Alterations of serum macro-minerals and trace elements are associated with major depressive disorder: a case-control study
Major depressive disorder (MDD) is a mixed disorder with the highly irregular course, inconsistent response to treatment and has no well-known mechanism for the pathophysiology. Major causes of depression are genetic, neurobiological, and environmental. However, over the past few years, altered seru...
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Published in | BMC psychiatry Vol. 18; no. 1; pp. 94 - 7 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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10.04.2018
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Abstract | Major depressive disorder (MDD) is a mixed disorder with the highly irregular course, inconsistent response to treatment and has no well-known mechanism for the pathophysiology. Major causes of depression are genetic, neurobiological, and environmental. However, over the past few years, altered serum levels of macro-minerals (MM) and trace elements (TE) have been recognized as major causative factors to the pathogenesis of many mental disorders. The purpose of this study was to determine the serum levels of MM (calcium and magnesium) and TE (copper, iron, manganese, selenium, and zinc) in MDD patients and find out their associations with depression risk.
This prospective case-control study recruited 247 patients and 248 healthy volunteers matched by age and sex. The serum levels of MM and TE were analyzed by atomic absorption spectroscopy (AAS). Statistical analysis was performed with independent sample t-tests and Pearson's correlation test.
We found significantly decreased concentrations of calcium and magnesium, iron, manganese, selenium, and zinc in MDD patients compared with control subjects (p < 0.05). But the concentration of copper was significantly increased in the patients than control subjects (p < 0.05). Data obtained from different inter-element relations in MDD patients and control subjects strongly suggest that there is a disturbance in the element homeostasis.
Our study suggests that altered serum concentrations of MM and TE are major contributing factors for the pathogenesis of MDD. Alterations of these elements in serum levels of MDD patients arise independently and they may provide a prognostic tool for the assessment of depression risk. |
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AbstractList | Major depressive disorder (MDD) is a mixed disorder with the highly irregular course, inconsistent response to treatment and has no well-known mechanism for the pathophysiology. Major causes of depression are genetic, neurobiological, and environmental. However, over the past few years, altered serum levels of macro-minerals (MM) and trace elements (TE) have been recognized as major causative factors to the pathogenesis of many mental disorders. The purpose of this study was to determine the serum levels of MM (calcium and magnesium) and TE (copper, iron, manganese, selenium, and zinc) in MDD patients and find out their associations with depression risk.BACKGROUNDMajor depressive disorder (MDD) is a mixed disorder with the highly irregular course, inconsistent response to treatment and has no well-known mechanism for the pathophysiology. Major causes of depression are genetic, neurobiological, and environmental. However, over the past few years, altered serum levels of macro-minerals (MM) and trace elements (TE) have been recognized as major causative factors to the pathogenesis of many mental disorders. The purpose of this study was to determine the serum levels of MM (calcium and magnesium) and TE (copper, iron, manganese, selenium, and zinc) in MDD patients and find out their associations with depression risk.This prospective case-control study recruited 247 patients and 248 healthy volunteers matched by age and sex. The serum levels of MM and TE were analyzed by atomic absorption spectroscopy (AAS). Statistical analysis was performed with independent sample t-tests and Pearson's correlation test.METHODSThis prospective case-control study recruited 247 