Sex-specific associations of inflammation markers with cognitive decline
Background/objective: Inflammation is implicated in cognitive decline; however, there is a paucity of data for African American populations and for sex-specific associations.Design: Prospective cohort study.Setting: Genetic Epidemiology Network of Arteriopathy/Genetics of Microangiopathic Brain Inju...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
West, Nancy A. [verfasserIn] Kullo, Iftikhar J. [verfasserIn] Morris, M. Caroline [verfasserIn] Mosley, Thomas H. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2020 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Experimental gerontology - Amsterdam [u.a.] : Elsevier Science, 1964, 138 |
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| Übergeordnetes Werk: |
volume:138 |
| DOI / URN: |
10.1016/j.exger.2020.110986 |
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| Katalog-ID: |
ELV004404955 |
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| 100 | 1 | |a West, Nancy A. |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Sex-specific associations of inflammation markers with cognitive decline |
| 264 | 1 | |c 2020 | |
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| 337 | |a Computermedien |b c |2 rdamedia | ||
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| 520 | |a Background/objective: Inflammation is implicated in cognitive decline; however, there is a paucity of data for African American populations and for sex-specific associations.Design: Prospective cohort study.Setting: Genetic Epidemiology Network of Arteriopathy/Genetics of Microangiopathic Brain Injury studies.Participants: African-American sibships (N = 1010).Measurements: Neurocognitive tests assessed global cognition and four cognitive domains: processing speed, memory, language, and executive function at two time points over seven years. Circulating levels of C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor receptor (TNFR)-1 and TNFR2 were measured at study baseline. Linear mixed models were used to investigate the association between inflammation markers and cognitive decline.Results: Among men, a one SD increase in CRP was associated with an increased rate of decline over 7 years in global cognitive Z-score (adjusted difference in slopes = −0.31, p = 0.006) and in processing speed Z-score (adjusted difference in slopes = −0.10, p = 0.02), but not declines in memory, language, or executive function Z-scores. Also among men, a one SD increase in IL-6 was associated with an increased decline rate in global cognitive Z-score (adjusted difference in slopes = −0.33, p = 0.002) and in processing speed Z-score (adjusted difference in slopes = −0.12, p = 0.007). There was no difference in decline rates by CRP or IL-6 level in adjusted analyses among women for any cognitive scores. Among men and women combined, a one SD increase in baseline sTNFR1 was associated with a faster rate of decline in memory Z-score (adjusted difference in slopes = −0.09, p = 0.02). Baseline sTNFR2 levels did not significantly predict rate of cognitive decline in any cognitive domains.Conclusions: Circulating markers of CRP and IL-6 may be differential risk factors for men and women in relation to cognitive decline. A novel inflammation marker, sTNFR1, may be a useful predictor of memory decline in older adults. | ||
| 650 | 4 | |a Inflammation | |
| 650 | 4 | |a Cognitive decline | |
| 650 | 4 | |a CRP | |
| 650 | 4 | |a IL6 | |
| 650 | 4 | |a sTNFR1 | |
| 700 | 1 | |a Kullo, Iftikhar J. |e verfasserin |4 aut | |
| 700 | 1 | |a Morris, M. Caroline |e verfasserin |4 aut | |
| 700 | 1 | |a Mosley, Thomas H. |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Experimental gerontology |d Amsterdam [u.a.] : Elsevier Science, 1964 |g 138 |h Online-Ressource |w (DE-627)320445259 |w (DE-600)2005397-6 |w (DE-576)263808238 |x 1873-6815 |7 nnns |
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| 936 | b | k | |a 44.68 |j Gerontologie |j Geriatrie |
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10.1016/j.exger.2020.110986 doi (DE-627)ELV004404955 (ELSEVIER)S0531-5565(20)30334-X DE-627 ger DE-627 rda eng 610 DE-600 44.68 bkl West, Nancy A. verfasserin aut Sex-specific associations of inflammation markers with cognitive decline 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background/objective: Inflammation is implicated in cognitive decline; however, there is a paucity of data for African American populations and for sex-specific associations.Design: Prospective cohort study.Setting: Genetic Epidemiology Network of Arteriopathy/Genetics of Microangiopathic Brain Injury studies.Participants: African-American sibships (N = 1010).Measurements: Neurocognitive tests assessed global cognition and four cognitive domains: processing speed, memory, language, and executive function at two time points over seven years. Circulating levels of C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor receptor (TNFR)-1 and TNFR2 were measured at study baseline. Linear mixed models were used to