The present invention provides a biomarker composition for detecting
diabetic retinopathy comprising at least one
protein selected from the group consisting of proteins as set forth in SEQ ID NOS: 1 to 169. And also, the present invention provides a kit for diagnosing
diabetic retinopathy, comprising a molecule specifically binding to at least one
protein selected from the group consisting of proteins as set forth in SEQ ID NOS: 1 to 169. It has been newly found that 105 proteins as set forth in SEQ ID NOS: 1 to 105 are significantly over-expressed in the
vitreous humors obtained from PDR patients, while 64 proteins as set forth in SEQ ID NOS: 106 to 169 are significantly over-expressed in those obtained from
normal people. Therefore, the proteins can be used for biomarker capable of detecting
diabetic retinopathy. The biomarker can provide fundamental information in researching vitreoretinal disorders, such as diabetic
retinopathy. Especially, the newly found proteins may be applied to a kit for diagnosing diabetic
retinopathy with a molecule specifically binding thereto, e.g., a
monoclonal antibody. And also, it has been newly found that the levels of thyroxine-binding
globulin precursor (TBG) in both vitreous and
plasma of PDR and NPDR states and in
plasma of
diabetes mellitus state, are outstandingly higher than in non-diabetic control (MH or
normal control). Therefore, TBG may be applied to a
diabetes mellitus biomarker, and a kit for diagnosing
diabetes mellitus with a molecule specifically binding thereto.