Association between uremic toxins and depression in patients with chronic kidney disease undergoing maintenance hemodialysis

Patients with chronic kidney disease (CKD) who are undergoing maintenance hemodialysis have a higher prevalence of depression than the general population. The underlying cause of this association is unknown, but may be related to accumulation of uremic toxins. Little is known about the association o...

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Published inGeneral hospital psychiatry Vol. 35; no. 1; pp. 23 - 27
Main Authors Hsu, Heng-Jung, Yen, Chiung-Hui, Chen, Chih-Ken, Wu, I-Wen, Lee, Chin-Chan, Sun, Chiao-Yin, Chang, Shu-Ju, Chou, Chia-Chi, Hsieh, Ming-Fang, Chen, Chun-Yu, Hsu, Chiao-Ying, Tsai, Chi-Jen, Wu, Mai-Szu
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.01.2013
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Abstract Patients with chronic kidney disease (CKD) who are undergoing maintenance hemodialysis have a higher prevalence of depression than the general population. The underlying cause of this association is unknown, but may be related to accumulation of uremic toxins. Little is known about the association of accumulation of uremic toxins and depression in hemodialysis patients. We conducted a cross-sectional study of 209 CKD patients from a single institution to evaluate the associations of a soluble small uremic toxin (urea), a soluble large uremic toxin (β2 microglobulin) and two protein-bound uremic toxins [total p-cresol sulfate (PCS) and indoxyl sulfate (IS)] with the presence of depression. A total of 47 patients (22.4%) had depression. Depressive patients had lower body mass index, lower serum creatinine, lower serum albumin and lower total IS. Univariate and multivariate logistic regression analyses that adjusted for age, gender and other statistically significant variables indicated that depression was significantly and independently associated with lower serum albumin and lower total IS. The levels of urea, β2 microglobulin and PCS were not significantly associated with depression. Our results indicate that depression in patients with CKD was significantly and independently associated with lower serum albumin and lower total IS. However, the pathological mechanisms underlying these associations are unknown.
AbstractList Patients with chronic kidney disease (CKD) who are undergoing maintenance hemodialysis have a higher prevalence of depression than the general population. The underlying cause of this association is unknown, but may be related to accumulation of uremic toxins. Little is known about the association of accumulation of uremic toxins and depression in hemodialysis patients. We conducted a cross-sectional study of 209 CKD patients from a single institution to evaluate the associations of a soluble small uremic toxin (urea), a soluble large uremic toxin (β2 microglobulin) and two protein-bound uremic toxins [total p-cresol sulfate (PCS) and indoxyl sulfate (IS)] with the presence of depression. A total of 47 patients (22.4%) had depression. Depressive patients had lower body mass index, lower serum creatinine, lower serum albumin and lower total IS. Univariate and multivariate logistic regression analyses that adjusted for age, gender and other statistically significant variables indicated that depression was significantly and independently associated with lower serum albumin and lower total IS. The levels of urea, β2 microglobulin and PCS were not significantly associated with depression. Our results indicate that depression in patients with CKD was significantly and independently associated with lower serum albumin and lower total IS. However, the pathological mechanisms underlying these associations are unknown.
Abstract Objective Patients with chronic kidney disease (CKD) who are undergoing maintenance hemodialysis have a higher prevalence of depression than the general population. The underlying cause of this association is unknown, but may be related to accumulation of uremic toxins. Little is known about the association of accumulation of uremic toxins and depression in hemodialysis patients. Method We conducted a cross-sectional study of 209 CKD patients from a single institution to evaluate the associations of a soluble small uremic toxin (urea), a soluble large uremic toxin (β2 microglobulin) and two protein-bound uremic toxins [total p-cresol sulfate (PCS) and indoxyl sulfate (IS)] with the presence of depression. Results A total of 47 patients (22.4%) had depression. Depressive patients had lower body mass index, lower serum creatinine, lower serum albumin and lower total IS. Univariate and multivariate logistic regression analyses that adjusted for age, gender and other statistically significant variables indicated that depression was significantly and independently associated with lower serum albumin and lower total IS. The levels of urea, β2 microglobulin and PCS were not significantly associated with depression. Conclusion Our results indicate that depression in patients with CKD was significantly and independently associated with lower serum albumin and lower total IS. However, the pathological mechanisms underlying these associations are unknown.
