2018
DOI: 10.1016/j.acap.2018.02.011
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Calculating a Continuous Metabolic Syndrome Score Using Nationally Representative Reference Values

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Cited by 16 publications
(13 citation statements)
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“…Sedangkan untuk penilaian menggunakan skor sindrom metabolik adalah penilaian semua komponen sindrom metabolik menggunakan perhitungan z-score. Perhitungan skor sindrom metabolik (SSM) dilakukan untuk semua komponen sindrom metabolik (lingkar perut, tekanan darah, trigliserida, HDL, dan glukosa darah puasa) dengan menggunakan z-score yang mengacu pada penelitian sebelumnya 15 .…”
Section: Metodeunclassified
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“…Sedangkan untuk penilaian menggunakan skor sindrom metabolik adalah penilaian semua komponen sindrom metabolik menggunakan perhitungan z-score. Perhitungan skor sindrom metabolik (SSM) dilakukan untuk semua komponen sindrom metabolik (lingkar perut, tekanan darah, trigliserida, HDL, dan glukosa darah puasa) dengan menggunakan z-score yang mengacu pada penelitian sebelumnya 15 .…”
Section: Metodeunclassified
“…Skor sindrom metabolik (SSM) merupakan total Z-score semua komponen sindrom metabolik. Sistem skoring tekanan darah menggunakan : 15,6 .…”
Section: Metodeunclassified
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“…This statement highlighted the need to establish a full definition of MS that includes continuous variables in a multivariate scoring system [ 9 ]. Existing research relating to scoring a consistent MS measure has involved the use of various tools, including percentile ranking [ 10 ], Z-scores [ 11 , 12 , 13 , 14 ], principal component analysis [ 15 , 16 ], and confirmatory factor analysis [ 17 , 18 , 19 ].…”
Section: Introductionmentioning
confidence: 99%
“…However, the authors have derived cMetS score from the MS component z-score of their cohort of patients and hence, the risk score and cut-offs may not be applicable to other populations. One way to overcome this limitation would be to use ethnic nationally representative (rather than sample specific) data for z-scores of MS risk components [14]. Secondly, the cMetS risk score calculation is based on the assumption that all components of MS contribute equally to disease risk; however, it is known that MS components may influence risk differentially depending on gender and ethnicity [15].…”
mentioning
confidence: 99%