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Glypican-4 levels in different biofluids and correlation with clinical parameters. ( A – C ) <t>GPC-4</t> levels of PD patients and CTR in CSF ( A ), serum ( B ) and tear fluid ( C ). Mann–Whitney-U test, n.s., not significant. ( D – F ) Correlation analysis of GPC-4 levels and age of PD patients in CSF ( D ), serum ( E ) and tear fluid ( F ). ( G – I ) Correlation analysis of GPC-4 levels and MoCA score of PD patients in CSF ( G ), serum ( H ) and tear fluid ( I ). GPC-4, Glypican-4; PD, Parkinson’s disease; CTR, control subjects with similar age range; CSF, cerebrospinal fluid; TF, tear fluid; MoCA, Montreal cognitive assessment. r, Spearman’s Rho; ns, not significant. p < 0.05 was considered significant.
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Glypican-4 levels in different biofluids and correlation with clinical parameters. ( A – C ) <t>GPC-4</t> levels of PD patients and CTR in CSF ( A ), serum ( B ) and tear fluid ( C ). Mann–Whitney-U test, n.s., not significant. ( D – F ) Correlation analysis of GPC-4 levels and age of PD patients in CSF ( D ), serum ( E ) and tear fluid ( F ). ( G – I ) Correlation analysis of GPC-4 levels and MoCA score of PD patients in CSF ( G ), serum ( H ) and tear fluid ( I ). GPC-4, Glypican-4; PD, Parkinson’s disease; CTR, control subjects with similar age range; CSF, cerebrospinal fluid; TF, tear fluid; MoCA, Montreal cognitive assessment. r, Spearman’s Rho; ns, not significant. p < 0.05 was considered significant.
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Glypican-4 levels in different biofluids and correlation with clinical parameters. ( A – C ) <t>GPC-4</t> levels of PD patients and CTR in CSF ( A ), serum ( B ) and tear fluid ( C ). Mann–Whitney-U test, n.s., not significant. ( D – F ) Correlation analysis of GPC-4 levels and age of PD patients in CSF ( D ), serum ( E ) and tear fluid ( F ). ( G – I ) Correlation analysis of GPC-4 levels and MoCA score of PD patients in CSF ( G ), serum ( H ) and tear fluid ( I ). GPC-4, Glypican-4; PD, Parkinson’s disease; CTR, control subjects with similar age range; CSF, cerebrospinal fluid; TF, tear fluid; MoCA, Montreal cognitive assessment. r, Spearman’s Rho; ns, not significant. p < 0.05 was considered significant.
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Glypican-4 levels in different biofluids and correlation with clinical parameters. ( A – C ) <t>GPC-4</t> levels of PD patients and CTR in CSF ( A ), serum ( B ) and tear fluid ( C ). Mann–Whitney-U test, n.s., not significant. ( D – F ) Correlation analysis of GPC-4 levels and age of PD patients in CSF ( D ), serum ( E ) and tear fluid ( F ). ( G – I ) Correlation analysis of GPC-4 levels and MoCA score of PD patients in CSF ( G ), serum ( H ) and tear fluid ( I ). GPC-4, Glypican-4; PD, Parkinson’s disease; CTR, control subjects with similar age range; CSF, cerebrospinal fluid; TF, tear fluid; MoCA, Montreal cognitive assessment. r, Spearman’s Rho; ns, not significant. p < 0.05 was considered significant.
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Glypican-4 levels in different biofluids and correlation with clinical parameters. ( A – C ) <t>GPC-4</t> levels of PD patients and CTR in CSF ( A ), serum ( B ) and tear fluid ( C ). Mann–Whitney-U test, n.s., not significant. ( D – F ) Correlation analysis of GPC-4 levels and age of PD patients in CSF ( D ), serum ( E ) and tear fluid ( F ). ( G – I ) Correlation analysis of GPC-4 levels and MoCA score of PD patients in CSF ( G ), serum ( H ) and tear fluid ( I ). GPC-4, Glypican-4; PD, Parkinson’s disease; CTR, control subjects with similar age range; CSF, cerebrospinal fluid; TF, tear fluid; MoCA, Montreal cognitive assessment. r, Spearman’s Rho; ns, not significant. p < 0.05 was considered significant.
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Glypican-4 levels in different biofluids and correlation with clinical parameters. ( A – C ) GPC-4 levels of PD patients and CTR in CSF ( A ), serum ( B ) and tear fluid ( C ). Mann–Whitney-U test, n.s., not significant. ( D – F ) Correlation analysis of GPC-4 levels and age of PD patients in CSF ( D ), serum ( E ) and tear fluid ( F ). ( G – I ) Correlation analysis of GPC-4 levels and MoCA score of PD patients in CSF ( G ), serum ( H ) and tear fluid ( I ). GPC-4, Glypican-4; PD, Parkinson’s disease; CTR, control subjects with similar age range; CSF, cerebrospinal fluid; TF, tear fluid; MoCA, Montreal cognitive assessment. r, Spearman’s Rho; ns, not significant. p < 0.05 was considered significant.

Journal: Scientific Reports

Article Title: Glypican-4 serum levels are associated with cognitive dysfunction and vascular risk factors in Parkinson’s disease

doi: 10.1038/s41598-024-54800-8

Figure Lengend Snippet: Glypican-4 levels in different biofluids and correlation with clinical parameters. ( A – C ) GPC-4 levels of PD patients and CTR in CSF ( A ), serum ( B ) and tear fluid ( C ). Mann–Whitney-U test, n.s., not significant. ( D – F ) Correlation analysis of GPC-4 levels and age of PD patients in CSF ( D ), serum ( E ) and tear fluid ( F ). ( G – I ) Correlation analysis of GPC-4 levels and MoCA score of PD patients in CSF ( G ), serum ( H ) and tear fluid ( I ). GPC-4, Glypican-4; PD, Parkinson’s disease; CTR, control subjects with similar age range; CSF, cerebrospinal fluid; TF, tear fluid; MoCA, Montreal cognitive assessment. r, Spearman’s Rho; ns, not significant. p < 0.05 was considered significant.

Article Snippet: To assess GPC-4 levels in CSF and blood serum of PD patients and CTR we used a commercial ELISA assay with highly specific human GPC-4 antibodies (#SEA998Hu, Cloud-Clone Corp., Katy, TX).

Techniques: MANN-WHITNEY

Glypican-4 serum levels in PD patients stratified for vascular risk factors (coronary artery disease, hyperlipidemia, diabetes, stroke, microangiopathy and hypertension). Stratified groups were compared applying a linear model adjusted for age and sex. p < 0.05 was considered significant. PD, Parkinson’s disease; GPC-4, glypican-4; ns, not significant, * p = 0.026.

Journal: Scientific Reports

Article Title: Glypican-4 serum levels are associated with cognitive dysfunction and vascular risk factors in Parkinson’s disease

doi: 10.1038/s41598-024-54800-8

Figure Lengend Snippet: Glypican-4 serum levels in PD patients stratified for vascular risk factors (coronary artery disease, hyperlipidemia, diabetes, stroke, microangiopathy and hypertension). Stratified groups were compared applying a linear model adjusted for age and sex. p < 0.05 was considered significant. PD, Parkinson’s disease; GPC-4, glypican-4; ns, not significant, * p = 0.026.

Article Snippet: To assess GPC-4 levels in CSF and blood serum of PD patients and CTR we used a commercial ELISA assay with highly specific human GPC-4 antibodies (#SEA998Hu, Cloud-Clone Corp., Katy, TX).

Techniques: