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Mainstay Parkinson's Medication Sometimes "Wears Off" Faster for Women

Parkinson's Foundation Science News blogs

Levodopa, which helps with the movement symptoms of Parkinson’s, tends to work less well over time, especially for women. 

Parkinson's disease (PD) is a condition that gets worse over time, impacting the nervous system. It's caused by the gradual death of brain cells that produce dopamine, a crucial chemical messenger for controlling movement. When these cells are lost and dopamine levels drop, people with Parkinson's begin to experience noticeable symptoms like shaking or tremors, muscle stiffness, a general slowness of movement and problems with balance

A primary treatment for these movement symptoms is the drug levodopa. The body converts this medication into dopamine, helping to replenish the brain's supply. By doing so, levodopa can significantly reduce the physical challenges of the disease and improve a person's daily life. 

However, for many individuals with Parkinson's, the effectiveness of levodopa can begin to diminish between doses. In other words, it starts "wearing off." Patients may notice their movement symptoms, such as tremors and stiffness, gradually returning before their next scheduled dose. 

Woman taking medication

Parkinson’s also impacts men and women differently. Men are estimated to be 1.5 times more likely to develop Parkinson’s. Women with Parkinson's are often diagnosed at a later age and may have slightly different symptoms. These differences between men and women with Parkinson’s could be due to a variety of factors, including hormonal differences and genetics

To better understand how these gender differences impact experience with levodopa, a recent study tracked 216 individuals with Parkinson's over a two-year period. The goal was to investigate whether men and women experience levodopa wearing off at different rates and to examine the symptoms that occur while on this medication. 

Study Results 

Participants included 139 men and 77 women with Parkinson’s who began taking levodopa for the first time at the start of the study. After two years in the study, almost 65% of women experienced symptom fluctuations, or times when the medication's effects seem to "wear off" before the next dose is due. This was compared to about 53% of men. This suggests that for many women, the medication was less effective in managing symptoms and did not feel as consistent over time. 

In addition, more women in the study developed dyskinesia, a side effect of levodopa that leads to involuntary, uncontrolled movements. About 14% of women developed dyskinesia compared to only 5% of men. Taken together, these results suggest that there may be differences in how levodopa is processed in the body between men and women. 

The study concluded that being female was the strongest predictor for both the wearing-off effect and dyskinesia after taking levodopa for two years. This indicates that gender is an important factor when considering how a person might respond to this medication. 

Highlights 

  • The study followed 139 men and 77 women with Parkinson’s for two years after they started taking levodopa for the first time.  

  • During the two-year study period, 65% of women experienced times when the medication's effects seemed to "wear off" before the next dose. This was compared to about 53% of men. 

  • During the study, about 14% of women developed dyskinesia, compared to only 5% of men.  

  • The study concluded that female gender predicted the development of motor fluctuations and dyskinesia more than any other factor.  

What does this mean? 

Women’s experiences have been historically underrepresented in PD research. This study adds to increasing evidence that men and women often experience various aspects of PD differently, including in their response to the PD medication levodopa. Specifically, these results indicate that women may be more likely to have worse responses to levodopa treatment over time compared to men. However, the reasons for these differences between men and women are still unknown. Additionally, it is common for both men and women to have breakthrough symptoms on levodopa over time.  

What do these findings mean to people with PD right now? 

Knowing that men and women may react differently to prolonged levodopa treatment can help healthcare providers develop more effective treatment plans for patients. While more research needs to be done, the findings from this study suggest that more tailored, “gender-oriented” treatment recommendations may be needed. If you are struggling with symptoms related to levodopa treatment, talk to your doctor to discuss your treatment plan.  

Learn More 

The Parkinson’s Foundation believes in empowering the Parkinson’s community through education. Learn more about PD and the topics in this article through our below resources, or by calling our free Helpline at 1-800-4PD-INFO (1-800-473-4636) for answers to your Parkinson’s questions. 

