Serum Folate, Vitamin B12 Levels, and Systemic Immune-Inflammation Index Correlate With Motor Performance in Parkinson's Disease: A Cross-Sectional Study.

This study aimed to investigate the influence of serum folate, vitamin B12 (VitB12) levels, and inflammation-based scores on the motor performance status in Parkinson's disease (PD). We retrospectively collected data from 148 consecutive patients with idiopathic PD first admitted to our hospital. We measured whole blood count, albumin, lactate dehydrogenase, C-reactive protein, folate, and VitB12 levels and calculated the inflammation-based scores. The following scales were applied to assess the motor performance status: activity of daily living scale (ADL, the Barthel Index), the Unified Parkinson's Disease Rating Scale Part III (UPDRS-III), and Hoehn-Yahr (H-Y) classification. The geometric mean of folate and VitB12 levels were 11.87 (ng/ml) and 330.52 (pmol/L), respectively. Folate deficiency (serum level < 4.0 ng/ml) and VitB12 deficiency (serum level < 133 pg/ml) were present in 0.7 and 5.4% of the patients, respectively. The mean prognostic nutritional index (PNI) and systemic immune-inflammation index (SII) were 47.78 ± 4.42 and 470.81 ± 254.05, respectively. The multivariate analyses showed that serum VitB12 level (P = 0.002) and SII (P = 0.005) were significant factors for ADL score; serum folate (P = 0.027) and VitB12 (P = 0.037) levels for UPDRS-III score; and serum folate (P = 0.066) and VitB12 (P = 0.017) levels for H-Y classification. The elevated folate level did correlate with greater decline in UPDRS-III score (P = 0.023) and H-Y classification (P = 0.003), whereas there was an obvious increase in ADL score (P = 0.048). SII was negatively associated (P < 0.001) with the ADL score. The three-dimensional drawing, combined with the effect of folate and VitB12 levels, showed that the lowest level of folate was associated with the lowest ADL score and the highest UPDRS-III score and H-Y classification. This study indicates that serum folate, VitB12 levels, and SII are significant factors influencing the motor performance status in patients with PD. SII is negatively associated with ADL. Elevated serum folate level correlates with mild motor impairment in patients with PD.

Introduction

Parkinson's disease (PD) is the second most common neurodegenerative disorder, with ~700,000 predicted cases in the United States from 2000 to 2040 (1). The main pathological features of PD are the loss of dopamine (DA)-ergic neurons in the substantia nigra (SN) and the presence of Lewy bodies (LBs), which are composed mainly of alpha-synuclein (2). Previous studies have demonstrated that protein misfolding and aggregation, disruption of autophagic catabolism, mitochondrial dysfunction, and loss of calcium homeostasis are the critical factors leading to the death of SN DAergic neurons (3).

The cell-autonomous mechanisms of neurodegeneration, which arise from an interaction between genetic and environmental risk factors, play an important role in the development of PD (4, 5). However, the pathological progression of PD involves several non-cell-autonomous mechanisms that facilitate further degeneration. Principal among these non-cell-autonomous factors is neuroinflammation, which involves a series of immune-mediated cascades that are triggered by the loss of DAergic neurons (4, 5). In vivo experiments have revealed that glial cells, particularly microglia, can adopt a pro-inflammatory phenotype that is associated with the release of cytotoxic molecules, which lead to enhanced neurodegeneration (4). Our previous study indicated that macrophage migration inhibitory factor (MIF) mediated neuroprotective effects via suppressing inflammatory responses in PD. These findings might demonstrate a causal link between neuroinflammation and PD pathogenesis (6).

The blood–brain barrier was once thought to inhibit the entry of inflammatory cells and mediators from the peripheral circulation, but increasing evidence suggests that the blood–brain barrier is affected due to pathological conditions (7, 8). Therefore, the status of systemic inflammation can partially reflect the progress and prognosis of PD. Many inflammation-based prognostic scores were developed on the basis of systemic inflammatory responses, such as the Glasgow Prognostic Score (GPS) and modified Glasgow Prognostic Score (mGPS), both evaluated by combining serum C-reactive protein (CRP) and albumin (ALB) levels; Prognostic Nutritional Index (PNI), measured by the ALB level; and the lymphocyte count measured by neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and lymphocyte-to-monocyte ratio (LMR); and the SII, calculated by the neutrophil, lymphocyte, and platelet counts. These scores have shown the prognostic value in several types of cancer (9–11) and immune-inflammation-related diseases (12).

Folate is particularly critical during the early development of the brain and is essential for the maintenance of normal brain function during the later stages of development. Folate and vitamin B12 (VitB12) are required for the methionine synthase reaction in which a methyl group is transferred from methyltetrahydrofolate (methyl-H4-folate; also known as levomefolic acid) to homocysteine by methionine synthase, with methyl-VitB12 as a coenzyme to form methionine. The resulting H4-folate can then be returned to the folate pool and can be made available for the generation of methylene-H4-folate, the form required for de novo synthesis of thymidine, which is essential for DNA replication and repair. Hence, either folate or B12 deficiency results in the same biochemical perturbation in thymidine synthesis and DNA replication (13). Folate and VitB12 deficiency results in an increase in blood and intracellular levels of homocysteine. Homocysteine is readily and partly reversibly transformed into other compounds, termed as “total homocysteine (tHcy).” Folate deficiency and tHcy impair DNA repair in hippocampal neurons and sensitize them to oxidative damage (14). Low serum VitB12 level was associated with an accelerated rate of white matter damage and brain atrophy (15–17). A prospective study that included 5,289 participants with a mean follow-up of 9.7 years failed to identify any relationship between VitB12 level and the risk of development of PD (18). Conversely, a large cohort collected from participants with a double-blind, randomized trial of PD (DATATOP) showed that low VitB12 levels at baseline predicted greater worsening of mobility, meanwhile elevated tHcy predicted greater cognitive decline (19).

