BIOCHEMICAL ANALYSIS IN PATIENTS WITH MAJOR DEPRESSIVE DISORDER IN JAMMU POPULATION
HTML Full TextBIOCHEMICAL ANALYSIS IN PATIENTS WITH MAJOR DEPRESSIVE DISORDER IN JAMMU POPULATION
Anil Kumar 1, 2, Radhika Sharma*3, Manu Arora 4 and Ramesh Chander Gupta 2
Department of Biochemistry 1, Government Medical College, Jammu - 180001, Jammu and Kashmir, India.
Department of Biochemistry 2, NIMS Medical College, Nims University, Jaipur - 303121, Rajasthan, India.
Department of Zoology 3, MCM DAV College, Chandigarh - 160036, Punjab, India.
Department of Psychiatry 4, Government Medical College, Jammu - 180001, Jammu and Kashmir, India.
ABSTRACT: The study was conducted to study biochemical parameters in 42 major depressive disorder (MDD) patients, 22 males and 20 females (age range 18 - 55 years) visiting the Psychiatric Department, Government Medical College, Jammu. The smoking and alcohol intake was much lower (95.24% and 88.09%) in patients (both male and female) diagnosed with MDD. The well being status is also 76.19% satisfactory with 71.43% patients with no family history of psychiatry illness and 73.81% with absence of chronic morbidity. The levels of thyroid stimulating hormone (TSH), ferritin and insulin are in normal reference range while the Vitamin B and Vitamin D 25OH levels are observed to be lower in 54.76% patients. The present study concluded that there is need for awareness towards these biomarkers as they play an important role in brain functioning by planning awareness programs. Therefore, further study with large sample size to evaluate these biochemical parameters and other risk factors is required to mitigate the effect of depression in the population of Jammu.
Keywords: |
Major depressive disorder, Biochemical, Vitamin, Thyroid stimulating hormone
INTRODUCTION: Major depressive disorder (MDD), also known as, depression is a serious medical illness characterized by melancholic feeling of sadness or grief, which can decrease the person’s ability to work 1. Epidemiologist, national and international agencies have been sounding an alarm on rapidly rising burden of depression for past many years. According to WHO 2, in young people neuropsychiatric disorders are the leading causes of worldwide disability and second leading cause of death in 15 - 29 year.
Kessler et al., 3 found that approximately 16% of adults would experience depression in their lifetime. It is a major public health problem affecting in large number to human clan of any age: children, adolescents, middle- aged groups and the elderly; residing either in urban or rural areas and linked with premature death by suicide and other causes 4, disability and economic burden 5.
There are several factors responsible for depression, viz. biological, social, economic and cultural factors, out of all strongly associated factors with mental disorders are social deprivation and poverty 6 - 8. The rise of depression prevalence in recent years is due to demographic shifts to urban areas, rapid social and economic changes, sedentary lifestyles and earlier pubescence. According to Charles et al., 9 in India, there has been seen significant changes viz. globalization, urbanization, migration, and modernization coupled with rapid socio- demographic transition, which may likely to increase depression in the coming years. In India, one in 20 i.e. 5.25% people with age group over 18 years have suffered from depression at least once in their lifetime 10.
There are different mechanisms involved in developing depression. For many diseases and disorders, depression itself is both the cause and consequence and is also associated with today’s modern life style that may contribute to metabolic abnormalities. There are different risk factors involved- biochemical, genetics, personality and environmental factors. Nutritional deficiency in any form can lead to impairment of our nervous system, which may lead to depression to the people at any age 2. For development and functioning of brain, Vitamin D (a unique neurosteroid hormone) 11; iron 12, 13; thyroid stimulating hormone 14 are important as they are involved in many neurological processes including neuroimmuno-modulation, regulation of neurotrophic factors, neuroprotection, neuroplasticity and brain development 15 - 17, therefore, plays an important role in depression.