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Expert Briefing: Managing Nighttime Interruptions in Parkinson's Disease

May 14, 2025

Sleep disturbances are a common and often challenging symptom of Parkinson’s disease (PD). This program explores three prevalent nighttime interruptions—Restless Legs Syndrome (RLS), REM Sleep Behavior Disorder (RBD), and insomnia—that can affect individuals with PD and their care partners. This session will provide an in-depth look at the causes, symptoms, and practical management strategies for these sleep disorders.

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Roneil G. Malkani, MD
Associate Professor, Northwestern University Feinberg School of Medicine
Neurologist, Northwestern Memorial Hospital
Specializing in Sleep Medicine and Movement Disorders

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The Parkinson's Foundation is an official charity partner for the 2026 Cape Town Marathon. By signing up to run as a Parkinson's Champion you commit to raising funds and awareness for the Parkinson's Foundation, and in return you get access to a free entry (bib) to the race in addition to tons of other fun benefits and perks. Register to run now at PDChampionsCapeTown.org.

 

Fundraising Commitments:

  • Marathon - $2,250

*If you manage to purchase your own bib to the race and want to join the team as an Honorary Athlete, please email us at Run4PD@Parkinson.org

*Even though the 2025 race had to be canceled due to high winds, the 2026 Cape Town Marathon IS set to go as planned, and athletes WILL be eligible for an Abbott World Marathon Major Star for finishing the race once the event completes certification! There are some specific details about how this will all work on our Event Details page

 

As the newest Abbott World Major Marathon (set to be fully confirmed in 2026), and first ever on the continent of Africa, the Sanlam Cape Town Marathon is a global city race renowned for its beautiful, fast, and flat route that showcases Cape Town's ocean scenery, mountains, and cultural attractions. Experience the vibrant beauty of Cape Town and everything South Africa has to offer. 

If you have questions, send us an email at Run4PD@Parkinson.org. For more information about the race itself, visit the Cape Town Marathon Homepage.

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Expert Briefing: Parkinson's Medications 101

September 17, 2025

Medication plays a key role in managing Parkinson’s disease (PD), but it’s only one part of a comprehensive care plan. Participants will gain a deeper understanding of how medications work, their intended benefits, and common side effects. We will address the natural progression of Parkinson’s and the changes in medication regimens that may be necessary over time. By managing expectations, participants can build a more sustainable strategy for living well with PD.

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Danny Bega, MD, MSCI
Associate Professor of Neurology, Northwestern University Feinberg School of Medicine, A Parkinson's Foundation Center of Excellence
Director, Neurology Residency Program, Northwestern Medicine Parkinson's Disease & Movement Disorders Center
Medical Director, NM PDMDC
Director, Huntington's Disease Program, HDSA Center of Excellence

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Join us for a special Mindfulness Monday session designed with care for the Parkinson’s community. In this practice, Crista will guide you through gentle hand mudras, calming breath with sound, and a soothing guided imagery of an evening walk in nature. Together, we’ll explore simple ways to relax the body, steady the mind, and invite a sense of connection and peace.

This session requires no prior experience and can be done from a chair or any comfortable position. Come as you are—all you need is yourself, your breath, and a willingness to receive a moment of ease.

Whether this is your first mindfulness Monday, or you are a returning participant, these sessions are created with the intention of including everyone. There will be time for questions following the practice. 

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There is no charge to attend, but registration is required. This program is open to people with Parkinson's, their family, friends, and the community.

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There is no charge to attend, but registration is required. This program is open to people with Parkinson's, their family, friends and the community.

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Check-in begins at Noon with lunch and vendor visits. Program starts at 1 pm.

After many years of good symptom management, Parkinson’s disease may become more challenging. Learn how Parkinson’s symptoms may change over time and new strategies available for managing them.

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There is no charge to attend, but registration is required. This program is open to people with Parkinson's, their family, friends, and the community.

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En este webinar, diseñado para los aliados en el cuidado que enfrentan el agotamiento mientras apoyan a su ser querido, aprenderán a reconocer las señales de agotamiento del cuidador, comprender qué es y explorar herramientas y estrategias prácticas para manejar el estrés y mantener su bienestar mientras brindan cuidados.

