Risk factors and prodromal markers and the development of Parkinson’s disease
Abstract Identification of risk factors and prodromal markers for Parkinson’s disease (PD) and the understanding of the point in time of first occurrence is essential for the early detection of incident PD. In this three-center longitudinal, observational study, we evaluated the specific risk for PD...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Lerche, Stefanie [verfasserIn] Seppi, Klaus [verfasserIn] Behnke, Stefanie [verfasserIn] Liepelt-Scarfone, Inga [verfasserIn] Godau, Jana [verfasserIn] Mahlknecht, Philipp [verfasserIn] Gaenslen, Alexandra [verfasserIn] Brockmann, Kathrin [verfasserIn] Srulijes, Karin [verfasserIn] Huber, Heiko [verfasserIn] Wurster, Isabel [verfasserIn] Stockner, Heike [verfasserIn] Kiechl, Stefan [verfasserIn] Willeit, Johann [verfasserIn] Gasperi, Arno [verfasserIn] Fassbender, Klaus [verfasserIn] Poewe, Werner [verfasserIn] Berg, Daniela [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2013 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Journal of neurology - [Darmstadt] : Steinkopff, 1891, 261(2013), 1 vom: 05. Nov., Seite 180-187 |
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| Übergeordnetes Werk: |
volume:261 ; year:2013 ; number:1 ; day:05 ; month:11 ; pages:180-187 |
| Links: |
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| DOI / URN: |
10.1007/s00415-013-7171-0 |
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| Katalog-ID: |
SPR005355850 |
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| 520 | |a Abstract Identification of risk factors and prodromal markers for Parkinson’s disease (PD) and the understanding of the point in time of first occurrence is essential for the early detection of incident PD. In this three-center longitudinal, observational study, we evaluated the specific risk for PD associated with single or combinations of risk factors and prodromal markers. In addition, we evaluated which risk factors and prodromal markers emerge at which time before the diagnosis of PD. Of the 1,847 at-baseline PD-free individuals ≥50 years, 1,260 underwent the 5-year follow-up assessment. There were 21 cases of incident PD during the study period. Enlarged hyperechogenic substantia nigra was the most frequent baseline sign in individuals developing PD after 3 years (80.0 %) and 5 years (85.7 %) compared to healthy controls (17.5 %) followed by the occurrence of mild parkinsonian signs and hyposmia. Evaluation of the signs at the first follow-up assessment showed that individuals developing PD after two additional years showed the same pattern of signs as individuals who developed PD 3 years after baseline assessment. | ||
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| 650 | 4 | |a Prodromal marker |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Parkinson’s disease |7 (dpeaa)DE-He213 | |
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| 700 | 1 | |a Godau, Jana |e verfasserin |4 aut | |
| 700 | 1 | |a Mahlknecht, Philipp |e verfasserin |4 aut | |
| 700 | 1 | |a Gaenslen, Alexandra |e verfasserin |4 aut | |
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| 700 | 1 | |a Huber, Heiko |e verfasserin |4 aut | |
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| 700 | 1 | |a Kiechl, Stefan |e verfasserin |4 aut | |
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| 700 | 1 | |a Fassbender, Klaus |e verfasserin |4 aut | |
| 700 | 1 | |a Poewe, Werner |e verfasserin |4 aut | |
| 700 | 1 | |a Berg, Daniela |e verfasserin |4 aut | |
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10.1007/s00415-013-7171-0 doi (DE-627)SPR005355850 (SPR)s00415-013-7171-0-e DE-627 ger DE-627 rakwb eng 610 ASE 610 ASE 44.90 bkl Lerche, Stefanie verfasserin aut Risk factors and prodromal markers and the development of Parkinson’s disease 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Identification of risk factors and prodromal markers for Parkinson’s disease (PD) and the understanding of the point in time of first occurrence is essential for the early detection of incident PD. In this three-center longitudinal, observational study, we evaluated the specific risk for PD associated with single or combinations of risk factors and prodromal markers. In addition, we evaluated which risk factors and prodromal markers emerge at which time before the diagnosis of PD. Of the 1,847 at-baseline PD-free individuals ≥50 years, 1,260 underwent the 5-year follow-up assessment. There were 21 cases of incident PD during the study period. Enlarged hyperechogenic substantia nigra was the most frequent baseline sign in individuals