There might be an indirect regulation between folate/VitB12 and the inflammatory cells and mediators. Previous studies suggested that cobalamin (VitB12) conversely decreased the expression of neurotrophic epidermal growth factor (EGF) and increased the expression of neurotoxic tumor necrosis factor-alpha (TNF-alpha) both in serum and cerebrospinal fluid (CSF) (20, 21). The increase in TNF-alpha and NGF levels increased the nuclear factor-kappa B activity levels and indirectly modulated the expression of some neuroinflammatory cytokines (13).

This study aimed to investigate the influence of serum folate, VitB12 levels, and inflammation-based scores on the motor performance status in patients with PD.

Materials and Methods

Ethical Statement

This study was performed with the approval of the Ethics Committee of the Third Affiliated Hospital of Guangzhou Medical University and the Ethics Committee of Guangdong Provincial People's Hospital (No. 2021-006). Informed consent was obtained from all patients. This study has been conducted according to the principles expressed in the Declaration of Helsinki. All the collected data were stored according to the ethical guidelines of medical research.

Study Participants

We retrospectively collected data from 148 consecutive patients with idiopathic PD admitted to our hospital for the first time from January 2018 to June 2020 so that data could be collected before dopaminergic medication. Diagnosis of PD was evaluated by two experienced neurologists, strictly according to the United Kingdom Parkinson's Disease Society Brain Bank Clinical Diagnostic Criteria. Exclusion criteria were as follows: PD induced by chemical drugs, trauma, cerebrovascular disease, inflammatory bowel disease, and other reasons; patients with PD complicated with nephropathy, tumor, myocardial infarction, stroke, and recent infection or surgery; patients with PD complicated with non-neurodegenerative (Alzheimer's disease or cognitive impairments) nervous system disease; and patients with missing outcome assessment medical record were excluded. We collected data on patient characteristics, such as education status, smoking, alcohol consumption, diabetes mellitus, ABO blood type, PD duration, whole blood count, ALB, total bilirubin (TBIL), alanine transaminase (ALT), creatinine (Cr), uric acid (UA), lactate dehydrogenase (LDH), CRP, prothrombin time (PT), D-dimmer (D-D), fibrinogen, folate, and VitB12 levels. Serum folate level < 4.0 ng/mL and VitB12 level < 133.0 pg/mL were considered as deficient. The outcome assessment or PD performance status was assessed by the activity of daily living scale (ADL), the Unified Parkinson's Disease Rating Scale Part III (UPDRS-III), and the Hoehn–Yahr (H–Y) classification. We used the Barthel Index (BI) to measure the basic ADL function (self-maintenance skills, such as dressing, bathing, and grooming) of patients with PD. The BI consists of 10 items and is predominantly used with the patient population (22). The UPDRS-III is the most frequently used scale in the clinical motor examination of PD. Part of the UPDRS-III scores was extracted from the levodopa challenge test before taking Madopar. The test is widely used to assess motor symptom alleviation in unifying the drug administration (23). H–Y classification was commonly used to assess the severity and the stage of motor performance in patients with PD.

Inflammation-Based Prognostic Scores

Blood samples with routine laboratory measurements of CRP and ALB levels and white blood cell, neutrophil, lymphocyte, monocyte, and platelet counts were obtained at the time of recurrence. The GPS, mGPS, PNI, NLR, PLR, LMR, and SII scores were calculated and constructed as described in Table 1.

Table 1

Definition of the systemic inflammation-based scores.

Scoring systems	Score
Glasgow Prognostic Score (GPS)
CRP (≤10 mg/L) and ALB (≥35 g/L)	0
CRP (≤10 mg/L) and ALB (<35 g/L)	1
CRP (>10 mg/L) and ALB (≥35 g/L)	1
CRP (>10 mg/L) and ALB (<35 g/L)	2
Modified Glasgow Prognostic Score (mGPS)
CRP (≤10 mg/L) and ALB (≥35 g/L)	0
CRP (≤10 mg/L) and ALB (<35 g/L)	0
CRP (>10 mg/L)	1
CRP (>10 mg/L) and ALB (<35 g/L)	2
Prognostic Nutritional Index (PNI)	ALB (g/L) + 5 × lymphocyte count (×109/L)
Neutrophil to lymphocyte ratio (NLR)	Neutrophil count (×109/L): lymphocyte count (×109/L)
Platelet to lymphocyte ratio (PLR)	Platelet count (×109/L): lymphocyte count (×109/L)
Lymphocyte to monocyte ratio (LMR)	Lymphocyte count (×109/L): monocyte count (×109/L)
Systemic Immune-inflammation Index (SII)	Platelet count (×109/L) × neutrophil count (×109/L)/lymphocyte count (×109/L)

CRP, C-reactive protein; ALB, albumin.

