and Inflammatory Response in Individuals With Prediabetes and Type 2 Diabetes', DIABETES CARE, vol. 38, no. 7, pp. 1356-1364. https://doi.org/10.2337/dc14-3008

APA

Grossmann, V., Schmitt, V. H., Zeller, T., Panova-Noeva, M., Schulz, A., Laubert-Reh, D., Juenger, C., Schnabel, R. B., Abt, T. G. J., Laskowski, R., Wiltink, J., Schulz, E., Blankenberg, S., Lackner, K. J., Münzel, T., & Wild, P. S. (2015). Profile of the Immune and Inflammatory Response in Individuals With Prediabetes and Type 2 Diabetes. DIABETES CARE, 38(7), 1356-1364. https://doi.org/10.2337/dc14-3008

Vancouver

Bibtex

@article{46461d1efa454c4ebcf48309c798d5a0,
title = "Profile of the Immune and Inflammatory Response in Individuals With Prediabetes and Type 2 Diabetes",
abstract = "OBJECTIVE: The inflammatory and immune systems are altered in type 2 diabetes. Here, the aim was to profile the immune and inflammatory response in subjects with prediabetes and diabetes in a large population-representative sample.RESEARCH DESIGN AND METHODS: In total, 15,010 individuals were analyzed from the population-based Gutenberg Health Study. Glucose status was classified according to HbA1c concentration and history of diagnosis. All samples were analyzed for white blood cells (WBCs), granulocytes, lymphocytes, monocytes, platelets, C-reactive protein (CRP), albumin, fibrinogen, and hematocrit. Interleukin-18 (IL-18), IL-1 receptor antagonist (IL-1RA), and neopterin concentrations were determined in a subcohort.RESULTS: In total, 7,584 men and 7,426 women were analyzed (range 35-74 years), with 1,425 and 1,299 having prediabetes and diabetes, respectively. Biomarkers showed varying dynamics from normoglycemic via subjects with prediabetes to subjects with diabetes: 1) gradual increase (WBCs, granulocytes, monocytes, IL-1RA, IL-18, and fibrinogen), 2) increase with subclinical disease only (lymphocytes and CRP), 3) increase from prediabetes to diabetes only (neopterin), and 4) no variation with glucose status (hematocrit). The strongest relative differences were found for CRP, IL-1RA, and fibrinogen concentrations. Several inflammatory and immune markers were associated with the glucose status independent from cardiovascular risk factors and comorbidities, varied with disease severity and the presence of disease-specific complications in the diabetes subcohort.CONCLUSIONS: The inflammatory and immune biomarker profile varies with the development and progression of type 2 diabetes. Markers of inflammation and immunity enable differentiation between the early preclinical and clinical phases of the disease, disease complications, and progression.",
keywords = "Adult, Aged, Biomarkers/blood, C-Reactive Protein/metabolism, Cardiovascular Diseases/blood, Comorbidity, Diabetes Mellitus, Type 2/blood, Disease Progression, Female, Humans, Immunity, Inflammation/blood, Male, Middle Aged, Prediabetic State/blood, Risk Factors",
author = "Vera Grossmann and Schmitt, {Volker H} and Tanja Zeller and Marina Panova-Noeva and Andreas Schulz and Dagmar Laubert-Reh and Claus Juenger and Schnabel, {Renate B} and Abt, {Tobias G J} and Rafael Laskowski and J{\"o}rg Wiltink and Eberhard Schulz and Stefan Blankenberg and Lackner, {Karl J} and Thomas M{\"u}nzel and Wild, {Philipp S}",
note = "{\textcopyright} 2015 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered.",
year = "2015",
month = jul,
doi = "10.2337/dc14-3008",
language = "English",
volume = "38",
pages = "1356--1364",
journal = "DIABETES CARE",
issn = "0149-5992",
publisher = "American Diabetes Association Inc.",
number = "7",

}

RIS

TY - JOUR

T1 - Profile of the Immune and Inflammatory Response in Individuals With Prediabetes and Type 2 Diabetes

AU - Grossmann, Vera

AU - Schmitt, Volker H

AU - Zeller, Tanja

AU - Panova-Noeva, Marina

AU - Schulz, Andreas

AU - Laubert-Reh, Dagmar

AU - Juenger, Claus

AU - Schnabel, Renate B

AU - Abt, Tobias G J

AU - Laskowski, Rafael

AU - Wiltink, Jörg

AU - Schulz, Eberhard

AU - Blankenberg, Stefan

AU - Lackner, Karl J

AU - Münzel, Thomas

AU - Wild, Philipp S

N1 - © 2015 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered.