developing PD after 3 years (80.0 %) and 5 years (85.7 %) compared to healthy controls (17.5 %) followed by the occurrence of mild parkinsonian signs and hyposmia. Evaluation of the signs at the first follow-up assessment showed that individuals developing PD after two additional years showed the same pattern of signs as individuals who developed PD 3 years after baseline assessment. Risk factor (dpeaa)DE-He213 Prodromal marker (dpeaa)DE-He213 Parkinson’s disease (dpeaa)DE-He213 Seppi, Klaus verfasserin aut Behnke, Stefanie verfasserin aut Liepelt-Scarfone, Inga verfasserin aut Godau, Jana verfasserin aut Mahlknecht, Philipp verfasserin aut Gaenslen, Alexandra verfasserin aut Brockmann, Kathrin verfasserin aut Srulijes, Karin verfasserin aut Huber, Heiko verfasserin aut Wurster, Isabel verfasserin aut Stockner, Heike verfasserin aut Kiechl, Stefan verfasserin aut Willeit, Johann verfasserin aut Gasperi, Arno verfasserin aut Fassbender, Klaus verfasserin aut Poewe, Werner verfasserin aut Berg, Daniela verfasserin aut Enthalten in Journal of neurology [Darmstadt] : Steinkopff, 1891 261(2013), 1 vom: 05. Nov., Seite 180-187 (DE-627)242065155 (DE-600)1421299-7 1432-1459 nnns volume:261 year:2013 number:1 day:05 month:11 pages:180-187 https://dx.doi.org/10.1007/s00415-013-7171-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 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_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 261 2013 1 05 11 180-187 |
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10.1007/s00415-013-7171-0 doi (DE-627)SPR005355850 (SPR)s00415-013-7171-0-e DE-627 ger DE-627 rakwb eng 610 ASE 610 ASE 44.90 bkl Lerche, Stefanie verfasserin aut Risk factors and prodromal markers and the development of Parkinson’s disease 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Identification of risk factors and prodromal markers for Parkinson’s disease (PD) and the understanding of the point in time of first occurrence is essential for the early detection of incident PD. In this three-center longitudinal, observational study, we evaluated the specific risk for PD associated with single or combinations of risk factors and prodromal markers. In addition, we evaluated which risk factors and prodromal markers emerge at which time before the diagnosis of PD. Of the 1,847 at-baseline PD-free individuals ≥50 years, 1,260 underwent the 5-year follow-up assessment. There were 21 cases of incident PD during the study period. Enlarged hyperechogenic substantia nigra was the most frequent baseline sign in individuals developing PD after 3 years (80.0 %) and 5 years (85.7 %) compared to healthy controls (17.5 %) followed by the occurrence of mild parkinsonian signs and hyposmia. Evaluation of the signs at the first follow-up assessment showed that individuals developing PD after two additional years showed the same pattern of signs as individuals who developed PD 3 years after baseline assessment. Risk factor (dpeaa)DE-He213 Prodromal marker (dpeaa)DE-He213 Parkinson’s disease (dpeaa)DE-He213 Seppi, Klaus verfasserin aut Behnke, Stefanie verfasserin aut Liepelt-Scarfone, Inga verfasserin aut Godau, Jana verfasserin aut Mahlknecht, Philipp verfasserin aut Gaenslen, Alexandra verfasserin aut Brockmann, Kathrin verfasserin aut Srulijes, Karin verfasserin aut Huber, Heiko verfasserin aut Wurster, Isabel verfasserin aut Stockner, Heike verfasserin aut Kiechl, Stefan verfasserin aut Willeit, Johann verfasserin aut Gasperi, Arno verfasserin aut Fassbender, Klaus verfasserin aut Poewe, Werner verfasserin aut Berg, Daniela verfasserin aut Enthalten in Journal of neurology [Darmstadt] : Steinkopff, 1891 261(2013), 1 vom: 05. Nov., Seite 180-187 (DE-627)242065155 (DE-600)1421299-7 1432-1459 nnns volume:261 year:2013 number:1 day:05 month:11 pages:180-187 https://dx.doi.org/10.1007/s00415-013-7171-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 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_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 261 2013 1 05 11 180-187 |
