Kidney function changes and their relation with the progression of cerebral small vessel disease and cognitive decline

We aimed to study whether worsening in markers of kidney function parallels the progression in cerebral small vessel disease (cSVD) and cognitive decline. Data from the ISSYS (Investigating Silent Strokes in Hypertensives Study), a longitudinal population-based study in hypertensives aged 50–70 and...

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Published inJournal of the neurological sciences Vol. 409; p. 116635
Main Authors Jiménez-Balado, Joan, Riba-Llena, Iolanda, Pizarro, Jesús, Palasí, Antoni, Penalba, Anna, Ramírez, Clara, Maisterra, Olga, Espinel, Eugenia, Ramos, Natalia, Pujadas, Francesc, Serón, Daniel, Delgado, Pilar
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 15.02.2020
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Online AccessGet full text
ISSN0022-510X
1878-5883
1878-5883
DOI10.1016/j.jns.2019.116635

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Abstract We aimed to study whether worsening in markers of kidney function parallels the progression in cerebral small vessel disease (cSVD) and cognitive decline. Data from the ISSYS (Investigating Silent Strokes in Hypertensives Study), a longitudinal population-based study in hypertensives aged 50–70 and dementia and stroke-free at baseline. At both visits, patients underwent a brain MRI, a cognitive diagnosis (normal aging or mild cognitive impairment, [MCI]) and urine and blood sampling collection. We assessed the incidence of infarcts and cerebral microbleeds, and the progression of white matter hyperintensities at periventricular (PVH) and deep areas. We determined changes in albumin-creatinine ratio and estimated glomerular filtration rate (eGFR). These changes were dichotomized into microalbuminuria at follow-up —either in subjects with or without baseline microalbuminuria— and significant decline in eGFR —lowest quintile of eGFR change (−10.57 mL/min/1.73m2)—. 360 patients were followed-up for 4 years. 80 (23%) patients presented microalbuminuria at follow-up and 68 (20.1%) experienced a significant eGFR decline. Considering cSVD change, we found a relationship between microalbuminuria at follow-up and progression in PVH (β = 0.31, P-value = .01). Regarding cognitive decline, presence of microalbuminuria at follow-up related to a steeper decrease in memory function (β = −0.36, P-value<.01). Moreover, patients with significant decline in eGFR were at higher risk of incident MCI (OR = 3.54, P-value = .02). These associations were independent of progression of cSVD. The worsening in markers of kidney function paralleled the decrease in cognition and the progression of cSVD, and this may be explained by common shared underlying risk factors. •We studied the changes in markers of kidney function, cognition and vascular lesions.•Microalbuminuria was associated with progression of periventricular hyperintensities.•We found a correlation between the increase in albuminuria and memory decline.•Decline in kidney function predicted the incidence of mild cognitive impairment.•The relationship between brain and kidney may be explained by shared etiologies.
AbstractList AbstractAimsWe aimed to study whether worsening in markers of kidney function parallels the progression in cerebral small vessel disease (cSVD) and cognitive decline. MethodsData from the ISSYS (Investigating Silent Strokes in Hypertensives Study), a longitudinal population-based study in hypertensives aged 50–70 and dementia and stroke-free at baseline. At both visits, patients underwent a brain MRI, a cognitive diagnosis (normal aging or mild cognitive impairment, [MCI]) and urine and blood sampling collection. We assessed the incidence of infarcts and cerebral microbleeds, and the progression of white matter hyperintensities at periventricular (PVH) and deep areas. We determined changes in albumin-creatinine ratio and estimated glomerular filtration rate (eGFR). These changes were dichotomized into microalbuminuria at follow-up —either in subjects with or without baseline microalbuminuria— and significant decline in eGFR —lowest quintile of eGFR change (−10.57 ml/min/1.73)—. Results360 patients were followed-up for 4 years. 80 (23%) patients presented microalbuminuria at follow-up and 68 (20.1%) experienced a significant eGFR decline. Considering cSVD change, we found a relationship between microalbuminuria at follow-up and progression in PVH (β = 0.31, P-value = .01). Regarding cognitive decline, presence of microalbuminuria at follow-up related to a steeper decrease in memory function (β = −0.36, P-value<.01). Moreover, patients with significant decline in eGFR were at higher risk of incident MCI (OR = 3.54, P-value = .02). These associations were independent of progression of cSVD. ConclusionThe worsening in markers of kidney function paralleled the decrease in cognition and the progression of cSVD, and this may be explained by common shared underlying risk factors.
