METHOD FOR ANALYZING INFORMATION FOR DIAGNOSIS AND KIT THEREFOR
    1.
    发明申请
    METHOD FOR ANALYZING INFORMATION FOR DIAGNOSIS AND KIT THEREFOR 审中-公开
    用于分析诊断信息的方法及其套件

    公开(公告)号:US20160313337A1

    公开(公告)日:2016-10-27

    申请号:US15108283

    申请日:2013-12-27

    Abstract: A method of analyzing diagnostic information, the method including: measuring a concentration of a mucin-1 (Tn-MUC1), which is reactive with a lectin that recognizes and binds to an N-acetyl-D-galactosamine→serine (threonine) residue, in a blood sample originated from a subject to be diagnosed; comparing the measured value with a threshold value; and estimating that a disease affecting the subject to be diagnosed is not prostate cancer but a benign prostate disease when the measured value of the concentration of Tn-MUC1 is greater than the threshold value.

    Abstract translation: 一种分析诊断信息的方法,所述方法包括:测量与识别并结合N-乙酰基-D-半乳糖胺→丝氨酸(苏氨酸)残基的凝集素反应的粘蛋白-1(Tn-MUC1)的浓度 来自待诊断对象的血液样本; 将测量值与阈值进行比较; 并且当Tn-MUC1的浓度的测量值大于阈值时,估计影响待诊断对象的疾病不是前列腺癌而是良性前列腺疾病。

    METHOD FOR DISCRIMINATING BETWEEN PROSTATE CANCER AND A BENIGN PROSTATE DISEASE

    公开(公告)号:US20190310257A1

    公开(公告)日:2019-10-10

    申请号:US16446526

    申请日:2019-06-19

    Abstract: A method of analyzing diagnostic information for estimating which of a benign prostate disease and prostate cancer is affecting a subject to be diagnosed combines two methods of analyzing diagnostic information. The first method includes measuring a concentration of a mucin-1 (Tn-MUC1), reactive with a lectin that recognizes and binds to an N-acetyl-D-galactosamine->serine(threonine) residue, in a subject blood sample, comparing the measured value with a threshold value, and estimating that a disease affecting the subject is benign prostate disease when the measured value is greater than the threshold value. The second method includes measuring a concentration of a prostate-specific antigen (LacdiNAc-PSA), reactive with a lectin that recognizes and binds to an N-acetyl-D-galactosamine B1-4 N-acetylglucosamine residue in the blood sample, comparing the measured value with a threshold value, and estimating that the disease affecting the subject is prostate cancer when the measured value of LacdiNAc-PSA is greater than the threshold value.

    METHOD FOR ACQUIRING AUXILIARY INFORMATION

    公开(公告)号:US20210318317A1

    公开(公告)日:2021-10-14

    申请号:US17272848

    申请日:2019-09-25

    Abstract: The present invention provides a method for acquiring auxiliary information useful to assist a diagnosis or treatment of prostate cancer. The method for acquiring auxiliary information of the present invention is a method for acquiring auxiliary information to assist a diagnosis or treatment of prostate cancer, and includes a step (C) of dividing a concentration value of a prostate specific antigen having a β-N-acetylgalactosamine residue at a non-reducing terminal of a sugar chain, contained in a sample derived from a living body, by a volume value of prostate of the living body to calculate the concentration value of the GalNAc-PSA per prostate volume.

    METHOD FOR ANALYZING INFORMATION FOR DIAGNOSIS AND KIT THEREFOR
    7.
    发明申请
    METHOD FOR ANALYZING INFORMATION FOR DIAGNOSIS AND KIT THEREFOR 审中-公开
    用于分析诊断信息的方法及其套件

    公开(公告)号:US20160305960A1

    公开(公告)日:2016-10-20

    申请号:US15108286

    申请日:2013-12-27

    Abstract: A method of analyzing diagnostic information, the method including: measuring the concentration of all mucin-1s (total MUC1) in a blood sample originated from a subject to be diagnosed; comparing the measured value with a threshold value; and estimating that a disease affecting the subject to be diagnosed is not prostate cancer but a benign prostate disease when the measured value of the concentration of total MUC1 is greater than the threshold value.

    Abstract translation: 一种分析诊断信息的方法,所述方法包括:测量源自待诊断对象的血液样品中所有粘蛋白-1(总MUC1)的浓度; 将测量值与阈值进行比较; 并且当总MUC1的浓度的测量值大于阈值时,估计影响待诊断对象的疾病不是前列腺癌而是良性前列腺疾病。

    DIFFRACTED LIGHT REMOVAL SLIT AND OPTICAL SAMPLE DETECTION SYSTEM USING SAME

    公开(公告)号:US20200319104A1

    公开(公告)日:2020-10-08

    申请号:US16754231

    申请日:2018-09-20

    Abstract: The present invention is to provide a diffracted light removal slit and an optical sample detection system including the same, in which diffracted light of excitation light can be reliably removed without affecting reflected light of the excitation light in a sample detection device utilizing the reflected light of the excitation light. A diffracted light removal slit is provided between a light source unit and an excitation light reflector in an optical sample detection system that emits excitation light from the light source unit and also performs predetermined measurement using reflected light of the excitation light reflected at the excitation light reflector. The diffracted light removal slit includes: a main portion provided in a direction substantially perpendicular to an optical path of the excitation light; and a sidewall portion extending from an end portion of the main portion and inclined toward an upstream side in an optical path direction of the excitation light.

    MEASUREMENT DEVICE
    9.
    发明申请
    MEASUREMENT DEVICE 审中-公开

    公开(公告)号:US20200150035A1

    公开(公告)日:2020-05-14

    申请号:US16610707

    申请日:2018-04-20

    Abstract: A measurement device is for measuring a sample arranged on a thick film transparent medium. In the measurement device, a light projecting surface, a light receiving surface, the thick film transparent medium, and a sample are set so as to satisfy the following formula (α) for eliminating noise light reflected from a back surface of the thick film transparent medium: h

    METHOD FOR ESTIMATING PATHOLOGICAL TISSUE DIAGNOSIS RESULT (GLEASON SCORE) OF PROSTATE CANCER

    公开(公告)号:US20180348223A1

    公开(公告)日:2018-12-06

    申请号:US15761637

    申请日:2016-09-02

    CPC classification number: G01N33/57434 G01N33/53 G01N33/543

    Abstract: Provided is a method of obtaining an index value used for pathological tissue diagnosis of prostate cancer, which method has low invasiveness and can be performed at a low cost. The method is a method of estimating a Gleason score that represents the malignancy of prostate cancer, which method includes: measuring the content of a prostate-specific antigen having an N-acetylgalactosamine residue at a non-reducing terminal of a sugar chain in a sample; and estimating that the Gleason score is 7 or higher when the thus measured value is larger than a threshold value, or estimating that the Gleason score is 6 or lower when the measured value is smaller than a threshold value. The prostate-specific antigen is preferably quantified by a method including the step of binding a molecule having an affinity for β-N-acetylgalactosamine residue, such as Wisteria floribunda lectin, soybean agglutinin, Vicia Villosa lectin or an anti-β-N-acetylgalactosamine antibody, to the prostate-specific antigen.

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