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1.
J Diabetes Complications ; 32(3): 325-329, 2018 03.
Article in English | MEDLINE | ID: mdl-29395841

ABSTRACT

AIMS: Advanced glycation endproducts (AGEs) and altered extracellular matrix remodeling by matrix metalloproteinases (MMPs) and tissue inhibitor of metalloproteinase (TIMP) are associated with vascular complications in type 1 diabetes. Experimental studies have shown that AGEs regulate the production of MMPs and/or TIMP-1. Therefore, we investigated associations between specific AGEs and MMP-1, -2, -3, -9, and -10, and TIMP-1 in individuals with type 1 diabetes. METHODS: In 670 type 1 diabetic individuals we determined serum levels of protein-bound AGEs Nε-(carboxymethyl)lysine (CML), Nε-(carboxyethyl)lysine (CEL), 5-hydro-5-methylimidazolone (MG-H1) and pentosidine, and MMP-1, -2, -3, -9, and -10, and TIMP-1. We performed linear regression analyses to investigate associations between AGEs and markers of the MMP-TIMP system. Analyses were adjusted for age, sex, HbA1c and duration of diabetes, and additionally for other potential confounders and presence of vascular complication. RESULTS: After full adjustment, levels of CML were positively associated with levels of MMP-2 and inversely with MMP-9. CEL was positively associated with MMP-3 and TIMP-1. MG-H1 was only associated with TIMP-1, whereas pentosidine was not associated with MMPs or TIMP-1. CONCLUSIONS: We showed independent associations between several AGEs and markers of the MMP-TIMP system, which indicate specific AGE-MMP/TIMP-1 interactions potentially contributing to vascular complications in patients with type 1 diabetes.


Subject(s)
Diabetes Mellitus, Type 1/blood , Diabetes Mellitus, Type 1/enzymology , Diabetic Angiopathies/blood , Diabetic Angiopathies/enzymology , Glycation End Products, Advanced/blood , Matrix Metalloproteinases, Secreted/blood , Adult , Aged , Biomarkers/blood , Cross-Sectional Studies , Diabetes Mellitus, Type 1/complications , Diabetic Angiopathies/etiology , Female , Humans , Male , Middle Aged
2.
Cardiovasc Diabetol ; 16(1): 55, 2017 04 26.
Article in English | MEDLINE | ID: mdl-28446168

ABSTRACT

BACKGROUND: Altered regulation of extracellular matrix remodeling by matrix metalloproteinases (MMPs) and tissue inhibitor of metalloproteinase (TIMP) may contribute to vascular complications in type 1 diabetes. We investigated associations between plasma MMP-1, -2, -3, -9, -10 and TIMP-1, and cardiovascular events and all-cause mortality in type 1 diabetic patients. METHODS: We prospectively followed 337 type 1 diabetic patients [mean age 41.4 years (9.6), 39% female], 170 with and 167 without diabetic nephropathy, with median follow-up of 12.3 years. Survival analyses were applied to investigate differences in plasma MMP-1, -2, -3, -9, -10, and TIMP-1-levels in patients with and without a cardiovascular event and in those who died vs survivors. All analyses were adjusted for age, sex, duration of diabetes, HbA1c, nephropathy and for other conventional cardiovascular risk factors. RESULTS: After adjustment for potential confounders, higher MMP-2 plasma levels were significantly associated with higher incidence of cardiovascular events [HR 1.49 (95% CI 1.11; 1.99)], and higher plasma levels of MMP-1 [1.38 (1.07; 1.78)], MMP-2 [1.60 (1.19; 2.15)] and MMP-3 [1.39 (1.05; 1.85)] were associated with all-cause mortality. All associations were independent of low-grade inflammation and endothelial dysfunction as estimated by plasma markers. Associations between MMP-2 and cardiovascular events and between MMP-3 and mortality were attenuated after further adjustment for eGFR and changes in eGFR. CONCLUSIONS: Higher levels of MMP-2 are associated with CVD and higher MMP-1, -2 and -3 with all-cause mortality. In addition, associations between MMP-2 and CVD, and MMP-3 and mortality were attenuated after adjustment for eGFR while both MMPs were associated with eGFR decline, indicating a possible mediating role of eGFR.


Subject(s)
Cardiovascular Diseases/blood , Cardiovascular Diseases/mortality , Diabetes Mellitus, Type 1/blood , Diabetes Mellitus, Type 1/mortality , Matrix Metalloproteinases, Secreted/blood , Adult , Biomarkers/blood , Cardiovascular Diseases/diagnosis , Cardiovascular Diseases/enzymology , Cause of Death , Diabetes Mellitus, Type 1/diagnosis , Diabetes Mellitus, Type 1/enzymology , Female , Follow-Up Studies , Glomerular Filtration Rate , Humans , Incidence , Kidney/physiopathology , Male , Middle Aged , Netherlands/epidemiology , Predictive Value of Tests , Prognosis , Proportional Hazards Models , Prospective Studies , Risk Assessment , Risk Factors , Time Factors , Tissue Inhibitor of Metalloproteinase-1/blood
3.
Cochlear Implants Int ; 5(2): 58-70, 2004 Jun.
Article in English | MEDLINE | ID: mdl-18792196

ABSTRACT

Different individual test methods and protocols have been reported for the in-vitro evaluation of temporal bones implanted with newly designed cochlear implant electrodes, prior to human implantation. In practice, however, these methods may not always give the required information. In this study, a large battery of tests has been evaluated using the electrode as a fixed parameter. Standard clinical x-ray gave the best information to evaluate the electrode's position. Light microscopic evaluation and polishing technique studies proved to be the most valuable techniques to evaluate endocochlear damage.

4.
J Neurosci Methods ; 128(1-2): 143-50, 2003 Sep 30.
Article in English | MEDLINE | ID: mdl-12948557

ABSTRACT

A 48 contact cochlear implant electrode has been constructed for electrical stimulation of the auditory nerve. The stimulating contacts of this electrode are organised in two layers: 31 contacts on the upper surface directed towards the habenula perforata and 17 contacts connected together as one longitudinal contact on the underside. The design of the electrode carrier aims to make radial current flow possible in the cochlea. The mechanical structure of the newly designed electrode was optimised to obtain maximal insertion depth. Electrode insertion tests were performed in a transparent acrylic model of the human cochlea.


Subject(s)
Biomedical Engineering/instrumentation , Cochlear Implants , Scala Tympani/physiology , Biomedical Engineering/methods , Cochlear Implants/standards , Cochlear Nerve/physiology , Electric Stimulation/methods , Electrodes, Implanted/standards
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