dc.contributor.author |
Jolle, Anne |
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dc.contributor.author |
Midthjell, Kristian |
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dc.contributor.author |
Holmen, Jostein |
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dc.contributor.author |
Carlsen, Sven Magnus |
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dc.contributor.author |
Tuomilehto, Jaakko |
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dc.contributor.author |
Bjorngaard, Johan Håkon |
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dc.contributor.author |
Åsvold, Bjorn Olav |
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dc.date.accessioned |
2020-01-30T12:08:01Z |
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dc.date.available |
2020-01-30T12:08:01Z |
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dc.date.issued |
2019-10 |
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dc.identifier.citation |
Jolle , A , Midthjell , K , Holmen , J , Carlsen , S M , Tuomilehto , J , Bjorngaard , J H & Åsvold , B O 2019 , ' Validity of the FINDRISC as a prediction tool for diabetes in a contemporary Norwegian population : a 10-year follow-up of the HUNT study ' , BMJ Open Diabetes Research & Care , vol. 7 , no. 1 , 000769 . https://doi.org/10.1136/bmjdrc-2019-000769 |
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dc.identifier.other |
PURE: 131020910 |
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dc.identifier.other |
PURE UUID: 39c7c529-83eb-4b80-a3e6-ed14214a0e0c |
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dc.identifier.other |
WOS: 000506187100054 |
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dc.identifier.uri |
http://hdl.handle.net/10138/310671 |
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dc.description.abstract |
Objective The Finnish Diabetes Risk Score (FINDRISC) is a recommended tool for type 2 diabetes prediction. There is a lack of studies examining the performance of the current 0-26 point FINDRISC scale. We examined the validity of FINDRISC in a contemporary Norwegian risk environment. Research design and methods We followed 47 804 participants without known diabetes and aged >= 20 years in the HUNT3 survey (2006-2008) by linkage to information on glucose-lowering drug dispensing in the Norwegian Prescription Database (2004-2016). We estimated the C-statistic, sensitivity and specificity of FINDRISC as predictor of incident diabetes, as indicated by incident use of glucose-lowering drugs. We estimated the 10-year cumulative diabetes incidence by categories of FINDRISC. Results The C-statistic (95% CI) of FINDRISC in predicting future diabetes was 0.77 (0.76 to 0.78). FINDRISC >= 15 (the conventional cut-off value) had a sensitivity of 38% and a specificity of 90%. The 10-year cumulative diabetes incidence (95% CI) was 4.0% (3.8% to 4.2%) in the entire study population, 13.5% (12.5% to 14.5%) for people with FINDRISC >= 15 and 2.8% (2.6% to 3.0%) for people with FINDRISC = 15 had a positive predictive value of 13.5% and a negative predictive value of 97.2% for diabetes within the next 10 years. To approach a similar sensitivity as in the study in which FINDRISC was developed, we would have to lower the cut-off value for elevated FINDRISC to >= 11. This would yield a sensitivity of 73%, specificity of 67%, positive predictive value of 7.7% and negative predictive value of 98.5%. Conclusions The validity of FINDRISC and the risk of diabetes among people with FINDRISC >= 15 is substantially lower in the contemporary Norwegian population than assumed in official guidelines. To identify similar to 3/4 of those developing diabetes within the next 10 years, we would have to lower the threshold for elevated FINDRISC to >= 11, which would label similar to 1/3 of the entire adult population as having an elevated FINDRISC necessitating a glycemia assessment. |
en |
dc.format.extent |
9 |
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dc.language.iso |
eng |
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dc.relation.ispartof |
BMJ Open Diabetes Research & Care |
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dc.rights |
cc_by |
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dc.rights.uri |
info:eu-repo/semantics/openAccess |
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dc.subject |
IMPAIRED GLUCOSE-TOLERANCE |
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dc.subject |
RISK SCORE |
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dc.subject |
LIFE-STYLE |
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dc.subject |
PREVENTION |
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dc.subject |
MELLITUS |
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dc.subject |
QUESTIONNAIRE |
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dc.subject |
PREVALENCE |
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dc.subject |
DISEASE |
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dc.subject |
OBESITY |
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dc.subject |
TRENDS |
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dc.subject |
3121 General medicine, internal medicine and other clinical medicine |
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dc.subject |
3142 Public health care science, environmental and occupational health |
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dc.title |
Validity of the FINDRISC as a prediction tool for diabetes in a contemporary Norwegian population : a 10-year follow-up of the HUNT study |
en |
dc.type |
Article |
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dc.contributor.organization |
Clinicum |
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dc.contributor.organization |
Department of Public Health |
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dc.contributor.organization |
University of Helsinki |
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dc.description.reviewstatus |
Peer reviewed |
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dc.relation.doi |
https://doi.org/10.1136/bmjdrc-2019-000769 |
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dc.relation.issn |
2052-4897 |
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dc.rights.accesslevel |
openAccess |
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dc.type.version |
publishedVersion |
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