Late-Life Depression is Associated With Increased Levels of GDF-15, a Pro-Aging Mitokine
•What is the primary question addressed by this study? We sought to evaluate the circulating levels of growth differentiation factor-15 (GDF-15) in older adults with major depressive disorder and its association with depression severity, physical comorbidity burden, age of onset of first depressive...
Gespeichert in:
Veröffentlicht in: | The American journal of geriatric psychiatry 2023-01, Vol.31 (1), p.1-9 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 9 |
---|---|
container_issue | 1 |
container_start_page | 1 |
container_title | The American journal of geriatric psychiatry |
container_volume | 31 |
creator | Mastrobattista, Emma Lenze, Eric J. Reynolds, Charles F. Mulsant, Benoit H. Wetherell, Julie Wu, Gregory F. Blumberger, Daniel M. Karp, Jordan F. Butters, Meryl A. Mendes-Silva, Ana Paula Vieira, Erica L. Tseng, George Diniz, Breno S. |
description | •What is the primary question addressed by this study? We sought to evaluate the circulating levels of growth differentiation factor-15 (GDF-15) in older adults with major depressive disorder and its association with depression severity, physical comorbidity burden, age of onset of first depressive episode, and cognitive performance.•What is the main finding of this study? Depressed older adults had significantly higher GDF-15 serum levels than comparison individuals. Among depressed individuals, those with high GDF-15 had higher levels of comorbid physical illness, lower executive cognitive functioning, and higher likelihood of having late-onset depression.•What is the meaning of the finding? GDF-15 is a novel and potentially targetable biological pathway between depression and accelerated aging, including cognitive aging.
In older adults, major depressive disorder (MDD) is associated with accelerated physiological and cognitive aging, generating interest in uncovering biological pathways that may be targetable by interventions. Growth differentiation factor-15 (GDF-15) plays a significant role in biological aging via multiple biological pathways relevant to age and age-related diseases. Elevated levels of GDF-15 correlate with increasing chronological age, decreased telomerase activity, and increased mortality risk in older adults. We sought to evaluate the circulating levels of GDF-15 in older adults with MDD and its association with depression severity, physical comorbidity burden, age of onset of first depressive episode, and cognitive performance.
This study assayed circulating levels of GDF-15 in 393 older adults (mean ± SD age 70 ± 6.6 years, male:female ratio 1:1.54), 308 with MDD and 85 non-depressed comparison individuals.
After adjusting for confounding variables, depressed older adults had significantly higher GDF-15 serum levels (640.1 ± 501.5 ng/mL) than comparison individuals (431.90 ± 223.35 ng/mL) (t=3.75, d.f.= 391, p=0.0002). Among depressed individuals, those with high GDF-15 had higher levels of comorbid physical illness, lower executive cognitive functioning, and higher likelihood of having late-onset depression.
Our results suggest that depression in late life is associated with GDF-15, a marker of amplified age-related biological changes. GDF-15 is a novel and potentially targetable biological pathway between depression and accelerated aging, including cognitive aging. |
