Implementasi Permendagri Nomor 15 Tahun 2008 Tentang Pengarusutamaan Gender pada Jenjang Pendidikan Dasar di Kota Malang

Windra Rizkiyana1 & Wahyu Widodo21 Mahasiswa & 2Staf Pengajar Program Pasca Sarjana, Universitas Muhammadiyah MalangAlamat Korespondensi : Jl. Bandung No.1 MalangEmail: [email protected] education, still found a gender gap regarding both aspects of the expansion of educationalaccess and equity, quality and relevance of education and management. The purpose of this studywere: (1) describe the substance Permendagri No. 15 of 2008 on Gender Mainstreaming; (2) describethe implementation of Permendagri No. 15 of 2008 on Gender Mainstreaming in Elementary Educationin Malang; (3) Analyze the obstacles encountered in implementation Permendagri No. 15 of 2008 onGender Mainstreaming in Elementary Education in Malang. This type of research is a descriptiveanalysis, using a qualitative approach that is supported by a quantitative approach. And the techniquesof data acolllection through by interviews and the documents. Study sites are in Malang EducationDepartment. Analysis of the data used is descriptive analysis of qualitative and quantitative theorysupported by Gender Analysis Pathway (GAP), Content Analysis and Root Analysis. Implementationof Permendagri No 15 of 2008 about gender mainstreaming in basic education levels in Malang hasnot been optimal. These proved by the remains of gender inequality or gap that occurs in all threeaspects, that access and educational equity, quality and relevance of education, as well as accountabilityand governance. Constraints encountered in implementation Permendagri No. 15 of 2008 on gendermainstreaming in elementary education in Malang include: (a) Outreach activities that are specificallyabout the PUG in primary education has not been done; (b) The budget is not specifically formainstreaming activities; (c) newly formed working group PUG.Key word: Permendagri No. 15 of 2008, gender mainstreaming, basic educatio

table_3.doc

Objective<p>The aim of this study was to examine the fluctuations in CD4⁺ T cells, CD8⁺ T cells, and natural CD4⁺CD25⁺FoxP3⁺T-regulatory (Treg) cells following an oral glucose tolerance test (OGTT) in participants with and those without type 2 diabetes (T2DM).</p>Methods<p>19 Japanese participants with T2DM (DM group) and 21 participants without diabetes (non-DM group) were recruited and underwent a 75-g OGTT. The cell numbers of leukocytes, lymphocytes, and the T cell compartment, such as CD4⁺, CD8⁺, and Treg, were calculated for blood samples obtained after an overnight 12 h fast and during a 75-g OGTT at 60 and 120 min.</p>Results<p>Before glucose loading, no differences in the cell numbers of leukocytes, lymphocytes, CD4⁺, CD8⁺, and Treg were observed between the DM group and the non-DM group. The proportion of CD8⁺ was significantly reduced, whereas the proportion of CD4⁺ was significantly increased, after 120 min of glucose loading in both groups. The proportion of Treg was not affected. Furthermore, a significant positive correlation was observed between the AUC_{0–120 min} of CD8⁺ and the change in the free fatty acid level following the OGTT (ρ = 0.39, P < 0.05), but not that of glucose or insulin.</p>Conclusion<p>The proportion of CD4⁺ T cells was increased and that of CD8⁺ T cells was reduced after glucose loading in both subjects with and without diabetes. These findings suggest that glucose loading dynamically affects the balance of the circulating T lymphocyte subset, regardless of glucose tolerance.</p

table_12.doc

Objective<p>The aim of this study was to examine the fluctuations in CD4⁺ T cells, CD8⁺ T cells, and natural CD4⁺CD25⁺FoxP3⁺T-regulatory (Treg) cells following an oral glucose tolerance test (OGTT) in participants with and those without type 2 diabetes (T2DM).</p>Methods<p>19 Japanese participants with T2DM (DM group) and 21 participants without diabetes (non-DM group) were recruited and underwent a 75-g OGTT. The cell numbers of leukocytes, lymphocytes, and the T cell compartment, such as CD4⁺, CD8⁺, and Treg, were calculated for blood samples obtained after an overnight 12 h fast and during a 75-g OGTT at 60 and 120 min.</p>Results<p>Before glucose loading, no differences in the cell numbers of leukocytes, lymphocytes, CD4⁺, CD8⁺, and Treg were observed between the DM group and the non-DM group. The proportion of CD8⁺ was significantly reduced, whereas the proportion of CD4⁺ was significantly increased, after 120 min of glucose loading in both groups. The proportion of Treg was not affected. Furthermore, a significant positive correlation was observed between the AUC_{0–120 min} of CD8⁺ and the change in the free fatty acid level following the OGTT (ρ = 0.39, P < 0.05), but not that of glucose or insulin.</p>Conclusion<p>The proportion of CD4⁺ T cells was increased and that of CD8⁺ T cells was reduced after glucose loading in both subjects with and without diabetes. These findings suggest that glucose loading dynamically affects the balance of the circulating T lymphocyte subset, regardless of glucose tolerance.</p

Comparison of individual changes of FMD before and after administration of liraglutide and glargine.