There were many cross-sectional 18 - 20; interventional 21 - 22 studies conducted on association of Vitamin D with depression and have shown significant association in many studies 23 - 24. The association of some other Vitamin deficiencies viz. folic acid, Vitamin B12, niacin and Vitamin C with depression has also been observed 16. Thyroid and insulin also play an important role in manifestation of mental health, as with increase or decrease of these parameters can cause mood changes and disturbance at emotion level.
There are number of studies 25 - 30 carried out on Indian population which reported prevalence of depression in different geographical regions of India while till date no study has been conducted on scenario of depression in the Jammu city of J&K state. Therefore, keeping in mind the increasing prevalence of depression globally, the present study was conducted on the population of Udhampur, Jammu city with the following objectives:
- To analyze different biochemical parameters (Vitamin D25OH, Vitamin B12), iron (ferritin), thyroid stimulating hormone and insulin in MDD patients.
- To study the association of biochemical parameters with depression in MDD patients.
MATERIALS AND METHODS:
Study Design and Data Collection: The study was conducted after getting the approval from Institutional Ethical Committee on outpatients visiting the Psychiatric Department, Government Medical College, Jammu, from August 2016 to January 2017. During this duration, a total of 60 patients with current major depressive disorder were selected and 42 patients fulfill the criteria for the present study. The inclusion and exclusion criteria for the present study is as follows:
Inclusion Criteria: Patients aged between 18 to 55 years, diagnosed for mental disorders in accordance with Diagnostic and Statistical Manual 31 (DSM-V) with the use of neuropsychiatric interview.
Exclusion Criteria: The patients on any type of medication or with any other disorder were excluded from the present study. Patients suffering from lifetime history of mania or hypermania or any with concurrent psychotic symptoms or pregnant females were also not included.
After informed written consent, their socio-demographic information was recorded on the pre-designed questionnaire and the rate of severity of depression in MDD patients was measured using the Hamilton Rating Scale of Depression 32 (HRSD, 1960). The British Columbia Cognitive Complaints Inventory (BC-CCI) 33 is used to measure perceived cognitive problems in depression and Hindi Cognitive Screening Test 34 was calculated. For biochemical analyses, 5ml of intravenous blood sample was collected in centrifuge tubes.
Biochemical Analyses: Serum 25-OH Vitamin D, Insulin, Vitamin B12, Thyroid – stimulating hormone (TSH) and Ferritin levels were determined by ARCHITECT assay (Abbott Laboratories, Abbott Park, Illinois, US) an immunoassay using Chemiluminiscent Micro-particle Immunoassay (CMIA) technology, referred to as Chemiflex. The lab references are 20-60 ng/ml for 25-OH Vitamin D; 1 - 300 µU/mL for Insulin; 187 - 883 pg/ml for Vitamin B12 0.2700 - 4.2000 µIU/mL for TSH and 4.63 - 204.00 ng/mL for Ferritin.
Statistical Analysis: The statistical analysis was done using SPSS 15.0 version. The categorical variables in numbers were analyzed using the Chi-squared test for deviations (if any) between male and female participants. The continuous variables of demographic and biochemical parameters were presented as mean ± S.E.M. (standard error of mean). Pearson correlation analysis was carried out to find the association (if any) of the confounding (independent) variables with biochemical parameters (dependent variables). The significance was considered with p values less than 0.05.
RESULTS: A total of 42 MDD patients were studied with gender distribution of 22 males (52.38%) and 20 females (47.62%), age ranging from 18-55years with majority (85.71%) of the participants belonging to Hindu community. Descriptive data of the study population is presented in Table 1. Average ages of major depressive disorder male and female subjects were 40.68 ± 2.63 and 40.85 ± 2.18 years, respectively. The smoking and alcohol intake was much lower (95.24% and 88.09%) in patients (both male and female) diagnosed with MDD. The well being status of MDD patients in the present study is also 76.19% satisfactory with 71.43% patients with no family history of psychiatry illness and 73.81% with absence of chronic morbidity.
The chi-squared analysis revealed no statistical significant difference within male and female patient for religion, place of residence, educational status, family status (living in join or nuclear family), well being status, family history of depression or any psychiatric disorder, HRSD (depression) scale Table 1. Therefore, for further analysis the data was pooled. Table 2 represents the continuous variables of the present study as mean ± SEM.