doi_str_mv | 10.1016/j.jagp.2022.08.003 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9701166</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S106474812200495X</els_id><sourcerecordid>2717696941</sourcerecordid><originalsourceid>FETCH-LOGICAL-c455t-a4f45897c749fe9e26e56c6813cdf751393cdeb5eb5345ed6f992f25ea3c062b3</originalsourceid><addsrcrecordid>eNp9kU1rGzEQhkVIaRK3fyCHoGMO3Y2klbQrKAGTb9jSHlram5C1I0fueuVIa0P_fWTshORSGJgR8847Yh6ETikpKaHyYlEuzHxVMsJYSZqSkOoAHVPBRVEzyg9zTSQvat7QI3SS0oIQIpXkH9FRJamomCLH6E9rRiha7wBfwypCSj4M2Cc8TSlYn5sd_u3HR_ww2Agm5WcLG-gTDg7fXd8WVHzBBv-IoZjO_TDH3_wY_voBPqEPzvQJPu_zBP26vfl5dV-03-8erqZtYbkQY2G446JRta25cqCASRDSyoZWtnO1oJXKBcxEjooL6KRTijkmwFSWSDarJuhy57taz5bQWRjGaHq9in5p4j8djNfvO4N_1POw0aomlEqZDc73BjE8rSGNeumThb43A4R10qymdT6b4jRL2U5qY0gpgntdQ4neItELvUWit0g0aXRGkofO3n7wdeSFQRZ83QnyVWHjIepkPQwWOh_BjroL_n_-z20OnK4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2717696941</pqid></control><display><type>article</type><title>Late-Life Depression is Associated With Increased Levels of GDF-15, a Pro-Aging Mitokine</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Mastrobattista, Emma ; Lenze, Eric J. ; Reynolds, Charles F. ; Mulsant, Benoit H. ; Wetherell, Julie ; Wu, Gregory F. ; Blumberger, Daniel M. ; Karp, Jordan F. ; Butters, Meryl A. ; Mendes-Silva, Ana Paula ; Vieira, Erica L. ; Tseng, George ; Diniz, Breno S.</creator><creatorcontrib>Mastrobattista, Emma ; Lenze, Eric J. ; Reynolds, Charles F. ; Mulsant, Benoit H. ; Wetherell, Julie ; Wu, Gregory F. ; Blumberger, Daniel M. ; Karp, Jordan F. ; Butters, Meryl A. ; Mendes-Silva, Ana Paula ; Vieira, Erica L. ; Tseng, George ; Diniz, Breno S.</creatorcontrib><description>•What is the primary question addressed by this study? We sought to evaluate the circulating levels of growth differentiation factor-15 (GDF-15) in older adults with major depressive disorder and its association with depression severity, physical comorbidity burden, age of onset of first depressive episode, and cognitive performance.•What is the main finding of this study? Depressed older adults had significantly higher GDF-15 serum levels than comparison individuals. Among depressed individuals, those with high GDF-15 had higher levels of comorbid physical illness, lower executive cognitive functioning, and higher likelihood of having late-onset depression.•What is the meaning of the finding? GDF-15 is a novel and potentially targetable biological pathway between depression and accelerated aging, including cognitive aging.
In older adults, major depressive disorder (MDD) is associated with accelerated physiological and cognitive aging, generating interest in uncovering biological pathways that may be targetable by interventions. Growth differentiation factor-15 (GDF-15) plays a significant role in biological aging via multiple biological pathways relevant to age and age-related diseases. Elevated levels of GDF-15 correlate with increasing chronological age, decreased telomerase activity, and increased mortality risk in older adults. We sought to evaluate the circulating levels of GDF-15 in older adults with MDD and its association with depression severity, physical comorbidity burden, age of onset of first depressive episode, and cognitive performance.
This study assayed circulating levels of GDF-15 in 393 older adults (mean ± SD age 70 ± 6.6 years, male:female ratio 1:1.54), 308 with MDD and 85 non-depressed comparison individuals.
After adjusting for confounding variables, depressed older adults had significantly higher GDF-15 serum levels (640.1 ± 501.5 ng/mL) than comparison individuals (431.90 ± 223.35 ng/mL) (t=3.75, d.f.= 391, p=0.0002). Among depressed individuals, those with high GDF-15 had higher levels of comorbid physical illness, lower executive cognitive functioning, and higher likelihood of having late-onset depression.
