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December 31, 2024

Low Alkaline Phosphatase: Causes, Symptoms & Treatments

Written By
Dr. Sarah Daglis ND
Medically Reviewed by
Updated On
January 9, 2025

Alkaline phosphatase (ALP) is an enzyme found in multiple tissues throughout the body, including the liver, bones, kidneys, intestines, and the placenta during pregnancy.

Experts believe it is involved in various physiological processes, such as lipid metabolism and detoxification in the liver, bone mineralization and formation, and nutrient absorption in the intestines. Despite its diverse roles, much about ALP's precise functions remains under investigation.

Low alkaline phosphatase (low ALP) in laboratory results indicates reduced levels of this enzyme in the bloodstream. As ALP is mainly produced by the liver and bones, low levels may reflect nutrient deficiencies, certain metabolic disorders, or impaired bone and liver function.

This guide provides a comprehensive overview of low ALP for healthcare professionals and patients, describing its significance in health and disease.

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Understanding Alkaline Phosphatase

Alkaline phosphatases (ALPs) are enzymes found on the surface of cells that help remove phosphate groups from nucleotides, proteins, and other molecules. Zinc and magnesium are essential cofactors for these enzymes.

ALP is predominantly found in the liver, bones, and kidneys, with smaller contributions from other tissues like the intestines and placenta. In healthy individuals, the liver and bones contribute over 80% of the circulating ALP.

Despite its widespread distribution and decades of research, its full physiological role is still under investigation.

Here is what we currently know about its functions:

  • Liver: ALP plays a role in bile formation and secretion, which aids fat digestion, detoxification, cholesterol removal, and the circulation of nutrients and hormones.
  • Bones: ALP is linked to osteoblast activity, aiding in bone mineralization and turnover, which are critical for building and maintaining strong bones.
  • Kidneys: ALP contributes to phosphate metabolism and reabsorption, helping to maintain homeostasis that supports cellular functions and bone health.

Normal vs. Low Alkaline Phosphatase Levels

The standard reference range for serum ALP can vary depending on the laboratory, age, and sex, but typical adult values are commonly 44–147 IU/L or 30 to 120 IU/L.

ALP levels are higher in individuals over 60, with men having slightly higher levels than women until menopause, when women's levels may match or exceed men's. Pregnant women also have higher levels.

Children, especially during growth periods, have significantly elevated ALP levels due to bone development.

Levels below the normal range are considered low and may indicate conditions such as malnutrition, mineral deficiencies, hypothyroidism, or rare genetic disorders affecting ALP production.

Always consult with a healthcare provider for interpretation of your test results.

Role in Health Monitoring

ALP is a valuable biomarker for assessing liver function and bone health. Included in a comprehensive metabolic panel (CMP), this routine test provides insights into underlying health conditions, helping to guide diagnosis and treatment plans.

Causes of Low Alkaline Phosphatase Levels

Various factors can influence ALP levels, leading to lower-than-normal levels.

Common Causes

Though high ALP levels are much more common, some of the known causes of low ALP include:

Genetic Factors

Hypophosphatasia (HPP), caused by mutations in the ALPL gene, is the most common genetic cause of low ALP. This condition impairs the body's ability to mineralize bones and teeth correctly.

It can present with a wide range of clinical manifestations, from severe skeletal abnormalities in infants to musculoskeletal pain, motor impairment, and dental issues in adults.

Nutrient Deficiencies

Overall malnutrition or specific nutrient deficiencies can significantly affect ALP levels. 

The active form of vitamin B6 serves as a substrate for ALP, magnesium enhances its activity, and zinc is essential for the enzyme's proper function. Protein deficiency may also impact ALP levels.

Deficiencies may be seen in cases of poor diet, eating disorders, and malabsorption syndromes.

Associated Conditions

Health conditions linked to low ALP levels may include:

  • Osteoporosis treated with bisphosphonate therapy: Low ALP activity may be seen in osteoporosis when treated with antiresorptive drugs
  • Wilson's disease: This genetic disorder causes copper accumulation in the tissues, including the liver, leading to damage and decreased ALP synthesis.
  • Celiac disease: This autoimmune disorder can cause malabsorption and nutrient deficiencies, leading to lower ALP levels.
  • Hypothyroidism: Low thyroid hormone levels can lead to decreased ALP activity, possibly due to low serum magnesium and zinc or reduced ALP synthesis by osteoblasts, which require thyroid hormone to function correctly.
  • Pernicious anemia: This condition, caused by vitamin B12 deficiency, can lead to low ALP levels, potentially due to suppressed osteoblastic activity associated with the deficiency.

This list is not exhaustive; consulting a healthcare provider for a complete evaluation is crucial.