Statistical Analysis

Continuous data were recorded as mean ± SD. Incidence of nominal variables was reported as the number of cases (percentage). Analysis of variance (ANOVA) and the Chi-square test were used to compare continuous and categorical variables normally distributed, respectively, and non-parametric tests were used for non-normally distributed variables. Variables that achieved statistical significance in the univariate analysis were introduced into the multivariate regression analyses, linear regression analyses for ADL score and UPDRS-III score, and logistic regression analyses for H–Y classification. The crude correlation between independent variables and outcomes was reported in scatter-plot figures. Independent variables were also classified in tertiles to study their combined association with outcomes. SPSS v.23.0 statistical software (SPSS, Inc., Chicago, IL, United States) was used for statistical analysis. P < 0.05 was considered as a statistically significant difference.

Results

Patient Characteristics

Table 2A shows the demographics and clinical characteristics (including the inflammation-based scores) of the enrolled patients. A total of 148 patients were included in this study. The total population consisted of 56 (37.84%) males and 92 (62.16%) females with a mean age of 63.79 years. The mean interval from the onset of PD-related symptoms to seeking medical care in our hospital was 58.89 months. The geometric mean of WBC, ALB, LDH, CRP, folate, and VitB12 levels were 6.08 (109/L), 39.45 (g/L), 196.18 (U/L), 2.73 (mg/L), 11.87 (ng/mL), and 330.52 (pmol/L), respectively. Folate deficiency (serum level < 4.0 ng/mL) and VitB12 deficiency (serum level < 133 pg/mL) were present in 0.7% and 5.4% of the patients, respectively. Thus, further analysis of folate and VitB12 levels were stratified to tertiles. The mean PNI, NLR, PLR, LMR, and SII were 47.78 ± 4.42, 2.12 ± 0.87, 128.48 ± 52.10, 4.16 ± 1.30, and 470.81 ± 254.05, respectively. Patients were divided into three groups according to the H–Y classification: early stage (1–2 classification), medium stage (2.5–3 classification), and advanced stage (4–5 classification). Table 2B showed that H–Y classification was highly correlated with PD duration, ADL scores, and UPDRS-III scores.

Table 2A

Demographic and clinical characteristics of the enrolled patients (n = 148).

Variables	Values (n = 148)
Gender (Female/Male)	56/92 (37.84/62.16)
Age (years), mean ± SD	63.79 ± 11.07
Education status (0/1/2/3/4/5)	6/26/44/31/39/2 (4.05/17.57/29.73/20.95/26.35/1.35)
Smoking (Yes/No)	10/138 (6.76/93.24)
Alcohol consumption (Yes/No)	3/145 (2.03/97.97)
Diabetes mellitus (Yes/No)	16/132 (10.81/89.19)
ABO blood type (A/B/AB/O)	34/40/18/56 (22.97/27.03/12.16/37.84)
PD duration (months), mean ± SD	58.89 ± 51.23
WBC (109/L), mean ± SD	6.08 ± 1.55
HGB (g/L), mean ± SD	132.99 ± 15.64
Neutrophil (109/L), mean ± SD	3.62 ± 1.25
Lymphocyte (109/L), mean ± SD	1.80 ± 0.49
Monocyte (109/L), mean ± SD	0.47 ± 0.17
PLT (109/L), mean ± SD	218.51 ± 63.00
ALB (g/L), mean ± SD	39.45 ± 3.59
TBIL (μmol/L), mean ± SD	13.68 ± 5.68
ALT (U/L), mean ± SD	17.17 ± 10.70
Cr (μmol/L), mean ± SD	71.25 ± 16.60
UA (μmol/L), mean ± SD	324.01 ± 95.50
LDH (U/L), mean ± SD	196.18 ± 129.33
CRP (mg/L), mean ± SD	2.73 ± 4.74
PT (s), mean ± SD	13.59 ± 0.94
D-dimmer (ng/ml), mean ± SD	559.53 ± 589.94
Fibrinogen (g/L), mean ± SD	3.28 ± 1.27
Folate (ng/ml), mean ± SD	11.87 ± 5.36
VitB12 (pmol/L), mean ± SD	330.52 ± 197.10
UA/Cr, mean ± SD	4.72 ± 1.50
GPS (0/1/2)	131/15/2 (88.51/10.14//1.35)
mGPS (0/1/2)	136/10/2 (91.89/6.76/1.35)
PNI, mean ± SD	47.78 ± 4.42
NLR, mean ± SD	2.12 ± 0.87
PLR, mean ± SD	128.48 ± 52.10
LMR, mean ± SD	4.16 ± 1.30
SII, mean ± SD	470.81 ± 254.05

Values are presented as the mean ± SD or n (%).

PD, Parkinson's disease; WBC, white blood cell; HGB, hemoglobin; PLT, platelet; ALB, albumin; TBIL, total bilirubin; ALT, alanine transaminase; Cr, creatinine; UA, uric acid; LDH, lactate dehydrogenase; CRP, C-reactive protein; PT, prothrombin time; VitB12, vitamin B12; GPS, Glasgow Prognostic Score; mGPS, modified Glasgow Prognostic Score; PNI, prognostic nutritional index; NLR, neutrophil-to-lymphocyte ratio; PLr, platelet-to-lymphocyte ratio; LMR, lymphocyte-to-monocyte ratio; SII, systemic immune-inflammation index.

Table 2B

Disease duration, ADL scores, and UPDRS-III scores according to H-Y classification in PD patients (n = 148).

H-Y classification	Early stage	Medium stage	Advanced stage	Pearson correlation P
Cases	78	50	20
PD duration (months)	34.55 ± 32.82	76.02 ± 45.36	110.95 ± 67.64	<0.001
ADL scores	97.92 ± 4.28	82.50 ± 19.93	61.75 ± 21.72	<0.001
UPDRS-III scores	29.88 ± 11.88	51.40 ± 8.68	68.75 ± 4.24	<0.001

PD, Parkinson's disease; ADL, activity of daily living scale; UPDRS-III, the Unified Parkinson's Disease Rating Scale Part III; H-Y classification, Hoehn–Yahr classification.