Our results suggest that depression in late life is associated with GDF-15, a marker of amplified age-related biological changes. GDF-15 is a novel and potentially targetable biological pathway between depression and accelerated aging, including cognitive aging.</description><identifier>ISSN: 1064-7481</identifier><identifier>EISSN: 1545-7214</identifier><identifier>DOI: 10.1016/j.jagp.2022.08.003</identifier><identifier>PMID: 36153290</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Aged ; Aging ; biological markers ; Biomarkers ; Comorbidity ; Depression - epidemiology ; Depressive Disorder, Major - epidemiology ; Female ; GDF-15 ; Geroscience ; Growth Differentiation Factor 15 ; Humans ; Late life depression ; Male</subject><ispartof>The American journal of geriatric psychiatry, 2023-01, Vol.31 (1), p.1-9</ispartof><rights>2022 American Association for Geriatric Psychiatry</rights><rights>Copyright © 2022 American Association for Geriatric Psychiatry. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-a4f45897c749fe9e26e56c6813cdf751393cdeb5eb5345ed6f992f25ea3c062b3</citedby><cites>FETCH-LOGICAL-c455t-a4f45897c749fe9e26e56c6813cdf751393cdeb5eb5345ed6f992f25ea3c062b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36153290$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mastrobattista, Emma</creatorcontrib><creatorcontrib>Lenze, Eric J.</creatorcontrib><creatorcontrib>Reynolds, Charles F.</creatorcontrib><creatorcontrib>Mulsant, Benoit H.</creatorcontrib><creatorcontrib>Wetherell, Julie</creatorcontrib><creatorcontrib>Wu, Gregory F.</creatorcontrib><creatorcontrib>Blumberger, Daniel M.</creatorcontrib><creatorcontrib>Karp, Jordan F.</creatorcontrib><creatorcontrib>Butters, Meryl A.</creatorcontrib><creatorcontrib>Mendes-Silva, Ana Paula</creatorcontrib><creatorcontrib>Vieira, Erica L.</creatorcontrib><creatorcontrib>Tseng, George</creatorcontrib><creatorcontrib>Diniz, Breno S.</creatorcontrib><title>Late-Life Depression is Associated With Increased Levels of GDF-15, a Pro-Aging Mitokine</title><title>The American journal of geriatric psychiatry</title><addtitle>Am J Geriatr Psychiatry</addtitle><description>•What is the primary question addressed by this study? We sought to evaluate the circulating levels of growth differentiation factor-15 (GDF-15) in older adults with major depressive disorder and its association with depression severity, physical comorbidity burden, age of onset of first depressive episode, and cognitive performance.•What is the main finding of this study? Depressed older adults had significantly higher GDF-15 serum levels than comparison individuals. Among depressed individuals, those with high GDF-15 had higher levels of comorbid physical illness, lower executive cognitive functioning, and higher likelihood of having late-onset depression.•What is the meaning of the finding? GDF-15 is a novel and potentially targetable biological pathway between depression and accelerated aging, including cognitive aging.
In older adults, major depressive disorder (MDD) is associated with accelerated physiological and cognitive aging, generating interest in uncovering biological pathways that may be targetable by interventions. Growth differentiation factor-15 (GDF-15) plays a significant role in biological aging via multiple biological pathways relevant to age and age-related diseases. Elevated levels of GDF-15 correlate with increasing chronological age, decreased telomerase activity, and increased mortality risk in older adults. We sought to evaluate the circulating levels of GDF-15 in older adults with MDD and its association with depression severity, physical comorbidity burden, age of onset of first depressive episode, and cognitive performance.
This study assayed circulating levels of GDF-15 in 393 older adults (mean ± SD age 70 ± 6.6 years, male:female ratio 1:1.54), 308 with MDD and 85 non-depressed comparison individuals.
After adjusting for confounding variables, depressed older adults had significantly higher GDF-15 serum levels (640.1 ± 501.5 ng/mL) than comparison individuals (431.90 ± 223.35 ng/mL) (t=3.75, d.f.= 391, p=0.0002). Among depressed individuals, those with high GDF-15 had higher levels of comorbid physical illness, lower executive cognitive functioning, and higher likelihood of having late-onset depression.