investigate the association between inflammation markers and cognitive decline.Results: Among men, a one SD increase in CRP was associated with an increased rate of decline over 7 years in global cognitive Z-score (adjusted difference in slopes = −0.31, p = 0.006) and in processing speed Z-score (adjusted difference in slopes = −0.10, p = 0.02), but not declines in memory, language, or executive function Z-scores. Also among men, a one SD increase in IL-6 was associated with an increased decline rate in global cognitive Z-score (adjusted difference in slopes = −0.33, p = 0.002) and in processing speed Z-score (adjusted difference in slopes = −0.12, p = 0.007). There was no difference in decline rates by CRP or IL-6 level in adjusted analyses among women for any cognitive scores. Among men and women combined, a one SD increase in baseline sTNFR1 was associated with a faster rate of decline in memory Z-score (adjusted difference in slopes = −0.09, p = 0.02). Baseline sTNFR2 levels did not significantly predict rate of cognitive decline in any cognitive domains.Conclusions: Circulating markers of CRP and IL-6 may be differential risk factors for men and women in relation to cognitive decline. A novel inflammation marker, sTNFR1, may be a useful predictor of memory decline in older adults. Inflammation Cognitive decline CRP IL6 sTNFR1 Kullo, Iftikhar J. verfasserin aut Morris, M. Caroline verfasserin aut Mosley, Thomas H. verfasserin aut Enthalten in Experimental gerontology Amsterdam [u.a.] : Elsevier Science, 1964 138 Online-Ressource (DE-627)320445259 (DE-600)2005397-6 (DE-576)263808238 1873-6815 nnns volume:138 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2106 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.68 Gerontologie Geriatrie AR 138 |
| spelling |
10.1016/j.exger.2020.110986 doi (DE-627)ELV004404955 (ELSEVIER)S0531-5565(20)30334-X DE-627 ger DE-627 rda eng 610 DE-600 44.68 bkl West, Nancy A. verfasserin aut Sex-specific associations of inflammation markers with cognitive decline 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background/objective: Inflammation is implicated in cognitive decline; however, there is a paucity of data for African American populations and for sex-specific associations.Design: Prospective cohort study.Setting: Genetic Epidemiology Network of Arteriopathy/Genetics of Microangiopathic Brain Injury studies.Participants: African-American sibships (N = 1010).Measurements: Neurocognitive tests assessed global cognition and four cognitive domains: processing speed, memory, language, and executive function at two time points over seven years. Circulating levels of C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor receptor (TNFR)-1 and TNFR2 were measured at study baseline. Linear mixed models were used to investigate the association between inflammation markers and cognitive decline.Results: Among men, a one SD increase in CRP was associated with an increased rate of decline over 7 years in global cognitive Z-score (adjusted difference in slopes = −0.31, p = 0.006) and in processing speed Z-score (adjusted difference in slopes = −0.10, p = 0.02), but not declines in memory, language, or executive function Z-scores. Also among men, a one SD increase in IL-6 was associated with an increased decline rate in global cognitive Z-score (adjusted difference in slopes = −0.33, p = 0.002) and in processing speed Z-score (adjusted difference in slopes = −0.12, p = 0.007). There was no difference in decline rates by CRP or IL-6 level in adjusted analyses among women for any cognitive scores. Among men and women combined, a one SD increase in baseline sTNFR1 was associated with a faster rate of decline in memory Z-score (adjusted difference in slopes = −0.09, p = 0.02). Baseline sTNFR2 levels did not significantly predict rate of cognitive decline in any cognitive domains.Conclusions: Circulating markers of CRP and IL-6 may be differential risk factors for men and women in relation to cognitive decline. A novel inflammation marker, sTNFR1, may be a useful predictor of memory decline in older adults. Inflammation Cognitive decline CRP IL6 sTNFR1 Kullo, Iftikhar J. verfasserin aut Morris, M. Caroline verfasserin aut Mosley, Thomas H. verfasserin aut Enthalten in Experimental gerontology Amsterdam [u.a.] : Elsevier Science, 1964 138 Online-Ressource (DE-627)320445259 (DE-600)2005397-6 (DE-576)263808238 1873-6815 nnns volume:138 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2106 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.68 Gerontologie Geriatrie AR 138 |
| allfields_unstemmed |
