摘要:
Verwendung von Fragmenten des N-terminalen Teils der Carbamoylphosphat Synthetase (CPS 1) aus Körperflüssigkeiten oder Körpergeweben als Markerpeptide zum diagnostischen Nachweis und für die Verlaufsprognose sowie die Verlaufskontrolle von Entzündungen und Infektionen, einschließlich Sepsis.
摘要:
Verfahren zur Früherkennung und Erkennung, für die Verlaufsprognose und die Beurteilung des Schweregrads und zur therapiebegleitenden Verlaufsbeurteilung von Entzündungserkrankungen und Infektionen, insbesondere von Sepsis und sepsisähnlichen systemischen Infektionen sowie von Entzündungserkrankungen, die im Gehirn lokalisiert sind, einschließlich der Alzheimer Krankheit, oder die auf das Gehirn übergreifen, bei dem man die Anwesenheit und/oder Menge einer Expressionsform des Phosphoproteins LASP-1 in einer biologischen Flüssigkeit auf Blut- oder Liquorbasis oder in einer Gewebeprobe eines Patienten bestimmt und aus der Anwesenheit und/oder Menge von LASP-1 Schlüsse hinsichtlich des Vorliegens, des zu erwartenden Verlaufs, des Schweregrads oder des Erfolgs einer Therapie der Entzündungserkrankung oder der Infektion zieht.
摘要:
Verwendungen der Aldose-1-Epimerase (SEQ ID NO:3) aus Körperflüssigkeiten oder Körpergeweben in der Human- und Tiermedizin als Markerpeptid zum diagnostischen Nachweis, für die Verlaufsprognose und für die Verlaufskontrolle von Entzündungen und Infektionen und/oder als Target für die therapeutische Beeinflussung des Verlaufs von Entzündungen und/oder Infektionen.
摘要:
The invention relates to a method for determining auto-antibodies (TRAb) to the TSH receptor (TSH-R), formed in a biological sample obtained from a patient. According to said method, the sample or at least one antibody fraction of the sample is reacted in a known manner in a reaction mixture in the presence of a first immunoreagent in the form of a selective competitor, with a second immunoreagent in the form of a TSH-R preparation. The selective competitor and/or the TSH-R preparation is/are, or can be labelled. The presence and/or quantity of the TRAb sought in the sample is determined by means of the bond between the TSH-R preparation and the selective competitor. According to the invention, the TSH receptor blocking auto-antibody (TBAb) is selectively determined in such a way, that the selective competitor is for the first time chosen to bond at those binding sites of the TSH-R preparation, for which said competitor competes with the TBAb that is to be determined, not however with the TSAb.
摘要:
In vitro method for the risk stratification of patients with stable arteriosclerosis, especially stable coronary artery disease, wherein the concentration of procalcitonin is determined in the circulation of such patients using a highly sensitive PCT assay, and wherein within the range of PCT concentrations in the typical normal range of healthy individuals cutoff values are defined which distinguish groups of individual patients with stable arteriosclerosis in accordance with the personal cardiac risk, and the patients are allotted to one of said risk groups on the basis of their individual PCT concentrations
摘要:
Subject of the present invention is an in vitro method for the alternative assessment of peak oxygen consumption (VO 2 ) for a subject not having a heart failure by measuring Pro-Endothelin-1 (ProET-1) or fragments thereof.
摘要:
Disclosed is a method for controlling the therapeutic treatment of a patient suffering from cardiac insufficiency. In said method, it is determined how the concentration of at least one of the vasoactive peptides adrenomedullin (ADM), endothelin-1 (ET-1), and/or vasopressin (AVP) changes in the patient's blood after beginning the therapy, and the therapeutic measures are considered to be unsatisfactory and are modified in case said concentration does not decrease at all or not enough in relation to a threshold value for the respective vasoactive peptide.
摘要:
CSF diagnostic in vitro method for diagnosis of dementia and neuroinflammatory diseases, in which method a sample of cerebrospinal fluid (CSF) is taken from a patient who is suffering from a dementia or neuroinflammatory disease, or in whom such a disease is suspected, and the sample is examined to determine the procalcitonin immune reactivity (PCT immune reactivity), and, in the event of a measured PCT immune reactivity that lies above a threshold value typical of healthy control volunteers, conclusions are drawn regarding the presence, course and severity, or the success of treatment, of the dementia or neuroinflammatory disease.