We aimed to study whether worsening in markers of kidney function parallels the progression in cerebral small vessel disease (cSVD) and cognitive decline.AIMSWe aimed to study whether worsening in markers of kidney function parallels the progression in cerebral small vessel disease (cSVD) and cognitive decline.Data from the ISSYS (Investigating Silent Strokes in Hypertensives Study), a longitudinal population-based study in hypertensives aged 50-70 and dementia and stroke-free at baseline. At both visits, patients underwent a brain MRI, a cognitive diagnosis (normal aging or mild cognitive impairment, [MCI]) and urine and blood sampling collection. We assessed the incidence of infarcts and cerebral microbleeds, and the progression of white matter hyperintensities at periventricular (PVH) and deep areas. We determined changes in albumin-creatinine ratio and estimated glomerular filtration rate (eGFR). These changes were dichotomized into microalbuminuria at follow-up -either in subjects with or without baseline microalbuminuria- and significant decline in eGFR -lowest quintile of eGFR change (-10.57 mL/min/1.73m2)-.METHODSData from the ISSYS (Investigating Silent Strokes in Hypertensives Study), a longitudinal population-based study in hypertensives aged 50-70 and dementia and stroke-free at baseline. At both visits, patients underwent a brain MRI, a cognitive diagnosis (normal aging or mild cognitive impairment, [MCI]) and urine and blood sampling collection. We assessed the incidence of infarcts and cerebral microbleeds, and the progression of white matter hyperintensities at periventricular (PVH) and deep areas. We determined changes in albumin-creatinine ratio and estimated glomerular filtration rate (eGFR). These changes were dichotomized into microalbuminuria at follow-up -either in subjects with or without baseline microalbuminuria- and significant decline in eGFR -lowest quintile of eGFR change (-10.57 mL/min/1.73m2)-.360 patients were followed-up for 4 years. 80 (23%) patients presented microalbuminuria at follow-up and 68 (20.1%) experienced a significant eGFR decline. Considering cSVD change, we found a relationship between microalbuminuria at follow-up and progression in PVH (β = 0.31, P-value = .01). Regarding cognitive decline, presence of microalbuminuria at follow-up related to a steeper decrease in memory function (β = -0.36, P-value<.01). Moreover, patients with significant decline in eGFR were at higher risk of incident MCI (OR = 3.54, P-value = .02). These associations were independent of progression of cSVD.RESULTS360 patients were followed-up for 4 years. 80 (23%) patients presented microalbuminuria at follow-up and 68 (20.1%) experienced a significant eGFR decline. Considering cSVD change, we found a relationship between microalbuminuria at follow-up and progression in PVH (β = 0.31, P-value = .01). Regarding cognitive decline, presence of microalbuminuria at follow-up related to a steeper decrease in memory function (β = -0.36, P-value<.01). Moreover, patients with significant decline in eGFR were at higher risk of incident MCI (OR = 3.54, P-value = .02). These associations were independent of progression of cSVD.The worsening in markers of kidney function paralleled the decrease in cognition and the progression of cSVD, and this may be explained by common shared underlying risk factors.CONCLUSIONThe worsening in markers of kidney function paralleled the decrease in cognition and the progression of cSVD, and this may be explained by common shared underlying risk factors.