TABLE 1: DESCRIPTIVE VARIABLES OF THE MAJOR DEPRESSIVE DISORDER PATIENTS
Demographic | Category | Male (n=22) | Female (n=20) | χ2 (p value) | Total (%) | |
Religion | Hindu | 19 | 17 | 0.015
|
36 (90) | |
Muslim | 03 | 03 | 06 (10) | |||
Place of Residence | Rural | 14 | 11 | 0.324 (0.569) | 25 (59.52) | |
Urban | 08 | 09 | 17 (40.48) | |||
Marital Status | Unmarried | 04 | 00 | - | 04 (9.52) | |
Married | 18 | 16 | 34 (80.95) | |||
Widow | 00 | 04 | 04 (9.52) | |||
Employment | Employed | Professional | 03 | 02 | - | 05 (11.90) |
Skilled | 10 | 02 | 12 (28.57) | |||
Unskilled | 04 | 00 | 04 (9.52) | |||
Unemployed | - | 01 | 16 | 17 (40.48) | ||
Family status | Nuclear | 09 | 10 | 0.349 (0.554) | 19 (45.24) | |
Joint | 13 | 10 | 23 (54.76) | |||
Education | Literate | 05 | 09 | 2.338 (0.126) | 14 (33.33) | |
Illiterate | 17 | 11 | 28 (66.67) | |||
Socioeconomic Status | Lower | 10 | 09 | - | 19 (45.24) | |
Middle | 12 | 10 | 32 (76.19) | |||
Upper | 00 | 01 | 01 (2.38) | |||
Smoking | No | 20 | 20 | - | 20 (47.62) | |
Yes | 02 | 00 | 02 (4.76) | |||
Alcohol | No | 17 | 20 | - | 37 (88.09) | |
Yes | 05 | 00 | 05 (11.90) | |||
Chronic Morbidity | Present | 03 | 06 | 1.667
(0.196) |
09 (21.43) | |
Absent | 19 | 14 | 33 (78.57) | |||
Disease | Present | 05 | 06 | 0.286 (0.592) | 11 (26.19) | |
Absent | 17 | 14 | 31 (73.81) | |||
Wellbeing | Poor | 07 | 03 | 1.633 (0.201) | 10 (23.81) | |
Satisfactory | 15 | 17 | 22 (52.38) | |||
Family History | Absent | 17 | 13 | 0.773 (0.379) | 30 (71.43) | |
Present | 05 | 07 | 12 (28.57) | |||
Grades of Depression | Mild | 01 | 05 | 3.973 (0.264) | 06 (14.29) | |
Moderate | 12 | 07 | 19 (45.24) | |||
Severe | 07 | 06 | 13 (30.95) | |||
Very Severe | 02 | 02 | 04 (9.52) | |||
Cognitive behaviour | BC-CCI-Ea | Moderate | 00 | 01 | - | 01 (2.38) |
Not at all | 09 | 08 | 17 (40.48) | |||
Quite a bit | 02 | 02 | 04 (9.52) | |||
Some | 11 | 09 | 20 (47.62) | |||
HSCTb | Negative | 21 | 18 | 0.469 (0.493) | 39 (92.86) | |
Positive | 01 | 02 | 03 (7.14) | |||
Thyroid Stimulating Hormone (μIU/ml) | <0.27 | 00 | 01 | - | 01 (2.38) | |
0.27-4.2 | 22 | 18 | 40 (95.24) | |||
>4.2 | 00 | 01 | 01 (2.38) | |||
Ferritin (ng/ml) | <4.63 | 01 | 00 | - | 01 (2.38) | |
4.63-204 | 21 | 20 | 41 (97.62) | |||
>204 | 00 | 00 | 00 | |||
Vitamin B 12 (pg/ml) | <187 | 12 | 11 | - | 23 (54.76) | |
187-883 | 08 | 09 | 17 (40.48) | |||
>883 | 02 | 00 | 02 (4.76) | |||
Vitamin D 25OH (ng/ml) | <20 | 12 | 11 | - | 23 (54.76) | |
20-60 | 07 | 04 | 11 (26.19) | |||
>60 | 03 | 05 | 08 (19.05) | |||
Insulin (μIU/ml) | 1-300 | 22 | 20 | - | 42 (100) |
Chi-square test reveals no significant difference within male and female patients
aBC-CCI-E: British Columbia Cognitive Complaint Inventory; bHCST- Hindi Cognitive Screening Test
