Cross-sectional analysis of the Parkinson's disease Non-motor International Longitudinal Study baseline non-motor characteristics, geographical distribution and impact on quality of life

被引:27
作者
van Wamelen, Daniel J. [1 ,2 ,3 ,25 ]
Sauerbier, Anna [1 ,4 ]
Leta, Valentina [1 ,2 ]
Rodriguez-Blazquez, Carmen [5 ]
Falup-Pecurariu, Cristian [6 ]
Rodriguez-Violante, Mayela [7 ]
Rizos, Alexandra [1 ,2 ]
Tsuboi, Y. [8 ]
Metta, Vinod [2 ]
Bhidayasiri, Roongroj [9 ]
Bhattacharya, Kalyan [10 ,11 ]
Borgohain, Rupam [12 ]
Prashanth, L. K. [13 ,14 ]
Rosales, Raymond [15 ]
Lewis, Simon [16 ]
Fung, Victor [17 ,18 ]
Behari, Madhuri [19 ]
Goyal, Vinay [20 ]
Kishore, Asha [21 ]
Lloret, Santiago Perez [22 ,23 ]
Martinez-Martin, Pablo [24 ]
Chaudhuri, K. Ray [1 ,2 ]
机构
[1] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Basic & Clin Neurosci, London, England
[2] Kings Coll Hosp London, Parkinsons Fdn Ctr Excellence, Denmark Hill, London, England
[3] Radboud Univ Nijmegen, Med Ctr, Dept Neurol, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands
[4] Univ Cologne, Fac Med, Dept Neurol, Univ Hosp Cologne, Cologne, Germany
[5] Carlos III Inst Hlth, Natl Ctr Epidemiol, Ctr Networked Biomed Res Neurodegenerat Dis CIBER, Madrid, Spain
[6] Transilvania Univ, Cty Emergency Clin Hosp, Fac Med, Dept Neurol, Brasov, Romania
[7] Inst Nacl Neurol & Neurocirug, Movement Disorders Unit, Mexico City, DF, Mexico
[8] Fukuoka Univ, Fac Med, Dept Neurol, Fukuoka, Japan
[9] Chulalongkorn Univ Hosp, Bangkok, Thailand
[10] RG Kar Med Coll, Kolkata, India
[11] Inst Neurosci, Kolkata, India
[12] Nizams Inst Med Sci, Hyderabad, India
[13] Vikram Hosp, Ctr Parkinsons Dis & Movement Disorders Clin, Bangalore, Karnataka, India
[14] Parkinsons Dis & Movement Disorders Clin, Bangalore, Karnataka, India
[15] Univ Santo Tomas Hosp, Manila, Philippines
[16] Univ Sydney, Brain & Mind Ctr, ForeFront Parkinsons Dis Res Clin, Sydney, NSW, Australia
[17] Westmead Hosp, Neurol Dept, Movement Disorders Unit, Sydney, NSW, Australia
[18] Univ Sydney, Sydney Med Sch, Sydney, NSW, Australia
[19] All India Inst Med Sci, Cardiothorac & Neurosci Ctr, Dept Neurol, New Delhi, India
[20] All India Inst Med Sci, Dept Neurol, New Delhi, India
[21] Sree Chitra Tirunal Inst Med Sci & Technol, Trivandrum, Kerala, India
[22] Interamer Open Univ CAECIHS UAI, Natl Res Council CONICET, Biomed Res Ctr, Buenos Aires, DF, Argentina
[23] Univ Buenos Aires, Sch Med, Dept Physiol, Buenos Aires, DF, Argentina
[24] Carlos III Inst Hlth, Ctr Networked Biomed Res Neurodegenerat Dis CIBER, Madrid, Spain
[25] Inst Psychiat Psychol & Neurosci, Dept Basic & Clin Neurosci, De Crespigny Pk, London SE5 8AF, England
关键词
SYMPTOMS SCALE; RATING-SCALE; PREVALENCE; PROGRESSION; COHORT; MULTICENTER; DISABILITY;
D O I
10.1038/s41598-021-88651-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Growing evidence suggests that non-motor symptoms (NMS) in Parkinson's disease (PD) have differential progression patterns that have a different natural history from motor progression and may be geographically influenced. We conducted a cross-sectional analysis of 1607 PD patients of whom 1327 were from Europe, 208 from the Americas, and 72 from Asia. The primary objective was to assess baseline non-motor burden, defined by Non-Motor Symptoms Scale (NMSS) total scores. Other aims included identifying the factors predicting quality of life, differences in non-motor burden between drug-naive and non-drug-naive treated patients, and non-motor phenotypes across different geographical locations. Mean age was 65.9 +/- 10.8 years, mean disease duration 6.3 +/- 5.6 years, median Hoehn and Yahr stage was 2 (2-3), and 64.2% were male. In this cohort, mean NMSS scores were 46.7 +/- 37.2. Differences in non-motor burden and patterns differed significantly between drug-naive participants, those with a disease duration of less than five years, and those with a duration of five years or over (p <= 0.018). Significant differences were observed in geographical distribution (NMSS Europe: 46.4 +/- 36.3; Americas: 55.3 +/- 42.8; Asia: 26.6 +/- 25.1; p<0.001), with differences in sleep/fatigue, urinary, sexual, and miscellaneous domains (p<less than or equal to>0.020). The best predictor of quality of life was the mood/apathy domain (beta =0.308, p<0.001). This global study reveals that while non-motor symptoms are globally present with severe NMS burden impacting quality of life in PD, there appear to be differences depending on disease duration and geographical distribution.
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