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10.1007/s00415-013-7171-0 doi (DE-627)SPR005355850 (SPR)s00415-013-7171-0-e DE-627 ger DE-627 rakwb eng 610 ASE 610 ASE 44.90 bkl Lerche, Stefanie verfasserin aut Risk factors and prodromal markers and the development of Parkinson’s disease 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Identification of risk factors and prodromal markers for Parkinson’s disease (PD) and the understanding of the point in time of first occurrence is essential for the early detection of incident PD. In this three-center longitudinal, observational study, we evaluated the specific risk for PD associated with single or combinations of risk factors and prodromal markers. In addition, we evaluated which risk factors and prodromal markers emerge at which time before the diagnosis of PD. Of the 1,847 at-baseline PD-free individuals ≥50 years, 1,260 underwent the 5-year follow-up assessment. There were 21 cases of incident PD during the study period. Enlarged hyperechogenic substantia nigra was the most frequent baseline sign in individuals developing PD after 3 years (80.0 %) and 5 years (85.7 %) compared to healthy controls (17.5 %) followed by the occurrence of mild parkinsonian signs and hyposmia. Evaluation of the signs at the first follow-up assessment showed that individuals developing PD after two additional years showed the same pattern of signs as individuals who developed PD 3 years after baseline assessment. Risk factor (dpeaa)DE-He213 Prodromal marker (dpeaa)DE-He213 Parkinson’s disease (dpeaa)DE-He213 Seppi, Klaus verfasserin aut Behnke, Stefanie verfasserin aut Liepelt-Scarfone, Inga verfasserin aut Godau, Jana verfasserin aut Mahlknecht, Philipp verfasserin aut Gaenslen, Alexandra verfasserin aut Brockmann, Kathrin verfasserin aut Srulijes, Karin verfasserin aut Huber, Heiko verfasserin aut Wurster, Isabel verfasserin aut Stockner, Heike verfasserin aut Kiechl, Stefan verfasserin aut Willeit, Johann verfasserin aut Gasperi, Arno verfasserin aut Fassbender, Klaus verfasserin aut Poewe, Werner verfasserin aut Berg, Daniela verfasserin aut Enthalten in Journal of neurology [Darmstadt] : Steinkopff, 1891 261(2013), 1 vom: 05. Nov., Seite 180-187 (DE-627)242065155 (DE-600)1421299-7 1432-1459 nnns volume:261 year:2013 number:1 day:05 month:11 pages:180-187 https://dx.doi.org/10.1007/s00415-013-7171-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 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_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 261 2013 1 05 11 180-187 |
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10.1007/s00415-013-7171-0 doi (DE-627)SPR005355850 (SPR)s00415-013-7171-0-e DE-627 ger DE-627 rakwb eng 610 ASE 610 ASE 44.90 bkl Lerche, Stefanie verfasserin aut Risk factors and prodromal markers and the development of Parkinson’s disease 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Identification of risk factors and prodromal markers for Parkinson’s disease (PD) and the understanding of the point in time of first occurrence is essential for the early detection of incident PD. In this three-center longitudinal, observational study, we evaluated the specific risk for PD associated with single or combinations of risk factors and prodromal markers. In addition, we evaluated which risk factors and prodromal markers emerge at which time before the diagnosis of PD. Of the 1,847 at-baseline PD-free individuals ≥50 years, 1,260 underwent the 5-year follow-up assessment. There were 21 cases of incident PD during the study period. Enlarged hyperechogenic substantia nigra was the most frequent baseline sign in individuals developing PD after 3 years (80.0 %) and 5 years (85.7 %) compared to healthy controls (17.5 %) followed by the occurrence of mild parkinsonian signs and hyposmia. Evaluation of the signs at the first follow-up assessment showed that individuals developing PD after two additional years showed the same pattern of signs as individuals who developed PD 3 years after baseline assessment. Risk factor (dpeaa)DE-He213 Prodromal marker (dpeaa)DE-He213 Parkinson’s disease (dpeaa)DE-He213 Seppi, Klaus verfasserin aut Behnke, Stefanie verfasserin aut Liepelt-Scarfone, Inga verfasserin aut Godau, Jana verfasserin aut Mahlknecht, Philipp verfasserin aut Gaenslen, Alexandra verfasserin aut Brockmann, Kathrin verfasserin aut Srulijes, Karin verfasserin aut Huber, Heiko verfasserin aut Wurster, Isabel verfasserin aut Stockner, Heike verfasserin aut Kiechl, Stefan verfasserin aut Willeit, Johann verfasserin aut Gasperi, Arno verfasserin aut Fassbender, Klaus verfasserin aut Poewe, Werner verfasserin aut Berg, Daniela verfasserin aut Enthalten in Journal of neurology [Darmstadt] : Steinkopff, 1891 261(2013), 1 vom: 05. Nov., Seite 180-187 (DE-627)242065155 (DE-600)1421299-7 1432-1459 nnns volume:261 year:2013 number:1 day:05 month:11 pages:180-187 https://dx.doi.org/10.1007/s00415-013-7171-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 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_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 261 2013 1 05 11 180-187 |
