Determining a Diagnosis

An accurate diagnosis made after ruling out other possible explanations is essential for the successful treatment or management of any disease. As new medical treatments become available, early intervention will be more and more important. Regardless of medical treatments, the sooner patients and caregivers have an accurate diagnosis, the sooner they can plan for upcoming care. The steps listed below are the common steps a person will go through when being evaluated for memory loss, behavioral disorders, and other related problems.

Neurological Exam & History

Because memory loss, behavioral disorders, and other related problems are often complex, a comprehensive evaluation is necessary. At the UCSF Memory and Aging Center, patients undergo extensive neurological, neuropsychological, and nursing assessments that usually require several hours. Information from the caregiver is sought in every case. The evaluation may require two to three visits to determine the cause of the symptoms and recommend treatment.

After the evaluation, the medical team involved with each patient meets to discuss the diagnosis and potential treatments. After this meeting, the team discusses its findings with the patient and the family. In some cases, a diagnosis will be deferred until more information from blood tests or brain imaging is collected.

Neuropsychological Testing

Neuropsychological testing adds to the clinical assessment of a person. These tests evaluate behavior, language, visuospatial abilities, memory, abstraction, planning and mental control, motor skills, and intelligence. The patterns of strengths and weaknesses in a person help identify which areas of the brain are functioning well and which ones are doing poorly.

  • Tests of a person with frontotemporal dementia (FTD) may show visual and memory abilities intact. However, abstract thinking, word generation, motivation, and the ability to follow rules may be disrupted.

Laboratory Tests

Certain blood tests can help evaluate for treatable conditions that may be contributing to changes in thinking or memory. Some of the most common blood tests ordered as part of a diagnostic evaluation for someone with changes in thinking or memory include: CBC (complete blood count), CMP (comprehensive metabolic panel), TSH (thyroid stimulating hormone), vitamin B12, RPR (rapid plasma reagin), HIV (human immunodeficiency virus).

Neuroimaging

Structural Scans

One of the most useful tests in the evaluation of dementia is magnetic resonance imaging (MRI). MRI uses magnetic fields and radio waves, without any X-rays, to produce images of the inside of your body. It is non-invasive and considered very safe, but some people with metal implants and cardiac pacemakers are unable to have MRIs. Talk to your doctor or the imaging technician if you have any concerns about entering the magnet. Some people find lying in the scanner produces anxiety or claustrophobia because of the tube-like shape or the loud sounds during the scan. Sedation may be available to you if needed, but relaxation techniques like deep breathing, visualization, and meditation can also help. Some MRI scanners allow you to listen to music or watch a movie. To get the best pictures, you need to be as still as possible while in the scanner.

A computed tomography (CT) scan is similar to the MRI but does not image brain structure with the fine precision of MR. A CT scan is an X-ray technique that produces cross-sectional images of the inside of your body or head. Typically, scans last only a few minutes, during which time you should lie still. You may hear some whirring and clicking noises during this test, which is normal. In order to make the CT image, you will be briefly exposed to X-ray radiation, so be sure to discuss any concerns you have with your doctor.

Functional Scans

A SPECT scan shows how blood flows through arteries in the brain. A radioactive material (tracer) is injected into a vein in the arm, and then the scanner detects the movement of the tracer through the brain and computes the brain activity. Brain areas affected by the disease typically show diminished activity. As with any neuroimaging procedure, you will need to lie as still as possible so that the machine can obtain accurate pictures. After the scan, be sure to drink plenty of fluids. Most of the radioactive tracer leaves your body through your urine within a few hours after your SPECT scan. Talk to your doctor if you're concerned about your exposure to radiation during a SPECT scan.

Functional MRI (fMRI) is a special type of scan done in an MRI scanner. It shows changes in blood flow in the brain, which represent areas of the brain using more or less blood to perform certain tasks. The experience and equipment are similar to those of a structural MRI scan.