Our results suggest that depression in late life is associated with GDF-15, a marker of amplified age-related biological changes. GDF-15 is a novel and potentially targetable biological pathway between depression and accelerated aging, including cognitive aging.</description><subject>Aged</subject><subject>Aging</subject><subject>biological markers</subject><subject>Biomarkers</subject><subject>Comorbidity</subject><subject>Depression - epidemiology</subject><subject>Depressive Disorder, Major - epidemiology</subject><subject>Female</subject><subject>GDF-15</subject><subject>Geroscience</subject><subject>Growth Differentiation Factor 15</subject><subject>Humans</subject><subject>Late life depression</subject><subject>Male</subject><issn>1064-7481</issn><issn>1545-7214</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1rGzEQhkVIaRK3fyCHoGMO3Y2klbQrKAGTb9jSHlram5C1I0fueuVIa0P_fWTshORSGJgR8847Yh6ETikpKaHyYlEuzHxVMsJYSZqSkOoAHVPBRVEzyg9zTSQvat7QI3SS0oIQIpXkH9FRJamomCLH6E9rRiha7wBfwypCSj4M2Cc8TSlYn5sd_u3HR_ww2Agm5WcLG-gTDg7fXd8WVHzBBv-IoZjO_TDH3_wY_voBPqEPzvQJPu_zBP26vfl5dV-03-8erqZtYbkQY2G446JRta25cqCASRDSyoZWtnO1oJXKBcxEjooL6KRTijkmwFSWSDarJuhy57taz5bQWRjGaHq9in5p4j8djNfvO4N_1POw0aomlEqZDc73BjE8rSGNeumThb43A4R10qymdT6b4jRL2U5qY0gpgntdQ4neItELvUWit0g0aXRGkofO3n7wdeSFQRZ83QnyVWHjIepkPQwWOh_BjroL_n_-z20OnK4</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Mastrobattista, Emma</creator><creator>Lenze, Eric J.</creator><creator>Reynolds, Charles F.</creator><creator>Mulsant, Benoit H.</creator><creator>Wetherell, Julie</creator><creator>Wu, Gregory F.</creator><creator>Blumberger, Daniel M.</creator><creator>Karp, Jordan F.</creator><creator>Butters, Meryl A.</creator><creator>Mendes-Silva, Ana Paula</creator><creator>Vieira, Erica L.</creator><creator>Tseng, George</creator><creator>Diniz, Breno S.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20230101</creationdate><title>Late-Life Depression is Associated With Increased Levels of GDF-15, a Pro-Aging Mitokine</title><author>Mastrobattista, Emma ; Lenze, Eric J. ; Reynolds, Charles F. ; Mulsant, Benoit H. ; Wetherell, Julie ; Wu, Gregory F. ; Blumberger, Daniel M. ; Karp, Jordan F. ; Butters, Meryl A. ; Mendes-Silva, Ana Paula ; Vieira, Erica L. ; Tseng, George ; Diniz, Breno S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-a4f45897c749fe9e26e56c6813cdf751393cdeb5eb5345ed6f992f25ea3c062b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Aged</topic><topic>Aging</topic><topic>biological markers</topic><topic>Biomarkers</topic><topic>Comorbidity</topic><topic>Depression - epidemiology</topic><topic>Depressive Disorder, Major - epidemiology</topic><topic>Female</topic><topic>GDF-15</topic><topic>Geroscience</topic><topic>Growth Differentiation Factor 15</topic><topic>Humans</topic><topic>Late life depression</topic><topic>Male</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mastrobattista, Emma</creatorcontrib><creatorcontrib>Lenze, Eric J.</creatorcontrib><creatorcontrib>Reynolds, Charles F.</creatorcontrib><creatorcontrib>Mulsant, Benoit H.</creatorcontrib><creatorcontrib>Wetherell, Julie</creatorcontrib><creatorcontrib>Wu, Gregory F.</creatorcontrib><creatorcontrib>Blumberger, Daniel M.</creatorcontrib><creatorcontrib>Karp, Jordan F.</creatorcontrib><creatorcontrib>Butters, Meryl A.</creatorcontrib><creatorcontrib>Mendes-Silva, Ana Paula</creatorcontrib><creatorcontrib>Vieira, Erica L.</creatorcontrib><creatorcontrib>Tseng, George</creatorcontrib><creatorcontrib>Diniz, Breno S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of geriatric psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mastrobattista, Emma</au><au>Lenze, Eric J.</au><au>Reynolds, Charles F.</au><au>Mulsant, Benoit H.</au><au>Wetherell, Julie</au><au>Wu, Gregory F.</au><au>Blumberger, Daniel M.</au><au>Karp, Jordan F.</au><au>Butters, Meryl A.</au><au>Mendes-Silva, Ana Paula</au><au>Vieira, Erica L.