The Growing Child: 3-Year-Olds

Lead Poisoning in Children – Johns Hopkins Employer Health Programs (EHP)

The Growing Child: 3-Year-Olds | Johns Hopkins Medicine

Here are facts that can help you keep your children safe:

  • Lead poisoning is a totally preventable disease.
  • Lead exposure can harm young children and babies—even before they are born.
  • Even children who seem healthy can have high levels of lead in their bodies.
  • Children can get lead in their bodies by breathing or swallowing lead dust, or by eating soil or paint chips with lead in them.
  • Removing lead-based paint improperly can increase the danger to your family.
  • CDC estimates reveal that about half a million children between the ages of 1 and 5 living in the U.S. have an elevated level of lead in their blood.

Lead is more dangerous to children than adults because:

  • They often put their hands and other objects in their mouths that can have lead dust on them.
  • Their growing bodies absorb more lead.
  • Their brains and nervous systems are more sensitive to the damaging effects of lead.

Children between the ages of 1 and 3 who live in low-income housing built before 1978 are especially at risk. In early 2005, the Consumer Product Safety Commission announced a new policy addressing lead in children’s metal jewelry.

There have been cases where children who swallowed or repeatedly sucked on jewelry items containing lead developed high blood lead levels.

Since 2004, the Commission has recalled over 150 million pieces of toy jewelry that were sold in vending machines and through other outlets.

Effects of lead in the body

Lead poisoning can affect just about every system in the body yet often produces no definitive symptoms. The following are some of the most common symptoms of lead poisoning. However, each child may experience symptoms differently. Lead poisoning may cause:

  • Damage to the brain and nervous system
  • Behavior and learning problems, or slowed growth
  • Hearing problems
  • Headaches
  • Anemia

Lead is also harmful to adults, and may cause:

  • Difficulties during pregnancy
  • Reproductive problems in both men and women
  • Anemia
  • Kidney damage
  • High blood pressure
  • Digestive problems
  • Nerve disorders
  • Memory and concentration problems
  • Muscle and joint pain

High levels of lead may also cause seizures, coma, and death. The symptoms of lead poisoning may resemble other conditions or medical problems. Always talk with your child’s healthcare provider for a diagnosis.

Testing children for lead exposure

If you think your home has high levels of lead, get your children tested. A simple blood test can find high levels of lead, and is important for:

  • Children who are 6 months to 1 year old (6 months if you live in an older home that might have lead in the paint). If your child is older than 1 year, talk to your child’s healthcare provider about whether he or she needs testing.
  • Family members whom you think might have high levels of lead.

Your child’s healthcare provider can test your child’s blood levels. The tests are inexpensive or, in some cases, free. Your child’s healthcare provider will explain the test results. Treatment can range from changes in your diet to medicines or a hospital stay.

Take a quiz and test your knowledge about lead safety.

Source: https://www.ehp.org/plan-benefits/health-programs-and-resources/health-library/lead-poisoning-children/

Experimental drug can encourage bone growth in children with dwarfism

The Growing Child: 3-Year-Olds | Johns Hopkins Medicine

Researchers at Johns Hopkins Medicine, the Murdoch Children's Research Institute in Australia and seven other medical institutions report that an experimental drug called vosoritide, which interferes with certain proteins that block bone growth, allowed the average annual growth rate to increase in a study of 35 children and teenagers with achondroplasia, a form of dwarfism. The patients' average boost in height to about 6 centimeters (2.4 inches) per year is close to growth rates among children of average stature, and the side effects of the drug were mostly mild, according to the researchers.

Results of the four-year study are summarized online June 18 in the New England Journal of Medicine.

“An increase in the annual growth rate alone may have a positive effect on some patients' quality of life. For other patients, now and in the future, our hope is that the altered bone growth throughout the body could ease such problems as sleep apnea, neurological and leg and back problems, and improve their quality of life,” says Julie Hoover-Fong, M.D.

, Ph.D., associate professor and director of the Greenberg Center for Skeletal Dysplasias at the Johns Hopkins McKusick-Nathans Institute of Genetic Medicine. “Right now, the results of the study show an impact on growth, and this effect is sustained, at least over nearly four years in this trial. The potential long-term benefit will take more time to observe.

Achondroplasia, although rare, is the most common form of dwarfism worldwide, affecting an estimated 1 in 15,000-40,000 live births. The condition is caused by mutations in a gene called FGFR3 that result in the excess production of proteins that slow bone growth. The disorder is marked by disproportionate short stature with shortened limbs, near normal-sized torsos and enlarged heads.

About 20% of people with achondroplasia inherit the mutations, meaning most children born with it have parents of average height. People with achondroplasia are prone to develop sleep apnea, chronic ear infections, neurological problems, spinal stenosis and bowed legs, frequently requiring surgical treatments to relieve pain and other symptoms.