TABLE 2: CONTINUOUS VARIABLES OF PATIENTS WITH MAJOR DEPRESSIVE DISORDER
Biochemical Parameters | Total (n = 42) |
Thyroid Stimulating Hormone (μIU/ml) | 1.80 ± 0.16 |
Ferritin (ng/ml) | 36.45 ± 5.13 |
Vitamin B12 (pg/ml) | 296.57 ± 49.33 |
Vitamin D 25OH (ng/ml) | 32.71 ± 4.46 |
Insulin (μIU/ml) | 14.78 ± 1.18 |
Biochemical Parameter Analysis: The levels of thyroid stimulating hormone (TSH), ferritin and insulin are in normal range according to the reference ranges in major depressive disorder patients while the Vitamin B and Vitamin D 25OH levels are observed to be lower in 54.76% patients
Table 1. Table 3 represents the levels of different biochemical parameters in accordance with grade of depression and observed that the level of TSH is significantly higher in individuals with moderate depression.
TABLE 3: COMPARISON OF BIOCHEMICAL PARAMETERS USING STUDENTS t-TEST IN ACCORDANCE WITH GRADES OF DEPRESSION
Grades of
Depression |
Number of Patients | Thyroid Stimulating Hormone (μIU/ml) | Ferritin (ng/ml) | Vitamin B12 (pg/ml) | Vitamin D 25OH (ng/ml) | Insulin (μIU/ml) | |
HRSD |
Mild | 06 | 2.46 ± 0.55 | 26.20 ± 5.46 | 241.33 ± 90.04 | 26.50 ± 8.59 | 15.28 ± 2.46 |
Moderate | 19 | 2.02 ± 0.21*a | 38.28 ± 7.91 | 240.00 ± 36.93 | 36.68 ± 7.79 | 15.32 ± 1.98 | |
Severe | 13 | 1.28 ± 0.27a | 39.18 ± 11.01 | 439 ± 140.13 | 27.34 ± 6.72 | 15.32 ± 2.24 | |
Very severe | 04 | 1.44 ± 0.37 | 34.28 ± 16.47 | 185.25 ± 45.34 | 40.66 ± 16.11 | 9.73 ± 0.21 |
*a(p < 0.05)
Stress Level and Severity of Depression: There was no significant correlation of biochemical parameters observed with well-being of patient and severity of the depression observed (Table not shown).
DISCUSSION: The present study revealed decreased levels of Vitamin B12 and Vitamin D 25OH in MDD patients, that is similar to the observation by Schneider and co-workers 35, which reported lower Vitamin D levels in persons with schizophrenia and major depression when compared to healthy controls.
Wilkins et al., 36 also claimed association of Vitamin D deficiency with the presence of an active mood disorder as assessed by the depressive symptoms inventory. The mechanism explaining association of Vitamin D with mental disorders is not clearly understood, but there are studies reporting their association with brain development. Eyles et al., 37 reported that there are Vitamin D receptors in the hypothalamus, which may be important in neuroendocrine functioning. Some studies have reported that Vitamin D is important for brain development 38 - 39. The level of Vitamin D is lower in dark-skinned individuals, due to higher melanin levels. Therefore, they experience reduced subcutaneous Vitamin D synthesis in comparison to those with lighter pigmentation, making them another high-risk group for Vitamin D deficiency 40.
