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Rheumors Page
Rheumors Volume 8, Number 1: Summer 1997
ARA
GROWS IN PHYSICIAN AND LOCATION NUMBERS
In
January 1997, we enthusiastically opened a new office
at 2021 K Street NW, Suite 300, Washington, DC. Two Board
Certified Rheumatologists, David G. Borenstein, M.D. and
Vicki L. Star, M.D., previously members of the faculty
of the Division of Rheumatology at the George Washington
University School of Medicine, joined our practice and
began seeing patients in our new K Street office. This
brings the number of physicians in our group to seven
Board Certified Rheumatologists practicing in four locations.
Profiles of our new physicians appear elsewhere in this
issue of Rheumors.
Our new office is conveniently located in a modern, handicapped-accessible
building only two blocks from both the Farragut North
and the Farragut West Metro Stations. For those who prefer
to drive, there is ample parking available in a garage
located adjacent to our building.
For our patients' convenience, we offer x-ray, lab and
a select number of clinical research trials at our new
location. In addition, we have opened our third Osteoporosis
Assessment Center (OAC) to better serve our downtown patients.
OAC is housed within Suite 300 and contains a state-of-the-art
Lunar IQ DEXA machine. The same commitment to high quality
imaging, reporting and patient education that has become
synonymous with the other OAC locations remains our standard.
Please
be sure to inform your family and friends of our additional
location. We are striving to make visits to our physicians
as convenient as possible for those who live or travel
downtown.
WE'D
LIKE YOU TO MEET
Vicki L. Star, M.D. is a native of the Washington, DC
area who attended Walt Whitman High School. Her undergraduate
degree was earned at Boston University and her Doctor
of Medicine degree at Howard University in Washington,
DC. Internship and Residency programs were completed at
Sinai Hospital in Baltimore, MD and her fellowship training
in Rheumatology was served at the University of Maryland
Hospital in Baltimore. During her last year of training,
Dr. Star was awarded the "Senior Rheumatology Scholar
Award" by the American College of Rheumatology. This award
is presented to fellows in their last year in recognition
of superior achievements.
During
her fellowship training, Dr. Star was greatly involved
in both the treatment of patients with Osteoporosis and
clinical research relating to the disease. This ignited
an interest in the field which Dr. Star continues to pursue
today. Her interest is now enhanced by the introduction
of a third Osteoporosis Assessment Center (OAC) to the
Washington Metropolitan Area which is located in our new
office at 2021 K Street NW, Suite 300.
After completing her fellowship, Dr. Star returned to
the DC area where she became an Assistant Professor of
Medicine at The George Washington University Medical Center
in the Division of Rheumatology. She remained there for
3 ½ years before joining Arthritis and Rheumatism Associates,
P.C. (ARA) in private practice. Her attraction to the
world of academics was related to the unique opportunity
to combine clinic work with research and teaching.
Asked what excites her about private practice, Dr. Star
replied, "I like the aspect of dealing with patients with
long-term illnesses. I can really get to know my patients,
follow them closely and have the satisfaction of seeing
them improve and become more functional." Dr. Star is
currently conducting a clinical research trial in the
DC office involving a topical anti-inflammatory for osteoarthritis,
so she is able to continue her interest in research as
well.
The
youngest of three daughters, Dr. Star became interested
in the sub-specialty of Rheumatology because she, herself,
suffers from Juvenile Chronic Arthritis. As a young woman,
she participated in a research study involving Physical
Therapy which piqued her interest in research and patient
education.
Dr. Star is involved with many local organizations including
the Lupus Foundation, the Arthritis Foundation, the Medical
Society of DC, the Washington Bone Club (where she is
Secretary), and the Rheumatism Society of DC (where she
will be President). Dr. Star continues to teach at the
G.W.U. pm a part-time basis and lectures frequently. She
has also had articles published in Gout and Rheumatoid
Arthritis.
For enjoyment, Dr. Star cheers on the Redskins - she is
a BIG fan, does volunteer work for The United Jewish Appeal,
sews, fiddles with photography and computers and spends
time with her young nieces and nephews. She looks forward
to building a stimulating and successful career with ARA
beginning with helping to develop our new NW Washington
DC office.
