DASH Diet, Triglycerides and AIP in Parkinson's Disease

February 10, 2026 updated by: Nurefşan KONYALIGİL ÖZTÜRK, Abant Izzet Baysal University

DASH Diet and Cardiometabolic Risk in Parkinson's Disease: Lower Triglycerides and AIP With Higher Adherence

Participants who agreed to participate in the study were informed about the purpose of the research and obtained their consent to participate in the study using an informed consent form. The study was conducted on 70 patients with Parkinson's disease. Participants who volunteered to participate in the study were given a questionnaire form containing sociodemographic characteristics. In addition, participants' anthropometric measurements (body weight, height, waist and hip circumference, Body Mass Index (BMI)), biochemical parameters (fasting blood glucose, HbA1c, triglycerides, LDL cholesterol, triglycerides, total cholesterol, C-reactive protein (CRP), albumin, and hematology markers (hemoglobin (Hb), hematocrit (Htc), leukocytes and platelets, lymphocytes) and serum vitamin D, folic acid, vitamin B12) and nutritional status (food consumption frequency, DASH diet compliance) were obtained. New cardiovascular risk markers such as neutrophil/lymphocyte ratio (NLR), monocyte HDL ratio (MHR), and plasma atherogenic index (PAI) were calculated.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

70

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Bolu, Turkey (Türkiye)
        • Bolu Abant İzzet Baysal University, Faculty of Health Sciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

This study was designed as a cross-sectional descriptive study. The study included patients who presented to the Neurology Outpatient Clinic at BAİBÜ İzzet Baysal Education and Research Hospital and diagnosed with Parkinson's Disease

Description

Inclusion Criteria:

  • Individuals over 19 years of age
  • Individuals who are literate
  • Individuals diagnosed with Parkinson's Disease

Exclusion Criteria:

  • Individuals who have had an acute infection or inflammatory disease within the past month
  • Individuals with chronic infectious or inflammatory diseases
  • Individuals with cancer

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Individuals with Parkinson's disease
This cohort includes adult participants diagnosed with Parkinson's disease. No control group is included.
No intervention (observational study)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Questionnaire Form
Time Frame: 6 months
Sociodemographic characteristics of the individuals (age, constipation status, presence of comorbidities, gender, smoking and alcohol use) were questioned.
6 months
Body weight (BW)
Time Frame: 6 months
BW was measured using a calibrated digital scale placed on a flat, tiled surface. The scale was sensitive to 100 grams.
6 months
Height
Time Frame: 6 months
Height was measured using a stadiometer with the participant's head positioned in the Frankfort plane and feet placed together.
6 months
Waist Circumference (WC)
Time Frame: 6 months
WC was measured at the midpoint between the lowest rib and the iliac crest (cristal point) using a flexible measuring tape.
6 months
Hip Circumference (HC)
Time Frame: 6 months
HC was measured at the widest point of the hips using a flexible measuring tape.
6 months
Body Mass Index (BMI)
Time Frame: 6 months
BMI was calculated by dividing body weight (in kilograms) by the square of height (in meters): BMI = weight (kg) / height² (m²).
6 months
Fasting Blood Glucose
Time Frame: 6 months
Fasting blood glucose was measured using standard laboratory techniques during routine outpatient visits.
6 months
Triglycerides
Time Frame: 6 months
Triglyceride levels were measured via fasting blood samples analyzed in the outpatient clinic laboratory.
6 months
LDL-Cholesterol
Time Frame: 6 months
LDL-cholesterol was measured from fasting serum samples using standard enzymatic colorimetric methods.
6 months
HDL-Cholesterol
Time Frame: 6 months
HDL-cholesterol was measured from fasting serum samples using standard enzymatic colorimetric methods.
6 months
C-Reactive Protein (CRP)
Time Frame: 6 months
CRP levels were measured using routine laboratory procedures in outpatient visits.
6 months
Vitamin D
Time Frame: 6 months
Serum vitamin D (25(OH)D) levels were assessed using chemiluminescence immunoassay methods in the outpatient clinic laboratory.
6 months
Folic Acid
Time Frame: 6 months
Serum folic acid levels were measured using standard automated immunoassay techniques.immunoassay methods in the outpatient clinic laboratory.
6 months
Vitamin B12
Time Frame: 6 months
Serum vitamin B12 concentrations were measured using automated chemiluminescent immunoassay.immunoassay methods in the outpatient clinic laboratory.
6 months
Atherogenic Index of Plasma (AIP)
Time Frame: 6 months
AIP is a logarithmically transformed ratio of plasma triglycerides to high-density lipoprotein cholesterol [log₁₀(TG/HDL-C)], and it is used as a surrogate marker of atherogenicity and cardiovascular risk.
6 months
Monocyte-to-High-Density Lipoprotein Cholesterol Ratio
Time Frame: 6 months
A biomarker reflecting the balance between inflammatory status (monocytes) and anti-atherogenic lipid components (HDL-C); it has been proposed as an indicator of systemic inflammation and cardiovascular risk.
6 months
Total Cholesterol-to-High-Density Lipoprotein Cholesterol Ratio
Time Frame: 6 months
A widely used index of atherogenic risk, representing the balance between total cholesterol and protective HDL-C, with higher values indicating increased cardiovascular risk.
6 months
Neutrophil-to-Lymphocyte Ratio (NLR)
Time Frame: 6 months
A systemic inflammatory marker calculated as the ratio of neutrophils to lymphocytes, commonly used to assess inflammatory status and immune response.
6 months
Food consumption frequency
Time Frame: 6 months
Participants were asked about the foods they consumed in the past month from seven groups, including five basic food groups (meat and meat products, milk and dairy products, bread and grains, vegetables and fruits, sugars and fats), beverages, and fast food. Participants were asked how often and in what quantities they consumed these foods using eight options: "every meal," "every day," "5-6 days a week," "3-4 days a week," "1-2 days a week," "once every 15 days," "once a month," and "never." In evaluating food consumption records, responses regarding food consumption frequency were calculated using food consumption frequency. The amounts of food and beverages consumed were multiplied by "3" for "every meal," '1' for "every day," "0.7855" for "5-6 times a week," "0.498" for "3-4 times a week," "0.2145" for "1-2 times a week," "0.067" for "once every 15 days," and "0.033" for "once a month" to obtain the daily average amounts.
6 months
Food consumption record
Time Frame: 6 months
A single-day food consumption record was obtained using the 24-hour recall method to determine participants' food consumption patterns. The Food and Nutrition Photo Catalog was used to estimate portions to ensure that the amounts of food consumed were assessed accurately and reliably. Based on these records, daily energy and nutrient intakes were calculated using the Nutrition Information System (BEBİS) software, based on the type and amount of food consumed by individuals in the last 24 hours.
6 months
DASH diet compliance
Time Frame: 6 months
Individuals' DASH diet compliance scores were calculated based on their food consumption frequency after their energy requirements were calculated. The highest possible score on the DASH diet compliance scale is 8.0. A score of 4.5 or above is considered 'high compliance', while a score below 4.5 is considered 'low compliance'.
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Nurefşan Konyalıgil Öztürk, Abant Izzet Baysal University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 1, 2024

Primary Completion (Actual)

December 1, 2024

Study Completion (Actual)

December 1, 2024

Study Registration Dates

First Submitted

February 5, 2026

First Submitted That Met QC Criteria

February 5, 2026

First Posted (Actual)

February 11, 2026

Study Record Updates

Last Update Posted (Actual)

February 12, 2026

Last Update Submitted That Met QC Criteria

February 10, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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