Other Contributing Factors

Other factors that may impact ALP levels include:

  • Medications: Certain drugs, including oral contraceptives, steroids, and bisphosphonate therapy used for osteoporosis, may cause low ALP.
  • Age: ALP levels fluctuate with age, typically peaking during periods of rapid growth in childhood and adolescence and declining in adulthood. Those with low ALP levels, especially children, require further evaluation.
  • Lifestyle: Alcohol consumption has been associated with low ALP levels.

Understanding the wide range of causes of low ALP levels is essential for healthcare practitioners to make accurate diagnoses and successfully manage patients.

Symptoms and Health Risks Associated with Low ALP

Individuals with low ALP may be asymptomatic, and others may exhibit severe symptoms, depending on the underlying cause.

Symptoms of Low Alkaline Phosphatase

Possible symptoms may include:

  • Fatigue
  • Brain fog
  • Muscle weakness
  • Bone or joint pain
  • Fragile bones and frequent fractures that heal slowly
  • Skeletal deformities (e.g., bowed legs, short stature)
  • Premature loss of baby teeth
  • Failure to thrive (FTT) in infants

Potential Complications

Low ALP levels can have severe health implications if not managed promptly.

Risks for Bone and Liver Health

In some cases, low ALP levels may lead to impaired bone mineralization, such as rickets in children and osteomalacia in adults. This can cause bone pain, deformities, and increased fracture risk.

While low ALP is less commonly associated with liver disease compared to high levels, they can indicate underlying conditions such as Wilson's disease, where copper accumulation leads to liver damage.

Low levels may also suggest reduced bile production or flow (cholestasis), potentially leading to fat malabsorption, vitamin deficiencies, and liver dysfunction.

Implications for Growth in Children

In children, low ALP levels can lead to growth impairment and skeletal abnormalities due to poor bone development and mineralization. This can manifest as short stature, delayed closure of fontanelles, and delayed motor development.

These risks necessitate careful diagnosis and management to prevent long-term complications.

Diagnostic Approach for Low Alkaline Phosphatase

ALP testing and follow-up assessments depend on the symptoms presented and the severity of the abnormal results.

When to Test ALP Levels

ALP may be tested during routine exams through a comprehensive metabolic panel (CMP).

However, your provider may specifically order an ALP test to screen for, monitor, or help diagnose liver or biliary diseases, bone disorders, or other suspected conditions.

Signs and symptoms of liver disease that may prompt testing include:

  • Jaundice
  • Abdominal pain or swelling
  • Right upper quadrant (RUQ) pain
  • Easy bruising
  • Nausea or vomiting
  • Dark colored urine
  • Light colored stool

Signs and symptoms of bone disorders may include:

  • Bone or joint pain
  • Enlarged bones or malformations
  • Frequent bone fractures

Although definitive diagnoses are not made solely based on ALP levels, they are critical components of the diagnostic process.

Interpreting Alkaline Phosphatase Test Results

An abnormal lab value does not necessarily indicate a medical condition requiring treatment. Healthcare providers consider the result in the context of other factors, including:

  • Medical history
  • Symptoms
  • Current medications
  • The degree of abnormality in the low result
  • Results of other tests on the CMP, such as liver function tests (LFTs), calcium, and phosphate levels

Additional Diagnostic Tests

Your healthcare provider may recommend additional tests to identify or confirm the underlying cause of low ALP levels. The selection of tests will be based on clinical suspicion and presenting symptoms.

Nutritional Assessments

Vitamin or mineral assessments are useful, particularly if a nutritional imbalance is suspected. Causes may include poor diet, eating disorders, or celiac disease.

Imaging Studies

X-rays may be ordered to assess bone structure and identify potential abnormalities.

A DEXA scan can measure bone density and evaluate for conditions like osteoporosis.

Tests for Hypophosphatasia (HPP)

If this rare condition is suspected, the following tests can help confirm the diagnosis:

  • Vitamin B6: Elevated levels are consistent with HPP.
  • Phosphoethanolamine (PEA): Excessive urinary excretion can be a marker of HPP.
  • Pyridoxal 5’-Phosphate (PLP): Increased blood levels are often associated.
  • Genetic Testing: Identifies mutations in the ALPL gene, which are diagnostic for HPP.

Other targeted tests may be ordered to help pinpoint the root cause of low ALP and guide appropriate management.

Treatment and Management of Low Alkaline Phosphatase

Effective management of low ALP begins with identifying the cause.

Addressing Underlying Causes

A thorough medical evaluation, including blood tests and a review of symptoms and medical history, is essential to determine the underlying issue. 