LET
US INTRODUCE US TO
David
G. Borenstein, M.D. grew up in Miami Beach, Florida and
his family still lives in the Ft. Lauderdale area. He
traveled north to get his education beginning with undergraduate
studies at Columbia University in New York followed by
medical school, internship, residency and fellowship training
at the Johns Hopkins University School of Medicine and
the Johns Hopkins Hospital in Baltimore, Maryland.
Dr. Borenstein's interest in medicine was sparked by his
brother who is eight years his senior and is a neurologist.
His interest in rheumatology was inspired by two physicians
at Johns Hopkins University who became his mentors and
whom he decided to emulate. Dr. Borenstein came to Washington,
DC after his fellowship was completed and took a position
as part of the medical faculty, rising to the rank of
Professor of Medicine, at The George Washington University
Medical Center. He remained there for 18 years. What turned
him on about academic medicine? "The combination of teaching,
seeing patients and research. I trained at least 20 individuals
who became Rheumatologists and now practice in areas all
across the country." Now that Dr. Borenstein is in private
practice, will he miss teaching on a full-time basis?
"Teaching is in my blood," says Dr. Borenstein. "Doctors
are teachers. Now I will teach the public."
After Dr. Borenstein left Johns Hopkins, he expected Lupus
to be his area of specialization. But, in DC, he came
to find out that low back pain was a prevalent disorder.
He became very interested in the subject, and with much
encouragement from the Orthopedic Surgeons at G.W., he
began evaluating their patients. When he had enough experience
and felt he had enough important information to share
with others, he began to write about the topic. The result
is a book, now in its second edition, entitled Low
Back Pain Medical Diagnosis and Comprehensive Management.
This book is on the Selected List of Books and Journals
for the Small Medical Library. This list consists
of books that experts Brandon and Hill feel every medical
library should contain. There are only 14 books on Orthopedics
on their list and Dr. Borenstein's is one of them.
Dr.
Borenstein published a new book in 1996 entitled Neck
Pain Medical Diagnosis and Comprehensive Management
and in 1997; he authored the section on Connective
Tissue Disease for Conn's Current Therapy.
Among Dr. Borenstein's distinguished achievements is his
membership in the International Society for the Lumbar
Spine. Society membership is limited to 250 active members
throughout the world. One has to be elected to the Society
and currently Dr. Borenstein is one only six Rheumatologists
in the world to belong. Dr. Borenstein will travel to
Singapore in June to present a paper to the Society.
Dr. Borenstein lectures regularly around the country both
for the American College of Rheumatology and pharmaceutical
companies.
In his spare time, Dr. Borenstein plays squash, skis,
and listens to music. He is married to an attorney who
practices Family Law and has three daughters ages 19,
16 and 14. He is now comfortably steeled into private
practice with ARA where he sees patients daily at our
new NW Washington, DC office.
QUESTION
& ANSWERS
| Q. |
Does
an "arthritis cure" really exist? |
| A. |
RMillions
of patients with arthritis of all types have been
looking for a cure. Those who are more realistic
are looking forays to supplement their response
to more traditional medications. Recently, Dr. Jason
Theodosakis published his remedy for arthritis in
"The Arthritis Cure." Despite the injudicious title,
Dr. Theodosakis makes no wild claims for a cure.
He does promote the use of glucosamine (GA) and
chondroitin sulfate (CS) in combination with an
eight-point program to treat osteoarthritis (OA).
He does not claim that a cure for OA, or the over
100 other types of arthritis, exists. Rather, some
patients may get some benefit using the recommended
regimen.
GA
and CS are both synthesized by the body and are
important constituents of the cartilage that caps
the end of our bones at the joint. GA, taken orally,
does find its way to cartilage. European studies
done in the early 1980's suggested that GA could
slow cartilage breakdown. Subsequent studies of
the GA-CS combination suggest that OA symptoms may
be reduced and cartilage production may be stimulated.
