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Table of Contents
LETTER TO THE EDITOR
Year : 2019  |  Volume : 23  |  Issue : 1  |  Page : 168-170

Hypokalemic periodic paralysis and spectrum of thyroid disorders: Analysis of 7 cases from Northern India


1 Department of Endocrinology, Fortis Hospital, Shalimar Bagh, New Delhi, India
2 Department of Endocrinology, Sahara Hospital, Lucknow, Uttar Pradesh, India
3 Department of Endocrinology, Vidyasagar Institute of Mental Health and Sciences, Nehru Nagar, New Delhi, India
4 Department of Endocrinology, Artemis Hospital, Gurugram, Haryana, India
5 Department of Endocrinology, Dr. Khanna's Endocrinology Clinic, Amritsar, Punjab, India

Date of Web Publication18-Mar-2019

Correspondence Address:
Ajay Aggarwal
Department of Endocrinology, Fortis Hospital, Shalimar Bagh, New Delhi - 110 088
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijem.IJEM_619_18

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How to cite this article:
Aggarwal A, Wadhwa R, Pande A, Sahu M, Kapoor D, Khanna R. Hypokalemic periodic paralysis and spectrum of thyroid disorders: Analysis of 7 cases from Northern India. Indian J Endocr Metab 2019;23:168-70

How to cite this URL:
Aggarwal A, Wadhwa R, Pande A, Sahu M, Kapoor D, Khanna R. Hypokalemic periodic paralysis and spectrum of thyroid disorders: Analysis of 7 cases from Northern India. Indian J Endocr Metab [serial online] 2019 [cited 2019 Aug 22];23:168-70. Available from: http://www.ijem.in/text.asp?2019/23/1/168/254462



Sir,

Hypokalemic periodic paralysis (HPP), a life-threatening complication of hyperthyroidism, is characterized by episodes of acute muscle weakness due to hypokalemia. Studies have reported incidence of 2% among Asians vs. 0.1–0.2% among non-Asians with hyperthyroidism.[1],[2] The male to female ratio ranges from 17:1 to 76:1 among different ethnic groups.[2],[3],[4] Familial HPP and thyrotoxic periodic paralysis (TPP) are the most common cause of HPP among Caucasians and Asians, respectively.[5],[6] The clinical manifestations are similar in both conditions. Hyperthyroidism may be clinically silent and patients may suffer recurrent attacks long before diagnosis.[3],[7] Weakness is more common in lower limbs, with more severe proximal muscles involvement. Grave's disease (GD) is the most common cause of hyperthyroidism among patients with TPP, whereas other thyroid disorders have been implicated uncommonly. This case series highlights the presentation, precipitating factors, etiology of various thyroid disorders causing HPP, and the importance of early diagnosis and management in reducing morbidity and mortality.

This is a multi-center case series of 7 patients who presented with acute muscle weakness and hypokalemia at referral hospitals in New Delhi, Lucknow (UP), Gurugram (Haryana), and Amritsar (Punjab) in northern India. All of them were diagnosed to have thyroid disorders. Informed consent was obtained from all the patients. The baseline characteristics of all 7 patients are shown in [Table 1]. All were middle-aged Asian Indian men with more severe involvement of lower extremities. Three patients had multiple episodes of HPP, whereas 4 patients had only one episode at diagnosis. Out of the 3 patients with multiple episodes, 1 patient (patient 1) was on irregular treatment for GD for several years, and GD was diagnosed in 2 patients (patient 2 and 7) during second episode. Three patients presented in early morning hours.
Table 1: Baseline characteristics of patients presenting with HPP

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For all patients, serum potassium was below 3 mmol/l with abnormal electrocardiogram (ECG). The trigger was identified in 3 patients. The bowel, bladder, and respiratory muscles were spared. The 99mTc thyroid scan was done in all patients except patient 4. All patients were diagnosed with thyroid disorders: 4 patients had GD, 1 patient toxic multinodular goiter (MNG), 1 patient painless thyroiditis, and 1 patient presented with primary hypothyroidism. Except patient 4 and 5, all other were treated with methimazole/carbimazole and propranolol [Table 2]. Six patients needed hospitalization.
Table 2: Biochemistry, imaging, diagnosis, and treatment of patients with HPP

