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      Association between vitamin b 12 levels and melancholic depressive symptoms: a Finnish population-based study

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          Abstract

          Background

          An association between vitamin B 12 levels and depressive symptoms (DS) has been reported in several epidemiological studies. The purpose of this study was to evaluate vitamin B 12 levels in population-based samples with melancholic or non-melancholic DS as the relationship between vitamin B 12 levels and different subtypes of DS has not been evaluated in previous studies.

          Methods

          Subjects without previously known type 2 diabetes, aged 45–74 years were randomly selected from the National Population Register as a part of the Finnish diabetes prevention programme (FIN-D2D). The study population (N = 2806, participation rate 62%) consisted of 1328 men and 1478 women. The health examinations were carried out between October and December 2007 according to the WHO MONICA protocol. The assessment of DS was based on the Beck Depression Inventory (BDI, cut-off ≥10 points). A DSM-IV- criteria based summary score of melancholic items in the BDI was used in dividing the participants with DS (N = 429) into melancholic (N = 138) and non-melancholic DS (N = 291) subgroups. In the statistical analysis we used chi-squared test, t-test, permutation test, analysis of covariance, multivariate logistic regression analysis and multinomial regression model.

          Results

          The mean vitamin B 12 level was 331±176 pmol/L in those without DS while the subjects with non-melancholic DS had a mean vitamin B 12 level of 324 ± 135 pmol/L, and those with melancholic DS had the lowest mean vitamin B 12 level of 292±112 pmol/L (p < 0.001 after adjusted for age, sex, use of antidepressive medication and chronic diseases sum index). The adjusted difference of vitamin B 12 levels between the non-melancholic and the melancholic group was 33 pmol/L (95%CI 8 to 57, p = 0.008). Melancholic DS and vitamin B 12 levels showed an independent linearly inverse association. The relative risk ratio (RRR) for melancholic DS was 2.75 (95%CI 1.66 to 4.56) in the lowest vitamin B 12 level tertile versus the highest (p for linearity <0.001) when those without DS formed the reference group. The RRR in the non-melancholic subgroup was nonsignificant.

          Conclusions

          The vitamin B 12 level was associated with melancholic DS but not with non-melancholic DS.

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          Most cited references40

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          Lifetime and 12-month prevalence of DSM-III-R psychiatric disorders in the United States. Results from the National Comorbidity Survey.

          This study presents estimates of lifetime and 12-month prevalence of 14 DSM-III-R psychiatric disorders from the National Comorbidity Survey, the first survey to administer a structured psychiatric interview to a national probability sample in the United States. The DSM-III-R psychiatric disorders among persons aged 15 to 54 years in the noninstitutionalized civilian population of the United States were assessed with data collected by lay interviewers using a revised version of the Composite International Diagnostic Interview. Nearly 50% of respondents reported at least one lifetime disorder, and close to 30% reported at least one 12-month disorder. The most common disorders were major depressive episode, alcohol dependence, social phobia, and simple phobia. More than half of all lifetime disorders occurred in the 14% of the population who had a history of three or more comorbid disorders. These highly comorbid people also included the vast majority of people with severe disorders. Less than 40% of those with a lifetime disorder had ever received professional treatment, and less than 20% of those with a recent disorder had been in treatment during the past 12 months. Consistent with previous risk factor research, it was found that women had elevated rates of affective disorders and anxiety disorders, that men had elevated rates of substance use disorders and antisocial personality disorder, and that most disorders declined with age and with higher socioeconomic status. The prevalence of psychiatric disorders is greater than previously thought to be the case. Furthermore, this morbidity is more highly concentrated than previously recognized in roughly one sixth of the population who have a history of three or more comorbid disorders. This suggests that the causes and consequences of high comorbidity should be the focus of research attention. The majority of people with psychiatric disorders fail to obtain professional treatment. Even among people with a lifetime history of three or more comorbid disorders, the proportion who ever obtain specialty sector mental health treatment is less than 50%. These results argue for the importance of more outreach and more research on barriers to professional help-seeking.
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            Global burden of depressive disorders in the year 2000.

