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Impact of Parental Socioeconomic Status on Excess Mortality in a Population-Based Cohort of Subjects With Childhood-Onset Type 1 Diabetes
Umeå universitet, Medicinska fakulteten, Institutionen för klinisk vetenskap, Pediatrik.
Umeå universitet, Medicinska fakulteten, Institutionen för folkhälsa och klinisk medicin, Medicin.
Umeå universitet, Medicinska fakulteten, Institutionen för klinisk vetenskap, Pediatrik.
Umeå universitet, Samhällsvetenskapliga fakulteten, Handelshögskolan vid Umeå universitet, Statistik.
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2015 (Engelska)Ingår i: Diabetes Care, ISSN 0149-5992, E-ISSN 1935-5548, Vol. 38, nr 5, s. 827-832Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

OBJECTIVE: The aim of this study was to analyze the possible impact of parental and individual socioeconomic status (SES) on all-cause mortality in a population-based cohort of patients with childhood-onset type 1 diabetes.

RESEARCH DESIGN AND METHODS: Subjects recorded in the Swedish Childhood Diabetes Registry (SCDR) from 1 January 1978 to 31 December 2008 were included (n =14,647). The SCDR was linked to the Swedish Cause of Death Registry (CDR) and the Longitudinal Integration Database for Health Insurance and Labour Market Studies (LISA).

RESULTS: At a mean follow-up of 23.9 years (maximum 46.5 years), 238 deaths occurred in a total of 349,762 person-years at risk. In crude analyses, low maternal education predicted mortality for male patients only (P = 0.046), whereas parental income support predicted mortality in both sexes (P < 0.001 for both). In Cox models stratified by age-at-death group and adjusted for age at onset and sex, parental income support predicted mortality among young adults (≥18 years of age) but not for children. Including the adult patient’s own SES in a Cox model showed that individual income support to the patient predicted mortality occurring at ≥24 years of age when adjusting for age at onset, sex, and parental SES.

CONCLUSIONS: Exposure to low SES, mirrored by the need for income support, increases mortality risk in patients with childhood-onset type 1 diabetes who died after the age of 18 years.

Ort, förlag, år, upplaga, sidor
2015. Vol. 38, nr 5, s. 827-832
Nationell ämneskategori
Klinisk medicin Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi
Identifikatorer
URN: urn:nbn:se:umu:diva-101362DOI: 10.2337/dc14-1522ISI: 000353505600023Scopus ID: 2-s2.0-84958591961OAI: oai:DiVA.org:umu-101362DiVA, id: diva2:798937
Forskningsfinansiär
Vetenskapsrådet, 07531Tillgänglig från: 2015-03-27 Skapad: 2015-03-27 Senast uppdaterad: 2023-03-24Bibliografiskt granskad

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Berhan, YonasEliasson, MatsMöllsten, AnnaWaernbaum, IngeborgDahlquist, Gisela

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Berhan, YonasEliasson, MatsMöllsten, AnnaWaernbaum, IngeborgDahlquist, Gisela
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PediatrikMedicinStatistik
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Diabetes Care
Klinisk medicinFolkhälsovetenskap, global hälsa, socialmedicin och epidemiologi

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