patients and 248 healthy volunteers matched by age and sex. The serum levels of MM and TE were analyzed by atomic absorption spectroscopy (AAS). Statistical analysis was performed with independent sample t-tests and Pearson's correlation test.We found significantly decreased concentrations of calcium and magnesium, iron, manganese, selenium, and zinc in MDD patients compared with control subjects (p < 0.05). But the concentration of copper was significantly increased in the patients than control subjects (p < 0.05). Data obtained from different inter-element relations in MDD patients and control subjects strongly suggest that there is a disturbance in the element homeostasis.RESULTSWe found significantly decreased concentrations of calcium and magnesium, iron, manganese, selenium, and zinc in MDD patients compared with control subjects (p < 0.05). But the concentration of copper was significantly increased in the patients than control subjects (p < 0.05). Data obtained from different inter-element relations in MDD patients and control subjects strongly suggest that there is a disturbance in the element homeostasis.Our study suggests that altered serum concentrations of MM and TE are major contributing factors for the pathogenesis of MDD. Alterations of these elements in serum levels of MDD patients arise independently and they may provide a prognostic tool for the assessment of depression risk.CONCLUSIONOur study suggests that altered serum concentrations of MM and TE are major contributing factors for the pathogenesis of MDD. Alterations of these elements in serum levels of MDD patients arise independently and they may provide a prognostic tool for the assessment of depression risk. Major depressive disorder (MDD) is a mixed disorder with the highly irregular course, inconsistent response to treatment and has no well-known mechanism for the pathophysiology. Major causes of depression are genetic, neurobiological, and environmental. However, over the past few years, altered serum levels of macro-minerals (MM) and trace elements (TE) have been recognized as major causative factors to the pathogenesis of many mental disorders. The purpose of this study was to determine the serum levels of MM (calcium and magnesium) and TE (copper, iron, manganese, selenium, and zinc) in MDD patients and find out their associations with depression risk. This prospective case-control study recruited 247 patients and 248 healthy volunteers matched by age and sex. The serum levels of MM and TE were analyzed by atomic absorption spectroscopy (AAS). Statistical analysis was performed with independent sample t-tests and Pearson's correlation test. We found significantly decreased concentrations of calcium and magnesium, iron, manganese, selenium, and zinc in MDD patients compared with control subjects (p < 0.05). But the concentration of copper was significantly increased in the patients than control subjects (p < 0.05). Data obtained from different inter-element relations in MDD patients and control subjects strongly suggest that there is a disturbance in the element homeostasis. Our study suggests that altered serum concentrations of MM and TE are major contributing factors for the pathogenesis of MDD. Alterations of these elements in serum levels of MDD patients arise independently and they may provide a prognostic tool for the assessment of depression risk. Background Major depressive disorder (MDD) is a mixed disorder with the highly irregular course, inconsistent response to treatment and has no well-known mechanism for the pathophysiology. Major causes of depression are genetic, neurobiological, and environmental. However, over the past few years, altered serum levels of macro-minerals (MM) and trace elements (TE) have been recognized as major causative factors to the pathogenesis of many mental disorders. The purpose of this study was to determine the serum levels of MM (calcium and magnesium) and TE (copper, iron, manganese, selenium, and zinc) in MDD patients and find out their associations with depression risk. Methods This prospective case-control study recruited 247 patients and 248 healthy