Our results for TSH levels does not go with other studies showing significant increase of TSH levels in patients with unipolar depression 41, 42, with major depressive disorder 43. The comparison within depressed subjects with and without psychotic features showed significantly higher levels of TSH in subjects with psychotic symptoms 44. The levels of insulin and ferritin were within the normal range. Hunt and Pete 45 showed no significant association with depression while some studies reported significant iron deficiency in infants 46; mothers 47. Iron plays an important role in brain 48, as it is required for dopamine synthesis, an important neurotransmitter in mood disorders 49.
CONCLUSION: The cause and consequence of depression is several non-communicable diseases (NCDs) such as cancer, ischemic heart disease and diabetes, substances use disorders (alcohol and drugs) and nutritional disorders (under-nutrition, over-nutrition and obesity) and depressed people are more likely (1.5 times) to die than general population 50 due to untreated problem, which is expected to increase over twenty years 51.
Therefore, there is a need for the awareness to the population about these common biomarkers along with signs of sadness, loss of interest or pleasure, feeling of guilt or low esteem, disturbed sleep or appetite, tiredness and poor concentration, which affect our brain functioning and should be evaluated at early stage of illness. However, this study needed to be further established with multicenter and larger-scale study.
ACKNOWLEDGEMENT: Nil
CONFLICT OF INTEREST: The authors declare no conflict of interest for this research.
REFERENCES:
- Parekh R: What is depression? American Psychiatric Association 2017.
- Depression in India- Let’s talk: World Health Organization 2017.
- Kessler RC, Berglund P, Demler O, Jin R, Koretz D, Merikangas KR, Rush AJ, Walters EE and Wang PS: The epidemiology of major depressive disorder: results from the National Comorbidity Survey Replication (NCS-R). Journal of the American Medical Association 2003; 289: 3095-3105.
- Chesney E, Goodwin GM and Fazel S: Risks of all-cause and suicide mortality in mental disorders: a meta-review. World Psychiatry 2014; 13: 153-160.
- Chang SM, Hong JP and Cho MJ: Economic burden of depression in South Korea. Social Psychiatry and Psychiatric Epidemiology 2012; 27: 683-689.
- Chauhan P, Kokiwar PR, Shridevi K and Katkuri S: A study on prevalence and correlates of depression among elderly population of rural South India. International Journal of Community Medicine and Public Health 2016; 3: 236-239.
- Depression and other common mental disorders: Global Health Estimates. Geneva: World Health Organization, 2017.
- Sharma S: Impact of Globalisation on Mental Health in Low- and Middle-income Countries. Psychology and Developing Societies 2016; 28: 251-279.
- Charlson FJ, Baxter AJ, Cheng HG, Shidhaye R and Whiteford HA: The burden of mental, neurological, and substance use disorders in China and India: A systematic analysis of community representative epidemiological studies. Lancet 2016; 388: 376-389.
- National Mental Health Survey of India, 2015 - 16: Summary. Supported by Ministry of Health and Family Welfare Government of India
- Kesby JP, Eyles DW, Bume THJ and McGrath JJ: The effects of Vitamin D on brain development and adult brain function. Molecular and Cellular Endocrinology 2011; 347: 121-127.
- Georgieff MK: The role of iron in Neurodevelopment: Fetal iron deficiency and the developing Hippocampus. Biochem Soc Trans 2008; 36: 1267-1271.
- Fretham SJB, Carlson ES and Georgieff MK: The role of iron in learning and memory. Advances in Nutrition 2011; 2: 112-121.
- Bernal J: Thyroid hormone receptors in brain development and function. Nature Clinical Practice Endocrinology and Metabolism 2007; 3: 249-259.
- Fernandes de Abreu DA, Eyles D and Feron F: Vitamin D, a neuro- immunomodulator: Implications for neurodegenerative and autoimmune diseases. Psycho-neuroendocrinology 2009; 34: S265-277.
- Kaplan HI, Sadock BJ and Sadock VA: Kaplan and Sadock's Synopsis of Psychiatry. Philadelphia, PA: Lippincott Williams & Wilkins; Ninth Edition 2003.