PET scans show the activity of tissues by measuring the energy usage (metabolic activity) of your brain. Like a SPECT scan, PET combines a brain camera and a radioactive material (tracer). The tracer is what allows doctors to see how your body tissues absorb and use different chemicals in real-time. 30–45 minutes prior to the scan, a tracer is injected into your bloodstream. Once the tracer has had time to reach your brain, you'll lie on a table that moves slowly through the scanner. By detecting metabolic changes in the brain, your doctor can see which areas are healthy versus dysfunctional. Be sure to remain as still as possible so that the machine can get accurate pictures. Depending on the information your doctor needs, you may be asked to perform certain tasks, like reading or speaking, to activate specific areas of your brain. Once the scan is complete, be sure to drink plenty of fluids to flush out any tracer left in your body. Amyloid imaging with PET can tell whether the patient has a buildup of amyloid protein, a sign of Alzheimer’s disease. New tracers to show the buildup of tau protein are under development, but are not yet available.

Cerebrospinal Fluid (CSF) Exam

A doctor collects cerebrospinal fluid (CSF – the watery liquid that surrounds your brain and spinal cord) by doing a lumbar puncture (spinal tap) in which a very thin needle is gently inserted into your lower back between two vertebrae, the bony structures that make up your spine. The procedure is usually done in a doctor’s office and takes about 30–45 minutes, during which time it is important to remain still. Afterward, drink plenty of fluids to help prevent ‟lumbar puncture headache.” If you have a headache or develop a fever after a lumbar puncture, let your doctor know immediately, as there are things that can be done to make the headache go away.

Once the CSF has been collected, many different tests may be ordered to either rule out or investigate the possibility of various conditions. For instance, an elevated white blood cell count in the CSF may suggest a possible infection or inflammatory condition. Other CSF protein tests include neuron-specific enolase (NSE) and total tau protein (T-tau). So far, the data suggest that MRI and PET are better at identifying disease biomarkers, but CSF tests may indicate a rapid injury to nerve cells in the brain.

  • In all cases of rapidly progressive dementia, a CSF examination should be performed. In people with Creutzfeldt-Jakob disease (CJD), the results of the CSF test are usually normal, with the exception of a slightly increased total protein count. If there is an increased white blood cell count, your doctor should consider other neurological diseases, particularly infections such as encephalitis.
  • Although we cannot yet detect prions in the CSF of patients with CJD, detection of elevated levels of the 14-3-3 protein in the CSF has been reported to support a CJD diagnosis in the scientific literature. The UCSF doctors do not feel this test is a very good diagnostic test for CJD because many people with confirmed CJD have a negative or normal result, and many others who do not have CJD but have another neurological disease have a positive result. Only half of the patients diagnosed with CJD at UCSF have an elevated 14-3-3 protein. Furthermore, in about ⅓ of patients referred to UCSF with an elevated 14-3-3 protein, UCSF doctors identify another diagnosis, not CJD! In many cases, these other diagnoses are very treatable.

Lumbar punctures are also vital to our research efforts at the Memory and Aging Center. CSF collected through lumbar punctures is a primary source to measure markers from the brain in living humans. We now have reliable CSF markers for early detection of Alzheimer’s disease in the clinic and many more markers in exploratory stages to help us better understand how the brain ages and how neurodegenerative disease unfolds in humans. If you are interested in participating in a lumbar puncture as part of a research study, please read the FAQ below or click here.

Lumbar Puncture FAQ

What is a lumbar puncture (LP)?

Lumbar puncture is a procedure used in clinical and research settings in which a small amount of fluid is removed by inserting a needle in the lower back, far below where the spinal cord ends. This fluid, cerebrospinal fluid (CSF), bathes the brain and spinal cord.

Why is a lumbar puncture so important?

Lumbar punctures are essential to our research! The cerebrospinal fluid (CSF) we collect is a rich source of proteins and other molecules found in and around the brain. CSF directly reflects the status of the brain and central nervous system.

The brain is protected from the rest of the body by a barrier called the “blood-brain barrier.” Due to this barrier, we cannot capture molecules that are found in CSF directly from the blood. CSF contains some of the earliest markers of abnormal brain changes.