volunteers matched by age and sex. The serum levels of MM and TE were analyzed by atomic absorption spectroscopy (AAS). Statistical analysis was performed with independent sample t-tests and Pearson's correlation test. Results We found significantly decreased concentrations of calcium and magnesium, iron, manganese, selenium, and zinc in MDD patients compared with control subjects (p < 0.05). But the concentration of copper was significantly increased in the patients than control subjects (p < 0.05). Data obtained from different inter-element relations in MDD patients and control subjects strongly suggest that there is a disturbance in the element homeostasis. Conclusion Our study suggests that altered serum concentrations of MM and TE are major contributing factors for the pathogenesis of MDD. Alterations of these elements in serum levels of MDD patients arise independently and they may provide a prognostic tool for the assessment of depression risk. Keywords: Major depressive disorder, Macro-minerals, Trace elements, Case-control, Inter-element relations Major depressive disorder (MDD) is a mixed disorder with the highly irregular course, inconsistent response to treatment and has no well-known mechanism for the pathophysiology. Major causes of depression are genetic, neurobiological, and environmental. However, over the past few years, altered serum levels of macro-minerals (MM) and trace elements (TE) have been recognized as major causative factors to the pathogenesis of many mental disorders. The purpose of this study was to determine the serum levels of MM (calcium and magnesium) and TE (copper, iron, manganese, selenium, and zinc) in MDD patients and find out their associations with depression risk. This prospective case-control study recruited 247 patients and 248 healthy volunteers matched by age and sex. The serum levels of MM and TE were analyzed by atomic absorption spectroscopy (AAS). Statistical analysis was performed with independent sample t-tests and Pearson's correlation test. We found significantly decreased concentrations of calcium and magnesium, iron, manganese, selenium, and zinc in MDD patients compared with control subjects (p < 0.05). But the concentration of copper was significantly increased in the patients than control subjects (p < 0.05). Data obtained from different inter-element relations in MDD patients and control subjects strongly suggest that there is a disturbance in the element homeostasis. Our study suggests that altered serum concentrations of MM and TE are major contributing factors for the pathogenesis of MDD. Alterations of these elements in serum levels of MDD patients arise independently and they may provide a prognostic tool for the assessment of depression risk. Abstract Background Major depressive disorder (MDD) is a mixed disorder with the highly irregular course, inconsistent response to treatment and has no well-known mechanism for the pathophysiology. Major causes of depression are genetic, neurobiological, and environmental. However, over the past few years, altered serum levels of macro-minerals (MM) and trace elements (TE) have been recognized as major causative factors to the pathogenesis of many mental disorders. The purpose of this study was to determine the serum levels of MM (calcium and magnesium) and TE (copper, iron, manganese, selenium, and zinc) in MDD patients and find out their associations with depression risk. Methods This prospective case-control study recruited 247 patients and 248 healthy volunteers matched by age and sex. The serum levels of MM and TE were analyzed by atomic absorption spectroscopy (AAS). Statistical analysis was performed with independent sample t-tests and Pearson’s correlation test. Results We found significantly decreased concentrations of calcium and magnesium, iron, manganese, selenium, and zinc in MDD patients compared with control subjects (p < 0.05). But the concentration of copper was significantly increased in the patients than control subjects (p < 0.05). Data obtained from different inter-element relations in MDD patients and control subjects strongly suggest that there is a disturbance in the element homeostasis. Conclusion Our study suggests that altered serum concentrations of MM and TE are major contributing factors for the pathogenesis of MDD. Alterations of these elements in serum levels of MDD patients arise independently and they may provide a prognostic tool for the assessment of depression risk. |