Univariate and Multivariate Regression Analyses

The univariate analysis identified that age, diabetes mellitus, PD duration, HGB, lymphocyte, ALB, ALT, CRP, D-D, FIB, folate, VitB12 levels, PNI, NLR, PLR, LMR, and SII were significant factors associated with the ADL score. After the multivariate linear regression analyses, we found that only diabetes mellitus (HR = −11.995; 95% CI = −20.260–3.731; P = 0.005), PD duration (HR = −0.113; 95% CI = −0.166–0.060; P < 0.001), VitB12 level (HR = −0.021; 95% CI = −0.034–0.008; P = 0.002), NLR (HR = −9.370; 95% CI = −0.226–18.513; P = 0.045), and SII (HR = −0.059; 95% CI = −0.100–0.018; P = 0.005) were significant factors for ADL scores (Table 3).

Table 3

Univariate and multivariate regression analyses of the clinical characteristics for ADL scores in PD patients (n = 148).

Univariate	HR (95% CI)	P	Multivariate	HR (95% CI)	P
Gender	3.455 (−2.890–9.800)	0.284
Age	−0.579 (−0.842–0.315)	<0.001	Age	−0.226 (−0.490–0.037)	0.090
Education: illiteracy	Reference
Education: primary	7.288 (−9.682–24.258)	0.397
Education: junior	6.402 (−9.904–22.708)	0.439
Education: senior	−2.070 (−18.781–14.641)	0.807
Education: undergraduate	3.397 (−13.034–19.828)	0.683
Education status: post-graduate	0.833 (−29.759–31.426)	0.957
Smoking	5.552 (−6.723–17.827)	0.373
Alcohol consumption	12.429 (−9.400–34.258)	0.262
Diabetes mellitus	−12.275 (−22.020–2.530)	0.014	Diabetes mellitus	−11.995 (−20.260–3.731)	0.005
PD duration	−0.159 (−0.213–0.104)	<0.001	PD duration	−0.113 (−0.166–0.060)	<0.001
ABO blood type: A	Reference
ABO blood type: B	−2.392 (−11.160–6.376)	0.591
ABO blood type: AB	3.969 (−6.988–14.926)	0.475
ABO blood type: O	2.233 (−5.939–10.406)	0.590
WBC	−0.903 (−2.902–1.096)	0.373
HGB	0.220 (0.025–0.415)	0.027	HGB	−0.045 (−0.231–0.142)	0.636
Lymphocyte	5.723 (−0.543–11.989)	0.073	Lymphocyte	12.234 (−4.047–23.758)	0.163
Neutrophil	−1.935 (−4.392–0.522)	0.122
Monocyte	−12.662 (−30.706–5.382)	0.168
Platelet	−0.034 (−0.082–0.015)	0.177
ALB	1.373 (0.538–2.208)	0.001	ALB	0.476 (−0.342–1.293)	0.252
TBIL	0.303 (−0.240–0.847)	0.272
ALT	0.341 (0.057–0.625)	0.019	ALT	0.022 (−0.224–0.267)	0.862
CREA	0.023 (−0.164–0.210)	0.810
URIC	0.007 (−0.025–0.040)	0.661
LDH	−0.014 (−0.038–0.010)	0.250
CRP	−1.090 (−1.719–0.460)	0.001	CRP	−0.102 (−0.786–0.583)	0.770
PT	1.430 (−1.857–4.717)	0.391
D-D	−0.010 (−0.015–0.005)	<0.001	D-D	−0.004 (−0.009–0.000)	0.071
FIB	−2.054 (−4.468–0.359)	0.095	FIB	−1.482 (−3.590–0.626)	0.167
Folate	0.592 (0.022–1.162)	0.042	Folate	0.394 (−0.086–0.873)	0.107
VitB12	−0.026 (−0.041–0.011)	0.001	VitB12	−0.021 (−0.034–0.008)	0.002
GPS = 0.0	Reference
GPS = 1.0	−4.882 (−12.095–2.331)	0.183
GPS = 2.0	−32.912 (−54.217–11.608)	0.003	GPS = 2.0	2.865 (−27.793–33.522)	0.854
mGPS = 0.0	Reference
mGPS = 1.0	−12.850 (−29.264–3.564)	0.124
mGPS = 2.0	−43.850 (−69.534–18.165)	0.001	mGPS = 2.0	−24.048 (−65.454–17.358)	0.253
PNI	1.291 (0.612–1.971)	<0.001	PNI	0.476 (−0.342–1.293)	0.252
NLR	−4.264 (−7.563–0.965)	0.012	NLR	9.370 (0.226–18.513)	0.045
PLR	−0.092 (−0.157–0.027)	0.006	PLR	0.128 (−0.030–0.286)	0.112
LMR	1.812 (−0.241–3.864)	0.083	LMR	−0.540 (−2.593–1.514)	0.604
SII	−0.020 (−0.032–0.008)	0.001	SII	−0.059 (−0.100–0.018)	0.005
UA/Cr	0.697 (−1.402–2.797)	0.512

ADL, activity of daily living scale; PD, Parkinson's disease; HR, hazard ratio; CI, confidence interval; WBC, white blood cell; HGB, hemoglobin; PLT, platelet; ALB, albumin; TBIL, total bilirubin; ALT, alanine transaminase; Cr, creatinine; UA, uric acid; LDH, lactate dehydrogenase; CRP, C-reactive protein; PT, prothrombin time; VitB12, vitamin B12; GPS, Glasgow Prognostic Score; mGPS, modified Glasgow Prognostic Score; PNI, prognostic nutritional index; NLR, neutrophil-to-lymphocyte ratio; PLR, platelet-to-lymphocyte ratio; LMR, lymphocyte-to-monocyte rati; SII, systemic immune-inflammation index.

