White Matter Lesion Progression in LADIS: Frequency, Clinical Effects, and Sample Size Calculations

Reinhold Schmidt; Andrea Berghold; Hanna Jokinen; Alida A Gouw; Wiesje M van der Flier; Frederik Barkhof; Philip Scheltens; Katja Petrovic; Sofia Madureira; Ana Verdelho; Jose M Ferro; Gunhild Waldemar; Anders Wallin; Lars-Olof Wahlund; Anna Poggesi; Leonardo Pantoni; Domenico Inzitari; Franz Fazekas; Timo Erkinjuntti; on behalf of the LADIS Study Group

doi:10.1161/STROKEAHA.112.662593

White Matter Lesion Progression in LADIS: Frequency, Clinical Effects, and Sample Size Calculations

Reinhold Schmidt, Andrea Berghold, Hanna Jokinen, Alida A Gouw, Wiesje M van der Flier, Frederik Barkhof, Philip Scheltens, Katja Petrovic, Sofia Madureira, Ana Verdelho, Jose M Ferro, Gunhild Waldemar, Anders Wallin, Lars-Olof Wahlund, Anna Poggesi, Leonardo Pantoni, Domenico Inzitari, Franz Fazekas, Timo Erkinjuntti, on behalf of the LADIS Study Group

65 Citations (Scopus)

Abstract

BACKGROUND AND PURPOSE: White matter lesion (WML) progression has been advocated as a surrogate marker in intervention trials on cerebral small vessel disease. We assessed the rate of visually rated WML progression, studied correlations between lesion progression and cognition, and estimated sample sizes for clinical trials with pure WML progression vs combined WML progression-cognitive outcomes. METHODS: Those 394 participants of the Leukoaraiosis and Disability Study (LADIS) study with magnetic resonance imaging scanning at baseline and 3-year follow-up were analyzed. WML progression rating relied on the modified Rotterdam Progression Scale. The Vascular Dementia Assessment Scale global score and a composite score of specific executive function tests assessed longitudinal change in cognition. Sample size calculations were based on the assumption that treatment reduces WML progression by 1 grade on the Rotterdam Progression Scale. RESULTS: WML progression related to deterioration in cognitive functioning. This relationship was less pronounced in subjects with early confluent and confluent lesions. Consequently, studies in which the outcome is cognitive change resulting from treatment effects on lesion progression will need between 1809 subjects per treatment arm when using executive tests and up to 18 853 subjects when using the Vascular Dementia Assessment Scale score. Studies having WML progression as the sole outcome will need only 58 or 70 individuals per treatment arm. CONCLUSIONS: WML progression is an interesting outcome for proof-of-concept studies in cerebral small vessel disease. If cognitive outcome measures are added to protocols, then sample size estimates increase substantially. Our data support the use of an executive test battery rather than the Vascular Dementia Assessment Scale as the primary cognitive outcome measure.

Original language	English
Journal	Stroke
Volume	43
Issue number	10
Pages (from-to)	2643-2647
Number of pages	5
ISSN	0039-2499
DOIs	https://doi.org/10.1161/STROKEAHA.112.662593
Publication status	Published - Oct 2012

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10.1161/STROKEAHA.112.662593

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Schmidt, R., Berghold, A., Jokinen, H., Gouw, A. A., van der Flier, W. M., Barkhof, F., Scheltens, P., Petrovic, K., Madureira, S., Verdelho, A., Ferro, J. M., Waldemar, G., Wallin, A., Wahlund, L-O., Poggesi, A., Pantoni, L., Inzitari, D., Fazekas, F., Erkinjuntti, T., & on behalf of the LADIS Study Group (2012). White Matter Lesion Progression in LADIS: Frequency, Clinical Effects, and Sample Size Calculations. Stroke, 43(10), 2643-2647. https://doi.org/10.1161/STROKEAHA.112.662593

Schmidt, R, Berghold, A, Jokinen, H, Gouw, AA, van der Flier, WM, Barkhof, F, Scheltens, P, Petrovic, K, Madureira, S, Verdelho, A, Ferro, JM, Waldemar, G, Wallin, A, Wahlund, L-O, Poggesi, A, Pantoni, L, Inzitari, D, Fazekas, F, Erkinjuntti, T & on behalf of the LADIS Study Group 2012, 'White Matter Lesion Progression in LADIS: Frequency, Clinical Effects, and Sample Size Calculations', Stroke, vol. 43, no. 10, pp. 2643-2647. https://doi.org/10.1161/STROKEAHA.112.662593

@article{f520d8cef66b4450af67f5a46b209eb3,

title = "White Matter Lesion Progression in LADIS: Frequency, Clinical Effects, and Sample Size Calculations",

abstract = "BACKGROUND AND PURPOSE: White matter lesion (WML) progression has been advocated as a surrogate marker in intervention trials on cerebral small vessel disease. We assessed the rate of visually rated WML progression, studied correlations between lesion progression and cognition, and estimated sample sizes for clinical trials with pure WML progression vs combined WML progression-cognitive outcomes. METHODS: Those 394 participants of the Leukoaraiosis and Disability Study (LADIS) study with magnetic resonance imaging scanning at baseline and 3-year follow-up were analyzed. WML progression rating relied on the modified Rotterdam Progression Scale. The Vascular Dementia Assessment Scale global score and a composite score of specific executive function tests assessed longitudinal change in cognition. Sample size calculations were based on the assumption that treatment reduces WML progression by 1 grade on the Rotterdam Progression Scale. RESULTS: WML progression related to deterioration in cognitive functioning. This relationship was less pronounced in subjects with early confluent and confluent lesions. Consequently, studies in which the outcome is cognitive change resulting from treatment effects on lesion progression will need between 1809 subjects per treatment arm when using executive tests and up to 18 853 subjects when using the Vascular Dementia Assessment Scale score. Studies having WML progression as the sole outcome will need only 58 or 70 individuals per treatment arm. CONCLUSIONS: WML progression is an interesting outcome for proof-of-concept studies in cerebral small vessel disease. If cognitive outcome measures are added to protocols, then sample size estimates increase substantially. Our data support the use of an executive test battery rather than the Vascular Dementia Assessment Scale as the primary cognitive outcome measure.",