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10.1007/s00415-013-7171-0 doi (DE-627)SPR005355850 (SPR)s00415-013-7171-0-e DE-627 ger DE-627 rakwb eng 610 ASE 610 ASE 44.90 bkl Lerche, Stefanie verfasserin aut Risk factors and prodromal markers and the development of Parkinson’s disease 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Identification of risk factors and prodromal markers for Parkinson’s disease (PD) and the understanding of the point in time of first occurrence is essential for the early detection of incident PD. In this three-center longitudinal, observational study, we evaluated the specific risk for PD associated with single or combinations of risk factors and prodromal markers. In addition, we evaluated which risk factors and prodromal markers emerge at which time before the diagnosis of PD. Of the 1,847 at-baseline PD-free individuals ≥50 years, 1,260 underwent the 5-year follow-up assessment. There were 21 cases of incident PD during the study period. Enlarged hyperechogenic substantia nigra was the most frequent baseline sign in individuals developing PD after 3 years (80.0 %) and 5 years (85.7 %) compared to healthy controls (17.5 %) followed by the occurrence of mild parkinsonian signs and hyposmia. Evaluation of the signs at the first follow-up assessment showed that individuals developing PD after two additional years showed the same pattern of signs as individuals who developed PD 3 years after baseline assessment. Risk factor (dpeaa)DE-He213 Prodromal marker (dpeaa)DE-He213 Parkinson’s disease (dpeaa)DE-He213 Seppi, Klaus verfasserin aut Behnke, Stefanie verfasserin aut Liepelt-Scarfone, Inga verfasserin aut Godau, Jana verfasserin aut Mahlknecht, Philipp verfasserin aut Gaenslen, Alexandra verfasserin aut Brockmann, Kathrin verfasserin aut Srulijes, Karin verfasserin aut Huber, Heiko verfasserin aut Wurster, Isabel verfasserin aut Stockner, Heike verfasserin aut Kiechl, Stefan verfasserin aut Willeit, Johann verfasserin aut Gasperi, Arno verfasserin aut Fassbender, Klaus verfasserin aut Poewe, Werner verfasserin aut Berg, Daniela verfasserin aut Enthalten in Journal of neurology [Darmstadt] : Steinkopff, 1891 261(2013), 1 vom: 05. Nov., Seite 180-187 (DE-627)242065155 (DE-600)1421299-7 1432-1459 nnns volume:261 year:2013 number:1 day:05 month:11 pages:180-187 https://dx.doi.org/10.1007/s00415-013-7171-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 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_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 261 2013 1 05 11 180-187 |
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Enthalten in Journal of neurology 261(2013), 1 vom: 05. Nov., Seite 180-187 volume:261 year:2013 number:1 day:05 month:11 pages:180-187 |
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Enthalten in Journal of neurology 261(2013), 1 vom: 05. Nov., Seite 180-187 volume:261 year:2013 number:1 day:05 month:11 pages:180-187 |
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Risk factor Prodromal marker Parkinson’s disease |
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Lerche, Stefanie @@aut@@ Seppi, Klaus @@aut@@ Behnke, Stefanie @@aut@@ Liepelt-Scarfone, Inga @@aut@@ Godau, Jana @@aut@@ Mahlknecht, Philipp @@aut@@ Gaenslen, Alexandra @@aut@@ Brockmann, Kathrin @@aut@@ Srulijes, Karin @@aut@@ Huber, Heiko @@aut@@ Wurster, Isabel @@aut@@ Stockner, Heike @@aut@@ Kiechl, Stefan @@aut@@ Willeit, Johann @@aut@@ Gasperi, Arno @@aut@@ Fassbender, Klaus @@aut@@ Poewe, Werner @@aut@@ Berg, Daniela @@aut@@ |
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|
| author |
Lerche, Stefanie |
| spellingShingle |
Lerche, Stefanie ddc 610 bkl 44.90 misc Risk factor misc Prodromal marker misc Parkinson’s disease Risk factors and prodromal markers and the development of Parkinson’s disease |
| authorStr |
Lerche, Stefanie |
| ppnlink_with_tag_str_mv |
@@773@@(DE-627)242065155 |
| format |
electronic Article |
| dewey-ones |
610 - Medicine & health |
| delete_txt_mv |
keep |
| author_role |
aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut |
| collection |
springer |
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true |
| illustrated |
Not Illustrated |
| issn |
1432-1459 |
| topic_title |
610 ASE 44.90 bkl Risk factors and prodromal markers and the development of Parkinson’s disease Risk factor (dpeaa)DE-He213 Prodromal marker (dpeaa)DE-He213 Parkinson’s disease (dpeaa)DE-He213 |
| topic |
ddc 610 bkl 44.90 misc Risk factor misc Prodromal marker misc Parkinson’s disease |
| topic_unstemmed |
ddc 610 bkl 44.90 misc Risk factor misc Prodromal marker misc Parkinson’s disease |
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ddc 610 bkl 44.90 misc Risk factor misc Prodromal marker misc Parkinson’s disease |