The univariate analysis identified that age, PD duration, B blood type, lymphocyte, TBIL, CRP, D-D, folate, VitB12 levels, PNI, and NLR were significant factors associated with UPDRS-III score. After the multivariate linear regression analyses, we found that only age (HR = 0.348; 95% CI = 0.096–0.601; P = 0.007), PD duration (HR = 0.124; 95% CI = 0.075–0.174; P < 0.001), folate level (HR = −0.519; 95% CI = −0.979–0.060; P = 0.027), and VitB12 level (HR = 0.013; 95% CI = 0.01–0.026; P = 0.037) were significant factors for UPDRS-III scores (Table 4).

Table 4

Univariate and multivariate regression analyses of the clinical characteristics for UPDRS-III scores in PD patients (n = 148).

Univariate	HR (95% CI)	P	Multivariate	HR (95% CI)	P
Gender	0.422 (−5.461–6.306)	0.887
Age	0.478 (0.231–0.724)	<0.001	Age	0.348 (0.096–0.601)	0.007
Education: illiteracy	Reference
Education: primary	−2.885 (−18.693–12.924)	0.719
Education: junior	−6.318 (−21.509–8.872)	0.412
Education: senior	−4.177 (−19.745–11.391)	0.597
Education: undergraduate	−7.244 (−22.550–8.063)	0.351
Education status: post-graduate	5.500 (−23.000–34.000)	0.703
Smoking	−6.333 (−17.655–4.989)	0.271
Alcohol consumption	−8.920 (−29.117–11.278)	0.384
Diabetes mellitus	5.362 (−3.787–14.510)	0.249
PD duration	0.161 (0.112–0.210)	<0.001	PD duration	0.124 (0.075–0.174)	<0.001
ABO blood type: A	Reference
ABO blood type: B	6.972 (−1.098–15.042)	0.090	ABO blood type: B	2.218 (−3.188–7.625)	0.419
ABO blood type: AB	2.147 (−7.938–12.232)	0.675
ABO blood type: O	3.718 (−3.803–11.240)	0.330
WBC	0.231 (−1.620–2.082)	0.805
HGB	−0.093 (−0.276–0.089)	0.313
Lymphocyte	−5.247 (−11.036–0.542)	0.075	Lymphocyte	−4.215 (−12.086–3.656)	0.291
Neutrophil	1.016 (−1.266–3.299)	0.380
Monocyte	6.717 (−10.023–23.457)	0.429
Platelet	−0.021 (−0.066–0.024)	0.363
ALB	−0.498 (−1.292–0.297)	0.218
TBIL	−0.521 (−1.018–0.024)	0.040	TBIL	−0.412 (−0.854–0.030)	0.068
ALT	−0.189 (−0.454–0.077)	0.162
CREA	0.032 (−0.140–0.205)	0.714
URIC	0.001 (−0.029–0.031)	0.954
LDH	−0.009 (−0.031–0.013)	0.411
CRP	0.974 (0.391–1.557)	0.001	CRP	0.390 (−0.799–1.579)	0.518
PT	0.590 (−2.452–3.632)	0.702
D-D	0.006 (0.001–0.011)	0.011	D-D	0.002 (−0.003–0.006)	0.465
FIB	0.942 (−1.303–3.187)	0.408
Folate	−0.752 (−1.272–0.233)	0.005	Folate	−0.519 (−0.979–0.060)	0.027
VitB12	0.016 (0.002–0.030)	0.030	VitB12	0.013 (0.001–0.026)	0.037
GPS = 0.0	Reference
GPS = 1.0	5.171 (−1.624–11.966)	0.135
GPS = 2.0	16.414 (−3.657–36.484)	0.108
mGPS = 0.0	Reference
mGPS = 1.0	20.153 (4.789–35.518)	0.011	mGPS = 1.0	10.879 (−12.999–34.756)	0.369
mGPS = 2.0	20.553 (−3.489–44.596)	0.093	mGPS = 2.0	−6.698 (−43.607–30.211)	0.720
PNI	−0.668 (−1.316–0.020)	0.043	PNI	0.608 (−0.162–1.377)	0.121
NLR	3.045 (−0.029–6.120)	0.052	NLR	1.225 (−2.103–4.554)	0.468
PLR	0.021 (−0.041–0.083)	0.495
LMR	−1.212 (−3.117–0.693)	0.211
SII	0.008 (−0.004–0.019)	0.182
UA/Cr	−0.363 (−2.303–1.577)	0.712

UPDRS-III, the Unified Parkinson's Disease Rating Scale Part III; PD, Parkinson's disease; HR, hazard ratio; CI, confidence interval; WBC, white blood cell; HGB, hemoglobin; PLT, platelet; ALB, albumin; TBIL, total bilirubin; ALT, alanine transaminase; Cr, creatinine; UA, uric acid; LDH, lactate dehydrogenase; CRP, C-reactive protein; PT, prothrombin time; VitB12, vitamin B12; GPS, Glasgow Prognostic Score; mGPS, modified Glasgow Prognostic Score; PNI, prognostic nutritional index; NLR, neutrophil-to-lymphocyte ratio; PLR, platelet-to-lymphocyte ratio; LMR, lymphocyte-to-monocyte ratio; SII, systemic immune-inflammation index.