10.1016/j.exger.2020.110986 doi (DE-627)ELV004404955 (ELSEVIER)S0531-5565(20)30334-X DE-627 ger DE-627 rda eng 610 DE-600 44.68 bkl West, Nancy A. verfasserin aut Sex-specific associations of inflammation markers with cognitive decline 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background/objective: Inflammation is implicated in cognitive decline; however, there is a paucity of data for African American populations and for sex-specific associations.Design: Prospective cohort study.Setting: Genetic Epidemiology Network of Arteriopathy/Genetics of Microangiopathic Brain Injury studies.Participants: African-American sibships (N = 1010).Measurements: Neurocognitive tests assessed global cognition and four cognitive domains: processing speed, memory, language, and executive function at two time points over seven years. Circulating levels of C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor receptor (TNFR)-1 and TNFR2 were measured at study baseline. Linear mixed models were used to investigate the association between inflammation markers and cognitive decline.Results: Among men, a one SD increase in CRP was associated with an increased rate of decline over 7 years in global cognitive Z-score (adjusted difference in slopes = −0.31, p = 0.006) and in processing speed Z-score (adjusted difference in slopes = −0.10, p = 0.02), but not declines in memory, language, or executive function Z-scores. Also among men, a one SD increase in IL-6 was associated with an increased decline rate in global cognitive Z-score (adjusted difference in slopes = −0.33, p = 0.002) and in processing speed Z-score (adjusted difference in slopes = −0.12, p = 0.007). There was no difference in decline rates by CRP or IL-6 level in adjusted analyses among women for any cognitive scores. Among men and women combined, a one SD increase in baseline sTNFR1 was associated with a faster rate of decline in memory Z-score (adjusted difference in slopes = −0.09, p = 0.02). Baseline sTNFR2 levels did not significantly predict rate of cognitive decline in any cognitive domains.Conclusions: Circulating markers of CRP and IL-6 may be differential risk factors for men and women in relation to cognitive decline. A novel inflammation marker, sTNFR1, may be a useful predictor of memory decline in older adults. Inflammation Cognitive decline CRP IL6 sTNFR1 Kullo, Iftikhar J. verfasserin aut Morris, M. Caroline verfasserin aut Mosley, Thomas H. verfasserin aut Enthalten in Experimental gerontology Amsterdam [u.a.] : Elsevier Science, 1964 138 Online-Ressource (DE-627)320445259 (DE-600)2005397-6 (DE-576)263808238 1873-6815 nnns volume:138 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2106 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.68 Gerontologie Geriatrie AR 138 |
| allfieldsGer |
10.1016/j.exger.2020.110986 doi (DE-627)ELV004404955 (ELSEVIER)S0531-5565(20)30334-X DE-627 ger DE-627 rda eng 610 DE-600 44.68 bkl West, Nancy A. verfasserin aut Sex-specific associations of inflammation markers with cognitive decline 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background/objective: Inflammation is implicated in cognitive decline; however, there is a paucity of data for African American populations and for sex-specific associations.Design: Prospective cohort study.Setting: Genetic Epidemiology Network of Arteriopathy/Genetics of Microangiopathic Brain Injury studies.Participants: African-American sibships (N = 1010).Measurements: Neurocognitive tests assessed global cognition and four cognitive domains: processing speed, memory, language, and executive function at two time points over seven years. Circulating levels of C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor receptor (TNFR)-1 and TNFR2 were measured at study baseline. Linear mixed models were used to investigate the association between inflammation markers and cognitive decline.Results: Among men, a one SD increase in CRP was associated with an increased rate of decline over 7 years in global cognitive Z-score (adjusted difference in slopes = −0.31, p = 0.006) and in processing speed Z-score (adjusted difference in slopes = −0.10, p = 0.02), but not declines in memory, language, or executive function Z-scores. Also among men, a one SD increase in IL-6 was associated with an increased decline rate in global cognitive Z-score (adjusted difference in slopes = −0.33, p = 0.002) and in processing speed Z-score (adjusted difference in slopes = −0.12, p = 0.007). There was no difference in decline rates by CRP or IL-6 level in adjusted analyses among women for any cognitive scores. Among men and women combined, a one SD increase in baseline sTNFR1 was associated with a faster rate of decline in memory Z-score (adjusted difference in slopes = −0.09, p = 0.02). Baseline sTNFR2 levels did not significantly predict rate of cognitive decline in any cognitive domains.Conclusions: Circulating markers of CRP and IL-6 may be differential risk factors for men and women in relation to cognitive decline. A novel inflammation marker, sTNFR1, may be a useful predictor of memory decline in older adults. Inflammation Cognitive decline CRP IL6 sTNFR1 Kullo, Iftikhar J. verfasserin aut Morris, M. Caroline verfasserin aut Mosley, Thomas H. verfasserin aut Enthalten in Experimental gerontology Amsterdam [u.a.] : Elsevier Science, 1964 138 Online-Ressource (DE-627)320445259 (DE-600)2005397-6 (DE-576)263808238 1873-6815 nnns volume:138 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2106 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.68 Gerontologie Geriatrie AR 138 |
