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RU2001132335A - METHOD FOR ESTIMATING THE RISK OF A PEPTIC ULCER, INCLUDING THE STAGES OF QUANTITATIVE DETERMINATION OF THE CONCENTRATION OF PEPPSINOGEN I (PGI) AND GASTRIN-17 IN THE SERUM SAMPLE - Google Patents

METHOD FOR ESTIMATING THE RISK OF A PEPTIC ULCER, INCLUDING THE STAGES OF QUANTITATIVE DETERMINATION OF THE CONCENTRATION OF PEPPSINOGEN I (PGI) AND GASTRIN-17 IN THE SERUM SAMPLE

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Publication number
RU2001132335A
RU2001132335A RU2001132335/14A RU2001132335A RU2001132335A RU 2001132335 A RU2001132335 A RU 2001132335A RU 2001132335/14 A RU2001132335/14 A RU 2001132335/14A RU 2001132335 A RU2001132335 A RU 2001132335A RU 2001132335 A RU2001132335 A RU 2001132335A
Authority
RU
Russia
Prior art keywords
gastrin
concentration
pepsinogen
risk
serum
Prior art date
Application number
RU2001132335/14A
Other languages
Russian (ru)
Other versions
RU2225615C2 (en
Inventor
Пентти Сиппонен
Матти Хяркенен
Осмо Суованиеми
Эрик ФОРСБЛОМ
Original Assignee
Биохит Ойй
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from FI990992A external-priority patent/FI118653B/en
Application filed by Биохит Ойй filed Critical Биохит Ойй
Publication of RU2001132335A publication Critical patent/RU2001132335A/en
Application granted granted Critical
Publication of RU2225615C2 publication Critical patent/RU2225615C2/en

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Claims (9)

1. Способ оценки наличия риска пептической язвы у индивидуума, причем способ включает в себя этапы количественного определения концентрации пепсиногена I и гастрина-17 в образце сыворотки указанного индивидуума, выбора специфической для способа эталонной величины и величины отсечки для соответствующих анализируемых веществ, сравнения определяемых таким образом концентраций пепсиногена I и гастрина-17 со специфической для способа эталонной величиной и величиной отсечки, в результате которого сывороточная концентрация пепсиногена I и гастрина-17 выше верхнего предела соответствующей эталонной величины или сывороточная концентрация пепсиногена I выше верхнего предела ее эталонной величины в комбинации с концентрацией гастрина-17 в пределах эталонного диапазона или ниже ее величины отсечки, указывает на возросший риск пептической язвы у указанного индивидуума.1. A method for assessing the risk of peptic ulcer in an individual, the method comprising the steps of quantifying the concentration of pepsinogen I and gastrin-17 in a serum sample of the indicated individual, selecting a method-specific reference value and cut-off value for the corresponding analytes, comparing so determined concentrations of pepsinogen I and gastrin-17 with a method-specific reference value and cut-off value, as a result of which the serum concentration of pepsinogen I and ha trine-17 above the upper limit of respective reference value, or a serum pepsinogen I concentration above the upper limit of its reference value in combination with a gastrin-17 concentration within the reference range or below its cut-off value, indicates an increased risk of peptic ulcer in said individual. 2. Способ по п.1, при котором в образце сыворотки проводится также определение антитела к Helicobacter pylori.2. The method according to claim 1, in which the determination of antibodies to Helicobacter pylori is also carried out in a serum sample. 3. Способ по п.1, при котором концентрацию гастрина-17 в сыворотке также измеряют с использованием теста белковой стимуляции путем измерения указанной концентрации в ситуации до и после поглощения богатого белком стандартного блюда, причем отсутствие реакции указывает на риск развития язвы желудка.3. The method according to claim 1, in which the concentration of gastrin-17 in serum is also measured using the protein stimulation test by measuring the specified concentration in the situation before and after absorption of a protein-rich standard dish, and the absence of a reaction indicates a risk of gastric ulcer. 4. Способ по пп.1, 2 или 3, при котором пепсиноген I и гастрин-17 определяется иммунологически с использованием пластиковой, стеклянной или целлюлозной подложки.4. The method according to claims 1, 2 or 3, wherein pepsinogen I and gastrin-17 are determined immunologically using a plastic, glass or cellulose substrate. 5. Способ по п.4, при котором подложка представляет собой микропланшет.5. The method according to claim 4, wherein the substrate is a microplate. 6. Способ по любому из пп.1-5, при котором способ выявления, основанный на измерении оптического поглощения, флуоресценции или люминесценции, используется для определения пепсиногена I и гастрина-17.6. The method according to any one of claims 1 to 5, wherein the detection method, based on the measurement of optical absorption, fluorescence or luminescence, is used to determine pepsinogen I and gastrin-17. 7. Способ по любому из пп.4-6, при котором для определения концентрации пепсиногена I используется поликлональное или моноклональное антитело против пепсиногена I.7. The method according to any one of claims 4 to 6, wherein a polyclonal or monoclonal anti-pepsinogen I antibody is used to determine the concentration of pepsinogen I. 8. Способ по любому из пп.4-7, при котором для определения концентрации гастрина-17 используется поликлональное или моноклональное антитело против гастрина-17.8. The method according to any one of claims 4 to 7, wherein a polyclonal or monoclonal anti-gastrin-17 antibody is used to determine the concentration of gastrin-17. 9. Способ по любому из предшествующих пунктов, при котором способы определения пепсиногена I, гастрина-17 и Helicobacter pylori комбинируются в набор-способ, в котором определения осуществляются одновременно на микропланшете с использованием поликлональных или моноклональных антител, а также способов выявления, основанных на поглощении, флуоресценции или люминесценции.9. The method according to any one of the preceding paragraphs, wherein the methods for determining pepsinogen I, gastrin-17 and Helicobacter pylori are combined into a kit-method, in which the determination is carried out simultaneously on a microplate using polyclonal or monoclonal antibodies, as well as detection methods based on absorption fluorescence or luminescence.
RU2001132335/15A 1999-04-30 2000-04-28 Method for differentiation between the risk in developing gastric ulcer and duodenal ulcer RU2225615C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FI990992A FI118653B (en) 1999-04-30 1999-04-30 Procedure for determining the risk of peptic ulcer
FI990992 1999-04-30

Publications (2)

Publication Number Publication Date
RU2001132335A true RU2001132335A (en) 2003-08-27
RU2225615C2 RU2225615C2 (en) 2004-03-10

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Country Status (13)

Country Link
US (1) US6872543B1 (en)
EP (1) EP1173770B1 (en)
JP (1) JP4598959B2 (en)
CN (1) CN100573152C (en)
AT (1) ATE300053T1 (en)
AU (1) AU4299800A (en)
DE (1) DE60021369T2 (en)
DK (1) DK1173770T3 (en)
ES (1) ES2241597T3 (en)
FI (1) FI118653B (en)
PT (1) PT1173770E (en)
RU (1) RU2225615C2 (en)
WO (1) WO2000067035A1 (en)

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US8272265B2 (en) * 2005-07-12 2012-09-25 Technion Research And Development Foundation Ltd. System and method for active detection of asymmetry in rotating structures
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RU2465597C1 (en) * 2011-04-08 2012-10-27 Сергей Михайлович Котелевец Method for determining probability of developing stomach cancer
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