The univariate analysis identified that age, PD duration, B blood type, lymphocyte, TBIL, CRP, folate, VitB12 levels, PNI, NLR, and LMR were significant factors associated with H–Y classification. After the multivariate logistic regression analyses, we found that only age (HR = 0.049; 95% CI = 0.018–0.080; P = 0.002), PD duration (HR = 0.019; 95% CI = 0.013–0.026; P < 0.001), TBIL (HR = −0.065; 95% CI = −0.123–0.007; P = 0.029), folate level (HR = −0.055; 95% CI = −0.113–0.004; P = 0.066), and VitB12 level (HR = 0.002; 95% CI = 0.000–0.004; P = 0.017) were significant factors for H–Y classification (Table 5).

Table 5

Univariate and multivariate regression analyses of the clinical characteristics for Hoehn–Yahr (H-Y) classification of PD patients (n = 148).

Univariate	HR (95% CI)	P	Multivariate	HR (95% CI)	P
Gender	−0.159 (−0.752–0.433)	0.599
Age	0.051 (0.024–0.079)	<0.001	Age	0.049 (0.018–0.080)	0.002
Education: illiteracy	−0.566 (−3.416–2.283)	0.697
Education: primary	−1.226 (−3.793–1.342)	0.349
Education: junior	−1.344 (−3.875–1.187)	0.298
Education: senior	−0.852 (−3.401–1.697)	0.513
Education: undergraduate	−1.473 (−4.012–1.067)	0.256
Education status: post-graduate	Reference
Smoking	−0.330 (−1.479–0.819)	0.573
Alcohol consumption	−0.719 (−2.773–1.336)	0.493
Diabetes mellitus	0.682 (−0.245–1.610)	0.149
PD duration	0.022 (0.015–0.028)	<0.001	PD duration	0.019 (0.013–0.026)	<0.001
ABO blood type: A	−0.062 (−0.823–0.699)	0.873
ABO blood type: B	0.455 (−0.271–1.181)	0.219
ABO blood type: AB	−0.084 (−1.033–0.865)	0.862
ABO blood type: O	Reference
WBC	−0.008 (−0.195–0.178)	0.931
HGB	−0.015 (−0.033–0.004)	0.124
Lymphocyte	−0.668 (−1.267–0.069)	0.029	Lymphocyte	−0.347 (−1.337–0.642)	0.492
Neutrophil	0.092 (−0.139–0.322)	0.436
Monocyte	0.870 (−0.821–2.562)	0.313
Platelet	−0.002 (−0.006–0.003)	0.436
ALB	−0.065 (−0.146–0.016)	0.116
TBIL	−0.070 (−0.122–0.018)	0.008	TBIL	−0.065 (−0.123–0.007)	0.029
ALT	−0.020 (−0.047–0.007)	0.145
CREA	−0.006 (−0.023–0.012)	0.527
URIC	−0.001 (−0.004–0.002)	0.485
LDH	−0.001 (−0.004–0.001)	0.224
CRP	0.088 (0.025–0.151)	0.006	CRP	0.039 (−0.030–0.108)	0.269
PT	0.143 (−0.164–0.450)	0.361
D-D	0.000 (0.000–0.001)	0.188
FIB	0.048 (−0.178–0.274)	0.679
Folate	−0.067 (−0.122–0.012)	0.016	Folate	−0.055 (−0.113–0.004)	0.066
VitB12	0.002 (0.000–0.003)	0.011	VitB12	0.002 (0.000–0.004)	0.017
GPS = 0.0	−1.180 (−3.227–0.866)	0.258
GPS = 1.0	−0.505 (−2.608–1.597)	0.638
GPS = 2.0	Reference
mGPS = 0.0	−1.553 (−4.059–0.952)	0.224
mGPS = 1.0	0.510 (−2.429–3.449)	0.734
mGPS = 2.0	Reference
PNI	−0.092 (−0.160–0.025)	0.007	PNI	0.035 (−0.063–0.133)	0.485
NLR	0.369 (0.051–0.687)	0.023	NLR	0.147 (−0.314–0.608)	0.532
PLR	0.003 (−0.003–0.010)	0.303
LMR	−0.222 (−0.418–0.026)	0.027	LMR	−0.142 (−3.389–0.105)	0.259
SII	0.001 (0.000–0.002)	0.134
UA/Cr	−0.034 (−0.229–0.162)	0.736

H-Y classification, Hoehn–Yahr classification; PD, Parkinson's disease; HR, hazard ratio; CI, confidence interval; WBC, white blood cell; HGB, hemoglobin; PLT, platelet; ALB, albumin; TBIL, total bilirubin; ALT, alanine transaminase; Cr, creatinine; UA, uric acid; LDH, lactate dehydrogenase; CRP, C-reactive protein; PT, prothrombin time; VitB12, vitamin B12; GPS, Glasgow Prognostic Score; mGPS, modified Glasgow Prognostic Score; PNI, prognostic nutritional index; NLR, neutrophil-to-lymphocyte ratio; PLR, platelet-to-lymphocyte ratio; LMR, lymphocyte-to-monocyte ratio; SII, systemic immune-inflammation index.