GA-CS
is classified by the FDA as a food supplement, not
a drug. Therefore, it is available over the counter
(OTC) without a prescription. As a food supplement,
it is not regulated by the FDA for purity, safety,
or efficacy. Many people are surprised to hear that
OTC "food supplements," including vitamin and mineral
supplements, are not subject to regulation and therefore
are not standard preparations. Many of the GA-CS
preparations contain little of the active compounds
and are of dubious value. Thus far, safety of these
preparations does not seem to be an issue.
Patients
contemplating use of the GA-CS combination should
know that this is not a cure for osteoarthritis
or any other form of arthritis. Small studies have
suggested modest benefit and only larger controlled
studies will eventually determine if GA-CS offers
real help in treating OA. Even Dr. Theodosakis'
program includes the American College of Rheumatology
recommendations for weight reduction, muscle strengthening,
and proper diet. Many patients will improve with
these achievements alone. While we don't have a
cure for arthritis, the prospect for better management
is always improving.
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| Q. |
Can
antibiotics be used to treat arthritis? |
| A. |
Infectious
arthritis is caused by the direct invasion of the
joint by a bacteria or virus. Sometimes the body's
response to an infection elsewhere may result in
an immune response that causes inflammation with-in
the joint. Either way, infection can cause joint
swelling, pain, and even joint damage. Lyme disease,
post streptococcal arthritis, gonococcal arthritis,
and the arthritis of measles are all examples of
arthritis resulting from infection.
Antibiotics
are essential in treating and curing arthritis caused
by bacterial infection. However, the causes of most
types of arthritis, including the most common types
such as rheumatoid arthritis and osteoarthritis,
are unknown. Bacteria and other infections have
been postulated to play a role in the cause of many
types of arthritis, but their role has been unsubstantiated.
Despite this, antibiotics have been proposed as
treatment for many types of arthritis.
Recent
studies have evaluated the role of antibiotics in
both rheumatoid arthritis and osteoarthritis. Although
there is no evidence that either of these types
of arthritis is caused by infections, the studies
do suggest that the tetracycline class of antibiotics
may offer some benefit. In these cases the antibiotics,
minocycline and doxycycline help retard the activity
of the metalloproteinase and collagenase enzIn these
situations, the tetracyclines are not acting as
antibiotics, have relatively modest antiarthritis
activity, and must be continued long-term for continued
benefit. Only about 30% of patients will respond
and most will need to continue on standard arthritis
therapy. The tetracycline and antibiotic story is
interesting enough to warrant more research. The
NIH has on-going trials looking at the role of antibiotics
in arthritis treatment.ymes that lead to joint damage.
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| Q. |
How
are the dry eyes and dry mouth of Sjogren's Syndrome
treated? |
| A. |
Sjogren's
Syndrome (SS) is an autoimmune condition characterized
by dry eyes, dry mouth and often arthritis. The
dry eyes are best treated with eye drops that add
moisture to the eyes. Eye drops are available as
thin watery drops that moisten well, but need to
be applied frequently. More viscous eye drops last
longer, but may blur vision in some patients. These
are best used at night. Tears may last longer if
the tear drainage is blocked temporarily or permanently
with punctual occlusion performed by an ophthalmologist.
Goggles and humidification may also help keep eyes
moist.
Salivary
substitutes, frequent sips of water, and salivary
lubricants all help keep the mouth moist. Products
such as Glandosane and Salix SST can stimulate the
production of normal saliva provided there is some
residual salivary function. To prevent the complications
of dry mouth good dental care is necessary. Frequent
use of fluorinated toothpaste and mouthwash, as
well as regular dental care, including fluoride
applications, are necessary to prevent tooth decay.
Sugarless mints and candies may help stimulates
salivary flow. Sugar containing candies are to be
avoided, as they will promote rapid tooth decay.
Oral
pilocarpine (Salagen) is now available and often
will help stimulate saliva and tear production.
Patients
suffering from Sjogren's with dry eyes may be eligible
to participate in a clinical trial of anew agent
to treat dry eyes and mouth. Please ask your physician,
or contact our Clinical Research Department, for
details.