Research from our team and many others have found that changes in CSF predict future risk for cognitive decline and dementia. What we learn has been and continues to be used to develop diagnostic tools and preventative treatments for Alzheimer’s and other neurodegenerative diseases. We need more participants like you to advance these efforts!

What have we learned from lumbar punctures and CSF?

Line chart showing the relationship between amyloid, tau and neurodegeneration
Graph illustrating that only adults with low synaptic functioning showed a relationship between amyloid, tau and neurodegeneration.

Thanks to many of your LPs and generous CSF donations, there have been rapid advances in CSF biological markers. We now have reliable markers for early detection of Alzheimer’s disease processes for use in the clinic. These markers are leading to more precise clinical trials. We have many more markers in exploratory stages that are teaching us invaluable information about how the brain ages and how other neurodegenerative diseases unfold in humans. One recent finding from your group CSF data suggested that synaptic integrity (the presence of communication junctions between brain cells) may play a critical role in how the amyloid plaques and tau tangles of Alzheimer’s disease develop.

In a recent study of healthy adults in the Hillblom Aging cohort, we measured CSF levels for two major proteins in Alzheimer’s disease: amyloid “plaques” and tau “tangles.” In Alzheimer’s disease, amyloid is thought to lead to tau, which causes neurodegeneration (breakdown of brain cells). We also measured markers of synapse functioning in CSF. Synapses are the communication junctions between brain cells that transmit signals from one cell to another, and they allow the brain to function. We found that only adults with low synapse markers showed a relationship between amyloid, tau, and neurodegeneration.

Adults with high synapse markers did not show the adverse relationship between amyloid and tau. These data suggest that maintenance of synaptic functioning may play an important role in how Alzheimer’s disease markers develop. This study is leading to future projects on how to target synaptic functioning in order to prevent dementia.

Can my lumbar puncture results be shared with me?

At this time, we are still learning more about what CSF biomarkers can predict at a group level. We don’t have enough information to discuss most of the lumbar puncture results on the individual level. With these collective CSF samples, we are trying to tackle neurodegeneration at the earliest stage of change, instead of waiting for symptoms to emerge.

Who performs the lumbar puncture?

Lumbar punctures are performed by board-certified neurologists, who are highly experienced in carrying out this procedure. Many patients at the Memory and Aging Center have received an LP for diagnostic reasons or as part of research visits. Our neurologists are exceptionally trained to guide you throughout the procedure and answer any questions you may have.

What happens during a lumbar puncture?

lumbar puncture procedure
Lumbar puncture procedure. Illustration by Cancer Research UK - Wikimedia Commons

Before scheduling a lumbar puncture, we make sure it is a good fit for you. We first take a few extra samples of blood during one of your research blood draws with our center. This process checks for criteria such as clotting factors and platelet counts, and your results are cleared for safety by our neurologists.

During the procedure, you will be accompanied by one of our research coordinators, who is there to support you and provide additional assistance to the neurologist. During the lumbar puncture, you can either lie down on your side or sit upright. The neurologist will feel and massage your back to identify the correct place to insert the needle. This area is between two bones of the lower back (vertebrae L4 and L5), far below the spinal cord. Spinal cord nerves will not be disturbed or at risk of damage during the procedure.

Before inserting the needle, the neurologist will carefully sanitize your back and inject a local anesthetic (Lidocaine). This might feel like a numbing shot at the dentist, but the sensation is less noticeable since the lower back has fewer nerve endings. After the anesthetic kicks in, the neurologist will insert the collection needle. About 2 tablespoons of CSF will be allowed to naturally drip out. You may feel mild contact pressure at the insertion site, but you should not feel any sharp pain.

The procedure takes about 30 minutes. Once the lumbar puncture is complete, you will rest for about 1 hour. We will provide you with a snack and keep you company. Afterward, you should be able to drive home and go about your normal activities, though we advise avoiding strenuous physical activity for the next 24–48 hours.

What happens if I change my mind?

Your participation in research is always voluntary. You can change your mind about an LP any time leading up to the procedure!

What are the risks associated with a lumbar puncture?