PY - 2015/7

Y1 - 2015/7

N2 - OBJECTIVE: The inflammatory and immune systems are altered in type 2 diabetes. Here, the aim was to profile the immune and inflammatory response in subjects with prediabetes and diabetes in a large population-representative sample.RESEARCH DESIGN AND METHODS: In total, 15,010 individuals were analyzed from the population-based Gutenberg Health Study. Glucose status was classified according to HbA1c concentration and history of diagnosis. All samples were analyzed for white blood cells (WBCs), granulocytes, lymphocytes, monocytes, platelets, C-reactive protein (CRP), albumin, fibrinogen, and hematocrit. Interleukin-18 (IL-18), IL-1 receptor antagonist (IL-1RA), and neopterin concentrations were determined in a subcohort.RESULTS: In total, 7,584 men and 7,426 women were analyzed (range 35-74 years), with 1,425 and 1,299 having prediabetes and diabetes, respectively. Biomarkers showed varying dynamics from normoglycemic via subjects with prediabetes to subjects with diabetes: 1) gradual increase (WBCs, granulocytes, monocytes, IL-1RA, IL-18, and fibrinogen), 2) increase with subclinical disease only (lymphocytes and CRP), 3) increase from prediabetes to diabetes only (neopterin), and 4) no variation with glucose status (hematocrit). The strongest relative differences were found for CRP, IL-1RA, and fibrinogen concentrations. Several inflammatory and immune markers were associated with the glucose status independent from cardiovascular risk factors and comorbidities, varied with disease severity and the presence of disease-specific complications in the diabetes subcohort.CONCLUSIONS: The inflammatory and immune biomarker profile varies with the development and progression of type 2 diabetes. Markers of inflammation and immunity enable differentiation between the early preclinical and clinical phases of the disease, disease complications, and progression.

AB - OBJECTIVE: The inflammatory and immune systems are altered in type 2 diabetes. Here, the aim was to profile the immune and inflammatory response in subjects with prediabetes and diabetes in a large population-representative sample.RESEARCH DESIGN AND METHODS: In total, 15,010 individuals were analyzed from the population-based Gutenberg Health Study. Glucose status was classified according to HbA1c concentration and history of diagnosis. All samples were analyzed for white blood cells (WBCs), granulocytes, lymphocytes, monocytes, platelets, C-reactive protein (CRP), albumin, fibrinogen, and hematocrit. Interleukin-18 (IL-18), IL-1 receptor antagonist (IL-1RA), and neopterin concentrations were determined in a subcohort.RESULTS: In total, 7,584 men and 7,426 women were analyzed (range 35-74 years), with 1,425 and 1,299 having prediabetes and diabetes, respectively. Biomarkers showed varying dynamics from normoglycemic via subjects with prediabetes to subjects with diabetes: 1) gradual increase (WBCs, granulocytes, monocytes, IL-1RA, IL-18, and fibrinogen), 2) increase with subclinical disease only (lymphocytes and CRP), 3) increase from prediabetes to diabetes only (neopterin), and 4) no variation with glucose status (hematocrit). The strongest relative differences were found for CRP, IL-1RA, and fibrinogen concentrations. Several inflammatory and immune markers were associated with the glucose status independent from cardiovascular risk factors and comorbidities, varied with disease severity and the presence of disease-specific complications in the diabetes subcohort.CONCLUSIONS: The inflammatory and immune biomarker profile varies with the development and progression of type 2 diabetes. Markers of inflammation and immunity enable differentiation between the early preclinical and clinical phases of the disease, disease complications, and progression.

KW - Adult

KW - Aged

KW - Biomarkers/blood

KW - C-Reactive Protein/metabolism

KW - Cardiovascular Diseases/blood

KW - Comorbidity

KW - Diabetes Mellitus, Type 2/blood

KW - Disease Progression

KW - Female

KW - Humans

KW - Immunity

KW - Inflammation/blood

KW - Male

KW - Middle Aged

KW - Prediabetic State/blood

KW - Risk Factors

U2 - 10.2337/dc14-3008

DO - 10.2337/dc14-3008

M3 - SCORING: Journal article

C2 - 25877811

VL - 38

SP - 1356

EP - 1364

JO - DIABETES CARE

JF - DIABETES CARE

SN - 0149-5992

IS - 7

ER -