We aimed to study whether worsening in markers of kidney function parallels the progression in cerebral small vessel disease (cSVD) and cognitive decline. Data from the ISSYS (Investigating Silent Strokes in Hypertensives Study), a longitudinal population-based study in hypertensives aged 50–70 and dementia and stroke-free at baseline. At both visits, patients underwent a brain MRI, a cognitive diagnosis (normal aging or mild cognitive impairment, [MCI]) and urine and blood sampling collection. We assessed the incidence of infarcts and cerebral microbleeds, and the progression of white matter hyperintensities at periventricular (PVH) and deep areas. We determined changes in albumin-creatinine ratio and estimated glomerular filtration rate (eGFR). These changes were dichotomized into microalbuminuria at follow-up —either in subjects with or without baseline microalbuminuria— and significant decline in eGFR —lowest quintile of eGFR change (−10.57 mL/min/1.73m2)—. 360 patients were followed-up for 4 years. 80 (23%) patients presented microalbuminuria at follow-up and 68 (20.1%) experienced a significant eGFR decline. Considering cSVD change, we found a relationship between microalbuminuria at follow-up and progression in PVH (β = 0.31, P-value = .01). Regarding cognitive decline, presence of microalbuminuria at follow-up related to a steeper decrease in memory function (β = −0.36, P-value<.01). Moreover, patients with significant decline in eGFR were at higher risk of incident MCI (OR = 3.54, P-value = .02). These associations were independent of progression of cSVD. The worsening in markers of kidney function paralleled the decrease in cognition and the progression of cSVD, and this may be explained by common shared underlying risk factors. •We studied the changes in markers of kidney function, cognition and vascular lesions.•Microalbuminuria was associated with progression of periventricular hyperintensities.•We found a correlation between the increase in albuminuria and memory decline.•Decline in kidney function predicted the incidence of mild cognitive impairment.•The relationship between brain and kidney may be explained by shared etiologies.
We aimed to study whether worsening in markers of kidney function parallels the progression in cerebral small vessel disease (cSVD) and cognitive decline. Data from the ISSYS (Investigating Silent Strokes in Hypertensives Study), a longitudinal population-based study in hypertensives aged 50-70 and dementia and stroke-free at baseline. At both visits, patients underwent a brain MRI, a cognitive diagnosis (normal aging or mild cognitive impairment, [MCI]) and urine and blood sampling collection. We assessed the incidence of infarcts and cerebral microbleeds, and the progression of white matter hyperintensities at periventricular (PVH) and deep areas. We determined changes in albumin-creatinine ratio and estimated glomerular filtration rate (eGFR). These changes were dichotomized into microalbuminuria at follow-up -either in subjects with or without baseline microalbuminuria- and significant decline in eGFR -lowest quintile of eGFR change (-10.57 mL/min/1.73m )-. 360 patients were followed-up for 4 years. 80 (23%) patients presented microalbuminuria at follow-up and 68 (20.1%) experienced a significant eGFR decline. Considering cSVD change, we found a relationship between microalbuminuria at follow-up and progression in PVH (β = 0.31, P-value = .01). Regarding cognitive decline, presence of microalbuminuria at follow-up related to a steeper decrease in memory function (β = -0.36, P-value<.01). Moreover, patients with significant decline in eGFR were at higher risk of incident MCI (OR = 3.54, P-value = .02). These associations were independent of progression of cSVD. The worsening in markers of kidney function paralleled the decrease in cognition and the progression of cSVD, and this may be explained by common shared underlying risk factors.