“About half of these children will need spinal or other surgery, and this can mean a lot of time away from school as the child recovers and rehabilitates after surgery, which can affect important social connections,” says Ravi Savarirayan, M.B.B.S., M.D., clinical geneticist and group leader of skeletal biology and disease at Murdoch Children's Research Institute.

There are no treatments able to reverse achondroplasia or treat the genetic culprit itself. However, growth hormone has been approved to treat the condition in Japan and occasionally is used off label elsewhere, but is not considered very effective in achondroplasia.

Vosoritide is a synthetic version of a protein present in humans called C-type natriuretic peptide.

It is designed to bind to a specific receptor on the surface of chondrocytes, a type of cartilage cell found in the growth plates of bones.

Once joined, the vosoritide-receptor connection sends a signal inside the fibroblast to stanch the flow of negative growth factors that were triggered by the mutation in the FGFR3 gene.

“This is the first therapeutic option that targets the molecular cause of the condition,” says Hoover-Fong.

For the currently reported study, conducted between January 2014 and July 2018, investigators enrolled 35 children ages 5-14 and followed them for a midpoint of 42 months. There were 19 girls and 16 boys, including two Hispanics, seven Asians and two African Americans.

To enroll in the study, participants had previously been monitored for six months to determine their baseline growth rate. Then, for six months, participants received a daily vosoritide injection through the skin at doses ranging from 2.5-30 micrograms/kilogram.

Over the four-year study, two participants discontinued the trial because of anxiety with daily injections. One left the trial because their growth plates closed, and another withdrew for unknown reasons.

A fifth was withdrawn when doctors found during a routine electrocardiography that a participant had Wolff-Parkinson-White syndrome, a condition in the electrical circuits of heart muscles that causes rapid heartbeat.

At the end of six months, 30 participants opted to continue taking vosoritide. Participants who had earlier received the lowest doses of the drug received increased dosages, up to 15 micrograms/kg, and the other participants continued to receive their initial doses of 15 and 30 micrograms/kg. One of the 30 patients withdrew from the study to undergo limb-lengthening surgery.

Overall, the researchers found that, on average, the childrens' annual growth rate increased from below 4 centimeters per year to just below 6 centimeters per year. “They grew nearly 2 centimeters more, on average, per year, and this rate comes close to the annual growth of average stature people,” says Hoover-Fong.

The research team also found that the growth rate increase lasted over the nearly four-year study.

Moving forward, Hoover-Fong says all the remaining study participants will receive vosoritide until they reach their final adult height or they choose to withdraw from the study.

She says the sweet spot of vosoritide dose seems to be at 15 micrograms/kilogram as participants who received 30 micrograms/kilogram did not gain any growth velocity beyond those who received 15.

All 35 study participants had at least one side effect, considered mild and reversible, including injection site pain, swelling, headache, cough and low-grade fever.

One child was admitted to a hospital for surgery to remove their tonsils and adenoids, which is common in achondroplasia to treat sleep apnea, and another had enlarged tonsils.

One child had a congenital cyst in the neck and another had a fluid-filled cyst in the spinal cord.

“Importantly, none of the children experienced an anaphylactic reaction to the drug and none developed a low blood pressure problem that required medical intervention, which was a concern with this type of drug,” says Hoover-Fong.

Some of the participants were averse to needle sticks, but this became less of a problem as the study went on, she says.

There are ongoing clinical trials of vosoritide, including a randomized, double-blind, placebo-controlled study in more than 100 children and teenagers with achondroplasia worldwide. It is expected to end in 2019, and a global study of the drug in 70 children younger than 5 years is ongoing.

At least four other experimental drugs that target different molecular bone growth receptors or pathways are currently being tested in children and teenagers with achondroplasia at Johns Hopkins and elsewhere.

The cost of vosoritide has not been determined.

Story Source:

Materials provided by Johns Hopkins Medicine. Note: Content may be edited for style and length.

Journal Reference:

  1. Ravi Savarirayan, Melita Irving, Carlos A. Bacino, Bret Bostwick, Joel Charrow, Valerie Cormier-Daire, Kim-Hanh Le Quan Sang, Patricia Dickson, Paul Harmatz, John Phillips, Natalie Owen, Anu Cherukuri, Kala Jayaram, George S. Jeha, Kevin Larimore, Ming-Liang Chan, Alice Huntsman Labed, Jonathan Day, Julie Hoover-Fong. C-Type Natriuretic Peptide Analogue Therapy in Children with Achondroplasia. New England Journal of Medicine, 2019; DOI: 10.1056/NEJMoa1813446

Source: https://www.sciencedaily.com/releases/2019/06/190618102710.htm