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            <subfield code="a">10.1016/j.diabres.2019.02.017</subfield>
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            <subfield code="2">sideral</subfield>
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            <subfield code="a">eng</subfield>
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            <subfield code="a">Mavrogianni, C.</subfield>
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        <datafield tag="245" ind1=" " ind2=" ">
            <subfield code="a">Evaluation of the Finnish Diabetes Risk Score as a screening tool for undiagnosed type 2 diabetes and dysglycaemia among early middle-aged adults in a large-scale European cohort. The Feel4Diabetes-study</subfield>
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        <datafield tag="260" ind1=" " ind2=" ">
            <subfield code="c">2019</subfield>
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            <subfield code="f">Unrestricted</subfield>
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            <subfield code="a">Aim: To assess the diagnostic accuracy of the FINDRISC for undiagnosed type 2 diabetes mellitus (T2DM) and dysglycaemia (i.e. the presence of prediabetes or T2DM) among early middle-aged adults from vulnerable groups in a large-scale European cohort. Methods: Participants were recruited from low-socioeconomic areas in high-income countries (HICs) (Belgium-Finland) and in HICs under austerity measures (Greece-Spain) and from the overall population in low/middle-income countries (LMICs) (Bulgaria-Hungary). Study population comprised of 2116 parents of primary-school children from families identified at increased risk of T2DM, based on parental self-reported FINDRISC. Sensitivity (Se), specificity (Sp), area under the receiver operating characteristic curves (AUC-ROC) and the optimal cut-offs of FINDRISC that indicate an increased probability for undiagnosed T2DM or dysglycaemia were calculated. Results: The AUC-ROC for undiagnosed T2DM was 0.824 with optimal cut-off =14 (Se = 68%, Sp = 81.7%) for the total sample, 0.839 with optimal cut-off =15 (Se = 83.3%, Sp = 86.9%) for HICs, 0.794 with optimal cut-off =12 (Se = 83.3%, Sp = 61.1%) for HICs under austerity measures and 0.882 with optimal cut-off =14 (Se = 71.4%, Sp = 87.8%) for LMICs. The AUC-ROC for dysglycaemia was 0.663 with optimal cut-off =12 (Se = 58.3%, Sp = 65.7%) for the total sample, 0.656 with optimal cut-off =12 (Se = 54.5%, Sp = 64.8%) for HICs, 0.631 with optimal cut-off =12 (Se = 59.7%, Sp = 62.0%) for HICs under austerity measures and 0.735 with optimal cut-off =11 (Se = 72.7%, Sp = 70.2%) for LMICs. Conclusion: FINDRISC can be applied for screening primarily undiagnosed T2DM but also dysglycaemia among vulnerable groups across Europe, considering the use of different cut-offs for each subpopulation.</subfield>
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            <subfield code="9">info:eu-repo/grantAgreement/EC/H2020/643708/EU/Developing and implementing a community-based intervention to create a more supportive social and physical environment for lifestyle changes to prevent diabetes in vulnerable families across Europe/Feel4Diabetes</subfield>
            <subfield code="9">This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 643708-Feel4Diabetes</subfield>
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            <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
            <subfield code="a">All rights reserved</subfield>
            <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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        <datafield tag="590" ind1=" " ind2=" ">
            <subfield code="a">4.234</subfield>
            <subfield code="b">2019</subfield>
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            <subfield code="a">1.402</subfield>
            <subfield code="b">2019</subfield>
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            <subfield code="a">ENDOCRINOLOGY &amp; METABOLISM</subfield>
            <subfield code="b">34 / 143 = 0.238</subfield>
            <subfield code="c">2019</subfield>
            <subfield code="d">Q1</subfield>
            <subfield code="e">T1</subfield>
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            <subfield code="a">Endocrinology</subfield>
            <subfield code="c">2019</subfield>
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            <subfield code="a">Medicine (miscellaneous)</subfield>
            <subfield code="c">2019</subfield>
            <subfield code="d">Q1</subfield>
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            <subfield code="a">Internal Medicine</subfield>
            <subfield code="c">2019</subfield>
            <subfield code="d">Q1</subfield>
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        <datafield tag="593" ind1=" " ind2=" ">
            <subfield code="a">Endocrinology, Diabetes and Metabolism</subfield>
            <subfield code="c">2019</subfield>
            <subfield code="d">Q1</subfield>
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            <subfield code="a">Lambrinou, C.P.</subfield>
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            <subfield code="a">Androutsos, O.</subfield>
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            <subfield code="a">Lindström, J.</subfield>
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            <subfield code="a">Kivelä, J.</subfield>
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            <subfield code="a">Cardon, G.</subfield>
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            <subfield code="a">Huys, N.</subfield>
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            <subfield code="a">Tsochev, K.</subfield>
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            <subfield code="a">Iotova, V.</subfield>
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            <subfield code="a">Chakarova, N.</subfield>
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            <subfield code="a">Rurik, I.</subfield>
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            <subfield code="0">(orcid)0000-0003-0454-653X</subfield>
            <subfield code="a">Moreno, L.A.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="a">Liatis, S.</subfield>
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            <subfield code="a">Makrilakis, K.</subfield>
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            <subfield code="a">Manios, Y.</subfield>
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            <subfield code="1">1006</subfield>
            <subfield code="2">255</subfield>
            <subfield code="a">Universidad de Zaragoza</subfield>
            <subfield code="b">Dpto. Fisiatría y Enfermería</subfield>
            <subfield code="c">Área Enfermería</subfield>
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            <subfield code="g">150 (2019), 99-110</subfield>
            <subfield code="p">Diabetes res. clin. pract.</subfield>
            <subfield code="t">DIABETES RESEARCH AND CLINICAL PRACTICE</subfield>
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