- Smith G, Kramer E, Hermann C, Goldberg S, Ma Y, Dhawan V, Barnes A, Chaly T, Belakhleff A, Laghrissi-Thode F, Greenwald B, Eidelberg D and Pollock BG: Acute and chronic effects of citalopram on cerebral glucose metabolism in geriatric depression. American Journal of Geriatric Psychiatry 2002; 10: 715-723.
- Anglin RES, Samaan Z, Walter SD and McDonald SD: Vitamin D deficiency and depression in adults: systematic review and meta-analysis. British Journal of Psychiatry 2013; 100-107.
- Armstrong DJ, Meenagh GK, Bickle I, Lee AS, Curran ES and Finch MB: Vitamin D deficiency is associated with anxiety and depression in fibromyalgia. Clinical Rheumatology 2007; 26: 551-554.
- Hoogendijk WJ, Lips P, Dik MG, Deeg DJ, Beekman AT, Penninx BW: Depression is associated with decreased 25-hydroxy Vitamin D and increased parathyroid hormone levels in older adults. Archives of General Psychiatry 2008; 65: 508-512.
- Jorde R, Sneve M, Figenschau Y, Svartberg J and Waterloo K: Effects of Vitamin D supplementation on symptoms of depression in overweight and obese subjects: Randomized double blind trial. Journal of Internal Medicine 2008; 264: 599-609.
- Gloth FM, Alam W and Hollis B: Vitamin D vs broad spectrum phototherapy in the treatment of seasonal affective disorder. Journal of Nutrition Health and Aging 1999; 3: 5-7.
- Umhau JC, George DT, Heaney RP, Lewis MD, Ursano RJ, Heilig M, Hibbeln JR and Schwandt ML: Low Vitamin D status and suicide: A case-control study of active duty military service members. PLoS One 2013; 8: e51543.
- Hoang MT, Defina LF, Willis BL, Leonard DS, Weiner MF and Brown ES: Association between low serum 25-hydroxy Vitamin D and depression in a large sample of healthy adults: the Cooper Center longitudinal study. Mayo Clinic Proceedings 2011; 86: 1050-1055.
- Ferrari AJ, Charlson FJ, Norman RE, Patten SB, Freedman G, Murray CJ, Vos T and Whiteford HA: Burden of Depressive Disorders by Country, Sex, Age, and Year: Findings from the Global Burden of Disease Study 2010. PLOS Med 2013; 10(11): e1001547.
- Sathyanayarana RTS, Darshan MS, Tandon A, Raman R, Karthik KN, Saraswathi N, Das K, Harsha GT, Krishna VS and Ashok NC: Suttur study: An epidemiological study of psychiatric disorders in south Indian rural population. Indian Journal of Psychiatry 2014; 56: 238-245.
- Mathias K, Goicolea I, Kermode M, Singh L, Shidhaye R and Sebastian MS: Cross- sectional study of depression and help-seeking in Uttarakhand, North India. BMJ Open 2015; 5: e008992.
- Behera P, Sharan P, Mishra AK, Nongkynrih B, Kant S and Gupta SK: Prevalence and determinants of depression among elderly persons in a rural community from northern India. National Medical Journal of India. 2016; 29: 129-135.
- Charlson FJ, Baxter AJ, Cheng HG, Shidhaye R and Whiteford HA: The burden of mental, neurological, and substance use disorders in China and India: A systematic analysis of community representative epidemiological studies. Lancet 2016; 388: 376-389.
- Shidhaye R, Gangale S and Patel V: Prevalence and treatment coverage for depression: A population-based survey in Vidarbha, India. Social Psychiatry and Psychiatric Epidemiology 2016; 51: 993-1003.
- American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorder. American Psychiatric Association Publishing. Fifth Edition 2013.
- Hamilton M: A rating scale for depression. Journal of Neurology, Neurosurgery, and Psychiatry 1960; 23: 56-62.
- Rating Scales. The British Columbia Cognitive Complaint Inventory (BC-CCI). The University of British Columbia. (http://workingwithdepression.psychiatry.ubc.ca/leaps/the-british-columbia-cognitive-complaints-inventory-bc-cci/)
- Tiwari SC and Tripathi RK: Development of an Education and Culture Fair Hindi Cognitive Screening Test for the Elderly Population of India. Indian Journal of Geriatric Mental Health. 2011; 7(2): 83-96.