<p>White circles are mean ± SD.</p

table_1.doc

Objective<p>The aim of this study was to examine the fluctuations in CD4⁺ T cells, CD8⁺ T cells, and natural CD4⁺CD25⁺FoxP3⁺T-regulatory (Treg) cells following an oral glucose tolerance test (OGTT) in participants with and those without type 2 diabetes (T2DM).</p>Methods<p>19 Japanese participants with T2DM (DM group) and 21 participants without diabetes (non-DM group) were recruited and underwent a 75-g OGTT. The cell numbers of leukocytes, lymphocytes, and the T cell compartment, such as CD4⁺, CD8⁺, and Treg, were calculated for blood samples obtained after an overnight 12 h fast and during a 75-g OGTT at 60 and 120 min.</p>Results<p>Before glucose loading, no differences in the cell numbers of leukocytes, lymphocytes, CD4⁺, CD8⁺, and Treg were observed between the DM group and the non-DM group. The proportion of CD8⁺ was significantly reduced, whereas the proportion of CD4⁺ was significantly increased, after 120 min of glucose loading in both groups. The proportion of Treg was not affected. Furthermore, a significant positive correlation was observed between the AUC_{0–120 min} of CD8⁺ and the change in the free fatty acid level following the OGTT (ρ = 0.39, P < 0.05), but not that of glucose or insulin.</p>Conclusion<p>The proportion of CD4⁺ T cells was increased and that of CD8⁺ T cells was reduced after glucose loading in both subjects with and without diabetes. These findings suggest that glucose loading dynamically affects the balance of the circulating T lymphocyte subset, regardless of glucose tolerance.</p

table_15.doc

Objective<p>The aim of this study was to examine the fluctuations in CD4⁺ T cells, CD8⁺ T cells, and natural CD4⁺CD25⁺FoxP3⁺T-regulatory (Treg) cells following an oral glucose tolerance test (OGTT) in participants with and those without type 2 diabetes (T2DM).</p>Methods<p>19 Japanese participants with T2DM (DM group) and 21 participants without diabetes (non-DM group) were recruited and underwent a 75-g OGTT. The cell numbers of leukocytes, lymphocytes, and the T cell compartment, such as CD4⁺, CD8⁺, and Treg, were calculated for blood samples obtained after an overnight 12 h fast and during a 75-g OGTT at 60 and 120 min.</p>Results<p>Before glucose loading, no differences in the cell numbers of leukocytes, lymphocytes, CD4⁺, CD8⁺, and Treg were observed between the DM group and the non-DM group. The proportion of CD8⁺ was significantly reduced, whereas the proportion of CD4⁺ was significantly increased, after 120 min of glucose loading in both groups. The proportion of Treg was not affected. Furthermore, a significant positive correlation was observed between the AUC_{0–120 min} of CD8⁺ and the change in the free fatty acid level following the OGTT (ρ = 0.39, P < 0.05), but not that of glucose or insulin.</p>Conclusion<p>The proportion of CD4⁺ T cells was increased and that of CD8⁺ T cells was reduced after glucose loading in both subjects with and without diabetes. These findings suggest that glucose loading dynamically affects the balance of the circulating T lymphocyte subset, regardless of glucose tolerance.</p

table_4.doc

Objective<p>The aim of this study was to examine the fluctuations in CD4⁺ T cells, CD8⁺ T cells, and natural CD4⁺CD25⁺FoxP3⁺T-regulatory (Treg) cells following an oral glucose tolerance test (OGTT) in participants with and those without type 2 diabetes (T2DM).</p>Methods<p>19 Japanese participants with T2DM (DM group) and 21 participants without diabetes (non-DM group) were recruited and underwent a 75-g OGTT. The cell numbers of leukocytes, lymphocytes, and the T cell compartment, such as CD4⁺, CD8⁺, and Treg, were calculated for blood samples obtained after an overnight 12 h fast and during a 75-g OGTT at 60 and 120 min.</p>Results<p>Before glucose loading, no differences in the cell numbers of leukocytes, lymphocytes, CD4⁺, CD8⁺, and Treg were observed between the DM group and the non-DM group. The proportion of CD8⁺ was significantly reduced, whereas the proportion of CD4⁺ was significantly increased, after 120 min of glucose loading in both groups. The proportion of Treg was not affected. Furthermore, a significant positive correlation was observed between the AUC_{0–120 min} of CD8⁺ and the change in the free fatty acid level following the OGTT (ρ = 0.39, P < 0.05), but not that of glucose or insulin.</p>Conclusion<p>The proportion of CD4⁺ T cells was increased and that of CD8⁺ T cells was reduced after glucose loading in both subjects with and without diabetes. These findings suggest that glucose loading dynamically affects the balance of the circulating T lymphocyte subset, regardless of glucose tolerance.</p