Changes of Outcomes According to Tertiles of Folate and VitB12

Although only a small portion of patients showed folate or VitB12 deficiency, analysis of outcomes according to folate level tertiles showed that the elevated folate level did correlate with greater decline in UPDRS-III scores (U = 902.500; P = 0.023) and H–Y classification (U = 781.000; P = 0.003) and a dramatic increase in ADL scores (U = 929.000; P = 0.048) (Table 6). However, these changes were not observed in VitB12 level tertiles related to the outcomes (Table 7).

Table 6

Changes of outcomes according to tertiles of Folate in PD patients (n = 148).

	Folate tertile
Change outcomes	First (<8.90 ng/ml)	Second (8.90–13.61 ng/ml)	Third (>13.61 ng/ml)	U	P
ADL	84.90 ± 20.27	87.30 ± 19.15	91.28 ± 17.14	902.500	0.023
UPDRS-III	46.86 ± 16.65	43.56 ± 17.75	36.78 ± 16.91	781.000	0.003
H-Y classification	4.14 ± 1.98	4.06 ± 1.62	3.37 ± 1.72	929.000	0.048

PD, Parkinson's disease; ADL, activity of daily living scale; UPDRS-III, the Unified Parkinson's Disease Rating Scale Part III; H-Y classification, Hoehn–Yahr classification.

Table 7

Changes of outcomes according to tertiles of VitB12 in PD patients (n = 148).

	VitB12 tertile
Change outcomes	First (<236.33 pmol/L)	Second (236.33–339.33 pmol/L)	Third (>339.33 pmol/L)	U	P
ADL	90.87 ± 14.17	88.50 ± 18.22	84.08 ± 23.15	1068.000	0.316
UPDRS-III	41.80 ± 17.35	41.10 ± 17.37	44.35 ± 17.98	1087.500	0.422
H-Y classification	3.57 ± 1.61	3.82 ± 1.81	4.18 ± 1.94	978.500	0.102

VitB12, vitamin B12; PD, Parkinson's disease; ADL, activity of daily living scale; UPDRS-III, the Unified Parkinson's Disease Rating Scale Part III; H-Y classification, Hoehn–Yahr classification.

Correlation Between the Significant Factors and the Outcomes

According to the above regression analysis and stratified analysis, we performed correlation analysis of the significant factors and the outcomes. Figure 1 shows that SII was negatively associated (P < 0.001) with the ADL score. Folate level was also negatively associated with UPDRS-III score (P = 0.005) and H–Y classification (P = 0.015). The three-dimensional drawing (Figure 2) showed the combined effect of folate and VitB12 levels on the outcomes. It showed that the lowest level of folate was associated with the lowest ADL score, while the lowest level of folate was related to the highest UPDRS-III score and H–Y classification. The trend between each tertile of folate levels was more stable and obvious than that of the VitB12 levels.

Figure 1

Correlation analysis between the significant factors and the outcomes. (A) SII was negatively associated (P < 0.001) with ADL score. (B,C) Folate level was also negatively associated with UPDRS-III score (P < 0.001) and H–Y classification (P < 0.001).

Figure 2

The combined effect of serum folate and VitB12 levels on the outcomes. Red bar represents the highest combined effects to the outcomes, while the blue bar represents the lowest effects. (A) ADL score, (B) UPDRS-III score, and (C) H-Y classification.

Discussion

The relationship between several important inflammation-based scores and the severity of PD was first investigated in our present study. We found that PD duration and motor performance status (ADL scores and UPDRS-III scores) were highly correlated with H–Y classification stages. Folate deficiency (serum level < 4.0 ng/mL) and VitB12 deficiency (serum level < 133 pg/mL) were only present in 0.7 and 5.4% of the patients, respectively. NLR and SII were significant factors for ADL scores. Serum folate and VitB12 levels are significant factors influencing the motor performance status (ADL scores, UPDRS-III scores, and H-Y classification in PD). Dose–response analysis suggested that elevated folate level correlates with mild motor impairment in PD.

Although the underlying mechanism of neurodegeneration mediated by neuroinflammation is still rarely understood, increasing evidence suggests that the blood–brain barrier is affected under pathological conditions. Faucheux et al. (7) reported an increase in endothelial cell density in the SN of PD. Farkas et al. (8) reported pathological changes in the microanatomy of cerebral capillaries in patients with PD. Activated microglia release cytokines that may stimulate angiogenesis. Whether these cytokines can also induce brain capillary damage and changes in permeability, allowing peripheral cells, such as lymphocytes, to cross the blood–brain barrier into the brain, deserves further investigation. Studies related to the systemic inflammatory indexes have been published based on the neuroinflammation hypothesis of PD progression. Altered differential leukocyte count was involved in PD-related symptoms even though there was no sign of clinical inflammation. Relatively mild peripheral inflammation might play an important role in promoting mild disease phenotype in PD (24). A positive association between NLR and motor severity was observed in a tremor-dominant (TD) subgroup. Besides, NLR could negatively predict the striatal binding ratios in ipsilateral and contralateral putamen and caudate nuclei in a TD phenotype (25). However, other studies showed that there was no statistically significant difference between the NLR of patients with idiopathic PD (akinetic-rigid or TD subtypes) and controls (26). The present study also found that NLR was independently associated with ADL score. However, no significant association was found with UPDRS-III score and H–Y classification after multivariate analyses. As mentioned before, the complex indexes, such as PNI and SII, have proved to be more sensitive and reliable than single parameters in reflecting the immune-inflammation or nutritional status in different types of cancer (9–11) or inflammatory diseases (12). Nevertheless, these complex indexes have never been investigated in PD before. The present study showed that SII is a significant factor for ADL score. SII was negatively associated with the ADL score, indicating that patients with PD with a high SII score have a more severe motor impairment and poor performance status. The SII score, based on lymphocytes, neutrophils, and platelets, might serve as a useful tool for predicting the severity of motor impairment or prognosis in patients with PD.

