LWPES: Turner Syndrome Patients Need More than Growth Hormone
By Ed Susman, Contributing Writer, MedPage Today
Published: May 03, 2010
Reviewed by Dori F. Zaleznik, MD; Associate Clinical Professor of Medicine, Harvard Medical School, Boston and
Dorothy Caputo, MA, RN, BC-ADM, CDE, Nurse Planner
| LWPES: Turner Syndrome Patients Need More than Growth Hormone |
VANCOUVER -- Researchers here aid that girls
diagnosed with Turner Syndrome not only have growth
deficiency, but also are prone to obesity, diabetes
and other cardiovascular risk factors.
"Often
doctors will see a patient with Turner Syndrome and
prescribe human growth hormone treatment and may
consider that is all that is needed for these
children," said Zeina M. Nabhan, MD, of the James
Whitcomb Riley Hospital for Children at the Indiana
University School of Medicine in Indianapolis.
However, children with Turner Syndrome have a number
of other potential health risks, including the
tendency toward weight gain and obesity, Nabhan said
during a poster presentation on TS treatment at a
session of the Lawson Wilkins Pediatric Endocrine
Society, included in the Pediatric Academic Societies
annual meeting.
"While changes in medical practice have occurred
since establishment of the international Turner
syndrome guidelines," she wrote in her abstract,
"screening for associated comorbidities was deficient
in > 50% of our patients with TS."
Nabhan explained that Turner Syndrome is caused by
the complete or partial absence of an X chromosome in
girls.
"Although short stature is the most prominent
characteristic of this disorder, affected girls have
a wide range of medical problems, including cardiac,
renal, ovarian and hearing problems," she said. As a
result, she said, Turner Syndrome patients require
life-long surveillance.
In reviewing the medical records of 128 girls
identified with Turner Syndrome, Nabhan said the
average age of diagnosis was about age 4.
About half were diagnosed at birth because of
dysmorphic features, while 48% were identified at
about age 9 due to short stature.
At diagnosis, 37% of the girls had cardiac
abnormalities, detected either through
echocardiography or magnetic resonance imaging, while
32.4% exhibited renal abnormalities and 38% had
hyperlipidemia, Nabhan reported.
The girls were initiated on human growth hormone at
an average age of 7.3 years and they achieved their
final adult height after about 5.7 years of therapy.
In the study, she noted that at the patients' last
visit, 48.7% of the girl had body mass index levels
in the overweight range and of those girls, 57.3% had
a body mass index in the obese range.
Nabhan said the prevalence of co-morbidities in her
study was similar to that reported elsewhere.
"Our findings emphasize the need for continual
education for all physicians involved in the care of
girls with Turner Syndrome. Special emphasis should
be placed on routine screening for hyperlipidemia,
liver disease and cardiac health, particularly in
older girls," she said.
"Prospective studies, aimed not only on detection,
but also at prevention of co-morbidities associated
with Turner syndrome, are needed."
Nabhan
had no relevant disclosures.
Primary
source:
Pediatric Academic Societies
Source reference:
Nabhan Z, et al, "Medical care of girls with Turner
Syndrome; Where are we lacking?" PAS 2010; Abstract
1455.47.
