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Interaction between levothyroxine and calcium carbonate

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Vol 54: january • janVier 2008 Canadian Family PhysicianLe Médecin de famille canadien

39

Current Practice

Pratique courante

Case Report Case Report

Interaction between

levothyroxine and calcium carbonate

Elias E. Mazokopakis

MD PhD

  Triantafillos G. Giannakopoulos

MD

  Ioannis K. Starakis

MD PhD

L

evothyroxine (L-T4) is one of the most commonly pre- scribed  medications.  It  is  given  as  either  physiologic  replacement  therapy  in  patients  with  hypothyroidism  or  as interventional therapy to suppress thyroid-stimulating  hormone (TSH) secretion in patients with nodular thyroid  disease or thyroid cancer.

Patients  treated  with  L-T4  suppressive  therapy  (a  state  known as exogenous subclinical hyperthyroidism) might be  at increased risk for osteoporosis. Because of this, patients  are encouraged to take a calcium supplement, such as cal- cium  carbonate.1  Calcium  supplementation  is  especially  important  for  preventing  or  treating  osteoporosis  in  post- menopausal women. However, several conditions or drugs  might  alter  L-T4  requirements  for  both  replacement  and  interventional therapy.2 We report a case of clinically signifi- cant interaction between L-T4 and calcium carbonate.

Case description

A  64-year-old  woman  with  hypothyroidism  visited  our  hospital  because  of  clinically  significant  changes  shown  in  results  of  thyroid  function  tests.  For  many  years  her  hypothyroidism  was  well  controlled  with  88  µg/d  of  L-T4  (TSH  ≤  2  mIU/L;  normal  range  0.3  to  4  mIU/L). She had been diagnosed with osteopenia 1 year  earlier  and  was  treated  with  oral  calcium  carbonate  (2500  mg/d = 1  g  elemental  calcium/d).  Three  months  after the patient started taking calcium carbonate, a clin- ical examination and results of laboratory tests revealed  hypothyroidism; thyroid function test results showed an  increase in TSH serum level (9.8 mIU/L) and a decrease  in  serum  free  thyroxine  (FT4)  level  (0.2  ng/dL;  normal  range 0.8 to 2 ng/dL). The L-T4 dose was increased to  112 µg/d, which improved the patient’s symptoms dur-

ing the following months (TSH level 6.4 mIU/L).

Because  the  hypothyroidism  persisted,  the  L-T4  dose  was  increased  to  125  µg/d,  and  her  symptoms  slowly  resolved  (TSH  level  2.7  mIU/L).  The  patient  stopped  taking  calcium  carbonate  during  the  follow- ing  months,  without  medical  advice,  and  her  TSH  level  decreased  to  0.1  mIU/L  (exogenous  subclinical  hyperthyroidism).  Because  of  the  obvious  interaction  between  L-T4  and  calcium  carbonate  in  our  patient,  we  decreased  the  dose  of  L-T4  to  88  µg/d.  A  more  detailed  history  revealed  that  our  patient  was  tak- ing  the  calcium  carbonate  at  the  same  time  as  L-T4.  After  more  than  a  year  following  the  patient’s  initial  presentation, her TSH level reverted to and remained 

at normal limits. The patient refused to take calcium  carbonate again despite our recommendation.

Discussion

This  case  report  confirms  the  importance  of  timing  for  patients taking calcium carbonate and L-T4. Recent stud- ies3-5  have  shown  that  taking  calcium  carbonate  within  4  hours  of  L-T4  might  decrease  absorption  of  L-T4  by  nearly a third. Also, patients knowing about this interac- tion  seems  to  be  insufficient.6  Patients  who  have  taken  L-T4 with calcium carbonate consistently for years might  have had their doses adjusted so they remained at ther- apeutic  levels.  However,  patients  who  receive  calcium  carbonate  sporadically  or  inconsistently  might  unknow- ingly  change  the  absorption  of  L-T4,  causing  variations  in their medication levels.

Conclusion

It is important for patients and health care providers to  know that calcium carbonate can interact with L-T4 and  affect  its  absorption.  Education  and  warning  labels  on  bottles  of  L-T4  might  help  to  decrease  the  risk  of  this  clinically significant interaction. 

Dr Mazokopakis is Head and Dr Giannakopoulos is a clinical resident in the Department of Internal Medicine at Naval Hospital of Crete in Chania, Greece. Dr Starakis is an Assistant Professor of Medicine in the Department of Internal Medicine at Patras University Hospital in Rion, Greece.

Competing interests None declared

Correspondence to: Dr Elias Mazokopakis, Iroon Polytechniu 38A, Chania 73 132, Crete, Greece;

telephone 30 282 1082754; fax 30 282 1089307;

e-mail emazokopakis@yahoo.gr references

1. Mazokopakis EE, Starakis IK, Papadomanolaki MG, Batistakis AG, Papadakis JA. 

Changes of bone mineral density in pre-menopausal women with differentiated thyroid  cancer receiving L-thyroxine suppressive therapy. Curr Med Res Opin 2006;22:1369-73.

2. Mandel SJ, Brent GA, Larsen PR. Levothyroxine therapy in patients with thyroid dis- ease. Ann Intern Med 1993;119:492-502.

3. Singh N, Singh PN, Hershman JM. Effect of calcium carbonate on the absorption of  levothyroxine. JAMA 2000;283:2822-5.

4. Singh N, Weisler SL, Hershman JM. The acute effect of calcium carbonate on the  intestinal absorption of levothyroxine. Thyroid 2001;11:967-71.

5. Neafsey PJ. Levothyroxine and calcium interaction: timing is everything. Home Healthc Nurse 2004;22:338-9.

6. Mazokopakis EE. Counseling patients receiving levothyroxine (L-T4) and calcium  carbonate. Mil Med 2006;171:vii, 1094.

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