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TPP occurs commonly among Asian males in third to fifth decade of life.[2] Some studies have reported TPP among Hispanics and Whites.[8],[9] As TPP occurs commonly in males, androgens may have a role in pathogenesis. A Chinese study linked TPP episodes with elevated serum testosterone in men.[10] Higher muscle-to-body mass ratio because of testosterone leads to higher total amount of Na +/K +-ATPase in men, increasing their susceptibility.[11] In thyrotoxic patients with TPP, there is an increased number and activity of Na +/K +-ATPase pumps in skeletal muscle cell membranes compared to those without attacks, through both transcriptional and post-transcriptional mechanisms, leading to rapid and massive intracellular potassium shift.[12] The enhanced β-adrenergic response in thyrotoxicosis also increases Na +/K +-ATPase activity.

The triggers for attacks include carbohydrate or sodium rich meal, alcohol ingestion, strenuous exercise, trauma, emotional stress, infection, menses, cold exposure, etc.[13] These events may release epinephrine or insulin to cause intracellular potassium shift.[11] A lot of patients suffer from HPP without any trigger. We could identify trigger in only 3 (42.8%) patients in our study. Chang et al.[14] reported triggers in 34% patients, in a 10-year follow-up study of 135 patients. The most commonly identified triggers were high carbohydrate ingestion (12%), acute upper respiratory tract infections (URI)(8%), and strenuous exercise (7%).

The subtle symptoms of thyrotoxicosis may delay the diagnosis at initial presentation.[2],[7] The symptoms of thyroid disorders were subtle in our patients and attacks preceded the diagnosis of thyroid disorder in 6 patients. Most cases of HPP have been attributed to GD in studies.[8],[15] It may be because of the fact that GD is the most common cause of hyperthyroidism. Studies have reported association between HPP and other thyroid disorders such as painless thyroiditis, toxic MNG, toxic thyroid adenoma, and thyroid stimulating hormone (TSH) secreting pituitary adenoma.[11],[15] Although association between HPP and primary hypothyroidism has been reported,[16],[17] exact cause is not clear.

Our series suggests that hypokalemic paralysis can occur in the diverse setting of thyroid disorders. It is not a chance association, as normal potassium was maintained, without potassium replacement, only after the restoration of euthyroidism. If such observations are reported more in future, there may be merit in revising the term from “thyrotoxic periodic paralysis” (TPP) to “thyroid associated periodic paralysis” (TAPP).

The treatment of HPP includes immediate oral/intravenous potassium replacement therapy depending upon the severity of hypokalemia, along with non-specific β-blockers. Beta blockers cannot prevent attacks when given between attacks.[15],[18] The main treatment of HPP involves control of hyperthyroidism using anti-thyroid drugs, radioiodine ablation or thyroidectomy, and the restoration of euthyroidism in other thyroid disorders. Precipitating factors must be avoided.

The hallmark of TPP is hypokalemia; serum potassium is usually less than 3.0 mmol/l. The degree of initial hypokalemia has a direct correlation with the severity of attacks. Because of severe hypokalemia, our 6 patients needed hospitalization. Cardiac arrhythmias are common in TPP.[7] Typical changes of hypokalemia are seen in ECG such as atrial flutter/fibrillation, sinus tachycardia, atrial and ventricular ectopics, Paroxysmal supraventricular tachycardia (PSVT), and ventricular fibrillation. U waves and conduction defects have also been reported. ECG changes in our patients were consistent with those reported in hypokalemia. During acute attacks of TPP, immediate restoration of serum potassium through intravenous route is necessary along with oral propranolol. It results in more rapid response than oral supplementation.[19]

We conclude that quadriparesis due to TPP may be the first presentation of thyroid disorders. GD is the most common cause. Other thyroid disorders including primary hypothyroidism may also present as HPP. Because of the subtle signs and symptoms of thyroid disorders, diagnosis and treatment may be delayed. A thyroid function test should be done routinely while evaluating patients with hypokalemic paralysis.

Acknowledgments

We thank Dr. Vijay M Katekhaye, (Quest MedPharma Consultants, Nagpur, India) for his assistance in reviewing the article.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
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[PUBMED]  [Full text]  
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Cesur M, Bayram F, Temel MA, Ozkaya M, Kocer A, Ertorer ME, et al. Thyrotoxic hypokalemic periodic paralysis in a Turkish population: Three new case reports and analysis of case series. Clin Endocrinol 2008;68:143-52.  Back to cited text no. 19
    



 
 
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