- Schneider B, Weber B, Frensch A, Stein J and Fritze J: Vitamin D in schizophrenia, major depression and alcoholism. Journal of Neural Transmission 2000; 107: 839-842.
- Wilkins CH, Sheline YI, Roe CM, Birge SJ and Morris JC: Vitamin D deficiency is associated with low mood and worse cognitive performance in older adults. American Journal of Geriatric Psychiatry 2006; 14(12): 1032-1040.
- Eyles DW, Smith S, Kinobe R, Hewison M and McGrath JJ. Distribution of the Vitamin D receptor and 1 alpha-hydroxylase in human brain. Journal of Chemical Neuroanatomy 2005; 29: 21-30.
- Eyles D, Brown J, Mackay-Sim A, McGrath J and Feron F: Vitamin D3 and brain development. Neuroscience 2003; 118: 641-653.
- McCann JC and Ames BN: Is there convincing biological or behavioral evidence linking Vitamin D deficiency to brain dysfunction? FASEB Journal 2008: 22: 982.
- Harris S: Vitamin D and African Americans. Journal of Nutrition 2006; 136: 1126-1129.
- Boral GG, Ghosh AB, Pal SK, Ghosh KK and Nandi DN: Thyroid function in depression. Indian Journal of Psychiatry 1980; 22: 353-355.
- Saxena J, Singh PN, Srivastava U and Siddiqui AQ: A study of thyroid hormones (T3, T4 and TSH) in patients of depression. Indian Journal of Psychiatry 2000; 42: 243-246.
- Gupta S, Saha PK and Mukhopadhyay A: Prevalence of hypothyroidism and importance of cholesterol estimation in patients suffering from major depressive disorder. Journal of Indian Medical Association 2008; 106: 240-242.
- Chopra VK and Daya Ram: Basal Thyroid Functions in First Episode Depressive Illness: A Controlled Study. Indian Journal of Psychiatry 2001; 43: 61-66.
- Hunt DL and Peland JG: Iron and depression in premenopausal women. An MMPI study. Behavioral Medicine 1999; 25(2): 62-68.
- Lozell B, Jmenez E and Hajen J: Poorer behavorial and developmental outcome more than 10 years after treatment for iron deficiency in infancy. Pédiatre 2000; 105: 51.
- Beard JL, Hendricks MK and Prez EM: Maternal iron deficiency anemia affects popartum emotions and cognition. Journal of Nutrition 2005; 135: 267-272.
- Beard JL, Connor JR and Jones BC: Iron in the brain. Nutrition Reviews 1993; 51(6): 157-170.
- Paul I, Tumer RE and Ross D: Update Nutrition. John Pow Company: USA. Eight Edition 2002.
- Cuijpers P, Vogelzangs N, Twisk J, Kleiboer A, Li J and Penninx BW: Comprehensive Meta-Analysis of Excess Mortality in Depression in the General Community Versus Patients With Specific Illnesses. American Journal of Psychiatry. 2014; 171: 453-462.
- Cipriani A, La Ferla T, Furukawa TA, Signoretti A, Nakagawa A, Churchill R, McGuire H and Barbui C: Sertraline versus other antidepressive agents for depression. Cochrane Database of Systematic Reviews 2009; (2): CD006117.
How to cite this article:
Kumar A, Sharma R, Arora M and Gupta RC: Biochemical analysis in patients with major depressive disorder in Jammu population. Int J Pharm Sci Res 2018; 9(1): 354-60.doi: 10.13040/IJPSR.0975-8232.9(1).354-60.
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Article Information
47
354-360
435
979
English
IJPSR
A. Kumar, R. Sharma*, M. Arora and R. C. Gupta
Department of Zoology, MCM DAV College, Chandigarh, Punjab, India.
radhikachd24@gmail.com
09 May, 2017
25 October, 2017
23 December, 2017
10.13040/IJPSR.0975-8232.9(1).354-60
01 January, 2018