Once identified, treatment should be tailored to the specific cause, whether it involves correcting nutritional deficiencies, managing the diagnosed medical condition, or adjusting medications that may contribute to low ALP levels.

Dietary and Lifestyle Modifications

Improving nutrition and lifestyle habits can help manage low ALP levels. A diet abundant in nutrients that promote enzyme production and function is critical.

Nutrients and foods to prioritize include:

  • Vitamin B6: This nutrient, found in fish, poultry, chickpeas, potatoes, non-citrus fruits, and fortified cereals, supports enzymatic processes in the body.
  • Zinc: Oysters, beef, pumpkin seeds, oats, and dairy products are excellent sources of this mineral, which is critical for metabolic and immune function.
  • Magnesium: Leafy greens, nuts, seeds, legumes, and whole grains provide magnesium, contributing to numerous biochemical reactions, including enzyme activation.

Individuals with conditions such as celiac disease or other malabsorption syndromes may require additional dietary adjustments to address deficiencies. A healthcare provider can evaluate whether additional testing, supplementation, or modifications are necessary.

Lifestyle adjustments can further enhance metabolic function and enzyme activity. These include:

  • Maintaining a healthy weight through balanced nutrition and regular physical activity to support metabolic health.
  • Avoiding or minimizing alcohol intake, as excessive consumption can impact liver and enzyme function.

Dietary and lifestyle changes should be tailored to individual needs. Always consult a qualified healthcare provider to develop a personalized plan aligning with your health status and goals.

Supplements and Medication Options

Supplementation may be necessary in cases where dietary intake is insufficient or the body's absorption is impaired.

Options may include:

  • Multivitamin: A high-quality multivitamin can provide vital nutrients to promote optimal levels for enhanced wellness.
  • Vitamin B6: Pyridoxal-5-phosphate (P5P) is the active form.
  • Zinc supplements: Chelated forms like zinc glycinate, gluconate, or picolinate offer better absorption.
  • Magnesium: Forms such as magnesium citrate or glycinate are best absorbed.

Individual needs vary, so it's essential to exercise caution when considering supplementation.

If low ALP is related to a medical condition, treating the underlying issue often involves pharmaceutical therapies. For instance:

Consultation with a healthcare provider is essential to developing an appropriate treatment plan.

Monitoring and Follow-Up

Regular monitoring of ALP levels is vital to evaluating treatment effectiveness and ensuring long-term stability. This may include periodic blood tests and reassessments of symptoms. 

Long-term follow-up can help detect potential complications or changes in the underlying condition, allowing for timely adjustments to the treatment plan.

Collaborating with a healthcare provider ensures comprehensive care and optimal outcomes.

Frequently Asked Questions (FAQs)

Here are some frequently asked questions (FAQs) about low ALP.

What does a low alkaline phosphatase mean for my health?

Low ALP levels can indicate underlying health issues such as nutritional deficiencies, metabolic disorders, or certain medical conditions. Always consult with a healthcare provider for a comprehensive evaluation.

Can diet and supplements improve low ALP levels?

Improving your diet and incorporating specific supplements may help address low ALP levels, especially with nutrient deficiencies like vitamin B6, zinc, or magnesium. Always seek professional guidance to create a personalized plan.

Are children affected differently by low ALP than adults?

Yes. Low ALP levels in children may be associated with growth-related conditions or genetic disorders like hypophosphatasia (HPP). 

Since children are still growing and developing, low ALP can significantly impact their bone formation, growth plates, and overall development compared to adults. 

Work with a pediatric specialist to accurately diagnose the cause and ensure proper treatment to support their growth and long-term health.

What are the potential risks if low ALP is untreated?

If left untreated, low ALP can lead to complications depending on its cause, such as impaired bone health, delayed healing, or other metabolic imbalances. Early intervention can help mitigate these risks.

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Key Takeaways

  • Low alkaline phosphatase (ALP) levels may be due to nutrient deficiencies, genetic conditions, metabolic disorders, certain medications, or lifestyle factors.
  • Low ALP can lead to various symptoms, including fatigue, bone pain, muscle weakness, and impaired bone mineralization. In children, it can affect growth and bone development.
  • Managing low ALP involves treating the underlying cause. Supplementation with vitamin B6, zinc, and magnesium may be beneficial. For specific medical conditions, pharmaceutical therapies may be required.
  • Routine testing and follow-up are critical to assess treatment effectiveness and prevent complications.
  • Low ALP should be managed by a qualified healthcare professional to ensure optimal health outcomes and prevent long-term risks.
The information in this article is designed for educational purposes only and is not intended to be a substitute for informed medical advice or care. This information should not be used to diagnose or treat any health problems or illnesses without consulting a doctor. Consult with a health care practitioner before relying on any information in this article or on this website.

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