| allfieldsSound |
10.1016/j.exger.2020.110986 doi (DE-627)ELV004404955 (ELSEVIER)S0531-5565(20)30334-X DE-627 ger DE-627 rda eng 610 DE-600 44.68 bkl West, Nancy A. verfasserin aut Sex-specific associations of inflammation markers with cognitive decline 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background/objective: Inflammation is implicated in cognitive decline; however, there is a paucity of data for African American populations and for sex-specific associations.Design: Prospective cohort study.Setting: Genetic Epidemiology Network of Arteriopathy/Genetics of Microangiopathic Brain Injury studies.Participants: African-American sibships (N = 1010).Measurements: Neurocognitive tests assessed global cognition and four cognitive domains: processing speed, memory, language, and executive function at two time points over seven years. Circulating levels of C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor receptor (TNFR)-1 and TNFR2 were measured at study baseline. Linear mixed models were used to investigate the association between inflammation markers and cognitive decline.Results: Among men, a one SD increase in CRP was associated with an increased rate of decline over 7 years in global cognitive Z-score (adjusted difference in slopes = −0.31, p = 0.006) and in processing speed Z-score (adjusted difference in slopes = −0.10, p = 0.02), but not declines in memory, language, or executive function Z-scores. Also among men, a one SD increase in IL-6 was associated with an increased decline rate in global cognitive Z-score (adjusted difference in slopes = −0.33, p = 0.002) and in processing speed Z-score (adjusted difference in slopes = −0.12, p = 0.007). There was no difference in decline rates by CRP or IL-6 level in adjusted analyses among women for any cognitive scores. Among men and women combined, a one SD increase in baseline sTNFR1 was associated with a faster rate of decline in memory Z-score (adjusted difference in slopes = −0.09, p = 0.02). Baseline sTNFR2 levels did not significantly predict rate of cognitive decline in any cognitive domains.Conclusions: Circulating markers of CRP and IL-6 may be differential risk factors for men and women in relation to cognitive decline. A novel inflammation marker, sTNFR1, may be a useful predictor of memory decline in older adults. Inflammation Cognitive decline CRP IL6 sTNFR1 Kullo, Iftikhar J. verfasserin aut Morris, M. Caroline verfasserin aut Mosley, Thomas H. verfasserin aut Enthalten in Experimental gerontology Amsterdam [u.a.] : Elsevier Science, 1964 138 Online-Ressource (DE-627)320445259 (DE-600)2005397-6 (DE-576)263808238 1873-6815 nnns volume:138 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2106 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.68 Gerontologie Geriatrie AR 138 |
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West, Nancy A. @@aut@@ Kullo, Iftikhar J. @@aut@@ Morris, M. Caroline @@aut@@ Mosley, Thomas H. @@aut@@ |
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2020-01-01T00:00:00Z |
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West, Nancy A. |
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West, Nancy A. ddc 610 bkl 44.68 misc Inflammation misc Cognitive decline misc CRP misc IL6 misc sTNFR1 Sex-specific associations of inflammation markers with cognitive decline |
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Sex-specific associations of inflammation markers with cognitive decline |
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Sex-specific associations of inflammation markers with cognitive decline |
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10.1016/j.exger.2020.110986 |
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sex-specific associations of inflammation markers with cognitive decline |
| title_auth |
Sex-specific associations of inflammation markers with cognitive decline |
| abstract |
Background/objective: Inflammation is implicated in cognitive decline; however, there is a paucity of data for African American populations and for sex-specific associations.Design: Prospective cohort study.Setting: Genetic Epidemiology Network of Arteriopathy/Genetics of Microangiopathic Brain Injury studies.Participants: African-American sibships (N = 1010).Measurements: Neurocognitive tests assessed global cognition and four cognitive domains: processing speed, memory, language, and executive function at two time points over seven years. Circulating levels of C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor receptor (TNFR)-1 and TNFR2 were measured at study baseline. Linear mixed models were used to investigate the association between inflammation markers and cognitive decline.Results: Among men, a one SD increase in CRP was associated with an increased rate of decline over 7 years in global cognitive Z-score (adjusted difference in slopes = −0.31, p = 0.006) and in processing speed Z-score (adjusted difference in slopes = −0.10, p = 0.02), but not declines in memory, language, or