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dc.contributor.authorChang, Alex R.
dc.contributor.authorGrams, Morgan E.
dc.contributor.authorBallew, Shoshana H.
dc.contributor.authorBilo, Henk
dc.contributor.authorCorrea, Adolfo
dc.contributor.authorEvans, Marie
dc.contributor.authorGutierrez, Orlando M.
dc.contributor.authorHosseinpanah, Farhad
dc.contributor.authorIseki, Kunitoshi
dc.contributor.authorKenealy, Timothy
dc.contributor.authorKlein, Barbara
dc.contributor.authorKronenberg, Florian
dc.contributor.authorLee, Brian J.
dc.contributor.authorLi, Yuanying
dc.contributor.authorMiura, Katsuyuki
dc.contributor.authorNavaneethan, Sankar D.
dc.contributor.authorRoderick, Paul J.
dc.contributor.authorValdivielso, Jose M.
dc.contributor.authorVisseren, Frank L.J.
dc.contributor.authorZhang, Luxia
dc.contributor.authorGansevoort, Ron T.
dc.contributor.authorHallan, Stein
dc.contributor.authorLevey, Andrew S.
dc.contributor.authorMatsushita, Kunihiro
dc.contributor.authorShalev, Varda
dc.contributor.authorWoodward, Mark
dc.date.accessioned2020-01-31T14:34:59Z
dc.date.available2020-01-31T14:34:59Z
dc.date.created2019-05-06T13:20:30Z
dc.date.issued2019
dc.identifier.citationBMJ. British Medical Journal. 2019, 364:k5301 1-11.nb_NO
dc.identifier.issn1756-1833
dc.identifier.urihttp://hdl.handle.net/11250/2639127
dc.description.abstractObjective To evaluate the associations between adiposity measures (body mass index, waist circumference, and waist-to-height ratio) with decline in glomerular filtration rate (GFR) and with all cause mortality.Design Individual participant data meta-analysis. Setting Cohorts from 40 countries with data collected between 1970 and 2017. Participants Adults in 39 general population cohorts (n=5 459 014), of which 21 (n=594 496) had data on waist circumference; six cohorts with high cardiovascular risk (n=84 417); and 18 cohorts with chronic kidney disease (n=91 607). Main outcome measures GFR decline (estimated GFR decline ≥40%, initiation of kidney replacement therapy or estimated GFR <10 mL/min/1.73 m2) and all cause mortality. Results Over a mean follow-up of eight years, 246 607 (5.6%) individuals in the general population cohorts had GFR decline (18 118 (0.4%) end stage kidney disease events) and 782 329 (14.7%) died. Adjusting for age, sex, race, and current smoking, the hazard ratios for GFR decline comparing body mass indices 30, 35, and 40 with body mass index 25 were 1.18 (95% confidence interval 1.09 to 1.27), 1.69 (1.51 to 1.89), and 2.02 (1.80 to 2.27), respectively. Results were similar in all subgroups of estimated GFR. Associations weakened after adjustment for additional comorbidities, with respective hazard ratios of 1.03 (0.95 to 1.11), 1.28 (1.14 to 1.44), and 1.46 (1.28 to 1.67). The association between body mass index and death was J shaped, with the lowest risk at body mass index of 25. In the cohorts with high cardiovascular risk and chronic kidney disease (mean follow-up of six and four years, respectively), risk associations between higher body mass index and GFR decline were weaker than in the general population, and the association between body mass index and death was also J shaped, with the lowest risk between body mass index 25 and 30. In all cohort types, associations between higher waist circumference and higher waist-to-height ratio with GFR decline were similar to that of body mass index; however, increased risk of death was not associated with lower waist circumference or waist-to-height ratio, as was seen with body mass index. Conclusions Elevated body mass index, waist circumference, and waist-to-height ratio are independent risk factors for GFR decline and death in individuals who have normal or reduced levels of estimated GFR.nb_NO
dc.language.isoengnb_NO
dc.publisherBMJ Publishing Groupnb_NO
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleAdiposity and risk of decline in glomerular filtration rate: Meta-analysis of individual participant data in a global consortiumnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber1-11nb_NO
dc.source.volume364:k5301nb_NO
dc.source.journalBMJ. British Medical Journalnb_NO
dc.identifier.doi10.1136/bmj.k5301
dc.identifier.cristin1695792
dc.description.localcode“© Authors 2019 This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/nb_NO
cristin.unitcode194,65,15,0
cristin.unitcode1920,15,0,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.unitnameMedisinsk klinikk
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal