Risk Factors in Late Adolescence for Young-Onset Dementia in Men A Nationwide Cohort Study

被引:72
作者
Nordstrom, Peter [1 ]
Nordstrom, Anna [2 ]
Eriksson, Marie [3 ]
Wahlund, Lars-Olof [4 ]
Gustafson, Yngve [1 ]
机构
[1] Umea Univ, Dept Community Med & Rehabil, Geriatr Med Sect, S-90187 Umea, Sweden
[2] Umea Univ, Dept Surg & Perioperat Sci, Sect Sports Med, S-90187 Umea, Sweden
[3] Umea Univ, Dept Stat, Sch Business & Econ, S-90187 Umea, Sweden
[4] Karolinska Inst, Dept Neurobiol Care Sci & Soc, Div Clin Geriatr, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
FAMILIAL ALZHEIMERS-DISEASE; ALCOHOL-RELATED DEMENTIA; FRONTOTEMPORAL DEMENTIA; LATE-LIFE; GENE; PREVALENCE; MUTATIONS; MISSENSE; VALIDATION; DIAGNOSIS;
D O I
10.1001/jamainternmed.2013.9079
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCE Young-onset dementia (YOD), that is, dementia diagnosed before 65 years of age, has been related to genetic mutations in affected families. The identification of other risk factors could improve the understanding of this heterogeneous group of syndromes. OBJECTIVE To evaluate risk factors in late adolescence for the development of YOD later in life. DESIGN We identified the study cohort from the Swedish Military Service Conscription Register from January 1, 1969, through December 31, 1979. Potential risk factors, such as cognitive function and different physical characteristics, were assessed at conscription. We collected other risk factors, including dementia in parents, through national register linkage. PARTICIPANTS All Swedish men conscripted for mandatory military service (n = 488 484) with a mean age of 18 years. SETTING Predominantly Swedish men born from January 1, 1950, through December 31, 1960. EXPOSURE Potential risk factors for dementia based on those found in previous studies, data available, and quality of register data. MAIN OUTCOMES AND MEASURE All forms of YOD. RESULTS During a median follow-up of 37 years, 487 men were diagnosed as having YOD at a median age of 54 years. In multivariate Cox regression analysis, significant risk factors (all P < .05) for YOD included alcohol intoxication (hazard ratio, 4.82 [95% CI, 3.83-6.05]); population-attributable risk, 0.28), stroke (2.96 [2.02-4.35]; 0.04), use of antipsychotics (2.75 [2.09-3.60]; 0.12), depression (1.89 [1.53-2.34]; 0.28), father's dementia (1.65 [1.22-2.24]; 0.04), drug intoxication other than alcohol (1.54 [1.06-2.24]; 0.03), low cognitive function at conscription (1.26 per 1-SD decrease [1.14-1.40]; 0.29), low height at conscription (1.16 per 1-SD decrease [1.04-1.29]; 0.16), and high systolic blood pressure at conscription (0.90 per 1-SD decrease [0.82-0.99]; 0.06). The population-attributable risk associated with all 9 risk factors was 68%. Men with at least 2 of these risk factors and in the lowest third of overall cognitive function were found to have a 20-fold increased risk of YOD during follow-up (hazard ratio, 20.38 [95% CI, 13.64-30.44]). CONCLUSIONS AND RELEVANCE In this nationwide cohort, 9 independent risk factors were identified that accounted for most cases of YOD in men. These risk factors were multiplicative, most were potentially modifiable, and most could be traced to adolescence, suggesting excellent opportunities for early prevention.
引用
收藏
页码:1612 / 1618
页数:7
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