The risk of infection from a lumbar puncture is very low, even less than from a standard blood draw. The LP is done in an extremely sterile state with a sterilized kit, sterilized gloves and an antiseptic solution.

The most common side effect after the procedure is a minor headache within the first 24 hours. These headaches are usually position-dependent, so they tend to occur when you are sitting or standing upright. They typically don’t persist for more than a few days and go away when you are lying flat. To reduce your chance of getting headaches after a lumbar puncture, we use a very thin, specialized type of needle. Staying well-hydrated, laying down, drinking caffeinated beverages and taking over-the-counter pain medication are easy ways to relieve any headaches. If the headache persists or worsens, another option we offer is administering a “blood patch,” which works to clot and heal the lumbar puncture site faster.

Common lumbar puncture side effects include:

During Procedure:

  • Headache (17.1%)
  • Nerve pressure/tingling (14.2%)
  • Pain (8.6%) Nausea/dizziness (7.0%)

Post-Procedure:

  • Headache (5.5% total; mild 3.7%; moderate 1.4%; severe 0.4%)
  • Low back pain (8.5% total; mild 6.7%; moderate 1.8%; severe 0%)

Source: Wisconsin ADRC Lumbar Puncture participants (2021)

Will I be compensated for participating in a lumbar puncture?

We do realize this procedure is more invasive than some of our other procedures and can take a lot of consideration before participating. If you are enthusiastic and willing to complete a lumbar puncture with us, we will compensate participants with $100 for donating this time and CSF to our research.

EEG

An electroencephalogram (EEG) shows patterns of electrical activity produced by your brain as recorded by electrodes placed on your scalp. It is non-invasive and minimally uncomfortable (the electrodes may scratch or itch you and are held in place with a sticky paste). The electrodes do not generate any electricity; they only record electrical activity produced by your brain. You will need to be still with your eyes closed during the 20–40-minute recording in order to get a quality EEG.

  • In people with frontotemporal dementia (FTD), the EEG is usually normal or shows mild frontal slowing. Thus, a normal EEG does not mean that the behavioral manifestations are primarily the result of a psychiatric illness.

Other Issues to Rule Out Before Diagnosing a Neurodegenerative Disease

  • Reactions to medications. Some medications have side effects that mimic the symptoms of dementia. Even a single dose of a medicine may trigger such a reaction in an older person or in someone whose liver fails to eliminate the drug normally. Interactions among two or more drugs may lead to reversible symptoms of dementia as well.
  • Metabolic abnormalities. Decreased thyroid function (hypothyroidism) can result in apathy or depression that mimics dementia. Hypoglycemia, a condition in which there isn’t enough sugar in the bloodstream, can cause confusion or personality changes. Pernicious anemia caused by an inability to absorb vitamin B-12 also can cause cognitive changes. Similarly, changes in blood sodium, calcium, heavy metals or other compounds can cause a reversible dementia.
  • Nutritional deficiencies. Chronic alcoholism can be associated with deficiencies of thiamin (vitamin B-1), which can seriously impair mental abilities. Severe deficiency of niacin (vitamin B-3) may cause pellagra, a neurological illness with features of dementia. Dehydration also can cause confusion that may resemble dementia.
  • Emotional or psychiatric problems. The confusion, apathy and forgetfulness associated with depression are sometimes mistaken for dementia, particularly in older individuals. Depression is not common in people with frontotemporal dementia (FTD), but apathy and emotional withdrawal are and this can lead to the misdiagnosis of depression. Even though people with FTD may appear to be depressed, when you ask them about their mood, they often offer that they feel happy. Similarly, bipolar disorder, schizophrenia and obsessive-compulsive disorder can be misdiagnosed as FTD.
  • Infections. Meningitis and encephalitis, which are infections of the brain or the membrane that covers it, can cause confusion, memory loss or sudden dementia. Untreated syphilis can damage the brain and cause dementia.
  • Normal-pressure hydrocephalus. If cerebrospinal fluid builds up in the ventricles of the brain, the brain tissue is compressed even though the fluid pressure remains normal. This may cause dementia. If this condition is identified in time, it may be treated by draining the excess fluid via a tube (shunt).