executive function Z-scores. Also among men, a one SD increase in IL-6 was associated with an increased decline rate in global cognitive Z-score (adjusted difference in slopes = −0.33, p = 0.002) and in processing speed Z-score (adjusted difference in slopes = −0.12, p = 0.007). There was no difference in decline rates by CRP or IL-6 level in adjusted analyses among women for any cognitive scores. Among men and women combined, a one SD increase in baseline sTNFR1 was associated with a faster rate of decline in memory Z-score (adjusted difference in slopes = −0.09, p = 0.02). Baseline sTNFR2 levels did not significantly predict rate of cognitive decline in any cognitive domains.Conclusions: Circulating markers of CRP and IL-6 may be differential risk factors for men and women in relation to cognitive decline. A novel inflammation marker, sTNFR1, may be a useful predictor of memory decline in older adults. |
| abstractGer |
Background/objective: Inflammation is implicated in cognitive decline; however, there is a paucity of data for African American populations and for sex-specific associations.Design: Prospective cohort study.Setting: Genetic Epidemiology Network of Arteriopathy/Genetics of Microangiopathic Brain Injury studies.Participants: African-American sibships (N = 1010).Measurements: Neurocognitive tests assessed global cognition and four cognitive domains: processing speed, memory, language, and executive function at two time points over seven years. Circulating levels of C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor receptor (TNFR)-1 and TNFR2 were measured at study baseline. Linear mixed models were used to investigate the association between inflammation markers and cognitive decline.Results: Among men, a one SD increase in CRP was associated with an increased rate of decline over 7 years in global cognitive Z-score (adjusted difference in slopes = −0.31, p = 0.006) and in processing speed Z-score (adjusted difference in slopes = −0.10, p = 0.02), but not declines in memory, language, or executive function Z-scores. Also among men, a one SD increase in IL-6 was associated with an increased decline rate in global cognitive Z-score (adjusted difference in slopes = −0.33, p = 0.002) and in processing speed Z-score (adjusted difference in slopes = −0.12, p = 0.007). There was no difference in decline rates by CRP or IL-6 level in adjusted analyses among women for any cognitive scores. Among men and women combined, a one SD increase in baseline sTNFR1 was associated with a faster rate of decline in memory Z-score (adjusted difference in slopes = −0.09, p = 0.02). Baseline sTNFR2 levels did not significantly predict rate of cognitive decline in any cognitive domains.Conclusions: Circulating markers of CRP and IL-6 may be differential risk factors for men and women in relation to cognitive decline. A novel inflammation marker, sTNFR1, may be a useful predictor of memory decline in older adults. |
| abstract_unstemmed |
Background/objective: Inflammation is implicated in cognitive decline; however, there is a paucity of data for African American populations and for sex-specific associations.Design: Prospective cohort study.Setting: Genetic Epidemiology Network of Arteriopathy/Genetics of Microangiopathic Brain Injury studies.Participants: African-American sibships (N = 1010).Measurements: Neurocognitive tests assessed global cognition and four cognitive domains: processing speed, memory, language, and executive function at two time points over seven years. Circulating levels of C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor receptor (TNFR)-1 and TNFR2 were measured at study baseline. Linear mixed models were used to investigate the association between inflammation markers and cognitive decline.Results: Among men, a one SD increase in CRP was associated with an increased rate of decline over 7 years in global cognitive Z-score (adjusted difference in slopes = −0.31, p = 0.006) and in processing speed Z-score (adjusted difference in slopes = −0.10, p = 0.02), but not declines in memory, language, or executive function Z-scores. Also among men, a one SD increase in IL-6 was associated with an increased decline rate in global cognitive Z-score (adjusted difference in slopes = −0.33, p = 0.002) and in processing speed Z-score (adjusted difference in slopes = −0.12, p = 0.007). There was no difference in decline rates by CRP or IL-6 level in adjusted analyses among women for any cognitive scores. Among men and women combined, a one SD increase in baseline sTNFR1 was associated with a faster rate of decline in memory Z-score (adjusted difference in slopes = −0.09, p = 0.02). Baseline sTNFR2 levels did not significantly predict rate of cognitive decline in any cognitive domains.Conclusions: Circulating markers of CRP and IL-6 may be differential risk factors for men and women in relation to cognitive decline. A novel inflammation marker, sTNFR1, may be a useful predictor of memory decline in older adults. |
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| score |
7.4003525 |