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*Por favor, verifica su zonas horarias.*

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Gerente de programa, Programa de Educación para la Autogestión de Enfermedades Crónicas
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Panelistas

Margarita Monroy
Aliada en el cuidado

Martha Suárez Torres
Aliada en el cuidado
Terapeuta del lenguaje especialista en Parkinson 
Máster en enfermedades neurodegenerativas 
Certificada por la Parkinson’s Foundation en el Team Training Program For Parkinson´s y Team-Based Palliative Care Essentials for Parkinson´s 
Miembro de la Asociación Civil Parkinson Caracas y de la Sociedad de Trastornos del Movimiento.
Embajadora Líder de la Davis Phinney Foundation for Parkinson´s

¿En busca de algo más? Podrá encontrar todos nuestros videos de EP Salud en Casa en YouTube.


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Todos los eventos de “EP Salud en Casa" – Parkinson.org/EPSalud.

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Join the Parkinson’s Foundation to hear from keynote speaker Ray Dorsey, MD, co-author of “The Parkinson’s Plan.” The presentation will overview key points of the book including how prevention, better care, smarter policy and advocacy can change the future of Parkinson’s.

Come together with your community for the presentations, a resource fair, exercise demonstrations, “The Parkinson’s Plan” book signing (while supplies last), and more.

This event is free and open to people with Parkinson's and their families. Registration is required as in-person seating is limited.

Thank you to our event partner, the Greater Fresno Parkinson’s Support Group.

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Speakers:

Ray Dorsey, MD

Dr. Ray Dorsey is a neurologist, researcher, and public health advocate working to end Parkinson’s disease by addressing its root causes: toxic environmental exposures. He is the founding Director of the Center for the Brain & Environment at Atria Health and Research Institute and serves as Professor of Neurology at the University of Rochester. Dr. Dorsey has testified before Congress, advised the World Health Organization, and was recognized by the White House as a “Champion for Change.” He is the co-author of Ending Parkinson’s Disease (2020) and the New York Times bestseller, The Parkinson’s Plan: A New Path to Prevention and Treatment (2025).

 

 

 

Ray Dorsey, MD

Rafael Zuzuárregui, MD

Rafael Zuzuárregui is a neurologist who cares for patients with Parkinson's disease and other movement disorders. He specializes in using deep brain stimulation (electrodes implanted in the brain to regulate abnormal activity) and botulinum toxin therapy (injections that can relieve muscle contractions). He is also interested in diagnosing and treating rapid eye movement (REM) sleep behavior disorder (a condition in which patients physically act out vivid dreams).

Zuzuárregui's research focuses on the overlap between movement disorders, such as Parkinson's disease, and sleep disorders. He is particularly interested in how deep brain stimulation can help improve sleep in patients with these disorders. He also studies issues related to medical education.

At Boston University School of Medicine, Zuzuárregui earned his medical degree; completed a residency in neurology, serving as chief resident; and completed a fellowship in movement disorders. He then completed a fellowship in sleep disorders at Stanford University School of Medicine. He is a member of the American Academy of Neurology and International Parkinson and Movement Disorder Society.

Rafael Zuzuárregui, MD

Deborah Swerdlow

As Associate Vice President of Advocacy and State Policy for the Parkinson's Foundation, Deborah Swerdlow leads the Foundation's state policy work as well as efforts to engage people with Parkinson's, care partners, and other community members in support of both federal and state policies. Deborah comes to the Foundation with 15 years of experience in policy and advocacy, including her most recent government service as Chief of Staff at the U.S. Department of Agriculture's Food, Nutrition and Consumer Services mission area. She previously served as Deputy Director of the State Campaigns team at the Center on Budget and Policy Priorities, where she led national issue campaigns on tax policy, food assistance, pandemic relief and other anti-poverty priorities. Earlier in her career, she served as Grassroots Advocacy Coordinator for the American Association of University Women and as a program associate and legislative assistant at the Religious Action Center for Reform Judaism.

 

Deborah Swerdlow

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