ArticleNumber | 94 |
Audience | Academic |
Author | Islam, Md Rabiul Shalahuddin Qusar, M. M. A. Kabir, Md Humayun Islam, Md Saiful Islam, Md Reazul Islam, Mohammad Safiqul Hasnat, Abul Mustafizur Rahman, G. K. M. |
Author_xml | – sequence: 1 givenname: Md Rabiul surname: Islam fullname: Islam, Md Rabiul – sequence: 2 givenname: Md Reazul surname: Islam fullname: Islam, Md Reazul – sequence: 3 givenname: M. M. A. surname: Shalahuddin Qusar fullname: Shalahuddin Qusar, M. M. A. – sequence: 4 givenname: Mohammad Safiqul surname: Islam fullname: Islam, Mohammad Safiqul – sequence: 5 givenname: Md Humayun surname: Kabir fullname: Kabir, Md Humayun – sequence: 6 givenname: G. K. M. surname: Mustafizur Rahman fullname: Mustafizur Rahman, G. K. M. – sequence: 7 givenname: Md Saiful surname: Islam fullname: Islam, Md Saiful – sequence: 8 givenname: Abul surname: Hasnat fullname: Hasnat, Abul |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29631563$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1126/science.179.4073.588 10.1007/s12011-013-9721-9 10.1001/archpsyc.64.4.433 10.1007/s12011-016-0798-9 10.1074/jbc.M801522200 10.1385/BTER:73:1:37 10.1038/s41598-017-10593-7 10.1002/(SICI)1099-1077(199910)14:7<447::AID-HUP106>3.0.CO;2-F 10.1017/S0954579414001151 10.1155/2017/3178784 10.1007/s00403-015-1570-2 10.1007/BF02784278 10.1080/10937400600755911 10.1016/j.cca.2008.04.003 10.1159/000255462 10.1016/j.genhosppsych.2009.02.007 10.1111/jnc.13170 10.1016/j.mam.2005.07.010 10.1016/j.pnpbp.2010.05.004 10.1021/bi026918f 10.1016/S1734-1140(13)71512-3 10.1016/j.psychres.2013.10.037 10.1007/978-0-387-92271-3_28 10.1177/15648265070281S108 10.1192/bjp.115.529.1375 10.1007/s12011-009-8421-y 10.1002/nbm.2891 10.3390/ijerph7041342 10.1056/NEJM196804042781406 10.1016/j.jtemb.2014.04.006 10.1016/j.biochi.2009.04.009 10.1002/hup.231 10.1007/s12011-009-8441-7 10.1179/1476830512Y.0000000044 10.4103/2277-8632.158577 10.1371/journal.pone.0180067 10.1016/j.neuro.2006.12.001 10.1007/s12011-012-9371-3 10.1136/bmj.314.7077.360 10.1080/1028415021000055925 10.1016/S0165-0173(02)00234-5 10.1371/journal.pone.0093900 10.1016/j.mehy.2006.01.047 10.1016/j.jtemb.2010.11.004 10.1016/j.mam.2005.07.013 10.1371/journal.pone.0082793 10.1007/s12011-015-0542-x 10.1080/10408349408048824 |
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Keywords | Trace elements Inter-element relations Major depressive disorder Macro-minerals Case-control |
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References | M Maes (1685_CR42) 2011; 35 MS Mustak (1685_CR44) 2008; 394 D Frizel (1685_CR34) 1969; 115 CC Pfeiffer (1685_CR40) 1983; 12 S Wilson (1685_CR3) 2014; 26 F da Silva (1685_CR14) 1999 KJ Hsu (1685_CR2) 2014; 215 O Grønli (1685_CR43) 2013; 8 G Nowak (1685_CR52) 1999; 67 B Grünec ker (1685_CR21) 2013; 26 A Takeda (1685_CR19) 2003; 41 SJ Li (1685_CR20) 2014; 9 JH Freeland-Graves (1685_CR49) 2015; 31 G Nowak (1685_CR24) 2001; 58 RS Gibson (1685_CR48) 2007; 28 LM Plum (1685_CR23) 2010; 7 WE Wacker (1685_CR32) 1968; 278 M Siwek (1685_CR45) 2013; 65 Z Nahar (1685_CR8) 2010; 133 LC Jellen (1685_CR17) 2009; 91 BR Stern (1685_CR28) 2007; 10 T Fukushima (1685_CR9) 2010; 34 L Prashanth (1685_CR25) 2015; 4 D Benton (1685_CR41) 2002; 5 A Alimonti (1685_CR4) 2007; 28 A Błażewicz (1685_CR10) 2017; 2017 JT Rotruck (1685_CR22) 1973; 179 DL de Romaña (1685_CR50) 2011; 25 M Szkup (1685_CR12) 2017; 176 ML Derom (1685_CR36) 2013; 16 X Cao (1685_CR27) 2008; 283 GA Eby (1685_CR33) 2006; 67 JM Christensen (1685_CR53) 1994 H Shohag (1685_CR6) 2012; 148 R Frewin (1685_CR15) 1997; 314 A Zieba (1685_CR35) 2000; 15 M Schlegel-Zawadzka (1685_CR51) 2000; 73 MH Lam (1685_CR46) 2009; 31 S Caroli (1685_CR54) 1994; 24 M Arredondo (1685_CR39) 2005; 26 P Chen (1685_CR18) 2015; 134 MN Amin (1685_CR29) 2015; 307 MS Sarwar (1685_CR30) 2013; 154 JG Anderson (1685_CR31) 2011 YS Piao (1685_CR16) 2017; 7 A Rajizadeh (1685_CR37) 2016; 171 EK Tarleton (1685_CR13) 2017; 12 G Schaafsma (1685_CR47) 1997; 51 M Schlegel-Zawadzka (1685_CR38) 1999; 14 KI Jung (1685_CR11) 2010; 133 CG Fraga (1685_CR5) 2005; 26 DR Livesay (1685_CR26) 2003; 42 JC Wakefield (1685_CR1) 2007; 64 MS Mustak (1685_CR7) 2008; 394 |
