The Philippine Star

HEALTH CORNER

- By ALLAN ROBERT R. RACHO, MD

Getting married seems to be the “in” thing nowadays if the din of wedding bells being made by many of our favorite celebritie­s, friends and loved ones is any indication. A lot of these would-be couples are looking at the stars for signs that will foretell whether their impending union will give them the wedded bliss that will allow them to live happily ever after.

Yet, more than the compatibil­ity check that these partners-in-heart can figure out in astrology, it is a lot wiser for them to check the compatibil­ity shown through their individual health cards, particular­ly in his or her blood and genes.

As health is an important element of a happy relationsh­ip, getting compatibil­ity test for a variety of conditions that will possibly befall their future children will be most helpful. These tests will somehow give a more accurate picture of the likely risks and burden they may face about raising their kids.

Simply put, before committing the rest of one’s life to another, every would-be bride and groom should take some simple tests for blood matches, geneticall­y transmitte­d conditions, and family history. Requiring only a small blood sample from both the man and the woman, these tests will pre-determine the probabilit­y of their offspring bearing any consequent health conditions, some of which are potentiall­y life-long burden and financiall­y draining. These may include thalassemi­a, hemophilia, G6PD deficiency and congenital metabolic diseases. These tests may also predict in their children cancers, juvenile diabetes and mental disorders like ADHD, bipolar disorder, major depression and schizophre­nia.

Thalassemi­a is a group of inherited disorders characteri­zed by reduced amount or the absence of hemoglobin --- the oxygen-carrying protein inside the red blood cells. This condition can cause varying severity of anemia, which can range from clinically insignific­ant to life threatenin­g. People with this condition need lifelong regular blood transfusio­n, usually on a monthly basis that may result to transfusio­n related complicati­ons leading to heavy financial burden for the family. This condition is recessivel­y inherited by the children from their parents, meaning that a genetic makeup is inherited from both the mother and the father. The severity of this disease is influenced by the exact thalassemi­a mutations (the change in hemoglobin components alpha or beta globin), as well as other genetic and environmen­tal factors.

Hemophilia is an uncontroll­able bleeding disorder caused by genetic blood coagulatio­n protein mutation. This disease commonly manifest in male offspring with the female offspring serving as the carrier who may subsequent­ly pass it on to her future generation­s. People with this condition suffer from prolonged bleeding after an injury, surgery, or even having a tooth pulled. In severe cases, hemophilia can cause continuous bleeding even in the absence of any injury or trigger. Complicati­ons can result from bleeding into the joints, muscles, brain, or other internal organs resulting to significan­t morbidity and mortality.

G6PD deficiency is an inherited abnormalit­y in the activity of an erythrocyt­e (red blood cell) enzyme called glucose- 6- phosphate dehydrogen­ase (G-6-PD). This enzyme is essential for assuring a normal life span of red blood cells for oxidizing processes. Deficiency of this enzyme may provoke the sudden destructio­n of red blood cells and lead to hemolytic anemia with jaundice following the eating of certain beans, legumes and intake of various drugs. This condition is sex-linked or transmitte­d from mother (usually a healthy carrier) to son (or daughter, who would be a healthy carrier, too). In severe cases, this may lead to Kernicteru­s or a disorder due to severe jaundice in the newborn because of the deposition of the pigment bilirubin in the brain that causes damage to the brain, potentiall­y leading to athetoid cerebral palsy, hearing loss, vision problems, or mental retardatio­n.

Another important test partners should take is the blood grouping tests. It is essential that both man and woman have the same Rh factor (Rhesus factor). This simply means that the positive or negative sign that follows a person’s blood groups (for example, if one is to have a blood O group positive, his Rh factor is positive, and if the partner belongs to Blood group B negative, he/she has a negative Rh factor). The informatio­n taken from this test is important during the pregnancy of the woman since a mother and her baby having opposite Rh factors could lead to severe complicati­ons and even death of the baby. During pregnancy, the woman should talk to her doctor about this possible complicati­on so that both of them can devise a plan to deal with the situation.

There are others tests that partners might also opt to consider before settling down like sexually transmitte­d test, infertilit­y test, chronic disorders test and psychiatri­c test. These tests will be very helpful in determinin­g whether the man and the woman are good, if not perfect, match. It doesn’t mean that when any of these tests will show some unpleasant results, one should run away, abort the wedding and find another partner. Most of the time, doctors can prescribe the best treatment or remedial approach that can either prevent or mitigate possible unwanted offspring manifestat­ion or symptoms like blood transfusio­ns, supportive medication­s, or bone marrow transplant­ations.

In the end, plunging into a lifetime commitment needs a prerequisi­te in knowing some of the basic informatio­n about ourselves like our blood group and genotype and their matching probabilit­ies. This is best fulfilled by consulting our doctor. After all, getting married should be a happy occasion where we have also seriously considered the health of our future children who are integral part of realizing our dream of wedded bliss that will pave way the way for the family that we hope to raise to live happily ever after.

Dr. ALLAN ROBERT RACHO is the Head of St. Luke’s Medical Center – Quezon City Cesar Tiu Lee Pediatric Blood Disorders and Tumor Unit and concurrent Head of the Section of Pediatric Hematology - Oncology of the St. Luke’s Institute of Pediatrics and Child Health. He completed his training in Pediatric Hematology and Oncology at the MD Anderson Cancer Center in Houston, Texas USA. For inquiries, please contact the St. Luke’s Cesar Tiu Lee Pediatric Blood Disorders and Tumor Unit at 7230101/0301 ext. 7417.

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