The association of serum folate and VitB12 levels with PD have long been investigated, but the result regarding VitB12 level and PD was still inconsistent. Several meta-analyses have been released to address this question. Patients with PD with cognitive impairment were likely to have higher tHcy levels, lower folate, and VitB12 levels (27). However, all of the 27 included studies were conducted in China. The I-squared was extremely high across the studies, indicating heterogeneity, and the pooled result was not robust and convincible. Another meta-analysis, including 15 studies worldwide, drew a subdivided conclusion that serum tHcy level was higher in patients with PD compared with the control group, and lower folate and VitB12 levels were only observed in the PD cognitive impairment group compared with the cognitively normal group (28). On the contrary, a large community-based study found that hyperhomocysteinemia was not a risk factor for PD, as well as VitB12 and folate deficiency (29). Using CSF specimens, Christine et al. (30) found that low CSF VitB12 predicted greater worsening of the UPDRS “walking” item, whereas CSF tHcy was not associated with the progression of cognitive impairment. These findings were partially contradicted to their findings in serum, which show that low serum VitB12 at baseline predicted greater worsening of mobility, whereas elevated tHcy predicted greater cognitive decline (19). These ambiguous results were challenged by Cardoso (32). First, the metabolism of VitB12 could be induced by L-dopa (12, 13). Second, many factors might contribute to low VitB12 level. Genuine deficiency is only observed in few cases with extremely low levels. Finally, the measurement of VitB12 level should be adjusted for important confounding factors, especially the tHcy level (31, 32).

Animal model experiments showed that supplementation of folic acid could attenuate the severity of parkinsonism. While the supplement of vitamin B complex also had a beneficial effect and improved motor performance (33). Dietary folic acid provided protection against disparities in parkin mutation-induced PD via alleviating mitochondrial dysfunction (34). If we take up the point of view that high serum tHcy level and low serum VitB12 and folate levels were associated with progression of motor or cognitive impairment, what could be the basic underlying mechanism?—Schaffner et al. (35) uncovered that 5'-deoxyadenosylcobalamin (AdoCbl), the physiological form of VitB12, modulated PD leucine-rich repeat kinase-2 (LRRK2) kinase activity through allosteric regulation. Treatment with AdoCbl inhibited LRRK2 kinase activity and prevented neurotoxicity. AdoCbl also alleviated deficits in dopamine release sustainability caused by LRRK2 disease variants in mouse models (35).

Based on the ambiguous epidemiological studies and positive fundamental research, the plan for supplementation of folic acid or VitB12 might come up and be put into practice. However, no significant association was observed for dietary intake of folic acid and VitB12 with the risk of developing PD (36). Another large longitudinal study on patients with early PD showed that no significant differences in the progress of UPDRS scores were observed. However, a well-designed prospective nested case–control study showed that a low–folate density diet, 2–8 years before PD diagnosis, was significantly associated with olfactory dysfunction at the time of PD diagnosis (37).

The unbalanced gender distribution was observed in demographics, which was contradictory to the previous study (38). PD is usually more common in men than women, with a male-to-female ratio of about 1.5. The underlying mechanism is rarely understood. Possible explanations for this difference include more frequent occupational exposures in men, neuroprotection from estrogens in women, and X-linked genetic factors. However, gender is neither considered a protective factor nor a risk factor in an epidemiological study of PD. There might be recall and selection bias in the retrospective study. Based on the univariate or multivariate analysis in the present study, gender was not statistically significant. It is widely accepted that UA is a natural antioxidant that has protective effects of scavenging free radicals and antioxidation in neurological disorders. It has been reported that lower serum UA level was associated with the worsening of motor function (39). Serum UA and UA/Cr levels were negatively correlated with the H–Y classification of PD and are independent of negatively predicting biological indexes of PD incidence and progression (40). However, the univariate and multivariate analyses of the study did not reveal significant associations between serum UA and UA/Cr levels and the motor performance status of PD.

There are several limitations in the present study: First, this is a retrospective study design, where recall and selection bias might exist. Second, age- and gender-matched healthy controls are not included because the elderly or retired people seldom go for medical check-ups, and the conventional check-ups do not contain tests for folate or VitB12 levels and for the assessment of motor performance status or cognitive ability. Third, a powerful endpoint assessment tool, such as UPDRS-II, was not used. Fourth, adjustments for important confounding factors, such as tHcy levels, medication, and gastrectomy history, were not performed.

Conclusions

The present study indicates that serum folate, VitB12 levels, and SII are significant factors influencing the status of motor performance in PD. SII is negatively associated with the ADL. Elevated folate level correlates with mild motor impairment in PD. Well-designed (nested case–control, propensity score matching, or long-time follow-up prospective design), large sample size studies would be needed to further clarify the influence of these factors.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The studies involving human participants were reviewed and approved by the Ethics Committee of the Third Affiliated Hospital of Guangzhou Medical University and the Ethics Committee of Guangdong Provincial People's Hospital (No. 2021-006). The patients/participants provided their written informed consent to participate in this study.

Author Contributions

SL and LW designed the whole study and revised the manuscript. SL, QZ, and YL enrolled patients and extracted raw data. KN and YZ performed the statistical analyses and prepared tables and figures. SL wrote the manuscript. All authors read and approved the final manuscript.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.