References_xml | – volume: 179 start-page: 588 year: 1973 ident: 1685_CR22 publication-title: Science doi: 10.1126/science.179.4073.588 – volume: 154 start-page: 14 year: 2013 ident: 1685_CR30 publication-title: Biol Trace Elem Res doi: 10.1007/s12011-013-9721-9 – volume: 64 start-page: 433 year: 2007 ident: 1685_CR1 publication-title: Arch Gen Psychiatry doi: 10.1001/archpsyc.64.4.433 – volume: 51 start-page: S13 issue: Suppl 1 year: 1997 ident: 1685_CR47 publication-title: Eur J Clin Nutr – volume: 176 start-page: 56 year: 2017 ident: 1685_CR12 publication-title: Biol Trace Elem Res doi: 10.1007/s12011-016-0798-9 – volume: 283 start-page: 16169 year: 2008 ident: 1685_CR27 publication-title: J Biol Chem doi: 10.1074/jbc.M801522200 – volume: 73 start-page: 37 year: 2000 ident: 1685_CR51 publication-title: Biol Trace Elem Res doi: 10.1385/BTER:73:1:37 – volume: 7 year: 2017 ident: 1685_CR16 publication-title: Sci Rep doi: 10.1038/s41598-017-10593-7 – volume: 14 start-page: 447 year: 1999 ident: 1685_CR38 publication-title: Hum Psychopharmacol Clin Exp doi: 10.1002/(SICI)1099-1077(199910)14:7<447::AID-HUP106>3.0.CO;2-F – volume: 26 start-page: 1477 year: 2014 ident: 1685_CR3 publication-title: Dev Psychopathol doi: 10.1017/S0954579414001151 – volume: 2017 start-page: 3178784 year: 2017 ident: 1685_CR10 publication-title: Biomed Res Int doi: 10.1155/2017/3178784 – volume: 58 start-page: 73 year: 2001 ident: 1685_CR24 publication-title: Acta Pol Pharm – volume: 307 start-page: 617 year: 2015 ident: 1685_CR29 publication-title: Arch Dermatol Res doi: 10.1007/s00403-015-1570-2 – volume: 67 start-page: 85 year: 1999 ident: 1685_CR52 publication-title: Biol Trace Elem Res doi: 10.1007/BF02784278 – volume: 10 start-page: 157 year: 2007 ident: 1685_CR28 publication-title: J Toxicol Environ Health B Crit Rev doi: 10.1080/10937400600755911 – volume: 394 start-page: 47 year: 2008 ident: 1685_CR44 publication-title: Clin Chim Acta doi: 10.1016/j.cca.2008.04.003 – volume: 34 start-page: 18 year: 2010 ident: 1685_CR9 publication-title: Neuroepidemiology doi: 10.1159/000255462 – volume: 31 start-page: 262 year: 2009 ident: 1685_CR46 publication-title: Gen Hosp Psychiatry doi: 10.1016/j.genhosppsych.2009.02.007 – volume: 134 start-page: 601 year: 2015 ident: 1685_CR18 publication-title: J Neurochem doi: 10.1111/jnc.13170 – volume: 26 start-page: 313 year: 2005 ident: 1685_CR39 publication-title: Mol Asp Med doi: 10.1016/j.mam.2005.07.010 – volume: 35 start-page: 676 year: 2011 ident: 1685_CR42 publication-title: Prog Neuro-Psychopharmacol Biol Psychiatry doi: 10.1016/j.pnpbp.2010.05.004 – volume: 42 start-page: 3464 year: 2003 ident: 1685_CR26 publication-title: Biochemistry doi: 10.1021/bi026918f – volume: 65 start-page: 1512 year: 2013 ident: 1685_CR45 publication-title: Pharmacol Rep doi: 10.1016/S1734-1140(13)71512-3 – volume: 215 start-page: 87 year: 2014 ident: 1685_CR2 publication-title: Psychiatry Res doi: 10.1016/j.psychres.2013.10.037 – start-page: 423 volume-title: Handbook of behavior, food and nutrition year: 2011 ident: 1685_CR31 doi: 10.1007/978-0-387-92271-3_28 – volume: 28 start-page: S77 issue: Suppl 1 year: 2007 ident: 1685_CR48 publication-title: Food Nutr Bull doi: 10.1177/15648265070281S108 – volume: 115 start-page: 1375 year: 1969 ident: 1685_CR34 publication-title: Br J Psychiatry doi: 10.1192/bjp.115.529.1375 – volume: 394 start-page: 47 year: 2008 ident: 1685_CR7 publication-title: Clin Chim Acta doi: 10.1016/j.cca.2008.04.003 – volume: 133 start-page: 153 year: 2010 ident: 1685_CR11 publication-title: Biol Trace Elem Res doi: 10.1007/s12011-009-8421-y – volume: 26 start-page: 542 year: 2013 ident: 1685_CR21 publication-title: NMR Biomed doi: 10.1002/nbm.2891 – volume: 7 start-page: 1342 year: 2010 ident: 1685_CR23 