Patients with chronic kidney disease (CKD) who are undergoing maintenance hemodialysis have a higher prevalence of depression than the general population. The underlying cause of this association is unknown, but may be related to accumulation of uremic toxins. Little is known about the association of accumulation of uremic toxins and depression in hemodialysis patients.OBJECTIVEPatients with chronic kidney disease (CKD) who are undergoing maintenance hemodialysis have a higher prevalence of depression than the general population. The underlying cause of this association is unknown, but may be related to accumulation of uremic toxins. Little is known about the association of accumulation of uremic toxins and depression in hemodialysis patients.We conducted a cross-sectional study of 209 CKD patients from a single institution to evaluate the associations of a soluble small uremic toxin (urea), a soluble large uremic toxin (β2 microglobulin) and two protein-bound uremic toxins [total p-cresol sulfate (PCS) and indoxyl sulfate (IS)] with the presence of depression.METHODWe conducted a cross-sectional study of 209 CKD patients from a single institution to evaluate the associations of a soluble small uremic toxin (urea), a soluble large uremic toxin (β2 microglobulin) and two protein-bound uremic toxins [total p-cresol sulfate (PCS) and indoxyl sulfate (IS)] with the presence of depression.A total of 47 patients (22.4%) had depression. Depressive patients had lower body mass index, lower serum creatinine, lower serum albumin and lower total IS. Univariate and multivariate logistic regression analyses that adjusted for age, gender and other statistically significant variables indicated that depression was significantly and independently associated with lower serum albumin and lower total IS. The levels of urea, β2 microglobulin and PCS were not significantly associated with depression.RESULTSA total of 47 patients (22.4%) had depression. Depressive patients had lower body mass index, lower serum creatinine, lower serum albumin and lower total IS. Univariate and multivariate logistic regression analyses that adjusted for age, gender and other statistically significant variables indicated that depression was significantly and independently associated with lower serum albumin and lower total IS. The levels of urea, β2 microglobulin and PCS were not significantly associated with depression.Our results indicate that depression in patients with CKD was significantly and independently associated with lower serum albumin and lower total IS. However, the pathological mechanisms underlying these associations are unknown.CONCLUSIONOur results indicate that depression in patients with CKD was significantly and independently associated with lower serum albumin and lower total IS. However, the pathological mechanisms underlying these associations are unknown.
Author Chang, Shu-Ju
Hsu, Chiao-Ying
Chou, Chia-Chi
Sun, Chiao-Yin
Lee, Chin-Chan
Yen, Chiung-Hui
Chen, Chih-Ken
Chen, Chun-Yu
Wu, Mai-Szu
Hsieh, Ming-Fang
Hsu, Heng-Jung
Wu, I-Wen
Tsai, Chi-Jen
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  givenname: Mai-Szu
  surname: Wu
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  email: maiszuwu@gmail.com
  organization: Division of Nephrology, Chang Gung Memorial Hospital, Keelung, Taiwan
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Issue 1
Keywords Depression
β2 Microglobulin
Chronic kidney disease
Hemodialysis
P-Cresol sulfate
Indoxyl sulfate
Kidney disease
Mood disorder
Human
Urinary system disease
Maintenance hemodialysis
Sulfates
Concomitant disease
Cross sectional study
Renal failure
Language English
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CC BY 4.0
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Snippet Patients with chronic kidney disease (CKD) who are undergoing maintenance hemodialysis have a higher prevalence of depression than the general population. The...
Abstract Objective Patients with chronic kidney disease (CKD) who are undergoing maintenance hemodialysis have a higher prevalence of depression than the...
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SubjectTerms Adult
Adult and adolescent clinical studies
Aged
beta 2-Microglobulin - blood
Biological and medical sciences
Body Mass Index
Chronic kidney disease
Cohort Studies
Creatinine - blood
Cresols - blood
Cross-Sectional Studies
Depression
Depressive Disorder - blood
Depressive Disorder - epidemiology
Female
Hemodialysis
Humans
Indican - blood
Indoxyl sulfate
Kidney Failure, Chronic - blood
Kidney Failure, Chronic - complications
Kidney Failure, Chronic - psychology
Kidneys
Logistic Models
Male
Medical sciences
Middle Aged
Mood disorders
Nephrology. Urinary tract diseases
Nephropathies. Renovascular diseases. Renal failure
P-Cresol sulfate
Psychiatry
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Renal Dialysis - psychology
Renal failure
Serum Albumin - analysis
Sulfuric Acid Esters - blood
Urea - blood
Uremia - blood
Uremia - etiology
Uremia - psychology
Urinary system involvement in other diseases. Miscellaneous
β2 Microglobulin
Title Association between uremic toxins and depression in patients with chronic kidney disease undergoing maintenance hemodialysis
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https://www.clinicalkey.es/playcontent/1-s2.0-S0163834312002721
https://dx.doi.org/10.1016/j.genhosppsych.2012.08.009
https://www.ncbi.nlm.nih.gov/pubmed/23044245
https://www.proquest.com/docview/1273666383
Volume 35
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