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SHR Neuro Cancer Cardio Lipid Metab Microb

Mossbock, G; Weger, M; Meinitzer, A; Semmelrock, J; Schmut, O; Faschinger, C; Zimmermann, C; Renner, W; Stanger, O.
Asymmetric dimethylarginine and homocysteine in primary open angle glaucoma
SPEKTRUM AUGENHEILKD. 2009; 23(5): 333-336. Doi: 10.1007/s00717-009-0351-8
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Leading authors Med Uni Graz
Mossböck Georg
Co-authors Med Uni Graz
Faschinger Christoph
Meinitzer Andreas
Renner Wilfried
Schmut Otto
Semmelrock Hans-Jürgen
Weger Martin
Zimmermann-Roth Christina
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Abstract:
BACKGROUND: Endothelial dysfunction has been implicated in the pathogenesis of primary open angle glaucoma (POAG). Nitric oxide (NO), synthesized from L-arginine by nitric oxide synthase (NOS), is the most important endothelial derived vasodilative substance. Asymmetric dimethylarginine (ADMA), an endogenous NOS inhibitor, leads to decreased NO bio-availability, while homocysteine has been associated with increased ADMA plasma levels. Furthermore, due to its neurotoxic and gliotoxic properties, homocysteine has been suggested to be a risk factor for POAG. METHODS: The present case-control study comprised 44 patients with POAG and 44 control subjects, matched for age and gender. Plasma levels of ADMA and homocysteine were determined using high-performance liquid chromatography. RESULTS: No significant difference in either mean ADMA or homocysteine plasma levels was found between patients and control subjects. Mean plasma level of ADMA was 0.75 +/- 0.09 A mu mol/l in patients and 0.72 +/- 0.09 A mu mol/l in control subjects (p = 0.10), while mean plasma level of homocysteine was 14.6 +/- 5.1 A mu mol/l and 12.9 +/- 3.7 A mu mol/l (p = 0.21), respectively. CONCLUSIONS: The present study suggests that plasma levels of ADMA and homocysteine are not associated with increased risk for POAG.

Find related publications in this database (Keywords)
ADMA
homocysteine
NO
primary open-angle glaucoma
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