author = "Reinhold Schmidt and Andrea Berghold and Hanna Jokinen and Gouw, {Alida A} and {van der Flier}, {Wiesje M} and Frederik Barkhof and Philip Scheltens and Katja Petrovic and Sofia Madureira and Ana Verdelho and Ferro, {Jose M} and Gunhild Waldemar and Anders Wallin and Lars-Olof Wahlund and Anna Poggesi and Leonardo Pantoni and Domenico Inzitari and Franz Fazekas and Timo Erkinjuntti and Gunhild Waldemar",

year = "2012",

month = oct,

doi = "10.1161/STROKEAHA.112.662593",

language = "English",

volume = "43",

pages = "2643--2647",

journal = "Stroke",

issn = "0039-2499",

publisher = "Lippincott Williams & Wilkins",

number = "10",

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TY - JOUR

T1 - White Matter Lesion Progression in LADIS

T2 - Frequency, Clinical Effects, and Sample Size Calculations

AU - Schmidt, Reinhold

AU - Berghold, Andrea

AU - Jokinen, Hanna

AU - Gouw, Alida A

AU - van der Flier, Wiesje M

AU - Barkhof, Frederik

AU - Scheltens, Philip

AU - Petrovic, Katja

AU - Madureira, Sofia

AU - Verdelho, Ana

AU - Ferro, Jose M

AU - Waldemar, Gunhild

AU - Wallin, Anders

AU - Wahlund, Lars-Olof

AU - Poggesi, Anna

AU - Pantoni, Leonardo

AU - Inzitari, Domenico

AU - Fazekas, Franz

AU - Erkinjuntti, Timo

AU - on behalf of the LADIS Study Group

PY - 2012/10

Y1 - 2012/10

N2 - BACKGROUND AND PURPOSE: White matter lesion (WML) progression has been advocated as a surrogate marker in intervention trials on cerebral small vessel disease. We assessed the rate of visually rated WML progression, studied correlations between lesion progression and cognition, and estimated sample sizes for clinical trials with pure WML progression vs combined WML progression-cognitive outcomes. METHODS: Those 394 participants of the Leukoaraiosis and Disability Study (LADIS) study with magnetic resonance imaging scanning at baseline and 3-year follow-up were analyzed. WML progression rating relied on the modified Rotterdam Progression Scale. The Vascular Dementia Assessment Scale global score and a composite score of specific executive function tests assessed longitudinal change in cognition. Sample size calculations were based on the assumption that treatment reduces WML progression by 1 grade on the Rotterdam Progression Scale. RESULTS: WML progression related to deterioration in cognitive functioning. This relationship was less pronounced in subjects with early confluent and confluent lesions. Consequently, studies in which the outcome is cognitive change resulting from treatment effects on lesion progression will need between 1809 subjects per treatment arm when using executive tests and up to 18 853 subjects when using the Vascular Dementia Assessment Scale score. Studies having WML progression as the sole outcome will need only 58 or 70 individuals per treatment arm. CONCLUSIONS: WML progression is an interesting outcome for proof-of-concept studies in cerebral small vessel disease. If cognitive outcome measures are added to protocols, then sample size estimates increase substantially. Our data support the use of an executive test battery rather than the Vascular Dementia Assessment Scale as the primary cognitive outcome measure.

AB - BACKGROUND AND PURPOSE: White matter lesion (WML) progression has been advocated as a surrogate marker in intervention trials on cerebral small vessel disease. We assessed the rate of visually rated WML progression, studied correlations between lesion progression and cognition, and estimated sample sizes for clinical trials with pure WML progression vs combined WML progression-cognitive outcomes. METHODS: Those 394 participants of the Leukoaraiosis and Disability Study (LADIS) study with magnetic resonance imaging scanning at baseline and 3-year follow-up were analyzed. WML progression rating relied on the modified Rotterdam Progression Scale. The Vascular Dementia Assessment Scale global score and a composite score of specific executive function tests assessed longitudinal change in cognition. Sample size calculations were based on the assumption that treatment reduces WML progression by 1 grade on the Rotterdam Progression Scale. RESULTS: WML progression related to deterioration in cognitive functioning. This relationship was less pronounced in subjects with early confluent and confluent lesions. Consequently, studies in which the outcome is cognitive change resulting from treatment effects on lesion progression will need between 1809 subjects per treatment arm when using executive tests and up to 18 853 subjects when using the Vascular Dementia Assessment Scale score. Studies having WML progression as the sole outcome will need only 58 or 70 individuals per treatment arm. CONCLUSIONS: WML progression is an interesting outcome for proof-of-concept studies in cerebral small vessel disease. If cognitive outcome measures are added to protocols, then sample size estimates increase substantially. Our data support the use of an executive test battery rather than the Vascular Dementia Assessment Scale as the primary cognitive outcome measure.

U2 - 10.1161/STROKEAHA.112.662593

DO - 10.1161/STROKEAHA.112.662593

M3 - Journal article

C2 - 22879094

SN - 0039-2499

VL - 43

SP - 2643

EP - 2647

JO - Stroke

JF - Stroke

IS - 10

ER -

White Matter Lesion Progression in LADIS: Frequency, Clinical Effects, and Sample Size Calculations

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