</au><au>Tseng, George</au><au>Diniz, Breno S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Late-Life Depression is Associated With Increased Levels of GDF-15, a Pro-Aging Mitokine</atitle><jtitle>The American journal of geriatric psychiatry</jtitle><addtitle>Am J Geriatr Psychiatry</addtitle><date>2023-01-01</date><risdate>2023</risdate><volume>31</volume><issue>1</issue><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>1064-7481</issn><eissn>1545-7214</eissn><abstract>•What is the primary question addressed by this study? We sought to evaluate the circulating levels of growth differentiation factor-15 (GDF-15) in older adults with major depressive disorder and its association with depression severity, physical comorbidity burden, age of onset of first depressive episode, and cognitive performance.•What is the main finding of this study? Depressed older adults had significantly higher GDF-15 serum levels than comparison individuals. Among depressed individuals, those with high GDF-15 had higher levels of comorbid physical illness, lower executive cognitive functioning, and higher likelihood of having late-onset depression.•What is the meaning of the finding? GDF-15 is a novel and potentially targetable biological pathway between depression and accelerated aging, including cognitive aging.
In older adults, major depressive disorder (MDD) is associated with accelerated physiological and cognitive aging, generating interest in uncovering biological pathways that may be targetable by interventions. Growth differentiation factor-15 (GDF-15) plays a significant role in biological aging via multiple biological pathways relevant to age and age-related diseases. Elevated levels of GDF-15 correlate with increasing chronological age, decreased telomerase activity, and increased mortality risk in older adults. We sought to evaluate the circulating levels of GDF-15 in older adults with MDD and its association with depression severity, physical comorbidity burden, age of onset of first depressive episode, and cognitive performance.
This study assayed circulating levels of GDF-15 in 393 older adults (mean ± SD age 70 ± 6.6 years, male:female ratio 1:1.54), 308 with MDD and 85 non-depressed comparison individuals.
After adjusting for confounding variables, depressed older adults had significantly higher GDF-15 serum levels (640.1 ± 501.5 ng/mL) than comparison individuals (431.90 ± 223.35 ng/mL) (t=3.75, d.f.= 391, p=0.0002). Among depressed individuals, those with high GDF-15 had higher levels of comorbid physical illness, lower executive cognitive functioning, and higher likelihood of having late-onset depression.
Our results suggest that depression in late life is associated with GDF-15, a marker of amplified age-related biological changes. GDF-15 is a novel and potentially targetable biological pathway between depression and accelerated aging, including cognitive aging.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>36153290</pmid><doi>10.1016/j.jagp.2022.08.003</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1064-7481 |
ispartof | The American journal of geriatric psychiatry, 2023-01, Vol.31 (1), p.1-9 |
issn | 1064-7481 1545-7214 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9701166 |
source | MEDLINE; Alma/SFX Local Collection |
subjects | Aged Aging biological markers Biomarkers Comorbidity Depression - epidemiology Depressive Disorder, Major - epidemiology Female GDF-15 Geroscience Growth Differentiation Factor 15 Humans Late life depression Male |
title | Late-Life Depression is Associated With Increased Levels of GDF-15, a Pro-Aging Mitokine |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T21%3A43%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Late-Life%20Depression%20is%20Associated%20With%20Increased%20Levels%20of%20GDF-15,%20a%20Pro-Aging%20Mitokine&rft.jtitle=The%20American%20journal%20of%20geriatric%20psychiatry&rft.au=Mastrobattista,%20Emma&rft.date=2023-01-01&rft.volume=31&rft.issue=1&rft.spage=1&rft.epage=9&rft.pages=1-9&rft.issn=1064-7481&rft.eissn=1545-7214&rft_id=info:doi/10.1016/j.jagp.2022.08.003&rft_dat=%3Cproquest_pubme%3E2717696941%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2717696941&rft_id=info:pmid/36153290&rft_els_id=S106474812200495X&rfr_iscdi=true |