table_10.doc

Objective<p>The aim of this study was to examine the fluctuations in CD4⁺ T cells, CD8⁺ T cells, and natural CD4⁺CD25⁺FoxP3⁺T-regulatory (Treg) cells following an oral glucose tolerance test (OGTT) in participants with and those without type 2 diabetes (T2DM).</p>Methods<p>19 Japanese participants with T2DM (DM group) and 21 participants without diabetes (non-DM group) were recruited and underwent a 75-g OGTT. The cell numbers of leukocytes, lymphocytes, and the T cell compartment, such as CD4⁺, CD8⁺, and Treg, were calculated for blood samples obtained after an overnight 12 h fast and during a 75-g OGTT at 60 and 120 min.</p>Results<p>Before glucose loading, no differences in the cell numbers of leukocytes, lymphocytes, CD4⁺, CD8⁺, and Treg were observed between the DM group and the non-DM group. The proportion of CD8⁺ was significantly reduced, whereas the proportion of CD4⁺ was significantly increased, after 120 min of glucose loading in both groups. The proportion of Treg was not affected. Furthermore, a significant positive correlation was observed between the AUC_{0–120 min} of CD8⁺ and the change in the free fatty acid level following the OGTT (ρ = 0.39, P < 0.05), but not that of glucose or insulin.</p>Conclusion<p>The proportion of CD4⁺ T cells was increased and that of CD8⁺ T cells was reduced after glucose loading in both subjects with and without diabetes. These findings suggest that glucose loading dynamically affects the balance of the circulating T lymphocyte subset, regardless of glucose tolerance.</p

table_6.doc

Objective<p>The aim of this study was to examine the fluctuations in CD4⁺ T cells, CD8⁺ T cells, and natural CD4⁺CD25⁺FoxP3⁺T-regulatory (Treg) cells following an oral glucose tolerance test (OGTT) in participants with and those without type 2 diabetes (T2DM).</p>Methods<p>19 Japanese participants with T2DM (DM group) and 21 participants without diabetes (non-DM group) were recruited and underwent a 75-g OGTT. The cell numbers of leukocytes, lymphocytes, and the T cell compartment, such as CD4⁺, CD8⁺, and Treg, were calculated for blood samples obtained after an overnight 12 h fast and during a 75-g OGTT at 60 and 120 min.</p>Results<p>Before glucose loading, no differences in the cell numbers of leukocytes, lymphocytes, CD4⁺, CD8⁺, and Treg were observed between the DM group and the non-DM group. The proportion of CD8⁺ was significantly reduced, whereas the proportion of CD4⁺ was significantly increased, after 120 min of glucose loading in both groups. The proportion of Treg was not affected. Furthermore, a significant positive correlation was observed between the AUC_{0–120 min} of CD8⁺ and the change in the free fatty acid level following the OGTT (ρ = 0.39, P < 0.05), but not that of glucose or insulin.</p>Conclusion<p>The proportion of CD4⁺ T cells was increased and that of CD8⁺ T cells was reduced after glucose loading in both subjects with and without diabetes. These findings suggest that glucose loading dynamically affects the balance of the circulating T lymphocyte subset, regardless of glucose tolerance.</p

table_5.doc

Objective<p>The aim of this study was to examine the fluctuations in CD4⁺ T cells, CD8⁺ T cells, and natural CD4⁺CD25⁺FoxP3⁺T-regulatory (Treg) cells following an oral glucose tolerance test (OGTT) in participants with and those without type 2 diabetes (T2DM).</p>Methods<p>19 Japanese participants with T2DM (DM group) and 21 participants without diabetes (non-DM group) were recruited and underwent a 75-g OGTT. The cell numbers of leukocytes, lymphocytes, and the T cell compartment, such as CD4⁺, CD8⁺, and Treg, were calculated for blood samples obtained after an overnight 12 h fast and during a 75-g OGTT at 60 and 120 min.</p>Results<p>Before glucose loading, no differences in the cell numbers of leukocytes, lymphocytes, CD4⁺, CD8⁺, and Treg were observed between the DM group and the non-DM group. The proportion of CD8⁺ was significantly reduced, whereas the proportion of CD4⁺ was significantly increased, after 120 min of glucose loading in both groups. The proportion of Treg was not affected. Furthermore, a significant positive correlation was observed between the AUC_{0–120 min} of CD8⁺ and the change in the free fatty acid level following the OGTT (ρ = 0.39, P < 0.05), but not that of glucose or insulin.</p>Conclusion<p>The proportion of CD4⁺ T cells was increased and that of CD8⁺ T cells was reduced after glucose loading in both subjects with and without diabetes. These findings suggest that glucose loading dynamically affects the balance of the circulating T lymphocyte subset, regardless of glucose tolerance.</p