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Elektronische Aufsätze Aufsätze Elektronische Ressource |
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Risk factors and prodromal markers and the development of Parkinson’s disease |
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Risk factors and prodromal markers and the development of Parkinson’s disease |
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Lerche, Stefanie Seppi, Klaus Behnke, Stefanie Liepelt-Scarfone, Inga Godau, Jana Mahlknecht, Philipp Gaenslen, Alexandra Brockmann, Kathrin Srulijes, Karin Huber, Heiko Wurster, Isabel Stockner, Heike Kiechl, Stefan Willeit, Johann Gasperi, Arno Fassbender, Klaus Poewe, Werner Berg, Daniela |
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risk factors and prodromal markers and the development of parkinson’s disease |
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Risk factors and prodromal markers and the development of Parkinson’s disease |
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Abstract Identification of risk factors and prodromal markers for Parkinson’s disease (PD) and the understanding of the point in time of first occurrence is essential for the early detection of incident PD. In this three-center longitudinal, observational study, we evaluated the specific risk for PD associated with single or combinations of risk factors and prodromal markers. In addition, we evaluated which risk factors and prodromal markers emerge at which time before the diagnosis of PD. Of the 1,847 at-baseline PD-free individuals ≥50 years, 1,260 underwent the 5-year follow-up assessment. There were 21 cases of incident PD during the study period. Enlarged hyperechogenic substantia nigra was the most frequent baseline sign in individuals developing PD after 3 years (80.0 %) and 5 years (85.7 %) compared to healthy controls (17.5 %) followed by the occurrence of mild parkinsonian signs and hyposmia. Evaluation of the signs at the first follow-up assessment showed that individuals developing PD after two additional years showed the same pattern of signs as individuals who developed PD 3 years after baseline assessment. |
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Abstract Identification of risk factors and prodromal markers for Parkinson’s disease (PD) and the understanding of the point in time of first occurrence is essential for the early detection of incident PD. In this three-center longitudinal, observational study, we evaluated the specific risk for PD associated with single or combinations of risk factors and prodromal markers. In addition, we evaluated which risk factors and prodromal markers emerge at which time before the diagnosis of PD. Of the 1,847 at-baseline PD-free individuals ≥50 years, 1,260 underwent the 5-year follow-up assessment. There were 21 cases of incident PD during the study period. Enlarged hyperechogenic substantia nigra was the most frequent baseline sign in individuals developing PD after 3 years (80.0 %) and 5 years (85.7 %) compared to healthy controls (17.5 %) followed by the occurrence of mild parkinsonian signs and hyposmia. Evaluation of the signs at the first follow-up assessment showed that individuals developing PD after two additional years showed the same pattern of signs as individuals who developed PD 3 years after baseline assessment. |
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Abstract Identification of risk factors and prodromal markers for Parkinson’s disease (PD) and the understanding of the point in time of first occurrence is essential for the early detection of incident PD. In this three-center longitudinal, observational study, we evaluated the specific risk for PD associated with single or combinations of risk factors and prodromal markers. In addition, we evaluated which risk factors and prodromal markers emerge at which time before the diagnosis of PD. Of the 1,847 at-baseline PD-free individuals ≥50 years, 1,260 underwent the 5-year follow-up assessment. There were 21 cases of incident PD during the study period. Enlarged hyperechogenic substantia nigra was the most frequent baseline sign in individuals developing PD after 3 years (80.0 %) and 5 years (85.7 %) compared to healthy controls (17.5 %) followed by the occurrence of mild parkinsonian signs and hyposmia. Evaluation of the signs at the first follow-up assessment showed that individuals developing PD after two additional years showed the same pattern of signs as individuals who developed PD 3 years after baseline assessment. |
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| score |
7.398695 |