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POINTS
ON JOINTS
PREVENTION OF OSTEOPOROSIS:
AN OUNCE OF PREVENTION IS WORTH A POUND OF CURE
Vicki L. Star, M.D.
Normal bone is strong and resistant to fracture. Osteoporosis
is a disease that weakens bones, causing them to become
brittle and more likely to break. This is the result of
a loss of calcium, which in its most severe form can make
bones more susceptible to fracture with even minor trauma.
Osteoporosis
is a major health problem in the United States. It is
one of the most common bone diseases in developed countries.
Osteoporosis affects an estimated 20 million people in
the United States which results in 1.5 million fractures
per year with 250,000 of these being hip fractures. By
the year 2040, it is estimated that the number of hip
fractures will more than double and will cost over $240
billion in health care dollars.
Bone
growth and loss is a continuous cycle that occurs throughout
one's life. The strength of the bones is referred to as
the bone "density" or the bone "mass." Bone density is
built up until the end of adolescence, a time when bone
gain is greater than bone loss. After adolescence, bone
gain equals bone loss until the time of menopause. The
balance of bone growth and loss is changed at the time
of menopause primarily because of a decline in estrogen
levels, a hormone which helps to preserve bone mass. Women
may lose as much as 25% of their bone mass around the
time of menopause.
While
there are several causes of osteoporosis, the most common
is menopause in women. Menopause may either occur naturally
as part of the aging process, or at the time when the
ovaries are surgically removed. Other causes of osteoporosis
in men and women include corticosteroid (prednisone) therapy,
thyroid supplementation (if given at too high of a dose),
rheumatoid arthritis, systemic lupus erythematosus, parathyroid
abnormalities, and vitamin D deficiency, among multiple
others.
Bone
loss occurs without any symptoms until a fracture occurs.
Patients or their physicians may notice a decline in height
or the onset of curving of the upper spine, sometimes
called a dowager's hump. However, the patient is generally
unaware that their bones are weakening. Once enough bone
is lost, a minor fall, cough or sneeze may result in a
fracture.
There
are two main goals in the prevention of osteoporosis:
1] to attain maximum bone quantity during adolescence
and 2] to maintain bone during adulthood and prevent bone
loss at menopause.
There
are several ways to attain maximum bone mass during childhood.
Genetics plays an important part in the bone mass achieved,
along with several other factors. Adequate nutrition,
activity and weight are all crucial to reaching the goal
of maximum bone. Calcium during childhood is essential
for the development of bones. Children should consume
between 800-1200 mg. of calcium per day (see table 1)
while participating in regular exercise. Calcium may be
taken in the form of food products or supplements.
Recommendations
to prevent bone loss in the adult are similar to those
in the child and adolescent, with the addition of estrogens
after menopause if the patient is able. Calcium supplementation
still remains important in maintaining adult bone, however,
the requirements may differ (see table 1). In addition,
regular weight bearing activities, such as walking or
low impact aerobics may increase bone strength. Cigarette
smoking and excessive alcohol intake should be avoided.
Unfortunately, the above measures, if used alone, are
often inadequate to stop the rapid bone loss experienced
at the time of menopause. Estrogens are effective in controlling
the rapid bone loss that occurs around this time. For
patients who are not able to take estrogens, Alendronate
(Fosamax) has recently been approved by the Food and Drug
Administration for the prevention of osteoporosis.
Finally,
an ounce of prevention is worth a pound of cure. Preventing
osteoporosis by using the guidelines mentioned is the
most effective way to diminish bone loss and to decrease
the risk of fracturing a bone. It is much easier to prevent
bone loss before it occurs, than to treat osteoporosis
after a significant amount of bone has already been lost.
Preventive measures should begin in childhood and should
be maintained throughout one's life.

R
H E U M I N A T I O N S
CLINICAL TRIALS 1996-1997
Herbert S. B. Baraf, M.D., FACP,
The Center for Rheumatology and Bone Research is the new
name for our clinical research unit. Research studies
have been conducted in this practice for the past 15 years,
allowing our physicians to be at the vanguard of therapeutics
in Rheumatology and giving our patients unique access
to new treatments that would otherwise be unavailable.