ArticleNumber 116635
Author Penalba, Anna
Ramos, Natalia
Pizarro, Jesús
Riba-Llena, Iolanda
Palasí, Antoni
Jiménez-Balado, Joan
Serón, Daniel
Delgado, Pilar
Maisterra, Olga
Ramírez, Clara
Espinel, Eugenia
Pujadas, Francesc
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  givenname: Iolanda
  surname: Riba-Llena
  fullname: Riba-Llena, Iolanda
  email: iriba2010@gmail.com
  organization: Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona, Neurovascular Research Lab, Barcelona, Spain
– sequence: 3
  givenname: Jesús
  surname: Pizarro
  fullname: Pizarro, Jesús
  email: jesus.pizarro@vhir.org
  organization: Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona, Neurovascular Research Lab, Barcelona, Spain
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  givenname: Antoni
  surname: Palasí
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  givenname: Anna
  surname: Penalba
  fullname: Penalba, Anna
  email: anna.penalba@gmail.com
  organization: Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona, Neurovascular Research Lab, Barcelona, Spain
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  givenname: Clara
  surname: Ramírez
  fullname: Ramírez, Clara
  email: clramire@vhebron.net
  organization: Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona, Biochemistry Lab, Clinical Central Laboratories, Barcelona, Spain
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  givenname: Olga
  surname: Maisterra
  fullname: Maisterra, Olga
  email: omaiste@hotmail.com
  organization: Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona, Neurovascular Research Lab, Barcelona, Spain
– sequence: 8
  givenname: Eugenia
  surname: Espinel
  fullname: Espinel, Eugenia
  email: eespinel@vhebron.net
  organization: Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona, Department of Nephrology, Hypertension Unit, Barcelona, Spain
– sequence: 9
  givenname: Natalia
  surname: Ramos
  fullname: Ramos, Natalia
  email: nramos@vhebron.net
  organization: Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona, Department of Nephrology, Hypertension Unit, Barcelona, Spain
– sequence: 10
  givenname: Francesc
  surname: Pujadas
  fullname: Pujadas, Francesc
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  organization: Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona, Dementia Unit, Neurology Service, Barcelona, Spain
– sequence: 11
  givenname: Daniel
  surname: Serón
  fullname: Serón, Daniel
  email: dseron@vhebron.net
  organization: Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona, Department of Nephrology, Hypertension Unit, Barcelona, Spain
– sequence: 12
  givenname: Pilar
  surname: Delgado
  fullname: Delgado, Pilar
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  organization: Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona, Neurovascular Research Lab, Barcelona, Spain
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Keywords Hypertension
MCI (mild cognitive impairment)
Kidney function
Cerebral small vessel disease
Longitudinal study
Language English
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SSID ssj0006889
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Snippet We aimed to study whether worsening in markers of kidney function parallels the progression in cerebral small vessel disease (cSVD) and cognitive decline. Data...
AbstractAimsWe aimed to study whether worsening in markers of kidney function parallels the progression in cerebral small vessel disease (cSVD) and cognitive...
We aimed to study whether worsening in markers of kidney function parallels the progression in cerebral small vessel disease (cSVD) and cognitive...
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pubmed
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Enrichment Source
Publisher
StartPage 116635
SubjectTerms Aged
Albuminuria - diagnostic imaging
Albuminuria - epidemiology
Albuminuria - physiopathology
Cerebral small vessel disease
Cerebral Small Vessel Diseases - diagnostic imaging
Cerebral Small Vessel Diseases - epidemiology
Cerebral Small Vessel Diseases - physiopathology
Cognitive Dysfunction - diagnostic imaging
Cognitive Dysfunction - epidemiology
Cognitive Dysfunction - physiopathology
Disease Progression
Female
Follow-Up Studies
Glomerular Filtration Rate - physiology
Humans
Hypertension
Kidney - diagnostic imaging
Kidney - physiology
Kidney function
Longitudinal Studies
Longitudinal study
Male
MCI (mild cognitive impairment)
Middle Aged
Neurology
Risk Factors
Title Kidney function changes and their relation with the progression of cerebral small vessel disease and cognitive decline
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0022510X19324001
https://www.clinicalkey.es/playcontent/1-s2.0-S0022510X19324001
https://dx.doi.org/10.1016/j.jns.2019.116635
https://www.ncbi.nlm.nih.gov/pubmed/31869590
https://www.proquest.com/docview/2330337146
Volume 409
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