publication-title: Int J Environ Res Public Health doi: 10.3390/ijerph7041342 – volume: 278 start-page: 772 year: 1968 ident: 1685_CR32 publication-title: N Engl J Med doi: 10.1056/NEJM196804042781406 – volume: 31 start-page: 135 year: 2015 ident: 1685_CR49 publication-title: J Trace Elem Med Biol doi: 10.1016/j.jtemb.2014.04.006 – volume: 91 start-page: 1255 year: 2009 ident: 1685_CR17 publication-title: Biochimie doi: 10.1016/j.biochi.2009.04.009 – volume: 15 start-page: 631 year: 2000 ident: 1685_CR35 publication-title: Hum Psychopharmacol doi: 10.1002/hup.231 – volume: 133 start-page: 284 year: 2010 ident: 1685_CR8 publication-title: Biol Trace Elem Res doi: 10.1007/s12011-009-8441-7 – volume: 16 start-page: 191 year: 2013 ident: 1685_CR36 publication-title: Nutr Neurosci doi: 10.1179/1476830512Y.0000000044 – start-page: 418 volume-title: The biological chemistry of the elements. The inorganic chemistry of life year: 1999 ident: 1685_CR14 – volume: 4 start-page: 75 year: 2015 ident: 1685_CR25 publication-title: J NTR Univ Health Sci doi: 10.4103/2277-8632.158577 – volume: 12 start-page: 28 year: 1983 ident: 1685_CR40 publication-title: J Orthomol Psychiatry – volume: 12 start-page: e0180067 year: 2017 ident: 1685_CR13 publication-title: PLoS One doi: 10.1371/journal.pone.0180067 – volume: 28 start-page: 450 year: 2007 ident: 1685_CR4 publication-title: Neurotoxicology doi: 10.1016/j.neuro.2006.12.001 – volume: 148 start-page: 275 year: 2012 ident: 1685_CR6 publication-title: Biol Trace Elem Res doi: 10.1007/s12011-012-9371-3 – volume: 314 start-page: 360 year: 1997 ident: 1685_CR15 publication-title: BMJ doi: 10.1136/bmj.314.7077.360 – volume: 5 start-page: 363 year: 2002 ident: 1685_CR41 publication-title: Nutr Neurosci doi: 10.1080/1028415021000055925 – volume: 41 start-page: 79 year: 2003 ident: 1685_CR19 publication-title: Brain Res Brain Res Rev doi: 10.1016/S0165-0173(02)00234-5 – volume: 9 start-page: e93900 year: 2014 ident: 1685_CR20 publication-title: PLoS One doi: 10.1371/journal.pone.0093900 – volume: 67 start-page: 362 year: 2006 ident: 1685_CR33 publication-title: Med Hypotheses doi: 10.1016/j.mehy.2006.01.047 – volume: 25 start-page: 3 year: 2011 ident: 1685_CR50 publication-title: J Trace Elem Med Biol doi: 10.1016/j.jtemb.2010.11.004 – volume: 26 start-page: 235 year: 2005 ident: 1685_CR5 publication-title: Mol Asp Med doi: 10.1016/j.mam.2005.07.013 – volume: 8 start-page: e82793 year: 2013 ident: 1685_CR43 publication-title: PLoS One doi: 10.1371/journal.pone.0082793 – start-page: 217 volume-title: Handbook on metals in clinical and analytical chemistry year: 1994 ident: 1685_CR53 – volume: 171 start-page: 275 year: 2016 ident: 1685_CR37 publication-title: Biol Trace Elem Res doi: 10.1007/s12011-015-0542-x – volume: 24 start-page: 363 year: 1994 ident: 1685_CR54 publication-title: Crit Rev Anal Chem doi: 10.1080/10408349408048824 |
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Snippet | Major depressive disorder (MDD) is a mixed disorder with the highly irregular course, inconsistent response to treatment and has no well-known mechanism for... Background Major depressive disorder (MDD) is a mixed disorder with the highly irregular course, inconsistent response to treatment and has no well-known... Abstract Background Major depressive disorder (MDD) is a mixed disorder with the highly irregular course, inconsistent response to treatment and has no... |
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SubjectTerms | Adolescent Adult Case-control Case-Control Studies Depressive Disorder, Major - blood Development and progression Female Health aspects Humans Inter-element relations Macro-minerals Major depressive disorder Male Middle Aged Minerals - blood Prospective Studies Psychological aspects Risk factors Spectrophotometry, Atomic Trace elements Trace Elements - blood Trace minerals (Nutrients) Young Adult |
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Title | Alterations of serum macro-minerals and trace elements are associated with major depressive disorder: a case-control study |
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