This
spring the Center has been busier than ever. A number
of new medicines are actively under study by our physicians
and our Clinical Research Coordinators, June Carter, Maureen
Montgomery, Jennifer Rocca, and Debbie Schley. Some of
the Center's research involves treatments with newly developed
medicines for Osteoporosis, Rheumatoid Arthritis, Osteoarthritis
and Sjogren's Syndrome that have not yet received FDA
approval and are only available to patients through research
protocols. We have participated in many nationwide trials
that, over the years, have led to the release of a number
of new arthritis medications. We have assisted such companies
as Pfizer, Eli Lilly, Proctor & Gamble, Searle, Merck,
Immunex, Schering Plough, Upjohn and Wyeth-Ayerst.
For patients interested in participating in clinical research
we have a number of new protocols:
RHEUMATOID
ARTHRITIS (RA): We are currently recruiting patients
with early RA for participation in a study that compares
a new biologic agent to methotrexate. This agent inhibits
communication between the white blood cells which promote
inflammation in rheumatoid arthritis. Exciting reports
about this agent first made it into the national media
last fall when extraordinary results were reported at
the meetings of the American College of Rheumatology.
In
a second clinical trial, we are enrolling patients with
RA for less than six years who have had an incomplete
response to methotrexate therapy. These patients may be
eligible to enroll in a program comparing Methotrexate
alone to Methotrexate in a combination with a second immuno-suppressive
agent.
Finally,
we have been asked to participate in a trial of a genetically
engineered copy of a substance produced naturally by white
blood cells in humans, which can help turn off the chronic
inflammation seen in Rheumatoid Arthritis. To be eligible,
a patient must have Rheumatoid Arthritis and have failed
to respond to one or more disease modifying drugs.
OSTEOARTHRITIS
OF THE KNEE OR HIP: We are looking for patients currently
on stable treatment with anti-inflammatory agent (NSAIDS).
We have three different programs that are actively enrolling.
These protocols are designed to evaluate new NSAID drugs
that are anticipated to be free of gastro-intestinal side
effects (COX-2 NSAIDS)
SJOGREN'S
SYNDROME: Patients with dry eyes and dry mouth caused
by this condition may be eligible to participate in one
of two clinical trials evaluating a drug that is expected
to enhance salivation and tearing. In all of these programs
diagnostic testing, medication and physical visits are
free of charge. We would be delighted to review the specifics
of these program with you. Please feel free to discuss
your interest with your physician during your next visit
to the office.
PRACTICE
NOTES
- Dr.
David G. Borenstein will present a paper entitled "Mexiletine
Therapy for Persistent Neuropathic Radicular Pain; An
Open Trial of 11 Patients" to the International Society
for the Lumbar Spine when they meet in Singapore in
June.
-
Dr. Norman S. Koval and Dr. Herbert S.B. Baraf have
been appointed Clinical Associate Professors of Medicine,
Department of Rheumatology, at the University of Maryland
School of Medicine.
- Dr.
Robert L. Rosenberg is the immediate past president
of the Rheumatism Society of D.C.
- Dr.
Vicki L. Star is the incoming president of the Rheumatism
Society of D.C.
- Dr.
Evan L. Siegel is featured in a discussion of Arthritis
as part of the variety show "Tacoma Coffeehouse," seen
on The Montgomery County Channel (49/22) and the Tacoma
Park Channel (54/14) on Cable TV.
- Dr.
Herbert S.B. Baraf and Dr. Emma DiIorio were interviewed
for local news channels 8 and 9 regarding exciting new
arthritis medications currently being evaluated as part
of our drug study program
A quarterly
publication brought to you by Arthritis & Rheumatism Associates
Norman S. Koval, M.D. Herbert S. B. Baraf, M.D. Robert L.
Rosenberg, M.D. Evan L. Siegel, M.D. Margaret Dieckhoner,
Editor © 1990 Arthritis & Rheumatism Associates
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