            The initial Global Burden of Disease study found that depression was the fourth leading cause of disease burden, accounting for 3.7% of total disability adjusted life years (DALYs) in the world in 1990. To present the new estimates of depression burden for the year 2000. DALYs for depressive disorders in each world region were calculated, based on new estimates of mortality, prevalence, incidence, average age at onset, duration and disability severity. Depression is the fourth leading cause of disease burden, accounting for 4.4% of total DALYs in the year 2000, and it causes the largest amount of non-fatal burden, accounting for almost 12% of all total years lived with disability worldwide. These data on the burden of depression worldwide represent a major public health problem that affects patients and society.
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              The World Health Organization MONICA Project (monitoring trends and determinants in cardiovascular disease): a major international collaboration. WHO MONICA Project Principal Investigators.

              A World Health Organization Working Group has developed a major international collaborative study with the objective of measuring over 10 years, and in many different populations, the trends in, and determinants of, cardiovascular disease. Specifically the programme focuses on trends in event rates for validated fatal and non-fatal coronary heart attacks and strokes, and on trends in cardiovascular risk factors (blood pressure, cigarette smoking and serum cholesterol) in men and women aged 25-64 in the same defined communities. By this means it is hoped both to measure changes in cardiovascular mortality and to see how far they are explained; on the one hand by changes in incidence mediated by risk factor levels; and on the other by changes in case-fatality rates, related to medical care. Population centres need to be large and numerous; to reliably establish 10-year trends in event rates within a centre 200 or more fatal events in men per year are needed, while for the collaborative study a multiplicity of internally homogeneous centres showing differing trends will provide the best test of the hypotheses. Forty-one MONICA Collaborating Centres, using a standardized protocol, are studying 118 Reporting Units (subpopulations) with a total population aged 25-64 (both sexes) of about 15 million.
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                Author and article information

                Journal
                BMC Psychiatry
                BMC Psychiatry
                BMC Psychiatry
                BioMed Central
                1471-244X
                2013
                24 May 2013
                : 13
                : 145
                Affiliations
                [1 ]Department of Psychiatry, South-Savo Hospital District, Mikkeli, Finland
                [2 ]Department of Psychiatry, Institute of Clinical Medicine, University of Eastern Finland, P.O. Box 1627, Kuopio, 70211, Finland
                [3 ]Department of Psychiatry, Kuopio University Hospital, P.O. Box 1777, Kuopio, 70211, Finland
                [4 ]Unit of Family Practice, Central Finland Central Hospital, Jyväskylä, 40620, Finland
                [5 ]Unit of Primary Health Care, Kuopio University Hospital, P.O. Box 1777, Kuopio, 70211, Finland
                [6 ]Department of General Practice and Primary Health Care, University of Helsinki, P.O. Box 33, Helsinki, 00014, Finland
                [7 ]Unit of General Practice, Helsinki University General Hospital, P.O. Box 590, Helsinki, 00029, Finland
                [8 ]National Institute for Health and Welfare, P.O. Box 30, Helsinki, 00271, Finland
                [9 ]Folkhälsan Research Center, P.O. Box 63, Helsinki, 00014, Finland
                [10 ]Vasa Central Hospital, Vasa, 65130, Finland
                [11 ]Medical School, University of Tampere, Tampere, 33014, Finland
                [12 ]Department of Psychiatry, Seinäjoki Hospital District, Seinäjoki, 60220, Finland
                [13 ]Department of Chronic Disease Prevention, National Institute for Health and Welfare, P.O. Box 30, Helsinki, 00271, Finland
                [14 ]Institute of Clinical Medicine, General Practice, University of Turku, Turku, 20014, Finland
                [15 ]Unit of Primary Health Care, Turku University Hospital, Turku, 20520, Finland
                [16 ]Tampere University Hospital, P.O. Box 2000, Tampere, 33521, Finland
                [17 ]Private practices, Diacor, Helsinki, 00380, Finland
                [18 ]Medical School, University of Tampere, Tampere, 33014, Finland
                [19 ]Tampere Mental Health Center, P.O. Box 487, Tampere, 33101, Finland
                [20 ]Department of Psychiatry, South-Savo Hospital District, Moisiontie 10, Mikkeli, FIN, 50520, Finland
                Article
                1471-244X-13-145
                10.1186/1471-244X-13-145
                3674945
                23705786
                9698a5c9-5eca-46d6-93c1-3985e9507855
                Copyright ©2013 Seppälä et al.; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 27 November 2012
                : 15 May 2013
                Categories
                Research Article

                Clinical Psychology & Psychiatry
                beck depression inventory,melancholic depressive symptoms,non-melancholic depressive symptoms,population-based,vitamin b12

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